WO2004096838A1 - Template-fixed peptidomimetics as medicaments against hiv and cancer - Google Patents

Template-fixed peptidomimetics as medicaments against hiv and cancer Download PDF

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Publication number
WO2004096838A1
WO2004096838A1 PCT/EP2003/004641 EP0304641W WO2004096838A1 WO 2004096838 A1 WO2004096838 A1 WO 2004096838A1 EP 0304641 W EP0304641 W EP 0304641W WO 2004096838 A1 WO2004096838 A1 WO 2004096838A1
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Prior art keywords
lower alkyl
chr
alkenyl
alkyl
conr
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PCT/EP2003/004641
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French (fr)
Inventor
Jürg ZUMBRUNN
J. Steven Demarco
Sergio Lociuro
Jan Wim Vrijbloed
Frank Gombert
Reshmi Mukherjee
Kerstin Moehle
Daniel Obrecht
John Anthony Robinson
Barbara Romagnoli
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Polyphor Ag
Universität Zürich
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Priority to DE60321053T priority Critical patent/DE60321053D1/en
Priority to AT03816774T priority patent/ATE395355T1/en
Priority to AU2003232254A priority patent/AU2003232254A1/en
Priority to PCT/EP2003/004641 priority patent/WO2004096838A1/en
Priority to EP03816774A priority patent/EP1622930B9/en
Priority to US10/550,778 priority patent/US7838496B2/en
Priority to ES03816774T priority patent/ES2306924T3/en
Publication of WO2004096838A1 publication Critical patent/WO2004096838A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04—Linear peptides containing only normal peptide links
    • C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/001—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof by chemical synthesis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04—Linear peptides containing only normal peptide links
    • C07K7/08—Linear peptides containing only normal peptide links having 12 to 20 amino acids

Definitions

  • the present invention provides template-fixed ⁇ -hairpin peptidomimetics incorporating two template-fixed chains of 4 and 6 or 5 and 7 ⁇ -amino acid residues which, depending on their positions in the chains, are Gly or Pro, or of certain types, as defined herein below. These template-fixed ⁇ -hairpin mimetics have antagonizing CXCR4-activity.
  • the present invention provides an efficient synthetic process by which these compounds can, if desired, be made in parallel library-format.
  • These ⁇ -hairpin peptidomimetics show improved efficacy, bioavailability, half-life and most importantly a significantly enhanced ratio between antagonizing CXCR4 activity on the one hand, and hemolysis on red blood cells and cytotoxicity on the other.
  • HAART-therapy Mghly active anti retroviral therapy which involves a combination of reverse transcriptase/protease inhibitor
  • HAART-therapy which involves a combination of reverse transcriptase/protease inhibitor
  • multi drug resistance a combination of reverse transcriptase/protease inhibitor
  • anti HIV agents that block the HIV infection at an early stage of the infection, such as the viral entry.
  • CXCR4 inhibitors M. Schwarz, T. N. C. Wells, A.E.I. Proudfoot, Receptors and Channels, 2001, 7, 417-428
  • one emerging class is based on naturally occurring cationic peptide analogues derived from Polyphemusin II which have an antiparallel ⁇ -sheet structure, and a ⁇ -hairpin that is maintained by two disulfide bridges (H. Nakashima, M. Masuda, T. Murakami, Y. Koyanagi, A. Matsumoto, N. Fujii, N. Yamamoto, Antimicrobial Agents and Chemoth. 1992, 36, 1249-1255; H. Tamamura, M.
  • Non-Hodg ⁇ s Lymphoma F. Bertolini, C. DellAgnola, P. Manusco, C. Rabascio, A. Burlini, S. Monestiroli, A. Gobbi, G. Pruneri, G. Martinelli, Cancer Research 2002, 62, 3106-3112), or lung cancer (T. Kijima, G. Maulik, P. C. Ma, E. V. Tibaldi, R:E. Turner, B. Rollins, M. Sattler, B.E. Johnson, R.
  • Blocking the chemotactic activity with a CXCR4 inhibitor should stop the migration of cancer cells.
  • the mediation of recruitment of immunecells to sites of inflammation should be stopped by a CXCR4 inhibitor.
  • Particularly desired are agents for treatment of cancer or agents for treatment of inflammatory disorders.
  • a new strategy is introduced to stabilize beta -hairpin conformations in bridged-backbone peptide mimetic exhibiting high CXCR4 antagonizing activity and anticancer activity and anti inflammatory activity.
  • This involves transplanting the cationic and hydrophobic hairpin sequence onto a template, whose function is to restrain the peptide loop backbone into a hairpin geometry.
  • the rigidity of the hairpin may be further influenced by introducing a disulfide bridge.
  • Template-bound hairpin mimetic peptides have been described in the literature (D, Obrecht, M. Altorfer, J. A. Robinson, Adv. Med. Chem. 1999, 4, 1-68; J. A. Robinson, Syn. Lett.
  • ⁇ -hairpin peptidomimetics of the present invention are compounds of the general formula
  • R 1 is H; lower alkyl; or aryl-lower alkyl
  • R 2 is H; alkyl; alkenyl; -(CH 2 ) m (CHR 61 ) s OR 55 ; -(CH 2 ) ra (CHR 61 ) s SR 56 ;
  • R 4 is H; alkyl; alkenyl; -(CH 2 ) m (CHR 61 ) s OR 55 ; -(CH 2 ) m (CHR 61 ) s SR 56 ; - (CH 2 ) m (CHR 61 ) s NR 33 R 34 ; -(CH 2 ) ra (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) m (CHR 61 ) NR 20 CONR 33 R 82 ;
  • R 6 is H; alkyl; alkenyl; -(CH 2 ) 0 (CHR 6I ) s OR 55 ; -(CH 2 ) 0 (CHR 61 ) S SR 56 ; - (CH 2 ) o (CHR 6I ) s NR 33 R 34 ;
  • R 7 is alkyl; alkenyl; -(CH 2 ) q (CHR 61 ) s 0R 55 ; -(CH 2 ) q (CHR 61 ) s NR 33 R 34 ; -(CH 2 ) q (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) q (CHR 61 ) s NR 20 CONR 33 R 82 ; -(CH 2 ) r (CHR 61 ) s COOR 37 ; -(CH2) r (CHR 61 ) s CONR 58 R 59 ; -(CH 2 ) r (CHR 61 ) s PO(OR 60 ) 2 ; -(CH 2 ) r (CHR 6I ;
  • R 8 is H; CI; F; CF 3 ; N0 2 ; lower alkyl; lower alkenyl; aryl; aryl-lower alkyl; -(CH 2 ) 0 (CHR 6, ) s OR 55 ; -(CH 2 ) 0 (CHR 61 ) S SR 56 ; -(CH 2 ) 0 (CHR 61 )NR 33 R 34 ; -(CH 2 ) 0 (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 )o(CHR 61 ) NR 20 CONR 33 R 82 ; -(CH2)o(CHR 61 ) s COOR 57 ; -(CH2) 0 (CHR 6I ) s CONR 58 R 59 ; -(CH 2 )o(CHR 61 ) s PO(OR 60 ) 2 ; -(CH 2 ) 0 (CHR 61 ) s S
  • R 9 is alkyl; alkenyl; -(CH 2 ) 0 (CHR 61 ) s OR 55 ; -(CH 2 ) 0 (CHR 61 ) S SR 56 ; -(CH 2 ) 0 (CHR 61 ) S NR 33 R 34 ; -(CH 2 ) o (CHR 6I ) s OCONR 33 R 75 ; -(CH 2 ) o (CHR 6I ) s NR 20 CONR 33 R 82 ; -(CH2)o(CHR 61 ) s COOR 57 ; -(CH2) 0 (CHR 61 ) s CONR 58 R 59 ; -(CH 2 )o(CHR 61 ) s PO(OR 60 ) 2 ; -(CH 2 ) solicit(CHR 61 ) S S0 2 R 62 ; or -(CH 2 ) 0 (CHR 61 ) S C 6 H 4 R
  • R 14 is H; alkyl; alkenyl; -(CH 2 ) m (CHR 61 ) s OR 55 ; -(CH 2 ) m (CHR 61 ) s NR 33 R 34 ; -(CH 2 ) m (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) m (CHR 61 ) s NR 20 CONR 33 R 82 ; -(CH 2 ) q (CHR 61 ) s COOR 57 ; -(CH 2 ) q (CHR 61 ) s CONR 58 R 59 ; -(CH 2 ) q (CHR 61 ) s PO(OR 60 )2; -(CH 2 ) q (CHR 61 ) s S0 2 R 62 ; or -(CH 2 ) q (CHR 61 ) s C 6 H 4 R 8 ;
  • R 14 is H; al
  • R 15 is alkyl; alkenyl; -(CH 2 ) 0 (CHR 61 ) s OR 55 ; -(CH 2 ) 0 (CHR 61 ) S SR 56 ; -(CH 2 ) 0 (CHR 61 ) S NR 33 R 34 ; -(CH 2 ) o (CHR 61 ) s OCONR 33 R 75 ; -(CH2)o(CHR 61 ) NR 20 CONR 33 R 82 ; -(CH 2 ) o (CHR 61 ) s COOR 57 ; -(CH 2 ) o (CHR 61 ) s CONR 58 R 59 ; -(CH 2 ) o (CHR 6I ) s PO(OR
  • R 16 is alkyl; alkenyl; -(CH 2 ) 0 (CHR 61 ) s OR 55 ; -(CH 2 ) 0 (CHR 61 ) S SR 56 ; -(CH 2 ) 0 (CHR 61 ) S NR 33 R 34 ; -(CH 2 ) o (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) 0 (CHR 61 ) NR 20 CONR 33 R 82 ; -(CH 2 )o(CHR 61 ) s COOR 57 ; -(CH 2 ) o (CHR 61 ) s CONR 58 R 59 ; -(CH 2 ) o (CHR 6I ) s PO(OR 60 )2; -(CH 2 ) 0 (CHR 61 ) S S0 2 R 62 ; or -(CH 2 ) 0 (CHR 61 ) S C
  • R 20 is H; alkyl; alkenyl; or aryl-lower alkyl;
  • R 21 is H; alkyl; alkenyl; -(CH 2 ) 0 (CHR 61 ) s OR 55 ; -(CH 2 ) 0 (CHR 61 ) S SR 56 ; - (CH 2 ) 0 (CHR 61 ) S NR 33 R 34 ;
  • R 22 is H; alkyl; alkenyl; -(CH 2 ) 0 (CHR 6I ) S 0R 55 ; -(CH 2 ) 0 (CHR 61 ) S SR 56 ; - (CH 2 ) 0 (CHR 61 ) S NR 33 R 34 ;
  • R 23 is alkyl; alkenyl; -(CH 2 ) 0 (CHR 61 ) s OR 55 ; -(CH 2 ) 0 (CHR 6I ) S SR 56 ; -(CH 2 ) 0 (CHR 61 ) S NR 33 R 34 ; -(CH 2 ) o (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) o (CHR 61 ) NR 20 CONR 33 R 82 ; -(CH 2 ) o (CHR 61 ) s COOR 57 ; -(CH 2 ) o (CHR 61 ) s CONR 58 R 59 ; -(CH 2 ) o (CHR 6I ) s PO(OR 60 ) 2 ; -(CH 2 ) 0 (CHR 61 ) S S0 2 R 62 ; or -(CH 2 ) 0 (CHR 61 )
  • R 26 is H; alkyl; alkenyl; -(CH 2 ) m (CHR 61 ) s OR 55 ; -(CH 2 ) m (CHR 61 ) s SR 56 ; -(CH 2 ) m (CHR 61 ) s NR 33 R 34 ; -(CH 2 ) m (CHR 61 ) s NR 33 R 34 ; -(CH 2 ) m (CHR 61 ) NR 20 CONR 33 R 82 ; -(CH 2 ) o (CHR 61 ) s COOR 57 ; -(CH 2 ) o (CHR 6I ) s CONR 58 R 59 ; -(CH 2 ) o (CHR 61 ) s PO(OR 60 ) 2 ; -(CH 2 ) 0 (CHR 61 ) s S0 2 R 62 ; or -(CH 2 ) 0 (CHR
  • R 27 is H; alkyl; alkenyl; -(CH 2 ) 0 (CHR 61 ) S OR 55 ; -(CH 2 ) 0 (CHR 61 ) S SR 56 ; - (CH 2 ) o (CHR 6I ) s NR 33 R 34 ;
  • R 28 is alkyl; alkenyl; -(CH 2 ) 0 (CHR 61 ) s -0R 55 ; -(CH 2 ) 0 (CHR 61 ) S SR 56 ; -(CH 2 ) 0 (CHR 61 ) S NR 33 R 34 ;
  • R 29 is alkyl; alkenyl; -(CH 2 ) 0 (CHR 61 ) s OR 55 ; -(CH 2 ) 0 (CHR 61 ) S SR 56 ; -(CH 2 ) 0 (CHR 61 ) S NR 33 R 34 ; -(CH 2 ) administrat(CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) o (CHR 61 ) NR 20 CONR 33 R 82 ; -(CH 2 ) sniff(CHR 61 ) s COOR 57 ; -(CH2)o(CHR 6I ) s CONR 58 R 59 ; -(CH 2 ) o (CHR 61 ) s PO(OR 60
  • R 30 is H; alkyl; alkenyl; or aryl-lower alkyl;
  • R 31 is H; alkyl; alkenyl; -(CH 2 ) p (CHR 61 ) s OR 55 ; -(CH 2 ) P (CHR 61 ) S NR 33 R 34 ; -(CH 2 ) P (CHR 61 ) S OCONR 33 R 75 ; -(CH 2 ) P (CHR 6I ) S NR 20 CONR 33 R 82 ; -(CH 2 ) o (CHR 61 ) s COOR 57 ; -(CH 2 ) o (CHR 61 ) s CONR 58 R 59 ; -(CH 2 ) o (CHR 61 ) s PO(OR 60 ) 2 ; -(CH 2 ) 0 (CHR 61 ) s S0 2 R 62 ; or -(CH 2 ) 0 (CHR 6, ) S C 6 H 4 R 8 ;
  • R 32 is H; lower alkyl; or aryl-lower alkyl;
  • R 33 is H; alkyl, alkenyl; -(CH 2 ) m (CHR 61 ) s OR 55 ; -(CH 2 ) m (CHR 61 ) s NR 34 R 63 ; -(CH 2 ) m (CHR 61 ) s OCONR 75 R 82 ; -(CH 2 ) m (CHR 61 ) s NR 20 CONR 78 R 82 ; -(CH 2 ) o (CHR 61 ) s COR 64 ; -(CH 2 ) o (CHR 61 ) s -CONR 58 R 59 , -(CH 2 ) o (CHR 61 ) s PO(OR 60 ) 2 ; -(CH 2 ) 0 (CHR 61 ) S S0 2 R 62 ; or -(CH 2 ) 0 (CHR 61 ) S C 6 H 4 R 8 ;
  • R 34 is H; lower alkyl; aryl, or aryl-lower alkyl; R 33 and R 34 taken together can form: -(CH 2 ) 2 . 6 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or R 35 is H; alkyl; alkenyl; -(CH 2 ) m (CHR 61 ) s OR 55 ; -(CH 2 ) m (CHR 6I ) s NR 33 R 34 ; -(CH 2 ) m (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) m (CHR 61 ) NR 20 CONR 33 R 82 ; -(CH 2 ) p (CHR 61 ) s COOR 57 ; -(CH 2 ) p (CHR 61 ) s COKR 58 R 59 ;
  • R 37 is H; F; Br; CI; N0 2 ; CF 3 ; lower alkyl; -(CH 2 ) p (CHR 6I ) s 0R 55 ; -(CH 2 ) p (CHR 61 ) s NR 33 R 34 ; -(CH 2 ) p (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) p (CHR 61 ) NR 20 CONR
  • R 38 is H; F; Br; CI; N0 2 ; CF 3 ; alkyl; alkenyl; -(CH 2 ) p (CHR 61 ) s OR 55 ; -(CH 2 ) P (CHR 61 ) S NR 33 R 34 ; -(CH 2 ) p (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) p (CHR 61 ) NR 20 CONR 33 R 82 ; -(CH 2 )o(CHR 61 ) s COOR 57 ; -(CH2)o(CHR 61 ) s CONR 58 R 59 ; -(CH2)o(CHR 61 ) s PO(OR 60 )2; -
  • R 39 is H; alkyl; alkenyl; or aryl-lower alkyl;
  • R 40 is H; alkyl; alkenyl; or aryl-lower alkyl;
  • R 41 is H; F; Br; CI; N0 2 ; CF 3 ; alkyl; alkenyl; -(CH 2 ) p (CHR 61 ) s OR 55 ; -(CH 2 ) P (CHR 6, ) S NR 33 R 34 ; -(CH 2 ) p (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) p (CHR 61 ) NR 20 CONR 33 R 82 ; -(CH 2 ) o (CHR 6, ) s COOR 57 ; -(CH 2 ) 0 (CHR 61 ) S CONR 58 R 59 ; -(CH 2 ) 0 (CHR 61 ) S PO(OR 60 ) 2 ;
  • R 42 is H; F; Br; CI; N0 2 ; CF 3 ; alkyl; alkenyl; -(CH 2 ) p (CHR 61 ) s OR 55 ; -(CH 2 ) P (CHR 61 ) S NR 33 R 34 ; -(CH 2 ) p (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) p (CHR 61 ) NR 20 CONR 33 R 82 ; -(CH2)o(CHR 61 ) s COOR 57 ; -(CH2)o(CHR 61 ) s CONR 58 R 59 ; -(CH 2 )o(CHR 61 ) s PO(OR 60 )2; -
  • R 43 is H; alkyl; alkenyl; -(CH 2 ) m (CHR 61 ) s 0R 55 ; -(CH 2 ) ra (CHR 61 ) s NR 33 R 34 ; -(CH 2 ) m (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) m (CHR 61 ) s NR 20 CONR 33 R 82 ; -(CH 2 ) o (CHR 61 ) s COOR 57 ; -(CH 2 ) o (CHR 61 ) s CONR 58 R 59 ; -(CH 2 ) o (CHR 61 ) s PO(OR 60 ) 2 ; -(CH 2 ) 0 (CHR 61 ) s S0 2 R 62 ; or -(CH 2 ) 0 (CHR 6, ) S C 6 H 4 R 8 ; R 44 is alkyl
  • R 45 is H; alkyl; alkenyl; or -(CH 2 ) 0 (CHR 61 ) P C 6 H 4 R 8 ;
  • R 47 is H; alkyl; alkenyl; or -(CH 2 ) 0 (CHR 6I ) s OR 55 ;
  • R 48 is H; lower alkyl; lower alkenyl; or aryl-lower alkyl;
  • R 49 is H; alkyl; alkenyl; -(CHR 61 ) s COOR 57 ; (CHR 61 ) s CONR 58 R 59 ; (CHR 61 ) S PO(OR 60 ) 2 ; -(CHR 61 ) s SOR 62 ; or -(CHR ⁇ H ⁇ ;
  • R 50 is H; lower alkyl; or aryl-lower alkyl;
  • R 51 is H; alkyl; alkenyl; -(CH 2 ) m (CHR 61 ) s OR 55 ; -(CH 2 ) m (CHR 61 ) s SR 56 ; -(CH 2 ) m (CHR 61 ) s NR 33 R 34 ; -(CH 2 ) m (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) m (CHR 61 ) NR 20 CONR 33 R 82 ; -(CH 2 ) 0 (CHR 61 ) s COOR 57 ; -(CH 2 ) 0 (CHR 61 ) s CONR 58 R 59 ; -(CH 2 ) o (CHR 61 ) p PO(OR 60 ) 2 ;
  • R 52 is H; alkyl; alkenyl; -(CH 2 ) m (CHR 61 ) s OR 55 ; -(CH 2 ) m (CHR 61 ) s SR 56 ; -(CH 2 ) m (CHR 61 ) s NR 33 R 34 ; -(CH 2 ) m (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) m (CHR 61 ) NR 20 CONR 33 R 82 ; -(CH 2 ) 0 (CHR 61 ) s COOR 57 ; -(CH 2 ) 0 (CHR 61 ) s CONR 58 R 59 ; -(CH 2 ) o (CHR 61 )
  • R 53 is H; alkyl; alkenyl; -(CH 2 ) m (CHR 61 ) s OR 55 ; -(CH 2 ) m (CHR 61 ) s SR 55 ; - (CH 2 ) m (CHR 61 ) s NR 33 R 34 ; -(CH 2 ) m (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) m (CHR 61 ) NR 20 CONR 33 R 82 ; -(CH 2 ) 0 (CHR 61 ) s COOR 57 ; -(CH 2 ) o (CHR 6I ) s CONR 58 R 59 ; -(CH 2 ) o (CHR 61 ) )
  • R 54 is H; alkyl; alkenyl; -(CH 2 ) m (CHR 61 ) s OR 55 ; -(CH 2 ) m (CHR 61 ) s NR 33 R 34 ; -(CH 2 ) m (CHR 61 ) s OCONR 33 R 75 ; -(CH 2 ) m (CHR 61 ) s NR 20 CONR 33 R 82 ; -(CH 2 ) 0 (CHR 61 )COOR 57 ; -(CH 2 ) 0 (CHR 61 ) S CONR 58 R 59 ; or -(CH 2 ) 0 (CHR 61 ) S QsH ⁇ 8 ; R 55 is H; lower alkyl; lower alkenyl
  • R 56 is H; lower alkyl; lower alkenyl; aryl-lower alkyl; -(CH 2 ) m (CHR 61 ) s OR 57 ; -(CH 2 ) m (CHR 61 ) s NR 34 R 63 ; -(CH 2 ) m (CHR 61 ) s OCONR 75 R 82 ; -(CH 2 ) m (CHR 61 ) NR 20 CONR 78 R 82 ; -(CH 2 ) 0 (CHR 61 ) s NR 20 CONR 78 R 82 ; -(CH 2 ) 0 (CHR 61 ) s NR 20 CONR 78 R 82 ; -(CH 2 ) 0 (CHR 61 ) s NR 20 CONR 78 R 82 ; -(CH 2 ) 0 (CHR 61 ) s
  • R 58 is H; lower alkyl; lower alkenyl; aryl; heteroaryl; aryl-lower alkyl; or heteroaryl-lower alkyl;
  • R 59 is H; lower alkyl; lower alkenyl; aryl; heteroaryl; aryl-lower alkyl; or heteroaryl-lower alkyl; or R 58 and R 59 taken together can form: -(CH 2 ) 2 -6-; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; R 60 is H; lower alkyl; lower alkenyl; aryl; or aryl-lower alkyl;
  • R 61 is alkyl; alkenyl; aryl; heteroaryl; aryl-lower alkyl; heteroaryl-lower alkyl; -(CH ⁇ OR 55 ; -(CH 2 ) m NR 33 R 34 ; -(CH 2 ) m OCONR 75 R 82 ; -(CH 2 ) m NR 20 CONR 78 R 82 ; -(CH 2 ) 0 COOR 37 ; -(CH 2 ) 0 NR 58 R 59 ; or -(CH 2 ) o PO(COR 60 ) 2 ;
  • R 62 is lower alkyl; lower alkenyl; aryl, heteroaryl; or aryl-lower alkyl;
  • R 63 is H; lower alkyl; lower alkenyl; aryl, heteroaryl; aryl-lower alkyl; heteroaryl-lower alkyl;
  • -COR 64 ; -COOR 57 ; -CONR 58 R 59 ; -S0 2 R 62 ; or -PO(OR 60 ) 2 ; R 34 and R 63 taken together can form: -(CH 2 ) 2 . 6 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -;
  • R 64 is H; lower alkyl; lower alkenyl; aryl; heteroaryl; aryl-lower alkyl; heteroaryl-lower alkyl; -(CH 2 ) p (CHR 61 ) s OR 65 ; -(CH 2 ) P (CHR 61 ) S SR 66 ; or -(CH 2 ) P (CHR 61 ) S NR 34 R 63 ; -(CH 2 ) P (CHR 61 ) S OCONR 75 R 82 ; -(CH 2 ) P (CHR 61 ) S NR 20 CONR 78 R 82 ; R 65 is H; lower alkyl; lower alkenyl; aryl, aryl-lower alkyl; heteroaryl-lower alkyl; -COR 57 ; -COOR 57 ; or -CONR 58 R 59 ;
  • R 66 is H; lower alkyl; lower alkenyl; aryl; aryl-lower alkyl; heteroaryl-lower alkyl; or -CONR 58 R 59 ;
  • Z and Z 1 are chains of n and, respectively, n' ⁇ -amino acid residues whereby either n is 4 and n' is 6 or n is 5 and n' is 7, the positions of said amino acid residues in said chain Z being counted starting from the N-terminal amino acid and the positions of said amino acid residues in said chain Z 1 being counted starting from the C-terminal amino acid, whereby these amino acid residues are, depending on their position in the chains, Gly, or Pro, or of one of the types C: -NR 20 CH(R 72 )CO-; D: -NR 20 CH(R 73 )CO-; E: -NR 20 CH(R 74 )CO-; F: -NR 20 CH(R 84 )CO-; and H: -NR 20 -CH(CO-)-(CH 2 ) 4-7 -CH(CO-)-NR 20 -;
  • R 71 is lower alkenyl; -(CH 2 ) p (CHR 61 ) s OR 75 ; -(CH 2 ) P (CHR 61 ) S SR 75 ;
  • R 72 is H, lower alkyl; lower alkenyl; -(CH 2 ) p (CHR 6I ) s OR 85 ; or -(CH 2 ) p (CHR 61 ) s SR 85 ;
  • R 73 is -(CH 2 ) 0 R 77 ; -(CH 2 ) r O(CH 2 ) 0 R 77 ; -(CH ⁇ S CH,) ⁇ 77 ; or -(CH 2 ) r NR 20 (CH 2 ) complicatR 77 ;
  • -(CH 2 ) p N C(NR 78 R 80 )NR 79 R 80 ;-(CH 2 ) p C 6 H 4 NR 78 R 79 ; -(CH 2 ) p C 6 H 4 NR 77 R 80 ;
  • N C(NR 78 R 80 )NR 79 R 80 ; -(CH 2 ) r O(CH 2 ) m NR 78 R 79 ; -(CH 2 ) r O(CH 2 ) m NR 77 R 80 ;
  • R 75 is lower alkyl; lower alkenyl; or aryl-lower alkyl;
  • R 33 and R 75 taken together can form: -(CH 2 ) 2-6 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or
  • R 75 and R 82 taken together can form: -(CH 2 ) 2-6 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -;
  • R 76 is H; lower alkyl; lower alkenyl; aryl-lower alkyl; -(CH 2 ) 0 OR 72 ; -(CH 2 ) 0 SR 72 ;
  • R 77 is -C 6 R 67 R 68 R ⁇ 9 R 70 R 76 ; or a heteroaryl group of one of the formulae
  • H50 H51 H52 H53 H54 R 78 is H; lower alkyl; aryl; or aryl-lower alkyl;
  • R 78 and R 82 taken together can form: -(CH 2 ) M S -(CH 2 )2 ⁇ (CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; R 79 is H; lower alkyl; aryl; or aryl-lower alkyl; or
  • R 78 and R 79 taken together, can be -(CH 2 ) 2 . 7 -; -(CH 2 ) 2 0(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -;
  • R 80 is H; or lower alkyl
  • R 81 is H; lower alkyl; or aryl-lower alkyl;
  • R 82 is H; lower alkyl; aryl; heteroaryl; or aryl-lower alkyl; R 33 and R 82 taken together can form: -(CH 2 ) 2 -6-; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -;
  • R 83 is H; lower alkyl; aryl; or -NR 78 R 79 ;
  • R 84 is -(CH 2 ) p CONR 78 R 79 ; -(CH 2 ) P NR 80 CONR 78 R 79 ; -(CH 2 ) p C 6 H 4 CONR 78 R 79 ; or
  • R is lower alkyl; or lower alkenyl
  • P3 and P3' taken together, can form a group of type H;
  • PI of type C or of type D or of type E or of type F, or the residue is Pro
  • P2 of type E or of type F P3 of type F, or the residue is Pro
  • P4 of type F P5 of type E Pi': of type C or of type D or of type E or of type F, or the residue is Pro;
  • P2' of type F
  • P3' of type D or the residue is Pro
  • - P4' of type E or of type F
  • P5' of type D, or the residue is Pro
  • P6' of type E or of type F, or the residue is Pro
  • ⁇ -hairpin peptidomimetics can be prepared by a process which comprises
  • X is an N-protecting group or, if
  • step (fa) coupling the product obtained in step (e) with an appropriately N-protected derivative of an amino acid of the general formula
  • step (fa') coupling the product obtained in step (e) with an appropriately N-protected derivative of an amino acid of the above general formula III, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected; (fb') removing the N-protecting group from the product thus obtained; and
  • Introducing an amino acid residue of type I can, alternatively, be effected by coupling with a leaving group-containing acetylating agent, such as bromo, chloro or iodo acetic acid, followed by nucleophilic displacement with an amine of the formula H 2 NR 86 which, if necessary, is appropriately protected.
  • a leaving group-containing acetylating agent such as bromo, chloro or iodo acetic acid
  • the peptidomimetics of the present invention can also be enantiomers of the compounds of formula I. These enantiomers can be prepared by a modification of the above process in which enantiomers of all chiral starting materials are used.
  • alkyl designates saturated, straight-chain or branched hydrocarbon radicals having up to 24, preferably up to 12, carbon atoms.
  • alkenyl designates straight chain or branched hydrocarbon radicals having up to 24, preferably up to 12, carbon atoms and containing at least one or, depending on the chain length, up to four olefinic double bonds.
  • lower designates radicals and compounds having up to 6 carbon atoms.
  • lower alkyl designates saturated, straight-chain or branched hydrocarbon radicals having up to 6 carbon atoms, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert.- butyl and the like.
  • aryl designates aromatic carbocyclic hydrocarbon radicals containing one or two six-membered rings, such as phenyl or naphthyl, which may be substituted by up to three substituents such as Br, CI, F, CF 3 , N0 2 , lower alkyl or lower alkenyl.
  • heteroaryl designates aromatic heterocyclic radicals containing one or two five- and/or six-membered rings, at least one of them containing up to three heteroatoms selected from the group consisting of O, S and N and said ring(s) being optionally substituted; representative examples of such optionally substituted heteroaryl radicals are indicated hereinabove in connection with the definition of R 77 .
  • the structural element -A-CO- designates amino acid building blocks which in combination with the structural element -B-CO- form templates (al) and (a2).
  • the structural element -B- CO- forms either alone or in combination with another structural element -B-CO- templates (a4) and (a3).
  • Templates (a) through (p) constitute building blocks which have an N-terminus and a C-terminus oriented in space in such a way that the distance between those two groups may lie between 4.0-5.5A.
  • a peptide chain Z is linked to the C-terminus of the templates (a) through (p) via the N-terminus, and the corresponding N-terminus of the template is linked to the C-terminus of Z 1 to form a ⁇ -hairpin structure such as that depicted in formula I.
  • the template will induce the H-bond network necessary for the formation of a ⁇ -hairpin conformation within the peptide chain Z and _ ⁇ .
  • template and peptide chains form a ⁇ - hairpin mimetic.
  • the ⁇ -hairpin conformation is highly relevant for the CXCR4 antagonizing activity of the ⁇ -hairpin mimetics of the present invention.
  • Building blocks A1-A69 belong to a class of amino acids wherein the N-terminus is a secondary amine forming part of a ring. Among the genetically encoded amino acids only proline falls into this class.
  • the configuration of building block Al through A69 is (D), and they are combined with a building block -B-CO- of (L)-configuration.
  • Preferred combinations for templates (al) are- D Al-CO- L B-CO- to D A69-CO- L B-CO-.
  • D Pro- L Pro constitutes the prototype of templates (al).
  • templates (a2) are - L Al-CO- D B-CO- to L A69-CO- D B-CO-.
  • L Pro- D Pro constitutes a less preferred prototype of template (a2).
  • building blocks -Al-CO- to -A69-CO- in which A has (D)- configuration are carrying a group R 1 at the ⁇ -position to the N-terminus.
  • the preferred values for R 1 are H and lower alkyl with the most preferred values for R 1 being H and methyl.
  • A1-A69 are shown in (D)-configuration which, for R 1 being H and methyl, corresponds to the (Reconfiguration.
  • this configuration may also have to be expressed as (S).
  • R 1 building blocks -Al-CO- to -A69-CO- can carry an additional substituent designated as R 2 to R 17 .
  • This additional substituent can be H, and if it is other than H, it is preferably a small to medium-sized aliphatic or aromatic group.
  • R 2 to R 17 examples include: - R 2 : H; lower alkyl; lower alkenyl; (CH 2 ) m OR 55 (where R 55 : lower alkyl; or lower alkenyl); (CH 2 ) m SR 56 (where R 56 : lower alkyl; or lower alkenyl); (CH 2 ) m NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; R 33 and R 34 taken together form: -(CH 2 ) 2-6 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; R 57 : H; or lower alkyl); (CH 2 ) m OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl;
  • R 3 H; lower alkyl; lower alkenyl; -(CH 2 ) m OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m SR 56 (where R 5 ⁇ : lower alkyl; or lower alkenyl); -(CH 2 ) m NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: - (CH 2 ) 2-6 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); -(CH 2 ) m OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75
  • R 4 H; lower alkyl; lower alkenyl; -(CH 2 ) m OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) m NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: - (CH 2 ) 2 .
  • R 5 lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .
  • R 57 H; or lower alkyl
  • (CH 2 ) o N(R 20 )COR 64 where: R 20 : H; or lower alkyl; R 64 : alkyl; alkenyl; aryl; and aryl-lower alkyl; heteroaryl-lower alkyl); -(CH 2 ) 0 C00R 57 (where R 57 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 CONR 58 R 59 (where R 58 : lower alkyl; or lower alkenyl; and R 59 : H; or lower alkyl; or R 58 and R 59 taken together form: - (CH 2 ) 2 .
  • R 6 H; lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .
  • R 7 lower alkyl; lower alkenyl; -(CH 2 ) q OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) q SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) q NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2-6 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); -(CH 2 ) q OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 : lower alky
  • R 8 H; F; CI; CF 3 ; lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); (CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: - (CH 2 ) 2-6 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); -(CH 2 ) 0 OCONR 33 R 75 (where R 33 : H; or lower alkyl; or
  • R 9 lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .
  • R 10 lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2-6 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); -(CH 2 ) 0 OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 :
  • R 1 ' H; lower alkyl; lower alkenyl; -(CH 2 ) m OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) m NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: - (CH 2 ) 2 .6-; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); -(CH 2 ) m OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R
  • R 12 H; lower alkyl; lower alkenyl; -(CH 2 ) m OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) m NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: - (CH 2 ) 2 .
  • R 13 lower alkyl; lower alkenyl; -(CH 2 ) q OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) q SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) q NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .
  • R 8 H; F; CI; CF 3 ; lower alkyl; lower alkenyl; or lower alkoxy.
  • R 14 H; lower alkyl; lower alkenyl; -(CH 2 ) ra OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) m NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: - (CH 2 ) 2 - 6 -; -(CH 2 ) 2 ⁇ (CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -
  • R 15 lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .
  • R 16 lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2-6 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); -(CH 2 ) 0 OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 :
  • R 17 lower alkyl; lower alkenyl; -(CH 2 ) q 0R 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) q SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) q NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .6-; -(CH 2 )2 ⁇ (CH 2 )2-; -(CH 2 )2S(CH 2 )2-; or -(CH 2 ) 2 NR 57 (CH 2 )2-; where R 57 : H; or lower alkyl); -(CH 2 ) q OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 : lower alkyl; or
  • building blocks Al to A69 the following are preferred: A5 with R 2 being H, A8, A22, A25, A38 with R 2 being H, A42, A47, and A50. Most preferred are building blocks of type A8':
  • R >20 i • s T HT omen_r 1 lo flesh pressw rawer alkyl; an ,dJ r R»64 .
  • Building block A70 belongs to the class of open-chain ⁇ -substituted ⁇ -amino acids, building blocks A71 and A72 to the corresponding ⁇ -amino acid analogues and building blocks A73- 0 A104 to the cyclic analogues of A70.
  • Such amino acid derivatives have been shown to constrain small peptides in well defined reverse turn or U-shaped conformations (C. M. Venkatachalam, Biopolymers, 1968, 6, 1425-1434; W. Kabsch, C Sander, Biopolymers 1983, 22, 2577).
  • Such building blocks or templates are ideally suited for the stabilization of ⁇ -hairpin conformations in peptide loops (D. Obrecht, M. Altorfer, J. A.
  • templates (al) can also consist of -A70-CO- to A104-CO- where building block A70 to A104 is of either (D)- or (L)-conf ⁇ guration, in combination with a building block -B-CO- of (L)- configuration.
  • R 20 in A70 to A104 are H or lower alkyl with methyl being most preferred.
  • Preferred values for R 18 , R 19 and R 21 -R 29 in building blocks A70 to A104 are the following: R 18 : lower alkyl.
  • R 19 lower alkyl; lower alkenyl; -(CH 2 ) p OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) P SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) P NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form:
  • R 21 H; lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .
  • R 22 lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form:
  • R 23 H; lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) compassionSR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 )2-6-; -(CH 2 ) 2 0(CH 2 )2-; -(CH 2 )2S(CH 2 )2-; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); -(CH 2 ) 0 OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 : lower alkyl; or R
  • R 25 H; lower alkyl; lower alkenyl; -(CH 2 ) m OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .6-; -(CH 2 ) 2 ⁇ (CH 2 )2-; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); -(CH 2 ) m OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 : lower alkyl; or R 33 and R 75 taken together form: -(CH 2 ) 2 .6-; - (CH
  • R 26 H; lower alkyl; lower alkenyl; -(CH 2 ) m OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) .6-; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); -(CH 2 ) m OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 : lower alkyl; or R 33 and R 75 taken together form: -(CH 2 ) 2 - 6 -;
  • R 25 and R 26 taken together can be -(CH 2 ) 2 . 5 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl).
  • R 27 H; lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2-6 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); -(CH 2 ) 0 OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 :
  • R 28 lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form:
  • R 29 lower alkyl; lower alkenyl; -(CH 2 ) 0 0R 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 -6-; -(CH 2 )2 ⁇ (CH2) 2 -; -(CH2) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); -(CH 2 ) 0 OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 : lower alkyl;
  • R 8 H; F; Cl; CF 3 ; lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where
  • R 33 lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -
  • R 82 (where R 20 : H; or lower alkyl; R 33 : H; or lower alkyl; or lower alkenyl;
  • R 82 H; or lower alkyl; or R 33 and R 82 taken together form: -(CH 2 ) 2 . 6 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH2) 2 S(CH 2 ) 2 -; or -(CH 2 )2NR 57 (CH 2 )2-; where R 57 : H; or lower alkyl); -(CH 2 ) 0 N(R 20 )COR 64 (where: R 20 : H; or lower alkyl; R 64 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 COOR 57 (where R 57 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 CONR 58 R 59 (where R 58 : lower alkyl; or lower alkenyl; and R 59 : H; or lower alkyl; or R 58 and R 59 taken together form: -(CH 2 )
  • R 31 H; lower alkyl; lower alkenyl; -(CH 2 ) p OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) P NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .6-; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); -(CH 2 ) p OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 : lower alkyl; or R 33 and R 75 taken together form: -(CH 2 ) 2 .
  • R 33 lower alkyl; lower alkenyl; -(CH 2 ) m OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m NR 34 R 63 (where R 34 : lower alkyl; or lower alkenyl; R 63 : H; or lower alkyl; or R 34 and R 63 taken together form: -(CH 2 ) 2 .
  • R 34 H; or lower alkyl.
  • - R 35 H; lower alkyl; lower alkenyl; -(CH 2 ) m OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .
  • R 36 lower alkyl; lower alkenyl; or aryl-lower alkyl.
  • - R 37 H; lower alkyl; lower alkenyl; -(CH 2 ) p OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) P NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .
  • R 82 (where R 20 : H; or lower alkyl; R 33 : H; or lower alkyl; or lower alkenyl; R 82 : H; or lower alkyl; or R 33 and R 82 taken together form: -(CH 2 ) 2 .
  • R 38 H; lower alkyl; lower alkenyl; -(CH 2 ) p OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) P NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .
  • R 39 H; lower alkyl; lower alkenyl; -(CH 2 ) m 0R 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m N(R 20 )COR 64 (where: R 20 : H; or lower alkyl; R 64 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 COOR 57 (where R 57 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 CONR 58 R 59 (where R 58 : lower alkyl; or lower alkenyl; and R 59 : H; lower alkyl; or R 58 and R 59 taken together form: -(CH 2 ) 2 .
  • R 40 lower alkyl; lower alkenyl; or aryl-lower alkyl.
  • - R 41 H; lower alkyl; lower alkenyl; -(CH 2 ) p OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) p NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .
  • R 42 H; lower alkyl; lower alkenyl; -(CH 2 ) P 0R 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) P NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .
  • R 43 H; lower alkyl; lower alkenyl; -(CH 2 ) m OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) m NR 3 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form:
  • R 44 lower alkyl; lower alkenyl; -(CH 2 ) p OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) P SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) P NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .6-; -(CH 2 ) 2 0(CH 2 )2-; -(CH 2 ) 2 S(CH 2 )2-; or -(CH 2 )2NR S7 (CH 2 )2-; where R 57 : H; or lower alkyl); -(CH 2 ) p 0C0NR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 : lower alkyl; orR 33
  • R 45 H; lower alkyl; lower alkenyl; -(CH 2 ) 0 OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .
  • R 46 H; lower alkyl; lower alkenyl; -(CH 2 ) s OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) S SR 56 (where R 56 : lower alkyl; or lower alkenyl); -(CH 2 ) S NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 )2-6-; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 )2-; where R 57 : H; or lower alkyl); -(CH 2 ) s OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 : lower alkyl;
  • R 57 H; or lower alkyl
  • R 8 H; F; Cl; CF 3 ; lower alkyl; lower alkenyl; or lower alkoxy
  • R 47 H; or OR 55 (where R 55 : lower alkyl; or lower alkenyl).
  • R 48 H; or lower alkyl.
  • R 49 H;lower alkyl; -(CH 2 ) 0 COOR 57 (where R 57 : lower alkyl; or lower alkenyl); -(CH 2 ) 0 CONR 58 R 59 (where R 58 : lower alkyl; or lower alkenyl; and R 59 : H; lower alkyl; or R 58 and R 59 taken together form: -(CH 2 ) 2 .
  • R 57 H; or lower alkyl
  • R 8 H; F; Cl; CF 3 ; lower alkyl; lower alkenyl; or lower alkoxy.
  • R 50 H; methyl.
  • R 51 H; lower alkyl; lower alkenyl; -(CH 2 ) m OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2-5 -; -(CH 2 ) 2 0(CH2) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); (CH 2 ) m 0C0NR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 : lower alkyl; or R 33 and R 75 taken together form: -(CH 2 ) 2 .
  • R 52 H; lower alkyl; lower alkenyl; -(CH 2 ) m OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2-6 -; -(CH 2 ) 2 0(CH 2 ) 2 -; -(CH 2 ) 2 S(CH 2 ) 2 -; or -(CH 2 ) 2 NR 57 (CH 2 ) 2 -; where R 57 : H; or lower alkyl); -(CH 2 ) m OCONR 33 R 75 (where R 33 : H; or lower alkyl; or lower alkenyl; R 75 : lower alkyl; or R 33 and R 75 taken together form: -(CH 2 ) 2 .
  • R 53 H; lower alkyl; lower alkenyl; -(CH 2 ) m OR 55 (where R 55 : lower alkyl; or lower alkenyl); -(CH 2 ) m NR 33 R 34 (where R 33 : lower alkyl; or lower alkenyl; R 34 : H; or lower alkyl; or R 33 and R 34 taken together form: -(CH 2 ) 2 .
  • R 54 lower alkyl; lower alkenyl; or aryl-lower alkyl.
  • building blocks A70 to A104 the following are preferred: A74 with R 22 being H, A75, A76, A77 with R 22 being H, A78 and A79.
  • the building block -B-CO- within template (al) through (a4) designates an L-amino acid residue.
  • Preferred values for B are: -NR 20 CH(R 71 )- and enantiomers of groups A5 with R 2 being H, A8, A22, A25, A38 with R 2 being H, A42, A47, and A50. Most preferred are
  • an additional preferred value for the building block -B-CO- is AMPA 3-Aminomethyphenyl acetic acid
  • R 20 is H or lower alkyl and R 64 is alkyl; alkenyl; aryl; aryl-lower alkyl; or heteroaryl- lower alkyl; especially those wherein R 64 is n-hexyl (A8"-21); n-heptyl (A8"-22); 4-
  • phenylbenzyl (A8"-23); diphenylmethyl (A8"-24); 3-amino-propyl (A8"-25); 5-amino- pentyl (A8"-26); methyl (A8"-27); ethyl (A8"-28); isopropyl (A8'*-29); isobutyl (A8"-30); n- propyl (A8"-31); cyclohexyl (A8"-32); cyclohexylmethyl (A8"-33); n-butyl (A8"-34); phenyl (A8"-35); benzyl (A8"-36); (3-indolyl)methyl (A8"-37); 2-(3-indolyl)ethyl (A8"-38); (4- phenyl)phenyl (A8' '-39); and n-nonyl (A8' '-40).
  • peptidic chains Z and Z 1 of the ⁇ -hairpin mimetics described herein are generally defined in terms of amino acid residues belonging to one of the following groups:
  • Gly can also be an amino acid residue in chains Z and Z 1
  • Pro can be an amino acid residue in chains Z and Z 1 , too, with the exception of positions where interstrand linkages (H) are possible.
  • Group C comprises amino acid residues with small to medium-sized hydrophobic side chain groups according to the general definition for substituent R 72 .
  • a hydrophobic residue refers to an amino acid side chain that is uncharged at physiological pH and that is repelled by aqueous solution .
  • these side chains generally do not contain hydrogen bond donor groups, such as (but not limited to) primary and secondary amides, primary and secondary amines and the corresponding protonated salts thereof, thiols, alcohols, phosphonates, phosphates, ureas or thioureas.
  • ethers such as ethers, thioethers, esters, tertiary amides, alkyl- or aryl phosphonates and phosphates or tertiary amines.
  • Genetically encoded small-to-medium-sized amino acids include alanine, isoleucine, leucine, methionine and valine.
  • Group D comprises amino acid residues with aromatic and heteroaromatic side chain groups according to the general definition for substituent R 73 .
  • An aromatic amino acid residue refers to a hydrophobic amino acid having a side chain containing at least one ring having a conjugated ⁇ -electron system (aromatic group).
  • hydrogen bond donor groups such as (but not limited to) primary and secondary amides, primary and secondary amines and the corresponding protonated salts thereof, thiols, alcohols, phosphonates, phosphates, ureas or thioureas, and hydrogen bond acceptor groups such as (but not limited to) ethers, thioethers, esters, tetriary amides, alkyl- or aryl phosphonates -and phosphates or tertiary amines.
  • Genetically encoded aromatic amino acids include phenylalanine and tyrosine.
  • a heteroaromatic amino acid residue refers to a hydrophobic amino acid having a side chain containing at least one ring having a conjugated ⁇ -system incorporating at least one heteroatom such as (but not limited to) O, S and N according to the general definition for substituent R 77 .
  • residues may contain hydrogen bond donor groups such as (but not limited to) primary and secondary amides, primary and secondary amines and the corresponding protonated salts thereof, thiols, alcohols, phosphonates, phosphates, ureas or thioureas, and hydrogen bond acceptor groups such as (but not limited to) ethers, thioethers, esters, tetriary amides, alkyl- or aryl phosphonates -and phosphates or tertiary amines.
  • Hydro bond donor groups such as (but not limited to) primary and secondary amides, primary and secondary amines and the corresponding protonated salts thereof, thiols, alcohols, phosphonates, phosphates, ureas or thioureas, and hydrogen bond acceptor groups such as (but not limited to) ethers, thioethers, esters, tetriary amides, alkyl- or aryl phosphonates
  • Group E comprises amino acids containing side chains with polar-cationic, acylamino- and urea-derived residues according to the general definition for substituen R 74 .
  • Polar-cationic refers to a basic side chain which is protonated at physiological pH.
  • Genetically encoded polar- cationic amino acids include arginine, lysine and histidine.
  • CitruUine is an example for an urea derived amino acid residue.
  • Group F comprises amino acids containing side chains with polar-non-charged residues according to the general definition for substituent R 84 .
  • a polar-non-charged residue refers to a hydrophilic side chain that is uncharged at physiological pH, but that is not repelled by aqueous solutions.
  • Such side chains typically contain hydrogen bond donor groups such as (but not limited to) primary and secondary amides, primary and secondary amines, thiols, alcohols, phosphonates, phosphates, ureas or thioureas. These groups can form hydrogen bond networks with water molecules.
  • polar-non-charged amino acids include asparagine, cysteine, glutamine, serine and threonine.
  • Group H comprises side chains of preferably (L)-amino acids at opposite positions of the ⁇ - strand region that can form an interstrand linkage.
  • the most widely known linkage is the disulfide bridge formed by cysteines and homo-cysteines positioned at opposite positions of the ⁇ -strand.
  • Various methods are known to form disulfide linkages including those described by: J. P. Tarn et al. Synthesis 1979, 955-957; Stewart et al. , Solid Phase Peptide Synthesis, 2d Ed., Pierce Chemical Company, III., 1984; Ahmed et al. J. Biol. Chem.
  • disulfide linkages can be prepared using acetamidomethyl (Acm)- protective groups for cysteine.
  • a well established interstrand linkage consists in linking ornithines and lysines, respectively, with glutamic and aspartic acid residues located at opposite ⁇ -strand positions by means of an amide bond formation.
  • Preferred protective groups for the side chain amino-groups of omithine and lysine are allyloxycarbonyl (Alloc) and allylesters for aspartic and glutamic acid.
  • interstrand linkages can also be established by linking the amino groups of lysine and omithine located at opposite ⁇ -strand positions with reagents such as N,N-carbonylimidazole to form cyclic ureas.
  • Group I comprises glycine having the amino group substituted by chains containing polar- cationic residues according to the general definition for substituent R 86 .
  • Polar-cationic refers to a basic side chain which is protonated at physiological pH.
  • positions for interstrand linkages are the following: If n is 4 and n' is 6 Postitions P3 and P3' taken together
  • Such interstrand linkages are known to stabilize the ⁇ -hairpin conformations and thus constitute an important structural element for the design of ⁇ -hairpin mimetics.
  • amino acid residues in chains Z and Z 1 are those derived from natural ⁇ -amino acids.
  • amino acids which, or the residues of which, are suitable for the purposes of the present invention, the abbreviations corresponding to generally adopted usual practice:
  • residues for group C are: Ala L-Alanine
  • residues for group D are:
  • the peptidic chains Z and Z 1 within the ⁇ -hairpin mimetics of the invention comprise 4 and, respectively, 6 residues or 5 and, respectively, 7 residues.
  • the positions P 1 to P" and P 1 to P n of each amino acid residue in the chain Z and, respectively, Z 1 are unequivocally defined as follows: P 1 represents the first amino acid in the chain Z that is coupled with its C-terminus to the N-terminus of the templates (b)-(p) or of group -B-CO- in templates (al), (a3) or (a4) or of group -A-CO- in template (a2), and P n represents the last amino acid in the chain Z; P 1' represents the first amino acid in the chain Z 1 that is coupled with its N-terminus to the C-terminus of the corresponding templates (b)-(p) or of group -B- CO- in template (al), (a3) or (a4) or of group -A-CO- in template (a2), and P" represents the last amino acid in the
  • Each of the positions P 1 to P n or P 1 ' to P"' will preferably contain an amino acid residue belonging to one or two or three of the above types C, D, E, F I, or being Pro or Gly, as follows:
  • amino acid residues in positions 1 to 4 of Z and the amino acid residues in positions 1' to 6' of Z 1 are preferably:
  • PI of type D or of type E or of type F, or the residue is Pro
  • P3 of type F, or the residue is Pro
  • P3' of type F or the residue is Pro
  • P5' of type E, or of type F or the residue is Pro
  • P6' of type E or of type F, or the residue is Pro;
  • P3 and P3' taken together, can form a group of type H.
  • amino acid residues in positions 1 to 5 of Z and the amino acid residues in positions 1' to.7' of Z 1 are preferably:
  • PI of type D or of type E or of type F, or the residue is Pro
  • P3 of type F, or the residue is Pro
  • PI' of type D or of type E or of type F, or the residue is Pro
  • - PP22'' : of type F
  • P3' of type D or the residue is Pro
  • P4' of type F
  • P5' of type D, or the residue is Pro
  • P6' of type E or of type F, or the residue is Pro
  • - PP77'' oftype E or of type I, or the residue is Gly; or
  • P2 and P2' and or P4 and P4', taken together, can form a group of type H; at P7' also D-isomers being possible.
  • amino acid residues in positions 1 to 4 of Z and the amino acid residues in positions 1' to 6' of Z 1 are most preferably:
  • amino acid residues in positions 1 to 5 of Z and the amino acid residues in positions 1' to 7' of Z 1 are most preferably:
  • Particularly preferred ⁇ -peptidomimetics of the invention include those described in Examples 6, 7, 8, 10, 12, 15, 20, 21, 22.
  • the process of the invention can advantageously be carried out as parallel array synthesis to yield libraries of template-fixed ⁇ -hairpin peptidomimetics of the above general formula I.
  • Such parallel synthesis allows one to obtain arrays of numerous (normally 24 to 192, typically 96) compounds of general formula I in high yields and defined purities, minimizing the formation of dimeric and polymeric by-products.
  • the proper choice of the functionalized solid- support (i.e. solid support plus linker molecule), and the templates play thereby key roles.
  • the functionalized solid support is conveniently derived from polystyrene crosslinked with, preferably 1-5%, divinylbenzene; polystyrene coated with polyethyleneglycol spacers (Tentagel R ); and polyacrylamide resins (see also Obrecht, D.; Villalgordo, J.-M, "Solid- Supported Combinatorial and Parallel Synthesis of Small-Molecular-Weight Compound Libraries", Tetrahedron Organic Chemistry Series, Vol. 17, Pergamon, Elsevier Science, 1998).
  • the solid support is functionalized by means of a linker, i.e. a bifunctional spacer molecule which contains on one end an anchoring group for attachment to the solid support and on the other end a selectively cleavable functional group used for the subsequent chemical transformations and cleavage procedures.
  • a linker i.e. a bifunctional spacer molecule which contains on one end an anchoring group for attachment to the solid support and on the other end a selectively cleavable functional group used for the subsequent chemical transformations and cleavage procedures.
  • linker i.e. a bifunctional spacer molecule which contains on one end an anchoring group for attachment to the solid support and on the other end a selectively cleavable functional group used for the subsequent chemical transformations and cleavage procedures.
  • Type 1 linkers are designed to release the amide group under acid conditions (Rink H, Tetrahedron Lett. 1987, 28, 3783-3790). Linkers os this kind form amides of the carboxyl group of the amino acids; examples of resins functionalized by such linker structures include 4- [(((2,4-dimethoxyphenyl)Fmoc-aminomethyl)phenoxyacetamido) aminomethyl] PS resin, 4- [(((2,4-dimethoxyphenyl)Fmoc-aminomethyl)phenoxyacetamido) aminomethyl] -4- methylbenzydrylamine PS resin (Rink amide MBHA PS Resin), and 4-[(((2,4- dimethoxyphenyl)Fmoc-aminomethyl)phenoxyacetamido) aminomethyl] benzhydrylamine PS- resin (Rink amide BHA PS resin).
  • the support is derived from polystyrene crosslinked with, most preferably 1-5%, divinylbenzene and functionalized by means of the 4- (((2,4-dimethoxyphenyl)Fmoc-aminomethyl)phenoxyacetamido) linker.
  • Type 2 linkers are designed to eventually release the carboxyl group under acidic conditions.
  • Linkers of this kind form acid-labile esters with the carboxyl group of the amino acids, usually acid-labile benzyl, benzhydryl and trityl esters; examples of such linker structures include 2- methoxy-4-hydroxymethylphenoxy (Sasrin R linker), 4-(2,4-dimethoxyphenyl-hydroxymethyl)- phenoxy (Rink linker), 4-(4-hydroxymethyl-3-methoxyphenoxy)butyric acid (HMPB linker), trityl and 2-chlorotrityl.
  • the support is derived from polystyrene crosslinked with, most preferably 1-5%, divinylbenzene and functionalized by means of the 2-chlorotrityl linker.
  • reaction vessels normally 24 to 192, typically 96
  • 25 to 1000 mg preferably 100 mg
  • of the appropriate functionalized solid support preferably 1 to 3% cross linked polystyrene.
  • the solvent to be used must be capable of swelling the resin and includes, but is not limited to, dichloromethane (DCM), dimethylformamide (DMF), N-methylpyrrolidone (NMP), dioxane, toluene, tetrahydrofuran (THF), ethanol (EtOH), trifluoroethanol (TFE), isopropylalcohol and the like.
  • Solvent mixtures containing as at least one component a polar solvent e. g. 20% TFE/DCM, 35% THF/NMP
  • Both the Rink linker that releases the C-terminal carboxylic amide group under acidic conditions and the 2-chlorotrityl linker that releases the C-terminal carboxylic acid group under acidic conditions, are stable to Fmoc deprotection conditions during the peptide synthesis.
  • the simultaneous release of the side chain protecting groups of the peptide fragment and the release of the peptide from the resin type 1 and type 2 is performed with 95% TFA and dichloromethane and scavencers such as phenol or triisopropylsilane (Bernatowicz, S.B. et al, Tetrahedron Lett., 1989, 30, 4645-4648).
  • Suitable protecting groups for amino acids and, respectively, for their residues are, for example,
  • guanidino group (as is present e. g. in the side-chain of arginine)
  • the 9-fluorenylmethoxycarbonyl- (Fmoc)-protected amino acid derivatives are preferably used as the building blocks for the construction of the template-fixed ⁇ -hairpin loop mimetics of formula I.
  • For the deprotection, i. e. cleaving off of the Fmoc group 20% piperidine in DMF or 2% DBU/2% piperidine in DMF can be used.
  • N-substituted glycine derivatives (type I) used as building blocks for the construction of certain compounds of formula I are derived from 9-fluorenylmethoxycarbonyl- (Fmoc)-protected amino acid derivatives or alternatively built up in two steps from leaving group-containing glycine precursors, such as bromo, chloro or iodo acetic acid, and suitable primary amine building blocks NH 2 -R 86 .
  • the first synthesis step consists of the attachment of the leaving group-containing acetylating agent, such as bromo acetic acid, to the resin bound intermediate through formation of the amide bond.
  • the second reaction step - the nucleophilic displacement - is accomplished using the primary amine building blocks, wherein the residues are, if necessary, suitably protected with groups as described above for side chains of amino acids.
  • the quantity of the reactant i. e. of the amino acid derivative, is usually 1 to 20 equivalents based on the milliequivalents per gram (meq/g) loading of the functionalized solid support (typically 0.1 to 2.85 meq/g for polystyrene resins) originally weighed into the reaction tube. Additional equivalents of reactants can be used if required to drive the reaction to completion in a reasonable time.
  • the reaction tubes, in combination with the holder block and the manifold, are reinserted into the reservoir block and the apparatus is fastened together. Gas flow through the manifold is initiated to provide a controlled environment, for example, nitrogen, argon, air and the like. The gas flow may also be heated or chilled prior to flow through the manifold.
  • Heating or cooling of the reaction wells is achieved by heating the reaction block or cooling externally with isopropanol/dry ice and the like to bring about the desired synthetic reactions. Agitation is achieved by shaking or magnetic stirring (within the reaction tube).
  • the preferred workstations are Labsource's Combi-chem station and MultiSyn Tech's-Syro synthesizer. Amide bond formation requires the activation of the ⁇ -carboxyl group for the acylation step. When this activation is being carried out by means of the commonly used carbodiimides such as dicyclohexylcarbodiimide (DCC, Sheehan & Hess, J. Am. Chem. Soc.
  • Certain phosphonium reagents have been used as direct coupling reagents, such as benzotriazol-1-yl- oxy-tris-(dimethylamino)-phosphonium hexafluorophosphate (BOP) (Castro et al., Tetrahedron Lett. 1975, 14, 1219-1222; Synthesis, 1976, 751-752), or benzotriazol-1-yl-oxy-tris- pyrrolidino-phosphonium hexaflurophoshate (Py-BOP, Coste et al., Tetrahedron Lett.
  • BOP benzotriazol-1-yl- oxy-tris-(dimethylamino)-phosphonium hexafluorophosphate
  • Py-BOP Coste et al., Tetrahedron Lett.
  • DPP A More recently diphenoxyphosphoryl azide (DPP A) or 0-(7-aza- benzotriazol-l-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (TATU) or 0-(7-aza- benzotriazol-l-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate (HATU)/7-aza-l- hydroxy benzotriazole (HO At, Carpino et al., Tetrahedron Lett. 1994, 35, 2279-2281) have also been used as coupling reagents.
  • DPP A diphenoxyphosphoryl azide
  • TATU 0-(7-aza- benzotriazol-l-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate
  • HATU 0-aza-l- hydroxy benzotriazole
  • the resin-bound intermediate within each reaction tube is washed free of excess of retained reagents, of solvents, and of by-products by repetitive exposure to pure solvent(s) by one of the two following methods: 1) The reaction wells are filled with solvent (preferably 5 ml), the reaction tubes, in combination with the holder block and manifold, are immersed and agitated for 5 to 300 minutes, preferably 15 minutes, and drained by gravity followed by gas pressure applied through the manifold inlet (while closing the outlet) to expel the solvent;
  • Both of the above washing procedures are repeated up to about 50 times (preferably about 10 times), monitoring the efficiency of reagent, solvent, and byproduct removal by methods such as TLC, GC, or inspection of the washings.
  • Interstrand linkages and their formation have been discussed above, in connection with the explanations made regarding groups of the type H which can, for example, be disulfide bridges formed by cysteines and homocysteines at opposite positions of the ⁇ -strand, or glutamic and aspartic acid residues linking ornithines and, respectively, lysines located at opposite ⁇ -strand positions by amide bond formation.
  • groups of the type H which can, for example, be disulfide bridges formed by cysteines and homocysteines at opposite positions of the ⁇ -strand, or glutamic and aspartic acid residues linking ornithines and, respectively, lysines located at opposite ⁇ -strand positions by amide bond formation.
  • the formation of such interstrand linkages can be effected by methods well known in the art.
  • a solution of 10 equivalents of iodine solution in DMF is applied for 1.5 h. The procedure is repeated for another 3h after with a fresh solution after filtering of the iodine solution
  • Detachment and complete deprotection of the fully protected peptide from the solid support is achieved by immersion of the reaction tubes, in combination with the holder block and manifold, in reaction wells containing a solution of the cleavage reagent (preferably 3 to 5 ml). Gas flow, temperature control, agitation, and reaction monitoring are implemented as described above and as desired to effect the detachment reaction.
  • the reaction tubes, in combination with the holder block and manifold are disassembled from the reservoir block and raised above the solution level but below the upper lip of the reaction wells, and gas pressure is applied through the manifold inlet (while closing the outlet) to efficiently expel the final product solution into the reservoir wells.
  • the resin remaining in the reaction tubes is then washed 2 to 5 times as above with 3 to 5 ml of an appropriate solvent to extract (wash out) as much of the detached product as possible.
  • the product solutions thus obtained are combined, taking care to avoid cross-mixing.
  • the individual solutions/extracts are then manipulated as needed to isolate the final compounds. Typical manipulations include, but are not limited to, evaporation, concentration, liquid/liquid extraction, acidification, basification, neutralization or additional reactions in solution.
  • the fully protected peptide derivative of type I is treated with 95% TFA, 2.5% H 2 0, 2.5% TIS or another combination of scavengers for effecting the cleavage of protecting groups.
  • the cleavage reaction time is commonly 30 minutes to 12 hours, preferably about 3.5 hours.
  • the resin is filtered and the cleavage solution containing the peptide is evaporated.
  • the product is dissolved in an acid and water and extracted with isopropyl ether or other solvents which are suitable therefor.
  • the cyclic peptide derivative obtained as end-product can be isolated.
  • this peptide derivative can be used directly for biological assays, or it has to be further purified, for example by preparative HPLC.
  • the ⁇ -hairpin peptidomimetics of the invention can be used in a wide range of applications in order to prevent HIV infections in healthy individuals and to slow or halt viral progression in infected patients or to inhibit the growth of cancer cells or to treat inflammatory disorders.
  • ⁇ -hairpin peptidomimetics may be administered per se or may be applied as an appropriate formulations together with carriers, diluents or excipients well known in the art.
  • the ⁇ -hairpin peptidomimetics When used to treat or prevent HIV infections or cancer the ⁇ -hairpin peptidomimetics can be administered singly, as mixtures of several ⁇ -hairpin peptidomimetics, in combination with other anti-HIV agents, or antimicrobial agents or anti cancer agents, or in combination with other pharmaceutically active agents.
  • the ⁇ -hairpin peptidomimetics can be administered per se or as pharmaceutical compositions.
  • Pharmaceutical compositions comprising ⁇ -hairpin peptidomimetics of the invention may be manufactured by means of conventional mixing, dissolving, granulating, coated tablet-making, levigating, emulsifying, encapsulating, entrapping or lyophilizing processes.
  • compositions may be formulated in conventional manner using one or more physiologically acceptable carriers, diluents, excipients or auxilliaries which facilitate processing of the active ⁇ -hairpin peptidomimetics into preparations which can be used pharmaceutically. Proper formulation depends upon the method of administration chosen.
  • ⁇ -hairpin peptidomimetics of the invention may be formulated as solutions, gels, ointments, creams, suspensions, etc. as are well-known in the art.
  • Systemic formulations include those designed for administration by injection, e.g. subcutaneous, intravenous, intramuscular, intrathecal or intraperitoneal injection, as well as those designed for transdermal, transmucosal, oral or pulmonary administration.
  • the ⁇ -hairpin peptidomimetics of the invention may be formulated in adequate solutions, preferably in physiologically compatible buffers such as Hink's solution, Ringer's solution, or physiological saline buffer.
  • the solution may contain formulatory agents such as suspending, stabilizing and/or dispersing agents.
  • the ⁇ -hairpin peptidomimetics of the invention may be in powder form for combination with a suitable vehicle, e.g., sterile pyrogen-free water, before use.
  • penetrants appropriate to the barrier to be permeated are used in the formulation as known in the art.
  • the compounds can be readily formulated by combining the active ⁇ - hairpin peptidomimetics of the invention with pharmaceutically acceptable carriers well known in the art.
  • Such carriers enable the ⁇ -hairpin peptidomimetics of the invention to be formulated as tablets, pills, dragees, capsules, liquids, gels, syrups, slurries, suspensions etc., for oral ingestion of a patient to be treated.
  • suitable excipients include fillers such as sugars, such as lactose, sucrose, mannitol and sorbitol; cellulose preparations such as maize starch, wheat starch, rice starch, potato starch, gelatin, gum tragacanth, methyl cellulose, hydroxypropylmethyl cellulose, sodium carboxymethylcellulose, and or polyvinylpyrrolidone (PVP); granulating agents; and binding agents.
  • desintegrating agents may be added, such as cross-linked polyvinylpyrrolidones, agar, or alginic acid or a salt thereof, such as sodium alginate.
  • solid dosage forms may be sugar-coated or enteric-coated using standard techniques.
  • suitable carriers, excipients or diluents include water, glycols, oils, alcohols, etc.
  • flavoring agents, preservatives, coloring agents and the like may be added.
  • the composition may take the form of tablets, lozenges, etc. formulated as usual.
  • the ⁇ -hairpin peptidomimetics of the invention are conveniently delivered in form of an aeorosol spray from pressurized packs or a nebulizer, with the use of a suitable propellant, e.g. dichlorodifluoromethane, trichlorofluromethane, carbon dioxide or another suitable gas.
  • a suitable propellant e.g. dichlorodifluoromethane, trichlorofluromethane, carbon dioxide or another suitable gas.
  • the dose unit may be determined by providing a valve to deliver a metered amount.
  • Capsules and cartridges of e.g. gelatin for use in an inhaler or insufflator may be formulated containing a powder mix of the ⁇ - hai ⁇ in peptidomimetics of the invention and a suitable powder base such as lactose or starch.
  • the compounds may also be formulated in rectal or vaginal compositions such as suppositories together with appropriate suppository bases such as cocoa butter or other glycerides.
  • the ⁇ -hai ⁇ in peptidomimetics of the invention may also be formulated as depot preparations. Such long acting formulations may be administered by implantation (e.g. subcutaneously or intramuscularly) or by intramuscular injection.
  • the ⁇ -hai ⁇ in peptidomimetics of the invention may be formulated with suitable polymeric or hydrophobic materials (e.g. as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble salts.
  • ⁇ -hai ⁇ in peptidomimetics of the invention may be delivered using a sustained-release system, such as semipermeable matrices of solid polymers containing the therapeutic agent.
  • sustained-release materials have been established and are well known by those skilled in the art. Sustained-release capsules may, depending on their chemical nature, release the compounds for a few weeks up to over 100 days. Depending on the chemical nature and the biological stability of the therapeutic agent, additional strategies for protein stabilization may be employed.
  • ⁇ -hai ⁇ in pepdidomimetics of the invention may contain charged residues, they may be included in any of the above-described formulations as such or as pharmaceutically acceptable salts.
  • Pharmaceutically acceptable salts tend to be more soluble in aqueous and other protic solvents than are the corresponding free base forms.
  • ⁇ -hai ⁇ in peptidomimetics of the invention will generally be used in an amount effective to achieve the intended piupose. It is to be understood that the amount used will depend on a particular application.
  • a therapeutically effective dose can be determined using, for example, the in vitro assays provided in the examples.
  • the treatment may be applied while the infection is visible, or even when it is not visible.
  • An ordinary skilled expert will be able to determine therapeutically effective amounts to treat topical infections without undue experimentation.
  • a therapeutically effective dose can be estimated initially from in vitro assays.
  • a dose can be formulated in animal models to achieve a circulating ⁇ -hai ⁇ in peptidomimetic concentration range that includes the IC 50 as determined in the cell culture (i.e. the concentration of a test compound that is lethal to 50% of a cell culture). Such information can be used to more accurately determine useful doses in humans.
  • Initial dosages can also be determined from in vivo data, e.g. animal models, using techniques that are well known in the art. One having ordinary skills in the art could readily optimize administration to humans based on animal data. Dosage amount for applications as anti-HIV agents may be adjusted individually to provide plasma levels of the ⁇ -hai ⁇ in peptidomimetics of the invention which are sufficient to maintain the therapeutic effect. Therapeutically effective serum levels may be achieved by administering multiple doses each day.
  • the effective local concentration of the ⁇ - hai ⁇ in peptidomimetics of the invention may not be related to plasma concentration.
  • One having the skills in the art will be able to optimize therapeutically effective local dosages without undue experimentation.
  • the amount of ⁇ -hai ⁇ in peptidomimetics administered will, of course, be dependent on the subject being treated, on the subject's weight, the severity of the affliction, the manner of administration and the judgement of the prescribing physician.
  • the anti-HIV therapy may be repeated intermittently while infections are detectable or even when they are not detectable.
  • the therapy may be provided alone or in combination with other drugs, such as for example other anti-HIV agents or anti cancer agents, or anti inflammatory agents or other antimicrobial agents.
  • a therapeutically effective dose of the ⁇ -hairpin peptidomimetics described herein will provide therapeutic benefit without causing substantial toxicity.
  • Toxicity of the ⁇ -hai ⁇ in peptidomimetics of the invention herein can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., by determining the LD 50 (the dose lethal to 50% of the population) or the LDi oo (the dose lethal to 100% of the population).
  • the dose ratio between toxic and therapeutic effect is the therapeutic index. Compounds which exhibit high therapeutic indices are preferred.
  • the data obtained from these cell culture assays and animal studies can be used in formulating a dosage range that is not toxic for use in humans.
  • the dosage of the ⁇ -hai ⁇ in peptidomimetics of the invention lies preferably within a range of circulating concentrations that include the effective dose with little or no toxicity.
  • the dosage may vary within the range depending upon the dosage form employed and the route of administration utilized.
  • the exact formulation, route of administration and dose can be chosen by the individual physician in view of the patient's condition (see, e.g. Fingl et al. 1975, In : The Pharmacological Basis of Therapeutics, Ch.l, p.l).
  • HBTU 1-benzotriazol-l-yl-tetramethylurounium hexafluorophosphate (Knorr et al. Tetrahedron Lett. 1989, 30, 1927-1930);
  • HOBt 1-hydroxybenzotriazole
  • DIEA diisopropylethylamine
  • DIC diisopropylcarbodiimide
  • HATU 0-(7-aza-benzotriazole-l-yl)-N,N,N',N'-tetramethyluronoium hexafluorophosphate (Ca ⁇ ino et al. Tetrahedron Lett. 1994, 35, 2279-2281).
  • the Fmoc-group was removed by treatment with a solution of 40% piperidine in DMF (191 ml) for 45 min at 25°C, the resin was washed DMF (lx), and the treatment was repeated. The resin was washed with DMF (1 x) and CH 2 C1 2 (lx) and dried under vacuum for 12 hours. Loading was typically 0.7-0.85 mMol/g.
  • the following preloaded resin was prepared: Fmoc-Arg(Pbf)-NH-Rink amide resin.
  • the resin was shaken (CH 2 C1 2 /MeOH/DIEA : 17/2/1), 30 ml for 30 min; then washed in the following order with CH 2 C1 2 (lx), DMF (lx), CH 2 C1 2 (lx), MeOH (lx), CH 2 Cl 2 (lx), MeOH (lx), CH 2 C1 2 (2x), Et 2 0 (2x) and dried under vacuum for 6 hours. Loading was typically 0.6-0.7 mMol g.
  • the synthesis was carried out using a Syro-peptide synthesizer (Multisyntech) using 24 to 96 reaction vessels. In each vessel was placed 60 mg (weight of the resin before loading) of the above resin. The following reaction cycles were programmed and carried out:
  • Steps 3 to 6 are repeated to add each amino-acid.
  • peptide-carrying resin 0.05 mmol was swelled in 3 mL of dry DCM for 1 h and after filtering off the DCM, with dry DMF (3 mL) for overnight. Then 10 equivalents of iodine solution in DMF (6 mL) was added to the reactor and stirred for 1.5 h. The resin was filtered and the fresh solution of iodine (10 equivalents) in DMF (6 mL) was added and stirred for another 3 h. The resin was filtered and washed thoroughly several times with DMF and DCM.
  • the water phase was dried under vacuum and then the product purified by preparative reverse phase HPLC.
  • the products were analysed by ESI-MS and after lyophilisation the products were obtained as a white powder.
  • the analytical data comprising HPLC retention times and ESI-MS are shown in table 1 and table 2.
  • the peptides were synthesized starting with the amino acid Arg which was grafted to the resin.
  • Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above.
  • the linear peptides were synthesized on solid support according to procedure described above in the following sequence: Resin-P4-P3- P2-P1- L Pro - D Lys -Pl'-P2'-P3'-P4'-P5 , -P6'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention times (minutes) were determined using the gradient described above.
  • the peptides were synthesized starting with the amino acid Arg which was grafted to the resin.
  • Starting resin was Fmoc-Arg(Pbf)- Rink-amide resin, which was prepared as described above.
  • the linear peptides were synthesized on solid support according to procedure described above in the following sequence: Resin-P4-P3-P2-Pl- L Pro- D Pro-Pl'-P2'-P3'-P4'-P5'-P6'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention times (minutes) were determined using the gradient described above.
  • the peptide was synthesized starting with the amino acid Arg which was grafted to the resin.
  • Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above.
  • the linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P4-P3- P2-Pl- L Pro- L Lys-Pl '-P2'-P3'-P4'-P5'-P6'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention time (minutes) was determined using the gradient described above.
  • the peptides were synthesized starting with the amino acid Arg which was grafted to the resin.
  • Starting resin was Fmoc- Arg(Pbf)-Rink-amide resin, which was prepared as described above.
  • the linear peptides were synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4-P3-P2-Pl- L Pro- D Pro-Pl'-P2*-P3'-P4'-P5 , -P6'-P7'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention times (minutes) were determined using the gradient described above:
  • the peptide was synthesized starting with the amino acid Arg which was grafted to the resin.
  • Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above.
  • the linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4- P3-P2-Pl- Pro- D Pro-Pl'-P2*-P3'-P4'-P5'-P6'-P7', and the disulfide bridge was formed.
  • the resin was then swelled in dry DCM for 0.5 hrs. DCM was filtered off and 5 mL of dry DCM was added to the resin.
  • the peptide was synthesized starting with the amino acid Arg which was grafted to the resin.
  • Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above.
  • the linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4- P3-P2-Pl- L Pro- D Pro-Pr-P2'-P3'-P4'-P5'-P6'-P7' and the disulfide bridge was formed.
  • the peptide was synthesized starting with the amino acid Arg which was grafted to the resin.
  • Starting resin was Fmoc-Arg(Pbf)-chlorotrityl resin, which was prepared as described above.
  • the linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4-P3- P2-P1- L Pro- D Pro -Pl'-P2'-P3'-P4'-P5'-P6'-P7'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated.
  • HPLC-retention time was determined using the gradient described above: 4.35 minutes.
  • the peptide was synthesized starting with the amino acid Arg which was grafted to the resin.
  • Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above.
  • the linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4-
  • HPLC-retention time was determined using the gradient described above: 4.02 minutes. * Template [(bl)-154] is (2S,6S,9S)-6-amino-2-carboxymethyl-3,8-diazabicyclo-[4,3,0]- nonane-l,4-dione
  • the peptide was synthesized starting with the amino acid Arg which was grafted to the resin.
  • Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above.
  • the linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4- P3-P2-Pl-AMPA-Pr-P2'-P3'-P4'-P5'-P6'-P7'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention time was determined using the gradient described above: 4.62 minutes.
  • the peptide wassynthesized starting with the amino acid Arg which was grafted to the resin.
  • Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above.
  • the linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4- P3-P2-Pl- D Pro- L Pro-Pl'-P2'-P3'-P4'-P5'-P6'-P7'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention time was determined using the gradient described above: 4.13, 4.40* minutes. * The MS is showing the correct mass.
  • the peptide was synthesized starting with the amino acid Arg which was grafted to the resin.
  • Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above.
  • the linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4- P3-P2-Pl- L Pro- Pro-Pr-P2'-P3'-P4'-P5'-P6'-P7'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention time was determined using the gradient described above: 4.08 minutes.
  • the peptide was synthesized starting with the amino acid Arg which was grafted to the resin.
  • Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above.
  • the linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4- P3-P2-Pl- L Pro- D Pic-Pl'-P2'-P3'-P4'-P5'-P6'-P7'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention time was determined using the gradient described above: 4.47 minutes.
  • Lyophilized peptides were weighed on a Microbalance (Mettler MT5) and dissolved in sterile water to a final concentration of 1 mM unless stated otherwise. Stock solutions were kept at + 4°C, light protected.
  • the cells were washed free from Fura-2-AM with a platelet centrifuge and resuspended in 800 ⁇ l MSB containing 5 mM D-Glucose.
  • the peptides to be administered were diluted to a 100 fold end concentration in MSB/0.2 % PPL, and 8 ⁇ l were injected.
  • [Ca 2+ ]i-dependent fluorescence change in response to single or sequential stimulation with the peptide was recorded with a fluorimeter at an excitation wavelength of 340 nM and an end emission wavelength of 510 nM [see ref. 4, below]. Measurements were done under continuous stirring at 37°C.
  • the signal intension was calibrated with 3 mM CaCl 2 /l mM Ionomycin (maximal fura-2- acetoxymethylester saturation) and 10 ⁇ M MnCl 2 (minimal Fura-2-acetoxymethylester saturation) and [Ca 2+ ]j-changes are presented in % fura-2-acetoxymethylester saturation.
  • the rate of [Ca 2+ ]j-changes was calculated on the basis of the initial [Ca 2+ ];-changes and plotted in dependence of chemokine concentration to obtain a sigmoidal curve and to determine the IC 50 values.
  • Fura 2-acetoxymethylester 1 mM stock solution in dimethylsulfoxide.
  • the assay was performed according to ref. 5, below.
  • Stock dilutions of the peptides (10 mM) were prepared by dissolving in 10 mM Tris-HCl at room temperature. Stock solutions were kept at + 4°C, light protected.
  • Working dilutions were prepared extemporaneously by serial dilution in Phosphate Buffered Saline (PBS) and added in a final volume of 10 ⁇ L directly to the cell cultures. After 48 hours of co-cultivation the cultures were rinsed with PBS and then exposed to glutaraldehyde/ formaldehyde (0.2 % / 2 %) in PBS for five minutes.
  • PBS Phosphate Buffered Saline
  • the fixed cultures were subsequently incubated with ortho-nitro- phenyl-galactopyranoside (ONPG) as a ⁇ -galactosidase substrate, which was enzymatically converted into the chromophore ortho-nitrophenol (ONP).
  • ONPG ortho-nitro- phenyl-galactopyranoside
  • the read out is directly obtained by measuring optical density of wells at 405 nm in an iEMS 96well-plate reader.
  • cytotoxicity of the peptides to HELA cells (Acc57) and COS-7 cells (CRL-1651) was determined using the MTT reduction assay [see ref. 6 and 7, below]. Briefly the method was as follows: HELA cells and COS-7 cells were seeded at 7.0 0 3 and, respectively, 4.5'10 3 cells per well and grown in 96-well microtiter plates for 24 hours at 37°C at 5% C0 2 . At this point, time zero (Tz) was determined by MTT reduction (see below). The supernatant of the remaining wells was discarded and fresh medium and the peptides in serial dilutions of 12.5, 25 and 50 ⁇ M were pipeted into the wells.
  • Each peptide concentration was assayed in triplicate. Incubation of the cells was continued for 48 hours at 37°C at 5% C0 2 . Wells were then washed once with PBS and subsequently 100 ⁇ l MTT reagent (0.5 mg/mL in medium RPMI1640 and, respectively, DMEM) was added to the wells. This was incubated at 37°C for 2 hours and subsequently the medium was aspirated and 100 ⁇ l isopropanol was added to each well. The absorbance at 595 nm of the solubilized product was measured (0D 595 peptide). For each concentration averages were calculated from triplicates.
  • the percentage of growth was calculated as follows: (ODsgspeptide-ODsgsTz-ODsgsEmpty well) / (ODsgsTz-ODsgsEmpty well) x 100% and was plotted for each peptide concentration.
  • 'CCR5' cells were cultured in DMEM medium with 4500 mg mL glucose, 10 % fetal bovine serum (FBS), supplemented with 50 U/ml Penicillin and 50 ⁇ g mL Streptomycin (Pen/Strept).
  • Hut/4-3 cells were maintained in RPMI medium, 10% FBS, supplemented with Pen/Strept. and 10 mM HEPES.
  • HELA cells and CCRF-CEM cells were maintained in RPMI1640 plus 5% FBS, Pen/Strept and 2 mM L-Glutamine.
  • Cos-7 cells were grown in DMEM medium with 4500 mg/mL glucose supplemented with 10% FCS, Pen/Strept. and 2 mM L-Glutamine. All cell lines were grown at 37°C at 5% C0 2 .
  • HEPES, Pen/Strept., L-Glutamine and sera were purchased from Gibco (Pailsey, UK). All fine chemicals came from Merck (Darmstadt, Germany).
  • chemotactic response of CCRF-CEM cells to a gradient of stromal cell-derived factor l ⁇ (SDF-1) was measured using disposable assay plates from Neuroprobe (5 ⁇ pore size) (Gaithersburg, MD), according to the manufacturer's directions and references therein [especially ref. 8, below]. Briefly, one 175 cm 2 flask was washed once with Dubecco's phosphate buffered saline (DPBS), and trypsinized for 10 minutes or until cells had lifted.
  • DPBS Dubecco's phosphate buffered saline
  • the trypsin was neutralized by the addition of fresh medium containing serum and the cells were pelleted, washed once in DPBS, and resuspended at 1-0.5 X 10 7 cells/ml in RPMI + 0.5% bovine serum albumin (BSA). 45 ⁇ l of cell suspension were mixed with 5 ⁇ l of 10-fold concentrated PEM peptide diluted in the same assay medium. 35 ⁇ l of this mixture were applied to the top of the assay filter. The cells were allowed to migrate (at 37°) into the bottom chamber of the assay plate containing 1 nM SDF-1. After 4 hours, the filter was removed and MTT was added to the migrated cells to a final concentration of 0.5 mg/ml, and incubated for a further 4 hours.
  • BSA bovine serum albumin
  • ABS 595 optical absorbance at 595 nm
  • Magellan The optical absorbance at 595 nm
  • the number of cells migrated was determined by comparing ABS 595 values against a standard curve generated with a known number of cells in the assay plate and were plotted against SDF-1 concentration to obtain a sigmoidal curve and to determine the IC 50 values.
  • the values for IC50 were determined using the Trendline function in Microsoft Excel by fitting a logarithmic curve to the averaged datapoints.

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Abstract

Template-fixed ß-hairpin peptidomimetics of the General Formula (I); wherein Z1 and Z2 are template-fixed chains of4 and 6 or 5 and 7 α-amino acid residues which, depending on their positions in the chain are Gly, or Pro, or of certain types which, as the remaining symbols in the above formula, are defined in the description and the claims, and salts thereof, have the property to prevent or to reduce HIV infections or to inhibit the growth of cancer cells or to inhibit inflammation. They can be used as medicaments to treat or prevent HIV infections and/or cancer or inflammatory disorders. These β-sheet peptidomimetics can be manufactured by a process which is based on a mixed solid- and solution phase synthetic strategy.

Description

TEMPLATE- FIXED PEPTIDOMIMETICS AS MEDICAMENTS AGAINST HIV AND CANCER
The present invention provides template-fixed β-hairpin peptidomimetics incorporating two template-fixed chains of 4 and 6 or 5 and 7 α-amino acid residues which, depending on their positions in the chains, are Gly or Pro, or of certain types, as defined herein below. These template-fixed β-hairpin mimetics have antagonizing CXCR4-activity. In addition, the present invention provides an efficient synthetic process by which these compounds can, if desired, be made in parallel library-format. These β-hairpin peptidomimetics show improved efficacy, bioavailability, half-life and most importantly a significantly enhanced ratio between antagonizing CXCR4 activity on the one hand, and hemolysis on red blood cells and cytotoxicity on the other.
To date the available therapies for the treatment of HIV infections have been leading to a remarkable improvement in symptoms and recovery from disease in infected people. Although the Mghly active anti retroviral therapy (HAART-therapy) which involves a combination of reverse transcriptase/protease inhibitor has dramatically improved the clinical treatment of individuals with AIDS or HIV infection, there have still remained several serious problems including multi drug resistance, significant adverse effects and high costs. Particularly desired are anti HIV agents that block the HIV infection at an early stage of the infection, such as the viral entry.
It has recently been recognized that for efficient entry into target cell, human immunodeficiency viruses require the chemokine receptors CCR5 and CXCR4 as well as the primary receptor CD4 (N. Levy, Engl. J. Med., 335, 29, 1528-1530). Accordingly, an agent which could block the CXCR4 chemokine receptors should prevent infections in healthy individuals and slow or halt viral progression in infected patients (Science, 1997, 275, 1261- 1264).
Among the different types of CXCR4 inhibitors (M. Schwarz, T. N. C. Wells, A.E.I. Proudfoot, Receptors and Channels, 2001, 7, 417-428), one emerging class is based on naturally occurring cationic peptide analogues derived from Polyphemusin II which have an antiparallel β -sheet structure, and a β-hairpin that is maintained by two disulfide bridges (H. Nakashima, M. Masuda, T. Murakami, Y. Koyanagi, A. Matsumoto, N. Fujii, N. Yamamoto, Antimicrobial Agents and Chemoth. 1992, 36, 1249-1255; H. Tamamura, M. Kuroda, M. Masuda, A. Otaka, S. Funakoshi, H. Nakashima, N. Yamamoto, M. Waki, A. Matsumotu, J.M. Lancelin, D. Kohda, S. Tate, F. Inagaki, N. Fujii, Biochim. Biophys. Ada 1993, 209, 1163; WO 95/10534 Al).
Synthesis of structural analogs and structural studies by nuclear magnetic resonance (NMR) spectroscopy have shown that the cationic peptides adopt well defined β-hairpins conformations, due to the constraining effect of the single or two disulfide bridges (H. Tamamura, M. Sugioka, Y. Odagaki, A. Omagari, Y. Kahn, S. Oishi, H. Nakashima, N. Yamamoto, S.C. Peiper, N. Hamanaka, A. Otaka, N. Fujii, Bioorg. Med. Chem. Lett. 2001, 359-362).These results show that the β-hairpin structure plays an important role in antagonizing CXCR4-activity. Additional structural studies have also indicated that the antagonizing activity can also be influenced by modulating amphiphilic structure and the pharmacophore (H. Tamamura, A.
Omagari, K. Hiramatsu,. K. Gotoh, T. Kanamoto, Y. Xu, E. Kodama, M. Matsuoka, T. Hattori, N. Yamamoto, H. Nakashima, A. Otaka, N. Fujii, Bioorg. Med. Chem. Lett. 2001, 11, 897- 1902; H. Tamamura, A. Omagari, K. Hiramatsu, S. Oishi, H. Habashita, T. Kanamoto, K. Gotoh, N. Yamamoto, H. Nakashima, A. Otaka N. Fujii, Bioorg. Med.'Chem. 2002, 10, 1417- 1426; H. Tamamura, K. Hiramatsu, K. Miyamoto, A. Omagari, S. Oishi, H. Nakashima, N.
Yamamoto, Y. Kuroda, T. Nakagawa, A. Otaki, N. Fujii, Bioorg. Med. Chem. Letters 2002, 12, 923-928).
A key issue in the design of CXCR4 antagonizing peptides is selectivity. The Polyphemusin II derived analogs exert still a cytotoxicity despite improvements (K. Matsuzaki, M. Fukui, N. Fujii, K. Miyajima, Biochim. Biophys. Acta 1991, 259, 1070; A. Otaka, H. Tamamura, Y. Terakawa, M. Masuda, T. Koide, T. Murakami, H. Nakashima, K. Matsuzaki, K. Miyajima, T. Ibuka, M. Waki, A. Matsumoto, N. Yamamoto, N. Fujii Biol. Pharm. Bull. 1994, 17, 1669 and references cited above.
This cytotoxic activity essentially obviates use in vivo, and represents a serious disadvantage in clinical applications. Before intravenous use can be considered, the general toxicity, protein- binding activity in blood serum, as well as protease stability become serious issues which must be adequately addressed. In addition it has recently been discovered, that the CXCR4-receptor is involved in chemotactic activity of cancer cells, such as breast cancer metastasis or ovarian cancer (A. Muller, B. Homey, H. Soto, N. Ge, D. Catron, M.E. Buchanan, T. Mc Clanahan, E. Murphey, W. Yuan, S.N. Wagner, J. Luis Barrera, A. Mohar, E. Verastegui, A. Zlotnik, Nature 2001, 50, 410, J. M. Hall, K. S. Korach, Molecular Endocrinology, 2003, 1-47; ), Non-Hodgπ s Lymphoma ( F. Bertolini, C. DellAgnola, P. Manusco, C. Rabascio, A. Burlini, S. Monestiroli, A. Gobbi, G. Pruneri, G. Martinelli, Cancer Research 2002, 62, 3106-3112), or lung cancer (T. Kijima, G. Maulik, P. C. Ma, E. V. Tibaldi, R:E. Turner, B. Rollins, M. Sattler, B.E. Johnson, R. Salgia, Cancer Research 2002, 62, 6304-6311) or in inflammatory diseases e.g. such as rheumatoid arthritis, asthma, or multiple sclerose (K.R. Shadidi et al, Scandinavian Journal oflmmunolgy, 2003, 57, 192-198, J. A. Gonzalo J. Immunol. 2000, 165, 499-508, S. Hatse et al, FEBS Letters 2002 527, 255-262 and cited references). Blocking the chemotactic activity with a CXCR4 inhibitor should stop the migration of cancer cells. The mediation of recruitment of immunecells to sites of inflammation should be stopped by a CXCR4 inhibitor. Particularly desired are agents for treatment of cancer or agents for treatment of inflammatory disorders.
In the compounds described below, a new strategy is introduced to stabilize beta -hairpin conformations in bridged-backbone peptide mimetic exhibiting high CXCR4 antagonizing activity and anticancer activity and anti inflammatory activity. This involves transplanting the cationic and hydrophobic hairpin sequence onto a template, whose function is to restrain the peptide loop backbone into a hairpin geometry. The rigidity of the hairpin may be further influenced by introducing a disulfide bridge. Template-bound hairpin mimetic peptides have been described in the literature (D, Obrecht, M. Altorfer, J. A. Robinson, Adv. Med. Chem. 1999, 4, 1-68; J. A. Robinson, Syn. Lett. 2000, 4, 429-441), but such molecules have not previously been evaluated for development of CXCR4 antagonizing peptides. However, the ability to generate β-hairpin peptidomimetics using combinatorial and parallel synthesis methods has now been established (L. Jiang, K. Moehle, B. Dhanapal, D. Obrecht, J. A. Robinson, Helv. Chun. Acta. 2000, 83, 3097-3112).
These methods allow the synthesis and screening of large hairpin mimetic libraries, which in turn considerably facilitates structure-activity studies, and hence the discovery of new molecules with highly potent CXCR4 antagonizing activity or anti cancer activity or anti inflammatory activity and low hemolytic activity to human red blood blood cells. β-Hairpin peptidomimetics obtained by the approach described here are useful as Anti-HW agents and anticancer agents and anti-inflammatory agents.
The β-hairpin peptidomimetics of the present invention are compounds of the general formula
Figure imgf000005_0001
(I) wherein
Figure imgf000005_0002
is a group of one of the formulae
Figure imgf000005_0003
(a1) (a2)
Figure imgf000005_0004
(■3) (a4)
Figure imgf000006_0001
(c2) (c3) (d)
Figure imgf000006_0002
(h) (11) (i2)
Figure imgf000007_0001
(i3) (14) (j)
Figure imgf000007_0002
(n) (o) (P)
wherein
Figure imgf000007_0003
is the residue of an L-α-amino acid with B being a residue of formula -NR20CH(R71)-; or the enantiomer of one of the groups Al to A69 as defined hereinafter; or, in case the template is of type (a4), also a residue of an amino acid with B being a residue of formula -NR20-CH2-C6H4-CH2-;
I
is a group of one of the formulae
Figure imgf000008_0001
A1 A2 A3 A4
Figure imgf000008_0002
A5 A6 A7 A8 A9
Figure imgf000008_0003
A10 A11 A12 A13 A14
Figure imgf000008_0004
A15 A16 A18 A19
Figure imgf000008_0005
A20 A21 A22 A23 A24
Figure imgf000009_0001
A38 A39 A40 A41 A42
Figure imgf000009_0002
A43 A44 A45 A46 A47
A48 A49 A50 A51 A52
Figure imgf000010_0001
A53 A54 A55 A56 A57
Figure imgf000010_0002
A63 A64 A65 A66
Figure imgf000010_0003
A67 A68 A69
Figure imgf000010_0004
A70 A71 A72 A73 A74
Figure imgf000010_0005
A75 A76 A77 A78 A79
Figure imgf000011_0001
A80 A81 A82 A83 A84
Figure imgf000011_0002
R1 is H; lower alkyl; or aryl-lower alkyl;
R2 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)ra(CHR61)sSR56;
-(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75;
-(CH2)m(CHR61)sNR20CONR33R 2; -(CH2)0(CHR6!)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)o(CHR61)s S02R62; or -(CH2)0(CHR61)SC6H4R8; R3 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)sCOOR57 ;
-(CH2)0(CHR61)sCONR58R59 ; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)o(CHR61)s S02R62; or -(CH2)„(CHR61)SC6H4R8; R4 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; - (CH2)m(CHR61)sNR33R34; -(CH2)ra(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82;
-(CH2)p(CHR61)sCOOR57; -(CH2)p(CHR61)sCONR58R59; -(CH2)p(CHR61)sPO(OR60)2; -(CH2)P(CHR61)S S02R62; or
Figure imgf000012_0001
R5 is alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)sCOOR57; -(CH2)„(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2;
-(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R6 is H; alkyl; alkenyl; -(CH2)0(CHR6I)sOR55; -(CH2)0(CHR61)SSR56; - (CH2)o(CHR6I)sNR33R34;
-(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)sCOOR57; -(CH2)0(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2;
-(CH2)„(CHR6I)S S02R62; or -(CH2)„(CHR61)SC6H4R8; R7 is alkyl; alkenyl; -(CH2)q(CHR61)s0R55; -(CH2)q(CHR61)sNR33R34; -(CH2)q(CHR61)sOCONR33R75; -(CH2)q(CHR61)sNR20CONR33R82; -(CH2)r(CHR61)sCOOR37; -(CH2)r(CHR61)sCONR58R59; -(CH2)r(CHR61)sPO(OR60)2; -(CH2)r(CHR6I)sS02R62; or -(CH2)r(CHR61)s C6H4R8;
R8 is H; CI; F; CF3; N02; lower alkyl; lower alkenyl; aryl; aryl-lower alkyl; -(CH2)0(CHR6,)sOR55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)NR33R34 ; -(CH2)0(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)0(CHR6I)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)sS02R62; or -(CH2)0(CHR61)sCOR64;
R9 is alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)o(CHR6I)sOCONR33R75; -(CH2)o(CHR6I)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)0(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)„(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R10 is alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR6I)SNR33R34; -(CH2)o(CHR61)sOCONR33R75; -(CH2)„(CHR61)sNR20CONR33R82; -(CH2)o(CHR6I)sCOOR57; -(CH2)o(CHR6I)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; Rπ is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOORS7; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR6,)sPO(OR60)2; -(CH2)0(CHR61)sS02R62; or -(CH2)0(CHR61)S C6H4R8; R12 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75;
-(CH2)m(CHR61)sNR20CONR33R82; -(CH2)r(CHR61)sCOOR57; - (CH2)r(CHR61)sCONR58R59; -(CH2)r(CHR6I)sPO(OR60)2; -(CH2)r(CHR61)s S02R62; or - (CH2)r(CHR61)sC6H4R8; R13 is alkyl; alkenyl; -(CH2)q(CHR61)sOR55; -(CH2)q(CHR61)sSR56; -(CH2)q(CHR61)sNR33R34; -(CH2)q(CHR61)sOCONR33R75; -(CH2)q(CHR61)sNR20CONR33R82;
-(CH2)q(CHR61)sCOOR57; -(CH2)q(CHR61)sCONR58R59; -(CH2)q(CHR61)sPO(OR60)2; -(CH2)q(CHR61)s S02R62; or -(CH2)q(CHR61)sC6H4R8; R14 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)q(CHR61)sCOOR57; -(CH2)q(CHR6')sCONR58R59; -(CH2)q(CHR61)sPO(OR60)2;.
-(CH2)q(CHR61)sSOR62; or -(CH2)q(CHR61)s C6H4R8; R15 is alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR6I)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR )SC6H4R8;
R16 is alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)o(CHR61)sOCONR33R75; -(CH2)0(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR6I)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R17 is alkyl; alkenyl; -(CH2)q(CHR61)s0R55; -(CH2)q(CHR61)sSR56; -(CH2)q(CHR61)sNR33R34; -(CH2)q(CHR61)sOCONR33R75; -(CH2)q(CHR61)sNR20CONR33R82; -(CH2)q(CHR61)sCOOR57; -(CH2)q(CHR6I)sCONR58R59; -(CH2)q(CHR6I)sPO(OR60)2; -(CH2)q(CHR61)s S02R62; or -(CH2)q(CHR61)sC6H4R8; R18 is alkyl; alkenyl; -(CH2)p(CHR61)s0R55; -(CH2)P(CHR61)SSR56; -(CH2)P(CHR61)SNR33R34; -(CH2)p(CHR61)sOCONR33R75; -(CH2)p(CHR61)sNR20CONR33R82; -(CH2)p(CHR6I)sCOOR57; -(CH2)p(CHR61)sCONR58R59; -(CH2)p(CHR61)sPO(OR60)2; -(CH2)p(CHR61)s S02R62; or -(CH2)0(CHR61)SC6H4R8; R19 is lower alkyl; -(CH2)P(CHR61)sOR55; -(CH2)P(CHR61)SSR56; -(CH2)P(CHR61)SNR33R34; -(CH2)P(CHR61)S0C01S1R33R75; -(CH2)P(CHR61)SNR20CONR33R82;
-(CH2)P(CHR61)SCOOR57; -(CH2)P(CHR61)SCONR58R59; -(CH2)P(CHR61)SPO(OR60)2; -(CH2)P(CHR61)S S02R62; or -(CH2)0(CHR6,)SC6H4R8; or R18 and R19 taken together can form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; R20 is H; alkyl; alkenyl; or aryl-lower alkyl;
R21 is H; alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR61)SSR56; - (CH2)0(CHR61)SNR33R34;
-(CH2)0(CHR61)SOCONR33R75; -(CH2)0(CHR61)SNR20CONR33R82; -(CH2)0(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)o(CHR61)s S02R62; or -(CH2)0(CHR61)SC6H4R8;
R22 is H; alkyl; alkenyl; -(CH2)0(CHR6I)S0R55; -(CH2)0(CHR61)SSR56; - (CH2)0(CHR61)SNR33R34;
-(CH2)o(CHR6I)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR6I)sCOOR57; -(CH2)0(CHR61)sCONR58R59; -(CH2)0(CHR6I)sPO(OR60)2; -(CH2)„(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8;
R23 is alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR6I)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR6I)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R24 is alkyl; alkenyl; -(CH2)0(CHR61)s0R55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR6,)SC6H4R8; R25 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; -(CH2)m(CHR61)sNR33R34; -(CH2)ra(CHR61)sOCONR33R75;
-(CH2)m(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR6I)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)sS02R62; or -(CH2)0(CHR61)SC6H4R8; R26 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)sCOOR57; - (CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR6l)sPO(OR60)2; -(CH2)0(CHR6I)S S02R62; or -(CH2)0(CHR61)SC6H4R8; or R25 and R26 taken together can form: -(CH2)2.6-; -(CH2)rO(CH2)r-; -(CH2)rS(CH2)r-; or -(CH2)rNR57(CH2)r-; R27 is H; alkyl; alkenyl; -(CH2)0(CHR61)SOR55; -(CH2)0(CHR61)SSR56; - (CH2)o(CHR6I)sNR33R34;
-(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR6I)sCONR58R59; -(CH2)„(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sPO(OR60)2;
-(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R28 is alkyl; alkenyl; -(CH2)0(CHR61)s-0R55; -(CH2)0(CHR61)S SR56; -(CH2)0(CHR61)S NR33R34;
-(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)s COOR57; -(CH2)0(CHR61)S CONR58R59; -(CH2)0(CHR61)S PO(OR60)2;
-(CH2)o(CHR61)s S02R62; or -(CH2)0(CHR61)S C6H4R8; R29 is alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)„(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)„(CHR61)sCOOR57; -(CH2)o(CHR6I)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8;
R30 is H; alkyl; alkenyl; or aryl-lower alkyl;
R31 is H; alkyl; alkenyl; -(CH2)p(CHR61)sOR55; -(CH2)P(CHR61)SNR33R34; -(CH2)P(CHR61)SOCONR33R75; -(CH2)P(CHR6I)SNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)sS02R62; or -(CH2)0(CHR6,)S C6H4R8;
R32 is H; lower alkyl; or aryl-lower alkyl;
R33 is H; alkyl, alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sNR34R63; -(CH2)m(CHR61)sOCONR75R82; -(CH2)m(CHR61)sNR20CONR78R82; -(CH2)o(CHR61)sCOR64; -(CH2)o(CHR61)s-CONR58R59, -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8;
R34 is H; lower alkyl; aryl, or aryl-lower alkyl; R33 and R34 taken together can form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
Figure imgf000015_0001
R35 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR6I)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)p(CHR61)sCOOR57; -(CH2)p(CHR61)sCOKR58R59; -(CH2)p(CHR6l)sPO(OR60)2; -(CH2)p(CHR61)sS02R62; or -(CH2)P(CHR61)S C6H4R8; R36 is H, alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)P(CHR61)SNR33R34; -(CH2)p(CHR61)sOCONR33R75; -(CH2)P(CHR61)SNR20CONR33R82;
-(CH2)p(CHR61)sCOOR57; -(CH2)p(CHR61)sCONR58R59; -(CH2)p(CHR61)sPO(OR60)2; -(CH2)p(CHR61)sS02R62; or -(CH2)0(CHR61)S C6H4R8; R37 is H; F; Br; CI; N02; CF3; lower alkyl; -(CH2)p(CHR6I)s0R55; -(CH2)p(CHR61)sNR33R34; -(CH2)p(CHR61)sOCONR33R75; -(CH2)p(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)0(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2;
-(CH2)o(CHR61)sS02R62; or -(CH2)0(CHR61)S C6H4R8; R38 is H; F; Br; CI; N02; CF3; alkyl; alkenyl; -(CH2)p(CHR61)sOR55; -(CH2)P(CHR61)SNR33R34; -(CH2)p(CHR61)sOCONR33R75; -(CH2)p(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)o(CHR61)sS02R62; or -(CH2)0(CHR6I)SC6H4R8;
R39 is H; alkyl; alkenyl; or aryl-lower alkyl; R40 is H; alkyl; alkenyl; or aryl-lower alkyl;
R41 is H; F; Br; CI; N02; CF3; alkyl; alkenyl; -(CH2)p(CHR61)sOR55; -(CH2)P(CHR6,)SNR33R34; -(CH2)p(CHR61)sOCONR33R75; -(CH2)p(CHR61)sNR20CONR33R82; -(CH2)o(CHR6,)sCOOR57; -(CH2)0(CHR61)SCONR58R59; -(CH2)0(CHR61)SPO(OR60)2;
-(CH2)0(CHR61)sS02R62; or -(CH2)0(CHR61)S C6H4R8; R42 is H; F; Br; CI; N02; CF3; alkyl; alkenyl; -(CH2)p(CHR61)sOR55; -(CH2)P(CHR61)SNR33R34; -(CH2)p(CHR61)sOCONR33R75; -(CH2)p(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)sS02R62; or -(CH2)0(CHR61)S H4R8;
R43 is H; alkyl; alkenyl; -(CH2)m(CHR61)s0R55; -(CH2)ra(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)sS02R62; or -(CH2)0(CHR6,)S C6H4R8; R44 is alkyl; alkenyl; -(CH2)r(CHR61)s0R55; -(CH2)r(CHR61)sSR56; -(CH2)r(CHR61)sNR33R34; -(CH2)r(CHR61)sOCONR33R75; -(CH2)r(CHR61)sNR20CONR33R82; -(CH2)r(CHR61)sCOOR57; -(CH2)r(CHR6l)sCONR58R59; -(CH2)r(CHR61)sPO(OR60)2; -(CH2)r(CHR61)s S02R62; or -(CH2)r(CHR61)sC6H4R8; R45 is H; alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR6,)SSR56; - (CH2)0(CHR61)SNR33R34;
-(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)s(CHR61)sCONR58R59; -(CH2)s(CHR61)sPO(OR60)2; -(CH2)s(CHR61)s S02R62; or -(CH2)S(CHR61)SC6H4R8;
R45 is H; alkyl; alkenyl; or -(CH2)0(CHR61)PC6H4R8; R47 is H; alkyl; alkenyl; or -(CH2)0(CHR6I)sOR55; R48 is H; lower alkyl; lower alkenyl; or aryl-lower alkyl;
R49 is H; alkyl; alkenyl; -(CHR61)sCOOR57; (CHR61)sCONR58R59; (CHR61)SPO(OR60)2; -(CHR61)sSOR62; or -(CHR^ H^ ;
R50 is H; lower alkyl; or aryl-lower alkyl;
R51 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)sCOOR57; -(CH2)0(CHR61)sCONR58R59; -(CH2)o(CHR61)pPO(OR60)2;
-(CH2)P(CHR6,)S S02R62; or -(CH2)P(CHR61)SC6H4R8; R52 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)sCOOR57; -(CH2)0(CHR61)sCONR58R59; -(CH2)o(CHR61)pPO(OR60)2;
-(CH2)P(CHR61)S S02R62; or -(CH2)P(CHR61)SC6H4R8; R53 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR55; - (CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)sCOOR57; -(CH2)o(CHR6I)sCONR58R59; -(CH2)o(CHR61)pPO(OR60)2;
-(CH2)P(CHR61)S S02R62; or -(CH2)p(CHR61)sC6H4R8; R54 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)COOR57; -(CH2)0(CHR61)SCONR58R59; or -(CH2)0(CHR61)S QsH^8; R55 is H; lower alkyl; lower alkenyl; aryl-lower alkyl; -(CH2)m(CHR61)sOR57; -(CH2)m(CHR61)sNR34R63; -(CH2)m(CHR61)sOCONR75R82;
-(CH2)m(CHR61)sNR20CONR78R82; -(CH2)o(CHR61)s-COR64; -(CH2)0(CHR6,)COOR57; or -(CH2)o(CHR61)sCONR58R59; R56 is H; lower alkyl; lower alkenyl; aryl-lower alkyl; -(CH2)m(CHR61)sOR57; -(CH2)m(CHR61)sNR34R63; -(CH2)m(CHR61)sOCONR75R82; -(CH2)m(CHR61)sNR20CONR78R82; -(CH2)0(CHR61)s-COR64; or -(CH2)o(CHR61)sCONR58R59; R57 is H; lower alkyl; lower alkenyl; aryl lower alkyl; or heteroaryl lower alkyl;
R58 is H; lower alkyl; lower alkenyl; aryl; heteroaryl; aryl-lower alkyl; or heteroaryl-lower alkyl;
R59 is H; lower alkyl; lower alkenyl; aryl; heteroaryl; aryl-lower alkyl; or heteroaryl-lower alkyl; or R58 and R59 taken together can form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; R60 is H; lower alkyl; lower alkenyl; aryl; or aryl-lower alkyl;
R61 is alkyl; alkenyl; aryl; heteroaryl; aryl-lower alkyl; heteroaryl-lower alkyl; -(CH^OR55; -(CH2)mNR33R34; -(CH2)mOCONR75R82; -(CH2)mNR20CONR78R82; -(CH2)0COOR37; -(CH2)0NR58R59; or -(CH2)oPO(COR60)2;
R62 is lower alkyl; lower alkenyl; aryl, heteroaryl; or aryl-lower alkyl;
R63 is H; lower alkyl; lower alkenyl; aryl, heteroaryl; aryl-lower alkyl; heteroaryl-lower alkyl;
-COR64; -COOR57; -CONR58R59; -S02R62; or -PO(OR60)2; R34and R63 taken together can form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-;
R64 is H; lower alkyl; lower alkenyl; aryl; heteroaryl; aryl-lower alkyl; heteroaryl-lower alkyl; -(CH2)p(CHR61)sOR65; -(CH2)P(CHR61)SSR66; or -(CH2)P(CHR61)SNR34R63; -(CH2)P(CHR61)SOCONR75R82; -(CH2)P(CHR61)SNR20CONR78R82; R65 is H; lower alkyl; lower alkenyl; aryl, aryl-lower alkyl; heteroaryl-lower alkyl; -COR57; -COOR57; or -CONR58R59;
R66 is H; lower alkyl; lower alkenyl; aryl; aryl-lower alkyl; heteroaryl-lower alkyl; or -CONR58R59;
Z and Z1 are chains of n and, respectively, n' α-amino acid residues whereby either n is 4 and n' is 6 or n is 5 and n' is 7, the positions of said amino acid residues in said chain Z being counted starting from the N-terminal amino acid and the positions of said amino acid residues in said chain Z1 being counted starting from the C-terminal amino acid, whereby these amino acid residues are, depending on their position in the chains, Gly, or Pro, or of one of the types C: -NR20CH(R72)CO-; D: -NR20CH(R73)CO-; E: -NR20CH(R74)CO-; F: -NR20CH(R84)CO-; and H: -NR20-CH(CO-)-(CH2)4-7-CH(CO-)-NR20-;
-NR20-CH(CO-)-(CH2)pSS(CH2)p-CH(CO-)-NR20-;
-NR20-CH(CO-)-(-(CH2)pNR20CO(CH2)p-CH(CO-)-NR20-;
-NR20-CH(CO-)-(-(CH2)pNR20CONR20(CH2)p-CH(CO-)-NR20-; and I: -NR86CH2CO-; R71 is lower alkenyl; -(CH2)p(CHR61)sOR75; -(CH2)P(CHR61)SSR75;
-(CH2)p(CHR61)sOCONR33R75;
-(CH2)0(CHR61)sCOOR75; -(CH2)pCONR58R59; -(CH2)pPO(OR62)2; -(CH2)pS02R62; or
-(CH2)o-C6R67R68R69R70R76; R72 is H, lower alkyl; lower alkenyl; -(CH2)p(CHR6I)sOR85; or -(CH2)p(CHR61)sSR85; R73 is -(CH2)0R77; -(CH2)rO(CH2)0R77; -(CH^S CH,)^77; or -(CH2)rNR20(CH2)„R77;
R74 is -(CH2)pNR78R79; -(CH2)PNR77R80; -(CH2)PC(=NR80)NR78R79; -(CH2)PC(=NOR50)NR78R79;
-(CH2)pC(=NNR78R79)NR78R79; -(CH2)pNR80C(=NR80)NR78R79;
-(CH2)pN=C(NR78R80)NR79R80;-(CH2)pC6H4NR78R79; -(CH2)pC6H4NR77R80;
-(CH2)pC6H4C(=NR80)NR78R79; -(CH2)pC6H4C(=NOR50)NR78R79; -(CH2)PC6H4C(=N R78R79)NR78R79; -(CH2)PC6H4NR80C(=NR80)NR78R79;
-(CH2)pC6H4N=C(NR78R80)NR79R80; -(CH2)rO(CH2)mNR78R79; -(CH2)rO(CH2)mNR77R80;
-(CH2)rO(CH2)pC(=NR80)NR78R79; -(CH2)rO(CH2)pC(=NOR50)NR78R79;
-(CH2)rO(CH2)pC(=NNR78R79)NR78R79; -(CH2)rO(CH2)mNR80C(=NR80)NR78R79;
-(CH2)rO(CH2)mN=C(NR78R80)NR79R80; -(CH2)rO(CH2)pC6H4CNR78R79; -(CH2)rO(CH2)pC6H4C(=NR80)NR78R79; -(CH2)rO(CH2)pC6H4C(=NOR50)NR78R79;
-(CH2)rO(CH2)pC6H4C(=NNR78R79)NR78R79;
-(CH2)rO(CH2)pC6H4NR80C(=NR80)NR78R79; -(CH2)rS(CH2)raNR78R79;
-(CH2)rS(CH2)mNR77R80;-(CH2)rS(CH2)pC(=NR80)NR78R79;
-(CH2)rS(CH2)pC(=NOR50)NR78R79; -(CH2)rS(CH2)pC(=NNR78R79)NR78R79; -(CH2)rS(CH2)mNR8OC(=NR80)NR78R79; -(CH2)rS(CH2)mN=C(NR78R80)NR79R80;
-(CH2)rS(CH2)pC6H4CNR78R79; -(CH2)rS(CH2)pC6H4C(=NR80)NR78R79;
-(CH2)rS(CH2)pC6H4C(=NOR50)NR78R79; -(CH2)rS(CH2)pC6H4C(=NNR78R79)NR78R79;
-(CH2)rS(CH2)pC6H4NR80C(=NR80)NR78R79; -(CH2)pNR80COR 4; -(CH2)pNR80COR77;
-(CH2)PNR80CONR78R79; or -(CH2)PC6H4NR80CONR78R' 79. R75 is lower alkyl; lower alkenyl; or aryl-lower alkyl;
R33 and R75 taken together can form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; R75 and R82 taken together can form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-;
R76 is H; lower alkyl; lower alkenyl; aryl-lower alkyl; -(CH2)0OR72; -(CH2)0SR72;
-(CH2)0NR33R34; -(CH2)0OCONR33R75; -(CH2)oNR20CONR33R82;
-(CH2)0COOR75; -(CH2)0CONR58R59; -(CH2)oPO(OR60)2; -(CH2)PS02R62; or
-(CH2)oC0R64; R77 is -C6R67R68Rδ9R70R76; or a heteroaryl group of one of the formulae
Figure imgf000020_0001
H1 H2 H3 H4 H5
Figure imgf000020_0002
H6 H7 H8 H9 H10
Figure imgf000020_0003
H11 H12 H13 H14 H15
Figure imgf000020_0004
H16 H17 H18 H19 H20
Figure imgf000020_0005
H21 H22 H23 H24 H25
Figure imgf000021_0001
H26 H27 H28 H29
Figure imgf000021_0002
H30 H31 H32 H33
Figure imgf000021_0003
H34 H35 H36 H37
Figure imgf000021_0004
H42 H43 H44 H45
Figure imgf000021_0005
H46 H47 H48 H49
Figure imgf000021_0006
H50 H51 H52 H53 H54 R78 is H; lower alkyl; aryl; or aryl-lower alkyl;
R78 and R82 taken together can form: -(CH2)MS -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; R79 is H; lower alkyl; aryl; or aryl-lower alkyl; or
R78 and R79, taken together, can be -(CH2)2.7-; -(CH2)20(CH2)2-; or -(CH2)2NR57(CH2)2-;
R80 is H; or lower alkyl;
R81 is H; lower alkyl; or aryl-lower alkyl;
R82 is H; lower alkyl; aryl; heteroaryl; or aryl-lower alkyl; R33 and R82 taken together can form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-;
R83 is H; lower alkyl; aryl; or -NR78R79;
R84 is -(CH2)pCONR78R79; -(CH2)PNR80CONR78R79; -(CH2)pC6H4CONR78R79; or
-(CH2)PC6H4NR80CONR78R79;
R is lower alkyl; or lower alkenyl;
R86 is R74; -[(CH2)u-X]r(CH2)vNR78R79; -[(CH2)u-X]t-(CH2)v-C(=NR80)NR78R79; X is -0-, -NR20-, -S-, OCOO-, u is 1-3, t is 1-6, v is 1-3;
with the proviso that in said chains Z and Z1 of n and , respectively, n' α-amino acid residues
if n is 4 and n' is 6, the amino acid residues in positions 1 to 4 of Z and in positions 1' to 6' of
Z1 are:
of type C or of type D or of type E or of type F, or the residue is Pro; of type E or of type F; of type F, or the residue is Pro; of type E;
of type C or of type D or of type E or of type F, or the residue is Gly; of type D or of type C; of type F or the residue is Pro; of type D or of type C; of type E, or of type F or the residue is Pro; and of type E or of type F, or the residue is Pro; or
P3 and P3', taken together, can form a group of type H;
and
if n is 5 and n' is 7, the amino acid residues in positions 1 to 5 of Z and in positions 1' to 7 of Z1 are:
PI of type C or of type D or of type E or of type F, or the residue is Pro; P2 of type E or of type F; P3 of type F, or the residue is Pro; P4 of type F; P5 of type E Pi': of type C or of type D or of type E or of type F, or the residue is Pro;
P2': of type F;
P3': of type D or the residue is Pro; - P4': of type E or of type F;
P5': of type D, or the residue is Pro;
P6': of type E or of type F, or the residue is Pro; and
P7': oftype E or of type I, or the residue is Gly; or
- P2 and P2' and/or P4 and P4', taken together, can form a group of type H; at P7' also D-isomers being possible,
and pharmaceutically acceptable salts thereof.
In accordance with the present invention these β-hairpin peptidomimetics can be prepared by a process which comprises
(a) coupling an appropriately functionalized solid support with an appropriately N- protected derivative of that amino acid which in the desired end-product is in position 4 of Z if n is 4 or in position 5 of Z if n is 5, any functional group which may be present in said N- protected amino acid derivative being likewise appropriately protected;
(b) removing the N-protecting group from the product thus obtained;
(c) coupling the product thus obtained with an appropriately N-protected derivative of that amino acid which in Z of the desired end-product is one position nearer the N-terminal amino acid residue, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected;
(d) removing the N-protecting group from the product thus obtained;
(e) repeating steps (c) and (d) until the N-terminal amino acid residue of Z has been introduced; (f) coupling the product thus obtained with a compound of the general formula
Figure imgf000025_0001
II wherein
Figure imgf000025_0002
is as defined above and X is an N-protecting group or, if
Figure imgf000025_0003
is to be group (al), or (a2), above, alternatively
(fa) coupling the product obtained in step (e) with an appropriately N-protected derivative of an amino acid of the general formula
HOOC-B-H III or HOOC-A-H IV wherein B and A are as defined above , any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected;
(fb) removing the N-protecting group from the product thus obtained; and
(fc) coupling the product thus obtained with an appropriately N-protected derivative of an amino acid of the above general formula IV and, respectively, III, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected; or if
Figure imgf000026_0001
is to be group (a3), above, alternatively
(fa') coupling the product obtained in step (e) with an appropriately N-protected derivative of an amino acid of the above general formula III, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected; (fb') removing the N-protecting group from the product thus obtained; and
(fc') coupling the product thus obtained with an appropriately N-protected derivative of an amino acid of the above general formula III, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected; (g) removing the N-protecting group from the product obtained in step (f) or (fc) or (fc1); (h) coupling the product thus obtained with an appropriately N-protected derivative of that amino acid which in the desired end-product is in position 1 of Z1, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected; (i) removing the N-protecting group from the product thus obtained;
(j) coupling the product thus obtained with an appropriately N-protected derivative of that amino acid which in the desired end-product is one position farther away from position 1 of Z1, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected; (k) removing the N-protecting group from the product thus obtained;
(1) repeating steps (j) and (k) until all amino acid residues of Z1 have been introduced; (m) if desired, selectively deprotecting one or several protected functional group(s) present in the molecule and appropriately substituting the reactive group(s) thus liberated; (n) if desired, forming one or two interstrand linkage(s) between side-chains of appropriate amino acid residues at opposite positions of the β-strand region; (o) detaching the product thus obtained from the solid support and removing any protecting groups present on functional groups of any members of the chain of amino acid residues and, if desired, any protecting group(s) which may in addition be present in the molecule; and (p) if desired, converting the product thus obtained into a pharmaceutically acceptable salt or converting a pharmaceutically acceptable, or unacceptable, salt thus obtained into the corresponding free compound of formula I or into a different, pharmaceutically acceptable, salt..
Introducing an amino acid residue of type I can, alternatively, be effected by coupling with a leaving group-containing acetylating agent, such as bromo, chloro or iodo acetic acid, followed by nucleophilic displacement with an amine of the formula H2NR86 which, if necessary, is appropriately protected.
The peptidomimetics of the present invention can also be enantiomers of the compounds of formula I. These enantiomers can be prepared by a modification of the above process in which enantiomers of all chiral starting materials are used.
As used in this description, the term "alkyl", taken alone or in combinations, designates saturated, straight-chain or branched hydrocarbon radicals having up to 24, preferably up to 12, carbon atoms. Similarly, the term "alkenyl" designates straight chain or branched hydrocarbon radicals having up to 24, preferably up to 12, carbon atoms and containing at least one or, depending on the chain length, up to four olefinic double bonds. The term "lower" designates radicals and compounds having up to 6 carbon atoms. Thus, for example, the term "lower alkyl" designates saturated, straight-chain or branched hydrocarbon radicals having up to 6 carbon atoms, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert.- butyl and the like. The term "aryl" designates aromatic carbocyclic hydrocarbon radicals containing one or two six-membered rings, such as phenyl or naphthyl, which may be substituted by up to three substituents such as Br, CI, F, CF3, N02, lower alkyl or lower alkenyl. The term "heteroaryl" designates aromatic heterocyclic radicals containing one or two five- and/or six-membered rings, at least one of them containing up to three heteroatoms selected from the group consisting of O, S and N and said ring(s) being optionally substituted; representative examples of such optionally substituted heteroaryl radicals are indicated hereinabove in connection with the definition of R77. The structural element -A-CO- designates amino acid building blocks which in combination with the structural element -B-CO- form templates (al) and (a2). The structural element -B- CO- forms either alone or in combination with another structural element -B-CO- templates (a4) and (a3). Templates (a) through (p) constitute building blocks which have an N-terminus and a C-terminus oriented in space in such a way that the distance between those two groups may lie between 4.0-5.5A. A peptide chain Z is linked to the C-terminus of the templates (a) through (p) via the N-terminus, and the corresponding N-terminus of the template is linked to the C-terminus of Z1 to form a β-hairpin structure such as that depicted in formula I. In a case as here where the distance between the N- and C- termini of the template lies between 4.0-5.5A the template will induce the H-bond network necessary for the formation of a β-hairpin conformation within the peptide chain Z and _}. Thus template and peptide chains form a β- hairpin mimetic. The β-hairpin conformation is highly relevant for the CXCR4 antagonizing activity of the β-hairpin mimetics of the present invention.
Building blocks A1-A69 belong to a class of amino acids wherein the N-terminus is a secondary amine forming part of a ring. Among the genetically encoded amino acids only proline falls into this class. The configuration of building block Al through A69 is (D), and they are combined with a building block -B-CO- of (L)-configuration. Preferred combinations for templates (al) are-DAl-CO-LB-CO- to DA69-CO-LB-CO-. Thus, for example, DPro-LPro constitutes the prototype of templates (al). Less preferred, but also possible are combinations where templates (a2) are -LAl-CO-DB-CO- to LA69-CO-DB-CO-. Thus, for example, LPro- DPro constitutes a less preferred prototype of template (a2).
It will be appreciated that building blocks -Al-CO- to -A69-CO- in which A has (D)- configuration, are carrying a group R1 at the α-position to the N-terminus. The preferred values for R1 are H and lower alkyl with the most preferred values for R1 being H and methyl. It will be recognized by those skilled in the art, that A1-A69 are shown in (D)-configuration which, for R1 being H and methyl, corresponds to the (Reconfiguration. Depending on the priority of other values for R1 according to the Cahn, Ingold and Prelog-rules, this configuration may also have to be expressed as (S). hi addition to R1 building blocks -Al-CO- to -A69-CO- can carry an additional substituent designated as R2 to R17. This additional substituent can be H, and if it is other than H, it is preferably a small to medium-sized aliphatic or aromatic group. Examples of preferred values for R2 to R17 are: - R2: H; lower alkyl; lower alkenyl; (CH2)mOR55 (where R55: lower alkyl; or lower alkenyl); (CH2)mSR56 (where R56: lower alkyl; or lower alkenyl); (CH2)mNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; R33 and R34 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; R57: H; or lower alkyl); (CH2)mOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0N(R20)COR64(where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; or lower alkyl; or R58 and R59 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60 : lower alkyl; or lower alkenyl); -(CH2)0SO2R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R3: H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mSR56 (where R5δ: lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: - (CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); (CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or
Figure imgf000030_0001
(where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy). - R4: H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mSR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: - (CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mN(R20)COR64(where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; or lower alkyl; or R58 and R59 taken together form: -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl;or lower alkoxy).
R5: lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)00C0NR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; R57: where H; or lower alkyl); (CH2)0NR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); (CH2)oN(R20)COR64(where: R20: H; or lower alkyl; R64: alkyl; alkenyl; aryl; and aryl-lower alkyl; heteroaryl-lower alkyl); -(CH2)0C00R57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; or lower alkyl; or R58 and R59 taken together form: - (CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy). - R6: H; lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56 : lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; or lower alkyl; or R58 and R59 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60 : lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R7: lower alkyl; lower alkenyl; -(CH2)qOR55 (where R55 : lower alkyl; or lower alkenyl); -(CH2)qSR56 (where R56 : lower alkyl; or lower alkenyl); -(CH2)qNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)qOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); (CH2)qNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)qN(R20)COR6 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)rCOOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)qCONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; or lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)rPO(OR60)2 (where R60 : lower alkyl; or lower alkenyl); (CH2)rS02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy). - R8: H; F; CI; CF3; lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); (CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: - (CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0N(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl);
-(CH2)0COOR57 (where R57 : lower alkyl; or lower alkenyl); -(CH2)0CONRS8R59 (where R58 : lower alkyl; or lower alkenyl; and R59: H; or lower alkyl; or R58 and R59 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or
Figure imgf000032_0001
(where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R9: lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oN(R20)COR64(where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R5 : lower alkyl; or lower alkenyl; and R59: H; or lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy). - R10: lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0N(R20)COR64(where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R1 ' : H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mSR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: - (CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR6C))2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy). - R12: H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mSR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: - (CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)2O(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)rCOOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)rCONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; or lower alkyl; or R58 and R59 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)rPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R13: lower alkyl; lower alkenyl; -(CH2)qOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)qSR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)qNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)qOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; orR33 and R75 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)qNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)qN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)rC0057 (where R57: lower alkyl; or lower alkenyl); -(CH2)qCONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; or lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)rPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)rS02R62 (where R62: lower alkyl; or lower alkenyl); or
-(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy). - R14: H; lower alkyl; lower alkenyl; -(CH2)raOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mSR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: - (CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mN(R20)COR64 (where: R20: H; lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; or lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R15: lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0NR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); (CH2)oN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); particularly favoured are NR20COlower alkyl (R20=H; or lower alkyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl, or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60 : lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy). - R16: lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0NR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0N(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; or lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R17: lower alkyl; lower alkenyl; -(CH2)q0R55 (where R55: lower alkyl; or lower alkenyl); -(CH2)qSR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)qNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)qOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)qNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)qN(R20)COR64(where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)rCOOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)qCONR5 R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)rPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)rS02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy). >
Among the building blocks Al to A69 the following are preferred: A5 with R2 being H, A8, A22, A25, A38 with R2 being H, A42, A47, and A50. Most preferred are building blocks of type A8':
Figure imgf000037_0001
A8' 0 wherein R >20 i •s T HT o „_r 1 lo„„w„er alkyl; an ,dJ r R»64 . is alkyl; alkenyl; aryl; aryl-lower alkyl; or heteroaryl- lower alkyl; especially those wherein R64 is n-hexyl (A8'-l); n-heptyl (A8'-2); 4- (phenyl)benzyl (A8'-3); diphenylmethyl (A8'-4); 3-amino-propyl (A8'-5); 5-amino-pentyl (A8'-6); methyl (A8'-7); ethyl (A8*-8); isopropyl (A8'-9); isobutyl (A8*-10); n-propyl (A81- 11); cyclohexyl (A8'-12); cyclohexylmethyl (A8*-13); n-butyl (A8'-14); phenyl (A8'-15); 5 benzyl (A8'-16); (3-indolyl)methyl (A8'-17); 2-(3-indolyl)ethyl (A8'-18); (4-phenyl)phenyl (A8'-19); andn-nonyl (A8'-20).
Building block A70 belongs to the class of open-chain α-substituted α-amino acids, building blocks A71 and A72 to the corresponding β-amino acid analogues and building blocks A73- 0 A104 to the cyclic analogues of A70. Such amino acid derivatives have been shown to constrain small peptides in well defined reverse turn or U-shaped conformations (C. M. Venkatachalam, Biopolymers, 1968, 6, 1425-1434; W. Kabsch, C Sander, Biopolymers 1983, 22, 2577). Such building blocks or templates are ideally suited for the stabilization of β-hairpin conformations in peptide loops (D. Obrecht, M. Altorfer, J. A. Robinson, "Novel Peptide 5 Mimetic Building Blocks and Strategies for Efficient Lead Finding", Adv. Med Chem. 1999, Vol.4, 1-68; P. Balaram, "Non-standard amino acids in peptide design and protein engineering", Curr. Opin. Struct. Biol. 1992, 2, 845-851; M. Crisma, G. Valle, C. Toniolo, S. Prasad, R. B. Rao, P. Balaram, "β-turn conformations in crystal structures of model peptides containing α,α- disubstituted amino acids", Biopolymers 1995, 35, 1-9; V. J. Hruby, F. Al- Obeidi, W. Kazmierski, Biochem. J. 1990, 268, 249-262).
It has been shown that both enantiomers of building blocks -A70-CO- to A104-CO- in combination with a building block -B-CO- of L-configuration can efficiently stabilize and induce β-hairpin conformations (D. Obrecht, M. Altorfer, J. A. Robinson, "Novel Peptide Mimetic Building Blocks and Strategies for Efficient Lead Finding", Adv. Med Chem. 1999, Vol.4, 1-68; D. Obrecht, C. Spiegler, P. Schδnholzer, K. Mϋller, H. Heimgartner, F. Stierli, Helv. Chim. Acta 1992, 75, 1666-1696; D. Obrecht, U. Bohdal, J. Daly, C. Lehmann, P. Schόnholzer, K. Mϋller, Tetrahedron 1995, 51, 10883-10900; D. Obrecht, C. Lehmann, C. Ruffieux, P. Schδnholzer, K. Mϋller, Helv. Chim. Acta 1995, 78, 1567-1587; D. Obrecht, U. Bohdal, C. Broger, D. Bur, C. Lehmann, R. Ruffieux, P. Schδnholzer, C. Spiegler, Helv. Chim. Acta 1995, 78, 563-580; D. Obrecht, H. Karajiannis, C. Lehmann, P. Schδnholzer, C. Spiegler, Helv. Chim. Acta 1995, 78, 703-714).
Thus, for the purposes of the present invention templates (al) can also consist of -A70-CO- to A104-CO- where building block A70 to A104 is of either (D)- or (L)-confιguration, in combination with a building block -B-CO- of (L)- configuration.
Preferred values for R20 in A70 to A104 are H or lower alkyl with methyl being most preferred. Preferred values for R18, R19 and R21-R29 in building blocks A70 to A104 are the following: R18: lower alkyl.
R19: lower alkyl; lower alkenyl; -(CH2)pOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)PSR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)PNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form:
-(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)pOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)PNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)PN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)pCOOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)pCONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; or lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH )pS02R62 (where R62: lower alkyl; or lower alkenyl); or
Figure imgf000039_0001
(where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R21: H; lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl, or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); (CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or (CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R22: lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form:
-(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0NR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oN(R20)COR64(where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl, or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF; lower alkyl; lower alkenyl; or lower alkoxy).
R23: H; lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)„SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); particularly favoured are NR20COlower alkyl (R20=H; or lower alkyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl, or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0SO2R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy); R24: lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form:
-(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0N(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); particularly favoured are NR20COlower alkyl (R20=H ; or lower alkyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl, or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)DS02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R25: H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; - (CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R26: H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2) .6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 andR82 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mN(R20)COR6 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
Alternatively, R25 and R26 taken together can be -(CH2)2.5-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl).
R27: H; lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0N(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl, or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R28 : lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form:
-(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.5-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0NR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together foim: -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NRS7(CH2)2-; where R57: H; or lower alkyl); -(CH2)0N(R20)COR64(where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl, or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R29: lower alkyl; lower alkenyl; -(CH2)00R55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)αN(R20)COR64(where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); particularly favored are NR20COlower-alkyl (R20=H; or lower alkyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl, or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)oS02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; CI; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
For templates (b) to (p), such as (bl) and (cl), the preferred values for the various symbols are the following:
R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where
R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -
(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0OCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl);
-(CH2)0NR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl;
R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0N(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; or lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)oS02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy). R20: H; or lower alkyl. - R30: H, methyl.
R31: H; lower alkyl; lower alkenyl; -(CH2)pOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)PNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)pOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; - (CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)PNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)PN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl);
-(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); (-CH2)0CONR58R59 (where R58: lower alkyl, or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)rC6H4R8 (where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy); most preferred is -CH2CONR58R59 (R58: H; or lower alkyl; R59: lower alkyl; or lower alkenyl). R32: H, methyl.
R33: lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mNR34R63 (where R34: lower alkyl; or lower alkenyl; R63: H; or lower alkyl; or R34 and R63 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl) ; (CH2)mOCONR75R82(where R75: lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R75 and R82 taken together form: -(CH2)2-6-; - (CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR78R82 (where R20: H; or lower alkyl; R78: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R78 and R82 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl).
R34: H; or lower alkyl. - R35: H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)m0C0NR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl).
R36: lower alkyl; lower alkenyl; or aryl-lower alkyl. - R37: H; lower alkyl; lower alkenyl; -(CH2)pOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)PNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)P0C0NR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; - (CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl);
-(CH2)pNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)PN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57 : lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl, or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0PO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alky; or lower alkenyl); or
Figure imgf000046_0001
(where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R38: H; lower alkyl; lower alkenyl; -(CH2)pOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)PNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)p0C0NR33R75 (where R33 : H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R78 taken together form: -(CH2)2.6-; - (CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)pNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)PN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl, or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R39: H; lower alkyl; lower alkenyl; -(CH2)m0R55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl).
R40: lower alkyl; lower alkenyl; or aryl-lower alkyl. - R41 : H; lower alkyl; lower alkenyl; -(CH2)pOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)pNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)pOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2) ; where R57: H; or lower alkyl); -(CH2)PNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)pN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl, or lower alkenyl; and R59: H; lower alky; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0PO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R42: H; lower alkyl; lower alkenyl; -(CH2)P0R55 (where R55: lower alkyl; or lower alkenyl); -(CH2)PNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)pOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)pNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)PN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl, or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R43: H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mSR56 (where R56 : lower alkyl; or lower alkenyl); -(CH2)mNR 3R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form:
-(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)m0C0NR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0PO(OR60)2 (where R60: lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62: lower alkyl; or lower alkenyl); or -(CHsJqCβH+R8 (where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R44: lower alkyl; lower alkenyl; -(CH2)pOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)PSR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)PNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NRS7(CH2)2-; where R57: H; or lower alkyl); -(CH2)p0C0NR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; orR33 and R78 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)PNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)PN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)pCOOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)pCONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); or -(CH2)0C6H4R8 (where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R45: H; lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)sOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)0NR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)oN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); or -(CH2)SC6H4R8 (where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R46: H; lower alkyl; lower alkenyl; -(CH2)sOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)SSR56 (where R56: lower alkyl; or lower alkenyl); -(CH2)SNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)sOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)SNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)SN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); or -(CH2)SC6H4R8 (where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy). R47: H; or OR55 (where R55: lower alkyl; or lower alkenyl). R48: H; or lower alkyl.
R49: H;lower alkyl; -(CH2)0COOR57 (where R57 : lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); or (CH2)SC6H4R8 (where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy). R50: H; methyl. - R51 : H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2-5-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); (CH2)m0C0NR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)pCOOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)pCONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59 : H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); or
Figure imgf000050_0001
(where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R52: H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; R57: H; or lower alkyl); -(CH2)mN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)pCOOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)pCONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); or -(CH2)rC6H4R8 (where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R53: H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55: lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33: lower alkyl; or lower alkenyl; R34: H; or lower alkyl; or R33 and R34 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mOCONR33R75 (where R33: H; or lower alkyl; or lower alkenyl; R75: lower alkyl; or R33 and R75 taken together form: -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NRS7(CH2)2-; where R57: H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20: H; or lower alkyl; R33: H; or lower alkyl; or lower alkenyl; R82: H; or lower alkyl; or R33 and R82 taken together form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); -(CH2)mN(R20)COR64 (where: R20: H; or lower alkyl; R64: lower alkyl; or lower alkenyl); -(CH2)PCOOR57 (where R57: lower alkyl; or lower alkenyl); -(CH2)pCONR58R59 (where R58: lower alkyl; or lower alkenyl; and R59: H; lower alkyl; or R58 and R59 taken together form: -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H; or lower alkyl); or
Figure imgf000051_0001
(where R8: H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R54: lower alkyl; lower alkenyl; or aryl-lower alkyl.
Among the building blocks A70 to A104 the following are preferred: A74 with R22 being H, A75, A76, A77 with R22 being H, A78 and A79.
The building block -B-CO- within template (al) through (a4) designates an L-amino acid residue. Preferred values for B are: -NR20CH(R71)- and enantiomers of groups A5 with R2 being H, A8, A22, A25, A38 with R2 being H, A42, A47, and A50. Most preferred are
Asn L-Asparagine
Cys L-Cysteine
Gin L-Glutamine
His L-Histidine
Met L-Methionine
Phe L-Phenylalanine
Pro L-Proline
Ser L-Serine
Thr L-Threonine
Trp L-Tryptophan
Tyr L-Tyrosine
Sar Sarcosine
4AmPhe L-para-Aminophenylalanine
3AmPhe L-meta-Aminophenylalanine
2AmPhe L-ortho-Aminophenylalanine
Phe(mC(NH2)=NH) L-meta-Amidinophenylalanine
Phe(pC(NH2)=NH) L-para-Amidinophenylalanine
Phe(mNHC (NH2)=NH) L-meta-Guanidinophenylalanine
Phe(pNHC (NH2)=NH) L-para-Guanidinophenylalanine
Phg L-Phenylglycine Cha L-Cyclohexylalanine
C4al L-3-Cyclobutylalanine
Csal L-3-Cyclopentylalanine
2-Nal L-2-Naphthylalanine
1-Nal L-1 -Naphthylalanine
4C1-Phe L-4-Chlorophenylalanine
3C1-Phe L-3-Chlorophenylalanine
2C1-Phe L-2-Chlorophenylalanine
3,4C12-Phe L-3 ,4-Dichlorophenylalanine
4F-Phe L-4-Fluorophenylalanine
3F-Phe L-3-Fluorophenylalanine
2F-Phe L-2-Fluorophenylalanine
Tic L-1 ,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid
Thi L-β-2-Thienylalanine
Tza L-2-Thiazolylalanine
Mso L-Methionine sulfoxide
Y(Bzl) L-O-Benzyltyrosine
Bip L-Biphenylalanine
S(Bzl) L-O-Benzylserine
T(Bzl) L-O-Benzylthreonine hCha L-Homo-cyclohexylalanine hCys L-Homo-cysteine hSer L-Homo-serine hPhe L-Homo-phenylalanine
Bpa L-4-Benzoylphenylalanine
Pip L-Pipecolic acid
OctG L-Octylglycine
MePhe L-N-Methylphenylalanine
MeNle L-N-Methylnorleucine
MeAla L-N-Methylalanine
Melle L-N-Methylisoleucine
MeVal L-N-Methvaline
MeLeu L-N-Methylleucine In template (a4), an additional preferred value for the building block -B-CO- is AMPA 3-Aminomethyphenyl acetic acid
In addition, the most preferred values for B also include groups of type A8" of (L)- configuration:
Figure imgf000053_0001
A8" wherein R20 is H or lower alkyl and R64 is alkyl; alkenyl; aryl; aryl-lower alkyl; or heteroaryl- lower alkyl; especially those wherein R64 is n-hexyl (A8"-21); n-heptyl (A8"-22); 4-
(phenyl)benzyl (A8"-23); diphenylmethyl (A8"-24); 3-amino-propyl (A8"-25); 5-amino- pentyl (A8"-26); methyl (A8"-27); ethyl (A8"-28); isopropyl (A8'*-29); isobutyl (A8"-30); n- propyl (A8"-31); cyclohexyl (A8"-32); cyclohexylmethyl (A8"-33); n-butyl (A8"-34); phenyl (A8"-35); benzyl (A8"-36); (3-indolyl)methyl (A8"-37); 2-(3-indolyl)ethyl (A8"-38); (4- phenyl)phenyl (A8' '-39); and n-nonyl (A8' '-40).
The peptidic chains Z and Z1 of the β-hairpin mimetics described herein are generally defined in terms of amino acid residues belonging to one of the following groups:
Group C -NR20CH(R72)CO-; "hydrophobic: small to medium-sized" - Group D -NR20CH(R73)CO-; "hydrophobic: large aromatic or heteroaromatic" Group E -NR20CH(R74)CO-; "polar-cationic" and "urea-derived"
Group F -NR20CH(R84)CO-; "polar-non-charged"
Group H -NR20-CH(CO-)-(CH2)4.7-CH(CO-)-NR20-; -NR20-CH(CO-)-(CH2)pSS(CH2)p-CH(CO-)-NR20-;
-NR20-CH(CO-)-(-(CH2)pNR20CO(CH2)p-CH(CO-)-NR20-; and -NR20-CH(CO-)-(-(CH2)pNR20CONR20(CH2)p-CH(CO-)-NR20-; "interstrand linkage"
Group I -NR86CH2CO-; "polar-cationic" Furthermore, Gly can also be an amino acid residue in chains Z and Z1, and Pro can be an amino acid residue in chains Z and Z1, too, with the exception of positions where interstrand linkages (H) are possible.
Group C comprises amino acid residues with small to medium-sized hydrophobic side chain groups according to the general definition for substituent R72. A hydrophobic residue refers to an amino acid side chain that is uncharged at physiological pH and that is repelled by aqueous solution . Furthermore these side chains generally do not contain hydrogen bond donor groups, such as (but not limited to) primary and secondary amides, primary and secondary amines and the corresponding protonated salts thereof, thiols, alcohols, phosphonates, phosphates, ureas or thioureas. However, they may contain hydrogen bond acceptor groups such as ethers, thioethers, esters, tertiary amides, alkyl- or aryl phosphonates and phosphates or tertiary amines. Genetically encoded small-to-medium-sized amino acids include alanine, isoleucine, leucine, methionine and valine.
Group D comprises amino acid residues with aromatic and heteroaromatic side chain groups according to the general definition for substituent R73. An aromatic amino acid residue refers to a hydrophobic amino acid having a side chain containing at least one ring having a conjugated π-electron system (aromatic group). In addition they may contain hydrogen bond donor groups such as (but not limited to) primary and secondary amides, primary and secondary amines and the corresponding protonated salts thereof, thiols, alcohols, phosphonates, phosphates, ureas or thioureas, and hydrogen bond acceptor groups such as (but not limited to) ethers, thioethers, esters, tetriary amides, alkyl- or aryl phosphonates -and phosphates or tertiary amines. Genetically encoded aromatic amino acids include phenylalanine and tyrosine.
A heteroaromatic amino acid residue refers to a hydrophobic amino acid having a side chain containing at least one ring having a conjugated π-system incorporating at least one heteroatom such as (but not limited to) O, S and N according to the general definition for substituent R77. In addition such residues may contain hydrogen bond donor groups such as (but not limited to) primary and secondary amides, primary and secondary amines and the corresponding protonated salts thereof, thiols, alcohols, phosphonates, phosphates, ureas or thioureas, and hydrogen bond acceptor groups such as (but not limited to) ethers, thioethers, esters, tetriary amides, alkyl- or aryl phosphonates -and phosphates or tertiary amines. Genetically encoded heteroaromatic amino acids include tryptophan and histidine. Group E comprises amino acids containing side chains with polar-cationic, acylamino- and urea-derived residues according to the general definition for substituen R74. Polar-cationic refers to a basic side chain which is protonated at physiological pH. Genetically encoded polar- cationic amino acids include arginine, lysine and histidine. CitruUine is an example for an urea derived amino acid residue.
Group F comprises amino acids containing side chains with polar-non-charged residues according to the general definition for substituent R84. A polar-non-charged residue refers to a hydrophilic side chain that is uncharged at physiological pH, but that is not repelled by aqueous solutions. Such side chains typically contain hydrogen bond donor groups such as (but not limited to) primary and secondary amides, primary and secondary amines, thiols, alcohols, phosphonates, phosphates, ureas or thioureas. These groups can form hydrogen bond networks with water molecules. In addition they may also contain hydrogen bond acceptor groups such as (but not limited to) ethers, thioethers, esters, tetriary amides, alkyl- or aryl phosphonates - and phosphates or tertiary amines. Genetically encoded polar-non-charged amino acids include asparagine, cysteine, glutamine, serine and threonine.
Group H comprises side chains of preferably (L)-amino acids at opposite positions of the β- strand region that can form an interstrand linkage. The most widely known linkage is the disulfide bridge formed by cysteines and homo-cysteines positioned at opposite positions of the β-strand. Various methods are known to form disulfide linkages including those described by: J. P. Tarn et al. Synthesis 1979, 955-957; Stewart et al. , Solid Phase Peptide Synthesis, 2d Ed., Pierce Chemical Company, III., 1984; Ahmed et al. J. Biol. Chem. 1975, 250, 8477-8482 ; and Pennington et al., Peptides, pages 164-166, Giralt and Andreu, Eds., ESCOM Leiden, The Netherlands, 1990. Most advantageously, for the scope of the present invention, disulfide linkages can be prepared using acetamidomethyl (Acm)- protective groups for cysteine. A well established interstrand linkage consists in linking ornithines and lysines, respectively, with glutamic and aspartic acid residues located at opposite β-strand positions by means of an amide bond formation. Preferred protective groups for the side chain amino-groups of omithine and lysine are allyloxycarbonyl (Alloc) and allylesters for aspartic and glutamic acid. Finally, interstrand linkages can also be established by linking the amino groups of lysine and omithine located at opposite β-strand positions with reagents such as N,N-carbonylimidazole to form cyclic ureas.
Group I comprises glycine having the amino group substituted by chains containing polar- cationic residues according to the general definition for substituent R86. Polar-cationic refers to a basic side chain which is protonated at physiological pH.
As mentioned earlier, positions for interstrand linkages are the following: If n is 4 and n' is 6 Postitions P3 and P3' taken together
If n is 5 and n' is 7 Postitions P2 and P2' and/or P4 and P4', taken together
Such interstrand linkages are known to stabilize the β-hairpin conformations and thus constitute an important structural element for the design of β-hairpin mimetics.
Most preferred amino acid residues in chains Z and Z1 are those derived from natural α-amino acids. Hereinafter follows a list of amino acids which, or the residues of which, are suitable for the purposes of the present invention, the abbreviations corresponding to generally adopted usual practice:
three letter code one letter code
Ala L-Alanine A
Arg L-Arginine R
Asn L-Asparagine N
Asp L-Aspartic acid D
Cys L-Cysteine C
Glu L-Glutamic acid E
Gin L-Glutamine Q
Gly Glycine G
His L-Histidine H
He L-Isoleucine I
Leu L-Leucine L Lys L-Lysine K
Met L-Methionine M
Phe L-Phenylalanine F
Pro L-Proline P
DPro D-Proline DP
Ser L-Serine S
Thr L-Threonine T
Trp L-Tryptophan W
Tyr L-Tyrosine Y
Val L-Valine V
Other α-amino acids which, or the residues of which, are suitable for the pi present invention include:
Cit L-Citrulline
Orn L-Omithine tBuA L-t-Butylalanine
Sar Sarcosine
Pen L-Penicillamine t-BuG L-tert.-Butylglycine
4AmPhe L-para-Aminophenylalanine
3AmPhe L-meta-Aminophenylalanine
2AmPhe L-ortho-Aminophenylalanine
Phe(mC(NH2)=NH) L-meta-Amidinophenylalanine
Phe(pC(NH2)=NH) L-para-Amidinophenylalanine
Phe(mNHC (NH2)=NH) L-meta-Guanidinophenylalanine
Phe(pNHC (NH2)=NH) L-para-Guanidinophenylalanine
Phg L-Phenylglycine
Cha L-Cyclohexylalanine
C4al L-3-Cyclobutylalanine
C5al L-3 -Cyclopentylalanine
Nle L-Norleucine
2-Nal L-2-Naphthylalanine
1-Nal L-1 -Naphthylalanine
4C1-Phe L-4-Chlorophenylalanine C1-Phe L-3-Chlorophenylalanine C1-Phe L-2-Chlorophenylalanine
3,4C12-Phe L-3 ,4-Dichlorophenylalanine F-Phe L-4-Fluorophenylalanine
3F-Phe L-3 -Fluorophenylalanine
2F-Phe L-2-Fluorophenylalanine
Tic 1 ,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid
Thi L-β-2-Thienylalanine
Tza L-2-Thiazolylalanine
Mso L-Methionine sulfoxide
AcLys N-Acetyllysine
Dpr 2,3-Diaminopropionic acid
A2Bu 2,4-Diaminobutyric acid
Dbu (S)-2,3-Diaminobutyric acid
Abu γ-Aminobutyric acid (GABA)
Aha ε-Aminohexanoic acid
Aib α-Aminoisobutyric acid
Y(Bzl) L-O-Benzyltyrosine
Bip L-(4-phenyl)phenylalanine
S(Bzl) L-O-Benzylserine
T(Bzl) L-O-Benzylthreonine hCha L-Homo-cyclohexylalanine hCys L-Homo-cysteine hSer L-Homo-serine hArg L-Homo-arginine hPhe L-Homo-phenylalanine
Bpa L-4-Benzoylρhenylalanine
4-AmPyrrl (2S,4S)-4-Amino-pyrrolidine-L-carboxylic acid
4-AmPyrr2 (2S,4R)-4-Amino-pyrrolidine-L-carboxylic acid
4-PhePyrrl (2S,5R)-4-Phenyl-pyrrolidine-L-carboxylic acid
4-PhePyrr2 (2S,5S)-4-Phenyl-pyrrolidine-L-carboxylic acid 5-PhePyrrl (2S,5R)-5-Phenyl-pyrrolidine-L-carboxylic acid 5-PhePyrr2 (2S,5S)-5-Phenyl-pyrrolidine-L-carboxylic acid Pro(4-OH)l (4S)-L-Hydroxyproline
Pro(4-OH)2 (4R)-L-Hydroxyproline
Pip L-Pipecolic acid
DPip D-Pipecolic acid
OctG L-Octylglycine
MePhe L-N-Methylphenylalanine
MeNle L-N-Methylnorleucine
MeAla L-N-Methylalanine
Melle L-N-Methylisoleucine
MeVal L-N-Methylvaline
MeLeu L-N-Methylleucine
W(6-C1) L-6-Cl-Tryptophan
(EA)G N-(2-Aminoethyl)glycine
(PrA)G N-(3 - Amino-n-propyl)glycine
(BA)G N-(4-Amino-n-butyl)glycine
(PeA)G N-(5-Amino-n-pentyl)glycine
(EGU)G N-(2-Guanidinoethyl)glycine
(PrGU)G N-(3-Guanidino-n-propyl)glycine
(BGU)G N-(4-Guanidino-n-butyl)glycine
(PeGU)G N-(5-Guanidino-n-pentyl)glycine
(PEG3-NH2)G N-[(CH2)3θ-(CH2-CH2O)2-(CH2)3-NH2]glycine
Particularly preferred residues for group C are: Ala L-Alanine
He L-Isoleucine
Leu L-Leucine
Met L-Methionine
Val L-Valine tBuA L-t-Butylalanine t-BuG L-tert.-Butylglycine
Cha L-Cyclohexylalanine
C4al L-3-Cyclobutylalanine C5al L-3-Cyclopentylalanine
Nle L-Norleucine hCha L-Homo-cyclohexylalanine
OctG L-Octylglycine MePhe L-N-Methylphenylalanine
MeNle L-N-Methylnorleucine
MeAla L-N-Methylalanine
Melle L-N-Methylisoleucine
MeVal L-N-Methylvaline MeLeu L-N-Methylleucine
Particularly preferred residues for group D are:
His L-Histidine
Phe L-Phenylalanine Trp L-Tryptophan
Tyr L-Tyrosine
Phg L-Phenylglycine
2-Nal L-2-Naphthylalanine
1-Nal L-1-Naphthylalanine 4C1-Phe L-4-Chlorophenylalanine
3C1-Phe L-3-Chlorophenylalanine
2C1-Phe L-2-Chlorophenylalanine
3 ,4C12-Phe L-3 ,4-Dichlorophenylalanine
4F-Phe L-4-Fluorophenylalanine 3F-Phe L-3 -Fluorophenylalanine
2F-Phe L-2-Fluorophenylalanine
Thi L-β-2-Thienylalanine
Tza L-2-Thiazolylalanine
Y(Bzl) L-O-Benzyltyrosine Bip L-Biphenylalanine
S(Bzl) L-O-Benzylserine
T(Bzl) L-O-Benzylthreonine hPhe L-Homo-phenylalanine
Bpa L-4-Benzoylphenylalanine W(6-C1) L-6-Cl-Tryptophan
Particularly preferred residues for group E are
Arg L-Arginine
Lys L-Lysine
Om L-Omithine
Dpr L-2,3-Diaminopropionic acid
A2Bu L-2,4-Diaminobutyric acid
Dbu (S)-2,3-Diaminobutyric acid
F(pNH2) L-para-Aminophenylalanine
Phe(mNH2) L-meta-Aminophenylalanine
Phe(oNH2) L-ortho-Aminophenylalanine hArg L-Homo-arginine
Phe(mC(NH2)=NH) L-meta-Amidinophenylalanine
Phe(pC(NH2)=NH) L-para-Amidinophenylalanine
Phe(mNHC (NH2)=NH) L-meta-Guanidinophenylalanine
Phe(pNHC (NH2)=NH) L-para-Guanidinophenylalanine
Particularly preferred residues for group F are
Asn L-Asparagine
Cys L-Cysteine
Gin L-Glutamine
Ser L-Serine
Thr L-Threonine
Cit L-Citrulline
Pen L-Penicillamine
AcLys L-Nε-Acetyllysine hCys L-Homo-cysteine hSer L-Homo-serine
Particularly preferred residues for group I are
(EA)G N-(2-Aminoethyl)glycine (PrA)G N-(3 -Amino-n-propyl) glycine
(BA)G N-(4-Amino-n-butyl)glycine
(PeA)G N-(5-Amino-n-pentyl)glycine
(EGU)G N-(2-Guanidinoethyl)glycine
(PrGU)G N-(3-Guanidino-n-propyl)glycine
(BGU)G N-(4-Guanidino-n-butyl)glycine
(PeGU)G N-(5-Guanidino-n-pentyl)glycine
(PEG3-NH2)G N-[(CH2)30-(CH2-CH2O)2-(CH2)3-NH2]glycine
As mentioned earlier, the peptidic chains Z and Z1 within the β-hairpin mimetics of the invention comprise 4 and, respectively, 6 residues or 5 and, respectively, 7 residues. The positions P1 to P" and P1 to Pn of each amino acid residue in the chain Z and, respectively, Z1 are unequivocally defined as follows: P1 represents the first amino acid in the chain Z that is coupled with its C-terminus to the N-terminus of the templates (b)-(p) or of group -B-CO- in templates (al), (a3) or (a4) or of group -A-CO- in template (a2), and Pn represents the last amino acid in the chain Z; P1' represents the first amino acid in the chain Z1 that is coupled with its N-terminus to the C-terminus of the corresponding templates (b)-(p) or of group -B- CO- in template (al), (a3) or (a4) or of group -A-CO- in template (a2), and P" represents the last amino acid in the chain Z1.
Each of the positions P1 to Pn or P1' to P"' will preferably contain an amino acid residue belonging to one or two or three of the above types C, D, E, F I, or being Pro or Gly, as follows:
If n is 4 and n1 is 6, the amino acid residues in positions 1 to 4 of Z and the amino acid residues in positions 1' to 6' of Z1 are preferably:
PI of type D or of type E or of type F, or the residue is Pro; P2 of type E or of type F; P3 of type F, or the residue is Pro;
P4 of type E; PI': of type E or of type F, or the residue is Gly;
P2': of type D;
P3': of type F or the residue is Pro;
P4': of type D;
P5': of type E, or of type F or the residue is Pro; and
P6': of type E or of type F, or the residue is Pro; or
P3 and P3', taken together, can form a group of type H.
If n is 5 and n' is 7, the amino acid residues in positions 1 to 5 of Z and the amino acid residues in positions 1' to.7' of Z1 are preferably:
PI of type D or of type E or of type F, or the residue is Pro; P2 of type E or of type F; P3 of type F, or the residue is Pro; P4 of type F; P5 of type E
PI': of type D or of type E or of type F, or the residue is Pro; - PP22'':: of type F; P3': of type D or the residue is Pro; P4': of type F; P5': of type D, or the residue is Pro; P6': of type E or of type F, or the residue is Pro; and - PP77'':: oftype E or of type I, or the residue is Gly; or
P2 and P2' and or P4 and P4', taken together, can form a group of type H; at P7' also D-isomers being possible.
If n is 4 and n' is 6, the amino acid residues in positions 1 to 4 of Z and the amino acid residues in positions 1' to 6' of Z1 are most preferably:
PI Tyr, Arg; P2 Cit, Arg; P3 Cys; - P4: Arg-NH2;
- PI': Lys, Arg;
- P2': Tyr;
- P3': Cys;
- P4': 2-Nal;
- P5': Arg; and
- P6': Arg.
Cys at pos P3 and P3' form a disulfide bridge
Ifn is 5 and n ' is 7, the amino acid residues in positions 1 to 5 of Z and the amino acid residues in positions 1' to 7' of Z1 are most preferably:
- PI: Tyr;
- P2: Arg;
- P3: Cit;
- P4: Cys;
- P5: Arg; Arg-NH2;
- PI': Lys;
- P2': Cit;
- P3': Tyr;
- P4': Cys;
- P5': 2-Nal, Trp, F(pNH2), W(6-C1);
- P6': Arg; and
_ P7': DArg, Arg, Ac-Arg, iPr-Arg, (EA)G, (PrA)G, (BA)G, (EGU)G,
(PrGU)G, (BGU)G. Cys at pos 4 and pos 4' form a disulfide bridge
Particularly preferred β-peptidomimetics of the invention include those described in Examples 6, 7, 8, 10, 12, 15, 20, 21, 22.
The process of the invention can advantageously be carried out as parallel array synthesis to yield libraries of template-fixed β-hairpin peptidomimetics of the above general formula I. Such parallel synthesis allows one to obtain arrays of numerous (normally 24 to 192, typically 96) compounds of general formula I in high yields and defined purities, minimizing the formation of dimeric and polymeric by-products. The proper choice of the functionalized solid- support (i.e. solid support plus linker molecule), and the templates play thereby key roles.
The functionalized solid support is conveniently derived from polystyrene crosslinked with, preferably 1-5%, divinylbenzene; polystyrene coated with polyethyleneglycol spacers (TentagelR); and polyacrylamide resins (see also Obrecht, D.; Villalgordo, J.-M, "Solid- Supported Combinatorial and Parallel Synthesis of Small-Molecular-Weight Compound Libraries", Tetrahedron Organic Chemistry Series, Vol. 17, Pergamon, Elsevier Science, 1998).
The solid support is functionalized by means of a linker, i.e. a bifunctional spacer molecule which contains on one end an anchoring group for attachment to the solid support and on the other end a selectively cleavable functional group used for the subsequent chemical transformations and cleavage procedures. For the purposes of the present invention two types of linkers are used:
Type 1 linkers are designed to release the amide group under acid conditions (Rink H, Tetrahedron Lett. 1987, 28, 3783-3790). Linkers os this kind form amides of the carboxyl group of the amino acids; examples of resins functionalized by such linker structures include 4- [(((2,4-dimethoxyphenyl)Fmoc-aminomethyl)phenoxyacetamido) aminomethyl] PS resin, 4- [(((2,4-dimethoxyphenyl)Fmoc-aminomethyl)phenoxyacetamido) aminomethyl] -4- methylbenzydrylamine PS resin (Rink amide MBHA PS Resin), and 4-[(((2,4- dimethoxyphenyl)Fmoc-aminomethyl)phenoxyacetamido) aminomethyl] benzhydrylamine PS- resin (Rink amide BHA PS resin). Preferably, the support is derived from polystyrene crosslinked with, most preferably 1-5%, divinylbenzene and functionalized by means of the 4- (((2,4-dimethoxyphenyl)Fmoc-aminomethyl)phenoxyacetamido) linker.
Type 2 linkers are designed to eventually release the carboxyl group under acidic conditions. Linkers of this kind form acid-labile esters with the carboxyl group of the amino acids, usually acid-labile benzyl, benzhydryl and trityl esters; examples of such linker structures include 2- methoxy-4-hydroxymethylphenoxy (SasrinR linker), 4-(2,4-dimethoxyphenyl-hydroxymethyl)- phenoxy (Rink linker), 4-(4-hydroxymethyl-3-methoxyphenoxy)butyric acid (HMPB linker), trityl and 2-chlorotrityl. Preferably, the support is derived from polystyrene crosslinked with, most preferably 1-5%, divinylbenzene and functionalized by means of the 2-chlorotrityl linker.
When carried out as a parallel array synthesis the process of the invention can be advantageously carried out as described hereinbelow but it will be immediately apparent to those skilled in the art how these procedures will have to be modified in case it is desired to synthesize one single compound of the above formula I
A number of reaction vessels (normally 24 to 192, typically 96) equal to the total number of compounds to be synthesized by the parallel method are loaded with 25 to 1000 mg, preferably 100 mg, of the appropriate functionalized solid support, preferably 1 to 3% cross linked polystyrene.
The solvent to be used must be capable of swelling the resin and includes, but is not limited to, dichloromethane (DCM), dimethylformamide (DMF), N-methylpyrrolidone (NMP), dioxane, toluene, tetrahydrofuran (THF), ethanol (EtOH), trifluoroethanol (TFE), isopropylalcohol and the like. Solvent mixtures containing as at least one component a polar solvent (e. g. 20% TFE/DCM, 35% THF/NMP) are beneficial for ensuring high reactivity and solvation of the resin-bound peptide chains ( Fields, G. B., Fields, C. G., J. Am. Chem. Soc. 1991, 113, 4202- 4207).
Both the Rink linker that releases the C-terminal carboxylic amide group under acidic conditions and the 2-chlorotrityl linker that releases the C-terminal carboxylic acid group under acidic conditions, are stable to Fmoc deprotection conditions during the peptide synthesis.
The simultaneous release of the side chain protecting groups of the peptide fragment and the release of the peptide from the resin type 1 and type 2 is performed with 95% TFA and dichloromethane and scavencers such as phenol or triisopropylsilane (Bernatowicz, S.B. et al, Tetrahedron Lett., 1989, 30, 4645-4648).
Suitable protecting groups for amino acids and, respectively, for their residues are, for example,
for the amino group (as is present e. g. also in the side-chain of lysine) Cbz benzyloxycarbonyl Boc tert.-butyloxycarbonyl
Fmoc 9-fluorenylmethoxycarbonyl
Alloc allyloxycarbonyl
Teoc trimethylsilylethoxycarbonyl Tec trichloroethoxycarbonyl
Nps o-nitrophenylsulfonyl;
Trt triphenymethyl or trityl
for the carboxyl group (as is present e. g. also in the side-chain of aspartic and glutamic acid) by conversion into esters with the alcohol components
tBu tert-butyl
Bn benzyl
Me methyl
Ph phenyl
Pac Phenacyl
Allyl
Tse trimethylsilylethyl
Tee trichloroethyl;
for the guanidino group (as is present e. g. in the side-chain of arginine)
Pmc 2,2,5,7,8-pentamethylchroman-6-sulfonyl
Ts tosyl (i. e. p-toluenesulfonyl) Cbz benzyloxycarbonyl
Pbf pentamethyldihydrobenzofuran-5-sulfonyl
for the hydroxy group (as is present e. g. in the side-chain of threonine and serine)
tBu tert.-butyl
Bn benzyl
Trt trityl
and for the mercapto group (as is present e. g. in the side-chain of cysteine) Acm acetamidomethyl tBu tert.-butyl
Bn benzyl
Trt trityl
Mtr 4-methoxytrityl.
The 9-fluorenylmethoxycarbonyl- (Fmoc)-protected amino acid derivatives are preferably used as the building blocks for the construction of the template-fixed β-hairpin loop mimetics of formula I. For the deprotection, i. e. cleaving off of the Fmoc group, 20% piperidine in DMF or 2% DBU/2% piperidine in DMF can be used.
N-substituted glycine derivatives (type I) used as building blocks for the construction of certain compounds of formula I are derived from 9-fluorenylmethoxycarbonyl- (Fmoc)-protected amino acid derivatives or alternatively built up in two steps from leaving group-containing glycine precursors, such as bromo, chloro or iodo acetic acid, and suitable primary amine building blocks NH2-R86. The first synthesis step consists of the attachment of the leaving group-containing acetylating agent, such as bromo acetic acid, to the resin bound intermediate through formation of the amide bond. The second reaction step - the nucleophilic displacement - is accomplished using the primary amine building blocks, wherein the residues are, if necessary, suitably protected with groups as described above for side chains of amino acids.
The quantity of the reactant, i. e. of the amino acid derivative, is usually 1 to 20 equivalents based on the milliequivalents per gram (meq/g) loading of the functionalized solid support (typically 0.1 to 2.85 meq/g for polystyrene resins) originally weighed into the reaction tube. Additional equivalents of reactants can be used if required to drive the reaction to completion in a reasonable time. The reaction tubes, in combination with the holder block and the manifold, are reinserted into the reservoir block and the apparatus is fastened together. Gas flow through the manifold is initiated to provide a controlled environment, for example, nitrogen, argon, air and the like. The gas flow may also be heated or chilled prior to flow through the manifold. Heating or cooling of the reaction wells is achieved by heating the reaction block or cooling externally with isopropanol/dry ice and the like to bring about the desired synthetic reactions. Agitation is achieved by shaking or magnetic stirring (within the reaction tube). The preferred workstations (without, however, being limited thereto) are Labsource's Combi-chem station and MultiSyn Tech's-Syro synthesizer. Amide bond formation requires the activation of the α-carboxyl group for the acylation step. When this activation is being carried out by means of the commonly used carbodiimides such as dicyclohexylcarbodiimide (DCC, Sheehan & Hess, J. Am. Chem. Soc. 1955, 77, 1067-1068) or diisopropylcarbodiimide (DIC, Sarantakis et al Biochem. Biophys. Res. Commun.1976, 73, 336-342), the resulting dicyclohexylurea is insoluble and, respectively, diisopropylurea is soluble in the solvents generally used. In a variation of the carbodiimide method 1- hydroxybenzotriazole (HOBt, Kόnig & Geiger, Chem. Ber 1970, 103, 788-798) is included as an additive to the coupling mixture. HOBt prevents dehydration, suppresses racemization of the activated amino acids and acts as a catalyst to improve the sluggish coupling reactions. Certain phosphonium reagents have been used as direct coupling reagents, such as benzotriazol-1-yl- oxy-tris-(dimethylamino)-phosphonium hexafluorophosphate (BOP) (Castro et al., Tetrahedron Lett. 1975, 14, 1219-1222; Synthesis, 1976, 751-752), or benzotriazol-1-yl-oxy-tris- pyrrolidino-phosphonium hexaflurophoshate (Py-BOP, Coste et al., Tetrahedron Lett. 1990, 31, 205-208), or 2-(lH-benzotriazol-l-yl-)l,l,3,3-tetramethyluronium terafluoroborate (TBTU), or hexafluorophosphate (HBTU, Knorr et al., Tetrahedron Lett. 1989, 30, 1927-1930); these phosphonium reagents are also suitable for in situ formation of HOBt esters with the protected amino acid derivatives. More recently diphenoxyphosphoryl azide (DPP A) or 0-(7-aza- benzotriazol-l-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (TATU) or 0-(7-aza- benzotriazol-l-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate (HATU)/7-aza-l- hydroxy benzotriazole (HO At, Carpino et al., Tetrahedron Lett. 1994, 35, 2279-2281) have also been used as coupling reagents.
Due to the fact that near-quantitative coupling reactions are essential it is desirable to have experimental evidence for completion of the reactions. The ninhydrin test (Kaiser et al., Anal. Biochemistry 1970, 34, 595), where a positive colorimetric response to an aliquot of resin- bound peptide indicates qualitatively the presence of the primary amine, can easily and quickly be performed after each coupling step. Fmoc chemistry allows the spectrophotometric detection of the Fmoc chromophore when it is released with the base (Meienhofer et al., Int. J. Peptide Protein Res. 1979, 13, 35-42).
The resin-bound intermediate within each reaction tube is washed free of excess of retained reagents, of solvents, and of by-products by repetitive exposure to pure solvent(s) by one of the two following methods: 1) The reaction wells are filled with solvent (preferably 5 ml), the reaction tubes, in combination with the holder block and manifold, are immersed and agitated for 5 to 300 minutes, preferably 15 minutes, and drained by gravity followed by gas pressure applied through the manifold inlet (while closing the outlet) to expel the solvent;
2) The manifold is removed from the holder block, aliquots of solvent (preferably 5 ml) are dispensed through the top of the reaction tubes and drained by gravity through a filter into a receiving vessel such as a test tube or vial.
Both of the above washing procedures are repeated up to about 50 times (preferably about 10 times), monitoring the efficiency of reagent, solvent, and byproduct removal by methods such as TLC, GC, or inspection of the washings.
The above described procedure of reacting the resin-bound compound with reagents within the reaction wells followed by removal of excess reagents, by-products, and solvents is repeated with each successive transformation until the final resin-bound fully protected linear peptide has been obtained.
Before this fully protected linear peptide is detached from the solid support, it is possible, if desired, to selectively deprotect one or several protected functional group(s) present in the molecule and to appropriately substitute the reactive group(s) thus liberated. To this effect, the functional group(s) in question must initially be protected by a protecting group which can be selectively removed without affecting the remaining protecting groups present. Alloc (allyloxycarbonyl) is an example for such a protecting group for amino which can be selectively removed, e.g. by means of Pd° and phenylsilane in CH2C12, without affecting the remaining protecting groups, such as Fmoc, present in the molecule. The reactive group thus liberated can then be treated with an agent suitable for introducing the desired substituent. Thus, for example, an amino group can be acylated by means of an acylating agent corresponding to the acyl substituent to be introduced.
Before detaching the peptide from the resin and removing the protecting groups from the fully protected peptide, it is also possible, if desired, to cyclize the linear peptide by forming an interstrand linkage between side-chains of appropriate amino acid residues at opposite positions of the β-strand region.
Interstrand linkages and their formation have been discussed above, in connection with the explanations made regarding groups of the type H which can, for example, be disulfide bridges formed by cysteines and homocysteines at opposite positions of the β-strand, or glutamic and aspartic acid residues linking ornithines and, respectively, lysines located at opposite β-strand positions by amide bond formation. The formation of such interstrand linkages can be effected by methods well known in the art. For the formation of disulfide bridges preferably a solution of 10 equivalents of iodine solution in DMF is applied for 1.5 h. The procedure is repeated for another 3h after with a fresh solution after filtering of the iodine solution.
Detachment and complete deprotection of the fully protected peptide from the solid support is achieved by immersion of the reaction tubes, in combination with the holder block and manifold, in reaction wells containing a solution of the cleavage reagent (preferably 3 to 5 ml). Gas flow, temperature control, agitation, and reaction monitoring are implemented as described above and as desired to effect the detachment reaction. The reaction tubes, in combination with the holder block and manifold, are disassembled from the reservoir block and raised above the solution level but below the upper lip of the reaction wells, and gas pressure is applied through the manifold inlet (while closing the outlet) to efficiently expel the final product solution into the reservoir wells. The resin remaining in the reaction tubes is then washed 2 to 5 times as above with 3 to 5 ml of an appropriate solvent to extract (wash out) as much of the detached product as possible. The product solutions thus obtained are combined, taking care to avoid cross-mixing. The individual solutions/extracts are then manipulated as needed to isolate the final compounds. Typical manipulations include, but are not limited to, evaporation, concentration, liquid/liquid extraction, acidification, basification, neutralization or additional reactions in solution.
Alternatively the detachment and complete deprotection of the fully protected peptide from the solid support is achieved manually in glass vessels.
The fully protected peptide derivative of type I is treated with 95% TFA, 2.5% H20, 2.5% TIS or another combination of scavengers for effecting the cleavage of protecting groups. The cleavage reaction time is commonly 30 minutes to 12 hours, preferably about 3.5 hours. The resin is filtered and the cleavage solution containing the peptide is evaporated. The product is dissolved in an acid and water and extracted with isopropyl ether or other solvents which are suitable therefor. After collecting the aqueous layer and optionally oxidizing bridges of type H (Cysteine) by passing air through the aqueous layer and careful removal of the solvent, the cyclic peptide derivative obtained as end-product can be isolated. Depending on its purity, this peptide derivative can be used directly for biological assays, or it has to be further purified, for example by preparative HPLC.
As mentioned earlier, it is thereafter possible, if desired, to convert a fully deprotected product thus obtained into a pharmaceutically acceptable salt or to convert a pharmaceutically acceptable, or unacceptable, salt thus obtained into the corresponding free compound of formula I or into a different, pharmaceutically acceptable, salt. Any of these operations can be carried out by methods well known in the art.
The template starting materials of formula II used in the processes of the invention, pre-starting materials therefor, and the preparation of these starting and pre-starting materials are described in International Application PCT EP02/01711 of the same applicants, published as WO 02/070547 Al.
The starting materials of formula H NR86 are known or can be prepared by methods which are well known in the art.
The β-hairpin peptidomimetics of the invention can be used in a wide range of applications in order to prevent HIV infections in healthy individuals and to slow or halt viral progression in infected patients or to inhibit the growth of cancer cells or to treat inflammatory disorders.
The β-hairpin peptidomimetics may be administered per se or may be applied as an appropriate formulations together with carriers, diluents or excipients well known in the art.
When used to treat or prevent HIV infections or cancer the β-hairpin peptidomimetics can be administered singly, as mixtures of several β-hairpin peptidomimetics, in combination with other anti-HIV agents, or antimicrobial agents or anti cancer agents, or in combination with other pharmaceutically active agents. The β-hairpin peptidomimetics can be administered per se or as pharmaceutical compositions. Pharmaceutical compositions comprising β-hairpin peptidomimetics of the invention may be manufactured by means of conventional mixing, dissolving, granulating, coated tablet-making, levigating, emulsifying, encapsulating, entrapping or lyophilizing processes. Pharmaceutical compositions may be formulated in conventional manner using one or more physiologically acceptable carriers, diluents, excipients or auxilliaries which facilitate processing of the active β-hairpin peptidomimetics into preparations which can be used pharmaceutically. Proper formulation depends upon the method of administration chosen.
For topical administration the β-hairpin peptidomimetics of the invention may be formulated as solutions, gels, ointments, creams, suspensions, etc. as are well-known in the art.
Systemic formulations include those designed for administration by injection, e.g. subcutaneous, intravenous, intramuscular, intrathecal or intraperitoneal injection, as well as those designed for transdermal, transmucosal, oral or pulmonary administration.
For injections, the β-hairpin peptidomimetics of the invention maybe formulated in adequate solutions, preferably in physiologically compatible buffers such as Hink's solution, Ringer's solution, or physiological saline buffer. The solution may contain formulatory agents such as suspending, stabilizing and/or dispersing agents. Alternatively, the β-hairpin peptidomimetics of the invention may be in powder form for combination with a suitable vehicle, e.g., sterile pyrogen-free water, before use.
For transmucosal administration, penetrants appropriate to the barrier to be permeated are used in the formulation as known in the art.
For oral administration, the compounds can be readily formulated by combining the active β- hairpin peptidomimetics of the invention with pharmaceutically acceptable carriers well known in the art. Such carriers enable the β-hairpin peptidomimetics of the invention to be formulated as tablets, pills, dragees, capsules, liquids, gels, syrups, slurries, suspensions etc., for oral ingestion of a patient to be treated. For oral formulations such as, for example, powders, capsules and tablets, suitable excipients include fillers such as sugars, such as lactose, sucrose, mannitol and sorbitol; cellulose preparations such as maize starch, wheat starch, rice starch, potato starch, gelatin, gum tragacanth, methyl cellulose, hydroxypropylmethyl cellulose, sodium carboxymethylcellulose, and or polyvinylpyrrolidone (PVP); granulating agents; and binding agents. If desired, desintegrating agents may be added, such as cross-linked polyvinylpyrrolidones, agar, or alginic acid or a salt thereof, such as sodium alginate. If desired, solid dosage forms may be sugar-coated or enteric-coated using standard techniques.
For oral liquid preparations such as, for example, suspensions, elixirs and solutions, suitable carriers, excipients or diluents include water, glycols, oils, alcohols, etc. In addition, flavoring agents, preservatives, coloring agents and the like may be added.
For buccal administration, the composition may take the form of tablets, lozenges, etc. formulated as usual.
For administration by inhalation, the β-hairpin peptidomimetics of the invention are conveniently delivered in form of an aeorosol spray from pressurized packs or a nebulizer, with the use of a suitable propellant, e.g. dichlorodifluoromethane, trichlorofluromethane, carbon dioxide or another suitable gas. In the case of a pressurized aerosol the dose unit may be determined by providing a valve to deliver a metered amount. Capsules and cartridges of e.g. gelatin for use in an inhaler or insufflator may be formulated containing a powder mix of the β- haiφin peptidomimetics of the invention and a suitable powder base such as lactose or starch.
The compounds may also be formulated in rectal or vaginal compositions such as suppositories together with appropriate suppository bases such as cocoa butter or other glycerides.
In addition to the formulations described previously, the β-haiφin peptidomimetics of the invention may also be formulated as depot preparations. Such long acting formulations may be administered by implantation (e.g. subcutaneously or intramuscularly) or by intramuscular injection. For the manufacture of such depot preparations the β-haiφin peptidomimetics of the invention may be formulated with suitable polymeric or hydrophobic materials (e.g. as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble salts.
In addition, other pharmaceutical delivery systems may be employed such as liposomes and emulsions well known in the art. Certain organic solvents such as dimethylsulfoxide also may be employed. Additionally, the β-haiφin peptidomimetics of the invention may be delivered using a sustained-release system, such as semipermeable matrices of solid polymers containing the therapeutic agent. Various sustained-release materials have been established and are well known by those skilled in the art. Sustained-release capsules may, depending on their chemical nature, release the compounds for a few weeks up to over 100 days. Depending on the chemical nature and the biological stability of the therapeutic agent, additional strategies for protein stabilization may be employed.
As the β-haiφin pepdidomimetics of the invention may contain charged residues, they may be included in any of the above-described formulations as such or as pharmaceutically acceptable salts. Pharmaceutically acceptable salts tend to be more soluble in aqueous and other protic solvents than are the corresponding free base forms.
The β-haiφin peptidomimetics of the invention, or compositions thereof, will generally be used in an amount effective to achieve the intended piupose. It is to be understood that the amount used will depend on a particular application.
For topical administration to treat or prevent infections a therapeutically effective dose can be determined using, for example, the in vitro assays provided in the examples. The treatment may be applied while the infection is visible, or even when it is not visible. An ordinary skilled expert will be able to determine therapeutically effective amounts to treat topical infections without undue experimentation.
For systemic administration, a therapeutically effective dose can be estimated initially from in vitro assays. For example, a dose can be formulated in animal models to achieve a circulating β-haiφin peptidomimetic concentration range that includes the IC50 as determined in the cell culture (i.e. the concentration of a test compound that is lethal to 50% of a cell culture). Such information can be used to more accurately determine useful doses in humans.
Initial dosages can also be determined from in vivo data, e.g. animal models, using techniques that are well known in the art. One having ordinary skills in the art could readily optimize administration to humans based on animal data. Dosage amount for applications as anti-HIV agents may be adjusted individually to provide plasma levels of the β-haiφin peptidomimetics of the invention which are sufficient to maintain the therapeutic effect. Therapeutically effective serum levels may be achieved by administering multiple doses each day.
In cases of local administration or selective uptake, the effective local concentration of the β- haiφin peptidomimetics of the invention may not be related to plasma concentration. One having the skills in the art will be able to optimize therapeutically effective local dosages without undue experimentation.
The amount of β-haiφin peptidomimetics administered will, of course, be dependent on the subject being treated, on the subject's weight, the severity of the affliction, the manner of administration and the judgement of the prescribing physician.
The anti-HIV therapy may be repeated intermittently while infections are detectable or even when they are not detectable. The therapy may be provided alone or in combination with other drugs, such as for example other anti-HIV agents or anti cancer agents, or anti inflammatory agents or other antimicrobial agents.
Normally, a therapeutically effective dose of the β-hairpin peptidomimetics described herein will provide therapeutic benefit without causing substantial toxicity.
Toxicity of the β-haiφin peptidomimetics of the invention herein can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., by determining the LD50 (the dose lethal to 50% of the population) or the LDioo (the dose lethal to 100% of the population). The dose ratio between toxic and therapeutic effect is the therapeutic index. Compounds which exhibit high therapeutic indices are preferred. The data obtained from these cell culture assays and animal studies can be used in formulating a dosage range that is not toxic for use in humans. The dosage of the β-haiφin peptidomimetics of the invention lies preferably within a range of circulating concentrations that include the effective dose with little or no toxicity. The dosage may vary within the range depending upon the dosage form employed and the route of administration utilized. The exact formulation, route of administration and dose can be chosen by the individual physician in view of the patient's condition (see, e.g. Fingl et al. 1975, In : The Pharmacological Basis of Therapeutics, Ch.l, p.l).
The following Examples illustrate the invention in more detail but are not intended to limit its scope in any way. The following abbreviations are used in these Examples:
HBTU: 1-benzotriazol-l-yl-tetramethylurounium hexafluorophosphate (Knorr et al. Tetrahedron Lett. 1989, 30, 1927-1930);
HOBt: 1-hydroxybenzotriazole;
DIEA: diisopropylethylamine; DIC: diisopropylcarbodiimide;
HO AT: 7-aza-l -hydroxybenzotriazole;
HATU: 0-(7-aza-benzotriazole-l-yl)-N,N,N',N'-tetramethyluronoium hexafluorophosphate (Caφino et al. Tetrahedron Lett. 1994, 35, 2279-2281).
Examples
1. Peptide synthesis
Coupling of the first protected amino acid residue to the resin
The synthesis was carried out using a ACT 90 synthesizer (Advanced Chemtec)
A) Preparation of preloaded Rink amide resin:
11 g 1% DVB- Aminomethyl-PS (loading 1.14 mmol/g) from Rapp Polymer GmbH, Germany (H1020, no. 100/0002) was allowed to swell in CH2C12 (100 ml) for 12 h, the solvent was filtered off and the resin was suspended in DMF (100 ml) for 30 min. After filtering off DMF, a solution of 1.2 eq ρ-{(R,S)-α-[l-(9H-Fluoren-9-yl)- methoxyformamido]-2,4-dimethoxybenzyl}-phenoxyacetic acid (Fmoc Rink linker, Novabiochem, Switzerland), 1.2 eq HOBT and 1.2 eq. DIC in 50 ml DMF was given to the resin and shaken at 25 °C for 12h. The solution was filtered of and the resin was washed with DMF (3x) and CH2C12 (3x). The resin was dried under vacuum for 12 hours. The Fmoc-group was removed by treatment with a solution of 40% piperidine in DMF (191 ml) for 45 min at 25°C, the resin was washed DMF (lx), and the treatment was repeated. The resin was washed with DMF (1 x) and CH2C12 (lx) and dried under vacuum for 12 hours. Loading was typically 0.7-0.85 mMol/g.
1.0 g of Rink amide resin (0.85 mMol/g, 0.85 mmol) was filled into a dried flask. The resin was suspended in CH2C12 (50 ml) and allowed to swell at room temperature under constant stirring for 60 min, the solvent was filtered off and the resin was suspended in DMF (50 ml) for 5 hours. After filtering off the solvent, the resin was treated with 5eq of the first suitably protected amino acid residue (see below), 5eq HOBT, and 5eq DIC in DMF (40 ml), the mixture was shaken at 25°C for 12 hours. The resin then was washed in the following order with CH2C12 (lx), DMF (lx), CH2C12 (lx) and dried under vacuum for 5 hours. Loading was typically 0.4-0.55 mMol/g.
The following preloaded resin was prepared: Fmoc-Arg(Pbf)-NH-Rink amide resin.
B) Preparation of preloaded chlorotrityl resin
0.5 g of 2-chlorotritylchloride resin (Barlos et al. Tetrahedron Lett. 1989, 30, 3943-3946) (0.83 mMol/g, 0.415 mmol) was filled into a dried flask. The resin was suspended in CH2C12 (2.5 ml) and allowed to swell at room temperature under constant stirring for 30 min. The resin was treated with 0.415 mMol (leq) of the first suitably protected amino acid residue (see below) and 284 μl (4eq) of diisopropylethylamine (DIEA) in CH2C12 (2.5 ml), the mixture was shaken at 25°C for 4 hours. The resin colour changed to puφle and the solution remained yellowish. The resin was shaken (CH2C12 /MeOH/DIEA : 17/2/1), 30 ml for 30 min; then washed in the following order with CH2C12 (lx), DMF (lx), CH2C12 (lx), MeOH (lx), CH2Cl2(lx), MeOH (lx), CH2C12 (2x), Et20 (2x) and dried under vacuum for 6 hours. Loading was typically 0.6-0.7 mMol g.
The following preloaded resin was prepared: Fmoc-Arg(Pbf)O-chlorotritylresin. Synthesis of the fully protected peptide fragment
The synthesis was carried out using a Syro-peptide synthesizer (Multisyntech) using 24 to 96 reaction vessels. In each vessel was placed 60 mg (weight of the resin before loading) of the above resin. The following reaction cycles were programmed and carried out:
Step Reagent Time 1 1 C CHH2CC1122,, wwaasshh aanndd sswweellll ( (mmaannuuaall)) 3 x 1 min.
2 DMF, wash and swell 1 x 5 min
3 20 % piperidine DMF 1 x 5 min.
4 DMF, wash 5 2 min.
5 5 5 5 eeqquuiivv.. FFmmoocc aammiinnoo aacciidd//DDMMFF//NNMMPP 22//11
+ + 55 eeqq.. HHBBTTUU + + 55 eeqq.. HHOOBBtt
+ 5 eq. DIEA 1 x 120 min.
6 DMF, wash 4 x 2 min.
7 CH2C12, wash (at the end of the synthesis) 3 2 min.
Steps 3 to 6 are repeated to add each amino-acid.
Formation of disulfide bridge (interstrand linkage)
0.05 mmol of peptide-carrying resin was swelled in 3 mL of dry DCM for 1 h and after filtering off the DCM, with dry DMF (3 mL) for overnight. Then 10 equivalents of iodine solution in DMF (6 mL) was added to the reactor and stirred for 1.5 h. The resin was filtered and the fresh solution of iodine (10 equivalents) in DMF (6 mL) was added and stirred for another 3 h. The resin was filtered and washed thoroughly several times with DMF and DCM.
Cleavage and deprotection of the fully protected peptide fragment
Cleavage from the resin and full deprotection of the peptide were done by 7.5 mL of the cleavage mixture TFA:TIS:H20 (95:2.5:2.5) for 3.5 h. The resin was filtered and the cleaved peptide was collected in a tube and evaporated to dryness under vaccum. The crude peptide was dissolved in 20% AcOH in water (7 mL) and extracted with isopropyl ether (4 mL) for three times. The aqueous layer was collected and evaporated to dryness. For final oxidation of the cysteine (for formation of disulfide bridge), air was passed through the diluted solution of crude peptide in H20 (6 mL) for 12 h.
Purification of the end-product:
The water phase was dried under vacuum and then the product purified by preparative reverse phase HPLC.
The products were analysed by ESI-MS and after lyophilisation the products were obtained as a white powder. The analytical data comprising HPLC retention times and ESI-MS are shown in table 1 and table 2.
Analytical HPLC retention times (RT, in minutes) were determined using a VYDAC 218MS5215 column with the following solvents A (H20 + 0.02% TFA) and B (CH3CN) and the gradient: 0 min: 92%A, 8%B; 8 min: 62%A 38%B; 9-12 min: 0% A, 100%B.
Examples 1-3 (n = 4, n' = 6) are shown in table 1. The peptides were synthesized starting with the amino acid Arg which was grafted to the resin. Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above. The linear peptides were synthesized on solid support according to procedure described above in the following sequence: Resin-P4-P3- P2-P1- LPro -DLys -Pl'-P2'-P3'-P4'-P5,-P6'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention times (minutes) were determined using the gradient described above.
Examples 4 and 5 (n = 4, n' = 6) are shown in table 1. The peptides were synthesized starting with the amino acid Arg which was grafted to the resin. Starting resin was Fmoc-Arg(Pbf)- Rink-amide resin, which was prepared as described above. The linear peptides were synthesized on solid support according to procedure described above in the following sequence: Resin-P4-P3-P2-Pl-LPro- DPro-Pl'-P2'-P3'-P4'-P5'-P6'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention times (minutes) were determined using the gradient described above. Example 6 (n = 4, n' = 6) is shown in table 1. The peptide was synthesized starting with the amino acid Arg which was grafted to the resin. Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above. The linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P4-P3- P2-Pl-LPro- LLys-Pl '-P2'-P3'-P4'-P5'-P6'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention time (minutes) was determined using the gradient described above.
Example 7 and 10-19 (n = 5, n1 = 7) are shown in table 2. The peptides were synthesized starting with the amino acid Arg which was grafted to the resin. Starting resin was Fmoc- Arg(Pbf)-Rink-amide resin, which was prepared as described above. The linear peptides were synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4-P3-P2-Pl-LPro-DPro-Pl'-P2*-P3'-P4'-P5,-P6'-P7'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention times (minutes) were determined using the gradient described above:
Ex. 7 (4.27), Ex. 10 (4.13), Ex. 11 (3.68), Ex. 12 (2.28), Ex. 13 (4.13), Ex. 14 (5.96), Ex. 15 (5.76), Ex. 16 (5.82), Ex. 17 (5.90), Ex. 18 (5.90), Ex. 19 (5.84).
Example 8 (n = 5, n' = 7) is shown in table 2. The peptide was synthesized starting with the amino acid Arg which was grafted to the resin. Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above. The linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4- P3-P2-Pl- Pro-DPro-Pl'-P2*-P3'-P4'-P5'-P6'-P7', and the disulfide bridge was formed. The resin was then swelled in dry DCM for 0.5 hrs. DCM was filtered off and 5 mL of dry DCM was added to the resin. 0.5 mL (2.92 mmol) of DIPEA and 0.125 mL (1.32 mmol) of acetic anhydride were added to the resin and stirred for 4 hrs. The resin was filtered and washed thoroughly with DCM, DMF, DCM, MeOH, Et20 and dried in vaccum. The peptide was cleaved from the resin, deprotected and purified as indicated. HPLC-retention time was determined using the gradient described above: 4.33 minutes.
Example 9 (n = 5, n' = 7) is shown in table 2. The peptide was synthesized starting with the amino acid Arg which was grafted to the resin. Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above. The linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4- P3-P2-Pl-LPro-DPro-Pr-P2'-P3'-P4'-P5'-P6'-P7' and the disulfide bridge was formed. 2.5 mL of dry THF and 200 μL of acetone was added to the reactor followed by addition of 2.5 mL of 50:50 (H20: Acetic acid) and stirred for 4 hrs. The solution of NaCNBH3 (120 mg, 1.90 mmol) in THF (2 mL) was added to the reactor and stirred for 4 hrs. Then the solvent was filtered and washed with DCM, DMF, DCM, MeOH, Et20 and dried in vaccum. The peptide was cleaved from the resin, deprotected and purified as indicated. HPLC-retention times was determined using the gradient described above: 4.37 minutes.
Example 20 (n = 5, n' = 7) is shown in table 2. The peptide was synthesized starting with the amino acid Arg which was grafted to the resin. Starting resin was Fmoc-Arg(Pbf)-chlorotrityl resin, which was prepared as described above. The linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4-P3- P2-P1- LPro-DPro -Pl'-P2'-P3'-P4'-P5'-P6'-P7'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated.
HPLC-retention time was determined using the gradient described above: 4.35 minutes.
Example 21 (n = 5, n' = 7) is shown in table 2. The peptide was synthesized starting with the amino acid Arg which was grafted to the resin. Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above. The linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4-
P3-P2-Pl-[(bl)-154*]-Pl'-P2'-P3'-P4*-P5'-P6'-P7*; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated.
HPLC-retention time was determined using the gradient described above: 4.02 minutes. * Template [(bl)-154] is (2S,6S,9S)-6-amino-2-carboxymethyl-3,8-diazabicyclo-[4,3,0]- nonane-l,4-dione
Example 22 (n = 5, n' = 7) is shown in table 2. The peptide was synthesized starting with the amino acid Arg which was grafted to the resin. Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above. The linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4- P3-P2-Pl-AMPA-Pr-P2'-P3'-P4'-P5'-P6'-P7'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention time was determined using the gradient described above: 4.62 minutes.
Example 23 (n = 5, n' = 7) is shown in table 2. The peptide wassynthesized starting with the amino acid Arg which was grafted to the resin. Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above. The linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4- P3-P2-Pl-DPro-LPro-Pl'-P2'-P3'-P4'-P5'-P6'-P7'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention time was determined using the gradient described above: 4.13, 4.40* minutes. * The MS is showing the correct mass.
Example 24 (n = 5, n' = 7) is shown in table 2. The peptide was synthesized starting with the amino acid Arg which was grafted to the resin. Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above. The linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4- P3-P2-Pl-LPro- Pro-Pr-P2'-P3'-P4'-P5'-P6'-P7'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention time was determined using the gradient described above: 4.08 minutes.
Example 25 (n = 5, n' = 7) is shown in table 2. The peptide was synthesized starting with the amino acid Arg which was grafted to the resin. Starting resin was Fmoc-Arg(Pbf)-Rink- amide resin, which was prepared as described above. The linear peptide was synthesized on solid support according to procedure described above in the following sequence: Resin-P5-P4- P3-P2-Pl-LPro-DPic-Pl'-P2'-P3'-P4'-P5'-P6'-P7'; disulfide bridge formation, cleavage from the resin, deprotection and purification were effected as indicated. HPLC-retention time was determined using the gradient described above: 4.47 minutes.
S3
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2. Biological methods
2.1. Preparation of the peptides.
Lyophilized peptides were weighed on a Microbalance (Mettler MT5) and dissolved in sterile water to a final concentration of 1 mM unless stated otherwise. Stock solutions were kept at + 4°C, light protected.
2.2. Ca2+'assay: CXCR4-antagonizing activity of the peptides. 3-4 Mio CXCR4 transfected pre-B cells [see references 1, 2 and 3, below] per measurement were resuspended in 200 μl MSB (20 mM 4-(2-Hyddroxyethyl)-piperazin-l-ethansulfonic acid (HEPES), 136 mM NaCl, 4.8 mM KCl and 1 mM CaCl2) containing 5 mM D-Glucose and were loaded with 0.75 μl of 1 mM Fura-2-acetoxymethylester for 17 minutes at 37°C. The cells were washed free from Fura-2-AM with a platelet centrifuge and resuspended in 800 μl MSB containing 5 mM D-Glucose. The peptides to be administered were diluted to a 100 fold end concentration in MSB/0.2 % PPL, and 8 μl were injected. [Ca2+]i-dependent fluorescence change in response to single or sequential stimulation with the peptide was recorded with a fluorimeter at an excitation wavelength of 340 nM and an end emission wavelength of 510 nM [see ref. 4, below]. Measurements were done under continuous stirring at 37°C. The signal intension was calibrated with 3 mM CaCl2/l mM Ionomycin (maximal fura-2- acetoxymethylester saturation) and 10 μM MnCl2 (minimal Fura-2-acetoxymethylester saturation) and [Ca2+]j-changes are presented in % fura-2-acetoxymethylester saturation. The rate of [Ca2+]j-changes was calculated on the basis of the initial [Ca2+];-changes and plotted in dependence of chemokine concentration to obtain a sigmoidal curve and to determine the IC50 values.
MSB: 20 mM HEPES, 136 mM NaCl, 4.8 mM KCl, 1 mM CaCl2«2H20, pH 7.4; Osmolarity:
310 mOsm adjusted with NaOH or HCl, adjusted with dH20 or PBS.
MSB plus: 5 mM D-glucose in MSB (50 mg/50mL).
Fura 2-acetoxymethylester: 1 mM stock solution in dimethylsulfoxide.
2.3. FIGS-Assay™
The assay was performed according to ref. 5, below. Stock dilutions of the peptides (10 mM) were prepared by dissolving in 10 mM Tris-HCl at room temperature. Stock solutions were kept at + 4°C, light protected. Working dilutions were prepared extemporaneously by serial dilution in Phosphate Buffered Saline (PBS) and added in a final volume of 10μL directly to the cell cultures. After 48 hours of co-cultivation the cultures were rinsed with PBS and then exposed to glutaraldehyde/ formaldehyde (0.2 % / 2 %) in PBS for five minutes. For photometric quantification the fixed cultures were subsequently incubated with ortho-nitro- phenyl-galactopyranoside (ONPG) as a β-galactosidase substrate, which was enzymatically converted into the chromophore ortho-nitrophenol (ONP). The read out is directly obtained by measuring optical density of wells at 405 nm in an iEMS 96well-plate reader.
2.4. Cytotoxicity assay
The cytotoxicity of the peptides to HELA cells (Acc57) and COS-7 cells (CRL-1651) was determined using the MTT reduction assay [see ref. 6 and 7, below]. Briefly the method was as follows: HELA cells and COS-7 cells were seeded at 7.0 03 and, respectively, 4.5'103 cells per well and grown in 96-well microtiter plates for 24 hours at 37°C at 5% C02. At this point, time zero (Tz) was determined by MTT reduction (see below).The supernatant of the remaining wells was discarded and fresh medium and the peptides in serial dilutions of 12.5, 25 and 50 μM were pipeted into the wells. Each peptide concentration was assayed in triplicate. Incubation of the cells was continued for 48 hours at 37°C at 5% C02. Wells were then washed once with PBS and subsequently 100 μl MTT reagent (0.5 mg/mL in medium RPMI1640 and, respectively, DMEM) was added to the wells. This was incubated at 37°C for 2 hours and subsequently the medium was aspirated and 100 μl isopropanol was added to each well. The absorbance at 595 nm of the solubilized product was measured (0D595peptide). For each concentration averages were calculated from triplicates. The percentage of growth was calculated as follows: (ODsgspeptide-ODsgsTz-ODsgsEmpty well) / (ODsgsTz-ODsgsEmpty well) x 100% and was plotted for each peptide concentration.
The LC 50 values (Lethal Concentration, defined as the concentration that kills 50% of the cells) were determined for each peptide by using the trend line function of EXCEL (Microsoft Office 2000) for the concentrations (50, 25, 12.5 and 0 μM), the corresponding growth percentages and the value -50, (=TREND(C50:C0,%50:%0,-50))
2.5. Cell culture
'CCR5' cells were cultured in DMEM medium with 4500 mg mL glucose, 10 % fetal bovine serum (FBS), supplemented with 50 U/ml Penicillin and 50 μg mL Streptomycin (Pen/Strept). Hut/4-3 cells were maintained in RPMI medium, 10% FBS, supplemented with Pen/Strept. and 10 mM HEPES. HELA cells and CCRF-CEM cells were maintained in RPMI1640 plus 5% FBS, Pen/Strept and 2 mM L-Glutamine. Cos-7 cells were grown in DMEM medium with 4500 mg/mL glucose supplemented with 10% FCS, Pen/Strept. and 2 mM L-Glutamine. All cell lines were grown at 37°C at 5% C02. Cell media, media supplements, PBS-buffer,
HEPES, Pen/Strept., L-Glutamine and sera were purchased from Gibco (Pailsey, UK). All fine chemicals came from Merck (Darmstadt, Germany).
2.6. Hemolysis The peptides were tested for their hemolytic activity against human red blood cells (hRBC). Fresh hRBC were washed three times with phosphate buffered saline (PBS) by centrifugation for 10 min at 2000 x g. Peptides at a concentration of 100 μM were incubated with 20% v/v hRBC for 1 hour at 37°C. The final erythrocyte concentration was approximately 0.9xl09 cells per mL. A value of 0% resp. 100% cell lysis was determined by incubation of the hRBC in the presence of PBS alone and respectively 0.1% Triton X-100 in H20. The samples were centrifuged and the supernatant was 20-fold diluted in PBS buffer and the optical density (OD) of the sample at 540 nM was measured. The 100% lyses value (OD540H20) gave an OD540 of approximately 1.3-1.8. Percent hemolysis was calculated as follows: (OD540peptide/OD54oH20) xl00%.
2.7. Chemotactic Assay (Cell migration assay)
The chemotactic response of CCRF-CEM cells to a gradient of stromal cell-derived factor lα (SDF-1) was measured using disposable assay plates from Neuroprobe (5 μ pore size) (Gaithersburg, MD), according to the manufacturer's directions and references therein [especially ref. 8, below]. Briefly, one 175 cm2 flask was washed once with Dubecco's phosphate buffered saline (DPBS), and trypsinized for 10 minutes or until cells had lifted. The trypsin was neutralized by the addition of fresh medium containing serum and the cells were pelleted, washed once in DPBS, and resuspended at 1-0.5 X 107 cells/ml in RPMI + 0.5% bovine serum albumin (BSA). 45 μl of cell suspension were mixed with 5 μl of 10-fold concentrated PEM peptide diluted in the same assay medium. 35 μl of this mixture were applied to the top of the assay filter. The cells were allowed to migrate (at 37°) into the bottom chamber of the assay plate containing 1 nM SDF-1. After 4 hours, the filter was removed and MTT was added to the migrated cells to a final concentration of 0.5 mg/ml, and incubated for a further 4 hours. After labeling with MTT, all medium was removed and 100 μl of isopropanol + 10 mM HCl were added to the cells. The optical absorbance at 595 nm (ABS595) was read using a Tecan Genios plate reader with Magellan software. The number of cells migrated was determined by comparing ABS595 values against a standard curve generated with a known number of cells in the assay plate and were plotted against SDF-1 concentration to obtain a sigmoidal curve and to determine the IC50 values. The values for IC50 were determined using the Trendline function in Microsoft Excel by fitting a logarithmic curve to the averaged datapoints.
2.7. Results
The results of the experiments described above are indicated in Table 3 hereinbelow.
Figure imgf000089_0001
n.d.: not determined References
1. Oberlin E, Amara A, Bachelerie F, Bessia C, Virelizier J-L, Arenzana-Seisdedos F, Schwartz O, Heard J-M, Clark-Lewis I, Legler DF, Loetscher M, Baggiolini M, Moser B. Nature. 1996, 352:833-835 2. Loetscher M, Geiser T, O'Reilly T, Zwalen R, Baggiolini M, Moser B. J.Biol. Chem. 1994. 269:232-237
3. D'Apuuo M, Rolink A, Loetscher M, Hoxie JA, Clark-Lewis I, Melchors F, Baggiolini M, Moser B. EurJ Immunol. 1997. 27:1788-1793
4. von Tschamer V, Prodliom B, Baggiolini M, Reuter H. Nature. 1986. 324:369-72. 5. Hamy F, Felder ER, Heizmann G, Lazdins J, Aboul-ela F, Varani G, Kam J, Klimkait T. Proc.Natl.Acad.Sci. 1997. P :3548-3553.
6. Mossman T. J.Immunol.Meth. 1983, 65:55-63
7. Berridge MV, Tan AS. Arch.Biochem.Biophys. 1993, 303:474-482
8. Frevert CW, Wong VA, Goodman RV, Goodwin R, Martin TR, J.Immunol.Meth. 1998. 213: 41-52.

Claims

1. Compounds of the general formula
Figure imgf000091_0001
(I) wherein
Figure imgf000091_0002
is a group of one of the formulae
Figure imgf000091_0003
(a1) (a2)
Figure imgf000091_0004
( 3) (a4)
Figure imgf000092_0001
(b1) (b2) d)
Figure imgf000092_0002
(c2) (c3) (d)
Figure imgf000092_0003
(h) (i1) (i2)
Figure imgf000093_0001
(i3) (i4) (i)
Figure imgf000093_0002
(n) (o) (P)
wherein
Figure imgf000093_0003
is the residue of an L-α-amino acid with B being a residue of formula -NR20CH(R71)-; or the enantiomer of one of the groups Al to A69 as defined hereinafter; or, in case the template is of type (a4), also a residue of an amino acid with B being a residue of formula -NR20-CH2-C6H4-CH2-;
I s a group of one of the formulae
Figure imgf000094_0001
A1 A2 A3 A4
Figure imgf000094_0002
A5 A6 A7 Aδ A9
Figure imgf000094_0003
A10 A11 A12 A13 A14
Figure imgf000094_0004
Figure imgf000094_0005
A20 A21 A22 A23 A24
Figure imgf000095_0001
A38 A39 A40 A41 A42
Figure imgf000095_0002
A43 A44 A45 A46 A47
Figure imgf000095_0003
A48 A49 A50 A51 A52
Figure imgf000096_0001
A58 A59 A60 A61 A62
Figure imgf000096_0002
A63 A64 A65 A66
Figure imgf000096_0003
A70 A71 A72 A73 A74
Figure imgf000096_0004
A75 A76 A77 A78 A79
Figure imgf000097_0001
A80 A81 A82 A83 A84
Figure imgf000097_0002
A100 A101 A102 A103 A104
R1 is H; lower alkyl; or aryl-lower alkyl;
R2 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)SCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R3 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)SCOOR57 ;
-(CH2)0(CHR61)sCONR58R59 ; -(CH2)0(CHR61)SPO(OR60)2; -(CH2)0(CHR6I)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R4 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; - (CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82;
-(CH2)p(CHR61)sCOOR57; -(CH2)p(CHR61)sCONR58R59; -(CH2)p(CHR61)sPO(OR60)2; -(CH2)P(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R5 is alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR6I)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)0(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2;
-(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R6 is H; alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR6I)SSR56; - (CH2)0(CHR61)SNR33R34;
-(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)sCOOR57; -(CH2)0(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2;
-(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R7 is alkyl; alkenyl; -(CH2)q(CHR61)s0R55; -(CH2)q(CHR61)sNR33R34; -(CH2)q(CHR6I)sOCONR33R75; -(CH2)q(CHR61)sNR20CONR33R82; -(CH2)r(CHR61)sCOOR57; -(CH2)r(CHR61)sCONRS8R59; -(CH2)r(CHR61)sPO(OR60)2; -(CH2)r(CHR61)sS02R62; or -(CH2)r(CHR61)s C6H4R8;
R8 is H; Cl; F; CF3; N02; lower alkyl; lower alkenyl; aryl; aryl-lower alkyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)NR33R34 ; -(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR6I)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR6,)sS02R62; or -(CH2)0(CHR61)sCOR64;
R9 is alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR6!)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R10 is alkyl; alkenyl; -(CH2)0(CHR6,)sOR55; -(CH2)0(CHR6I)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR6l)sPO(OR60)2; -(CH2)o(CHR61)s S02R62; or -(CH2)0(CHR61)SC6H4R8; R" is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)ra(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR6I)sNR20CONR33R82; -(CH2)o(CHR6I)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)sS02R62; or -(CH2)0(CHR61)S C6H4R8; R12 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75;
-(CH2)m(CHR61)sNR20CONR33R82; -(CH2)r(CHR61)sCOOR57; - (CH2)r(CHR61)sCONR58R59; -(CH2)r(CHR6,)sPO(OR60)2; -(CH2)r(CHR61)s S02R62; or - (CH2)r(CHR61)sC6H4R8; R13 is alkyl; alkenyl; -(CH2)q(CHR61)sOR55; -(CH2)q(CHR61)sSR56; -(CH2)q(CHR61)sNR33R34; -(CH2)q(CHR61)sOCONR33R75; -(CH2)q(CHR61)sNR20CONR33R82;
-(CH2)q(CHR61)sCOOR57; -(CH2)q(CHR61)sCONR58R59; -(CH2)q(CHR61)sPO(OR60)2; -(CH2)q(CHR6I)s S02R62; or -(CH2)q(CHR61)sC6H4R8; R14 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)q(CHR61)sCOOR57; -(CH2)q(CHR61)sCONR58R59; -(CH2)q(CHR61)sPO(OR60)2;.
-(CH2)q(CHR61)sSOR62; or -(CH2)q(CHR61)s C6H4R8; R15 is alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR6l)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8;
R16 is alkyl; alkenyl; -(CH2)0(CHR61)s0R55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R17 is alkyl; alkenyl; -(CH2)q(CHR61)sOR55; -(CH2)q(CHR61)sSR56; -(CH2)q(CHR6l)sNR33R34; -(CH2)q(CHR6l)sOCONR33R7 ; -(CH2)q(CHR61)sNR20CONR33R82; -(CH2)q(CHR6I)sCOOR57; -(CH2)q(CHR61)sCONR58RS9; -(CH2)q(CHR61)sPO(OR60)2; -(CH2)q(CHR61)s S02R62; or -(CH2)q(CHR61)sC6H4R8; R18 is alkyl; alkenyl; -(CH2)p(CHR6,)sOR55; -(CH2)P(CHR61)SSR56; -(CH2)P(CHR61)SNR33R34; -(CH2)p(CHR61)sOCONR33R75; -(CH2)p(CHR61)sNR20CONR33R82; -(CH2)p(CHR61)sCOOR57; -(CH2)p(CHR61)sCONR58R59; -(CH2)p(CHR61)sPO(OR60)2; -(CH2)p(CHR61)s S02R62; or -(CH2)0(CHR6I)SC6H4R8; R19 is lower alkyl; -(CH2)p(CHR61)sOR55; -(CH2)P(CHR61)SSR56; -(CH2)P(CHR61)SNR33R34; -(CH2)P(CHR6I)sOCONR33R75; -(CH2)P(CHR61)SNR20CONR33R82;
-(CH2)p(CHR61)sCOOR57; -(CH2)p(CHR61)sCONR58R59; -(CH2)p(CHR61)sPO(OR60)2; -(CH2)P(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; or R18 and R19 taken together can form: -(CR2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; R20 is H; alkyl; alkenyl; or aryl-lower alkyl;
R21 is H; alkyl; alkenyl; -(CH2)0(CHR61)SOR55; -(CH2)0(CHR61)SSR56; - (CH2)o(CHR61)sNR33R34;
-(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8;
R22 is H; alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR61)SSR56; - (CH2)0(CHR61)SNR33R34;
-(CH2)o(CHR61)sOCONR33R75; -(CH2)o(CHR6I)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)o(CHR6,)s S02R62; or -(CH2)0(CHR61)SC6H4R8;
R23 is alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)o(CHR61)sOCONR33R75; -(CH2)0(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)0(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R24 is alkyl; alkenyl; -(CH2)0(CHR6I)sOR55; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)o(CHR61)sOCONR33R75; -(CH2)0(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR5 R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; R25 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75;
-(CH2)m(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)sS02R62; or -(CH2)0(CHR61)SC6H4R8;
R26 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR; 56. -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)sCOOR57; - (CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8; or R25 and R26 taken together can form: -(CH2)2.6-; -(CH2)rO(CH2)r-; -(CH2)rS(CH2)r-; or -(CH2)rNR57(CH2)r-; R27 is H; alkyl; alkenyl; -(CH2)0(CHR6I)SOR55; -(CH2)0(CHR61)SSR56; - (CH2)0(CHR61)SNR33R34;
-(CH2)0(CHR61)sCOOR57; -(CH2)0(CHR61)sCONR58R59; -(CH2)0(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sPO(OR60)2;
-(CH2)0(CHR6I)S S02R62; or -(CH2)0(CHR61)sC<ϊH4R8; R28 is alkyl; alkenyl; -(CH2)0(CHR61)s-OR55; -(CH2)0(CHR61)S SR56; -(CH2)0(CHR61)S NR33R34;
-(CH2)o(CHR61)sOCONR33R75; -(CH2)0(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)S COOR57; -(CH2)0(CHR61)S CONR58R59; -(CH2)0(CHR61)S PO(OR60)2;
-(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)S C6H4R8; R29 is alkyl; alkenyl; -(CH2)0(CHR61)sORS5; -(CH2)0(CHR61)SSR56; -(CH2)0(CHR61)SNR33R34; -(CH2)0(CHR61)SOCONR33R75; -(CH2)0(CHR61)SNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR6I)S S02R62; or -(CH2)0(CHR61)SC6H4R8;
R30 is H; alkyl; alkenyl; or aryl-lower alkyl;
R31 is H; alkyl; alkenyl; -(CH2)p(CHR61)sOR55; -(CH2)P(CHR61)SNR33R34; -(CH2)p(CHR61)sOCONR33R75; -(CH2)p(CHR6I)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR6I)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)sS02R62; or -(CH2)0(CHR61)S C6H4R8;
R32 is H; lower alkyl; or aryl-lower alkyl;
R33 is H; alkyl, alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sNR34R63; -(CH2)„,(CHR61)sOCONR75R82; -(CH2)m(CHR61)sNR20CONR78R82; -(CH2)o(CHR61)sCOR64; -(CH2)o(CHR6l)s-CONR58R59, -(CH2)o(CHR61)sPO(OR60)2; -(CH2)0(CHR61)S S02R62; or -(CH2)0(CHR61)SC6H4R8;
R34 is H; lower alkyl; aryl, or aryl-lower alkyl; R33 and R34 taken together can form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NRS7(CH2)2-; R35 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82; -(CH2)p(CHR61)sCOOR57; -(CH2)p(CHR61)sCONR58R59; -(CH2)p(CHR61)sPO(OR60)2; -(CH2)p(CHR6I)sS02R62; or -(CH2)P(CHR6I)S C6H4R8; R36 is H, alkyl; alkenyl; -(CH2)0(CHR61)sOR55; -(CH2)P(CHR61)SNR33R34; -(CH2)p(CHR61)sOCONR33R75; -(CH2)P(CHR6I)SNR20CONR33R82;
-(CH2)p(CHR61)sCOOR57; -(CH2)p(CHR61)sCONR58R59; -(CH2)p(CHR61)sPO(OR60)2; -(CH2)p(CHR61)sS02R62; or -(CH2)0(CHR61)S C6H4R8; R37 is H; F; Br; Cl; N02; CF3; lower alkyl; -(CH2)p(CHR6,)s0R55; -(CH2)P(CHR6I)SNR33R34; -(CH2)p(CHR61)sOCONR33R75; -(CH2)p(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)sCOOR57; -(CH2)0(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2;
-(CH2)0(CHR61)sS02R62; or -(CH2)0(CHR61)S C6H4R8; R38 is H; F; Br; Cl; N02; CF3; alkyl; alkenyl; -(CH2)p(CHR61)sOR55; - (CH2)P(CHR61)SNR33R34;
-(CH2)p(CHR61)sOCONR33R75; -(CH2)p(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)sCOOR57; -(CH2)0(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2;
-(CH2)0(CHR61)sS02R62; or -(CH2)0(CHR61)SC6H4R8; R39 is H; alkyl; alkenyl; or aryl-lower alkyl; R40 is H; alkyl; alkenyl; or aryl-lower alkyl; R41 is H; F; Br; Cl; N02; CF3; alkyl; alkenyl; -(CH2)p(CHR61)sOR55; - (CH2)p(CHR6,)sNR33R34;
-(CH2)P(CHR61)SOCONR33R75; -(CH2)P(CHR61)SNR20CONR33R82; -(CH2)o(CHR6I)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2;
-(CH2)0(CHR01)sSO2R0Z; or -(CH2)0(CHR )s C6H4R8;
R42 is H; F; Br; Cl; N02; CF3; alkyl; alkenyl; -(CH2 ))Pp((CHR61)sOR55; (CH2)P(CHR61)SNR33R34;
-(CH2)P(CHR61)SOCONR33R75; -(CH2)P(CHR61)SNR20CONR33R82;
-(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)sPO(OR60)2;
-(CH2)„(CHR6,)SS02R62; or -(CH2)0(CHR6I)S C6H4R8; R43 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82;
-(CH2)o(CHR61)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)0(CHR61)sPO(OR60)2;
-(CH2)0(CHR61)sSO2R62; or -(CH2)0(CHR61)S C6H4R8; R44 is alkyl; alkenyl; -(CH2)r(CHR61)sOR55; -(CH2)r(CHR61)sSR56; -(CH2)r(CHR61)sNR33R34;
-(CH2)r(CHR61)sOCONR33R75; -(CH2)r(CHR61)sNR20CONR33R82; -(CH2)r(CHR61)sCOOR57; -(CH2)r(CHR61)sCONR58R59; -(CH2)r(CHR61)sPO(OR60)2;
-(CH2)r(CHR61)s S02R62; or -(CH2)r(CHR61)sC6H4R8; R45 is H; alkyl; alkenyl; -(CH2)0(CHR6I)sOR55; -(CH2)0(CHR61)SSR56; -
(CH2)0(CHR61)SNR33R34; -(CH2)0(CHR61)sOCONR33R75; -(CH2)o(CHR61)sNR20CONR33R82;
-(CH2)o(CHR61)sCOOR57; -(CH2)s(CHR61)sCONR58R59; -(CH2)s(CHR61)sPO(OR60)2;
-(CH2)S(CHR61)S S02R62; or -(CH2)S(CHR6I)SC6H4R8; R46 is H; alkyl; alkenyl; or -(CH2)0(CHR61)PC6H4R8; R47 is H; alkyl; alkenyl; or -(CH2)0(CHR61)s0R55; R48 is H; lower alkyl; lower alkenyl; or aryl-lower alkyl;
R49 is H; alkyl; alkenyl; -(CHR61)sCOOR57; (CHR61)sCONR58R59; (CHR61)SPO(OR60)2;
-(CHR61)sSOR62; or -(CHR61)SC6H4R8; R50 is H; lower alkyl; or aryl-lower alkyl;
R51 is H; alkyl; alkenyl; -(CH2)ra(CHR61)sOR55; -(CH2)m(CHR61)sSR56; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75;
-(CH2)m(CHR61)sNR20CONR33R82; -(CH2)o(CHR61)sCOOR57;
-(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR61)pPO(OR60)2; -(CH2)P(CHR6I)S S02R62; or -(CH2)P(CHR6I)SC6H4R8; R52 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; -(CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75;
-(CH2)m(CHR61)sNR20CONR33R82; -(CH2)0(CHR61)sCOOR57; -(CH2)o(CHR6,)sCONR58R59; -(CH2)o(CHR6I)pPO(OR60)2; -(CH2)p(CHR61)s S02R62; or -(CH2)P(CHR61)SC6H4R8; R53 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR61)sSR56; - (CH2)m(CHR61)sNR33R34; -(CH2)m(CHR61)sOCONR33R75;
-(CH2)m(CHR6,)sNR20CONR33R82; -(CH2)o(CHR6l)sCOOR57; -(CH2)o(CHR61)sCONR58R59; -(CH2)o(CHR6I)pPO(OR60)2; -(CH2)P(CHR61)S S02R62; or -(CH2)P(CHR61)SC6H4R8; R54 is H; alkyl; alkenyl; -(CH2)m(CHR61)sOR55; -(CH2)m(CHR6I)sNR33R34; -(CH2)m(CHR6I)sOCONR33R75; -(CH2)m(CHR61)sNR20CONR33R82;
-(CH2)0(CHR6I)COOR57; -(CH2)0(CHR61)sCONR58R59; or -(CH2)0(CHR61)S C6H4R8; R55 is H; lower alkyl; lower alkenyl; aryl-lower alkyl; -(CH2)m(CHR6I)sOR57; -(CH2)m(CHR61)sNR34R63; -(CH2)m(CHR61)sOCONR75R82; -(CH2)m(CHR6I)sNR20CONR78R82; -(CH2)o(CHR61)s-COR64; -(CH2)o(CHR61)COOR57; or
-(CH2)0(CHR61)sCONR58R59; R56 is H; lower alkyl; lower alkenyl; aryl-lower alkyl; -(CH2)m(CHR61)sOR57; -(CH2)m(CHR6,)sNR34R63; -(CH2)m(CHR61)sOCONR75R82;
-(CH2)m(CHR61)sNR20CONR78R82; -(CH2)0(CHR61)s-COR64; or -(CH2)0(CHR61)sCONR58R59; R57 is H; lower alkyl; lower alkenyl; aryl lower alkyl; or heteroaryl lower alkyl; R58 is H; lower alkyl; lower alkenyl; aryl; heteroaryl; aryl-lower alkyl; or heteroaryl-lower alkyl;
R59 is H; lower alkyl; lower alkenyl; aryl; heteroaryl; aryl-lower alkyl; or heteroaryl-lower alkyl; or
R58 and R59 taken together can form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; R60 is H; lower alkyl; lower alkenyl; aryl; or aryl-lower alkyl;
R61 is alkyl; alkenyl; aryl; heteroaryl; aryl-lower alkyl; heteroaryl-lower alkyl; -(CH2)mOR55; -(CH2)mNR33R34; -(CH2)mOCONR75R82; -(CH2)mNR20CONR78R82; -(CH2)0COOR37; -(CH2)0NR58R59; or -(CH2)oPO(COR60)2; R62 is lower alkyl; lower alkenyl; aryl, heteroaryl; or aryl-lower alkyl; R63 is H; lower alkyl; lower alkenyl; aryl, heteroaryl; aryl-lower alkyl; heteroaryl-lower alkyl;
-COR64; -COOR57; -CONR58R59; -S02R62; or -PO(OR60)2; R34and R63 taken together can form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; R64 is H; lower alkyl; lower alkenyl; aryl; heteroaryl; aryl-lower alkyl; heteroaryl-lower alkyl;
-(CH2)p(CHR61)sOR65; -(CH2)P(CHR61)SSR66; or -(CH2)P(CHR61)SNR34R63; -(CH2)p(CHR61)sOCONR75R82; -(CH2)P(CHR6,)SNR20CONR78R82; R65 is H; lower alkyl; lower alkenyl; aryl, aryl-lower alkyl; heteroaryl-lower alkyl; -COR57; -COOR57; or -CONR58R59;
R66 is H; lower alkyl; lower alkenyl; aryl; aryl-lower alkyl; heteroaryl-lower alkyl; or -CONR58R59; Z and Z1 are chains of n and, respectively, n' α-amino acid residues whereby either n is 4 and n' is 6 or n is 5 and n' is 7, the positions of said amino acid residues in said chain Z being counted starting from the N-terminal amino acid and the positions of said amino acid residues in said chain Z1 being counted starting from the C-terminal amino acid, whereby these amino acid residues are, depending on their position in the chains, Gly, or Pro, or of one of the types
C: -NR20CH(R72)CO-; D: -NR20CH(R73)CO-; E: -NR20CH(R74)CO-; F: -NR20CH(R84)CO-; and
H: -NR20-CH(CO-)-(CH2)4.7-CH(CO-)-NR20-;
-NR20-CH(CO-)-(CH2)pSS(CH2)p-CH(CO-)-NR20-;
-NR20-CH(CO-)-(-(CH2)pNR20CO(CH2)p-CH(CO-)-NR20-;
-NR20-CH(CO-)-(-(CH2)pNR20CONR20(CH2)p-CH(CO-)-NR20-; and I: -NR86CH2CO-;
R71 is lower alkenyl; -(CH2)p(CHR61)sOR75; -(CH2)P(CHR61)SSR75;
-(CH2)p(CHR6,)sOCONR33R75;
-(CH2)o(CHR61)sCOOR75; -(CH2)PCONR5 R59; -(CH2)„PO(OR62)2; -(CH2)pS02R62; or
-(CH2)o-C6R67R68R69R70R76; R72 is H, lower alkyl; lower alkenyl; -(CH2)p(CHR6I)sOR85; or -(CH2)P(CHR61)SSR85; R73 is -(CH2)oR77; -(CH2)rO(CH2)0R77; -(CH2)rS(CH2)0R77; or -(CH2)rNR20(CH2)0R77; R74 is -(CH2)PNR78R79; -(CH2)PNR77R80; -(CH2)PC(=NR80)NR78R79; -(CH2)PC(=NOR50)NR78R79;
Figure imgf000105_0001
-(CH2)pN=C(NR78R80)NR79R 0;-(CH2)pC6H4NR7 R79; -(CH2)pC6H4NR77R80; -(CH2)pC6H4C(=NR80)NR78R79; -(CH2)pC6H4C(=NOR50)NR78R79;
-(CH2)pC6H4C(=NNR78R79)NR7 R79; -(CH2)pC6H4NR80C(=NR80)NR78R79;
-(CH2)pC6H4N=C(NR78R80)NR79R80; -(CH2)rO(CH2)mNR78R79; -(CH2)rO(CH2)mNR77R80;
-(CH2)rO(CH2)pC(=NR80)NR78R79; -(CH2)I.O(CH2)pC(=NOR50)NR78R79;
-(CH2)rO(CH2)pC(=NNR78R79)NR78R79; -(CH2)rO(CH2)mNR80C(=NR80)NR78R79; -(CH2)rO(CH2)mN=C(NR78R80)NR79R80; -(CH2)rO(CH2)pC6H4CNR78R79;
-(CH2)rO(CH2)pC6H4C(=NR80)NR78R79; -(CH2)rO(CH2)pC6H4C(=NOR50)NR78R79;
-(CH2)rO(CH2)pC6H4C(=NNR78R79)NR78R79;
-(CH2)rO(CH2)pC6H4NR80C(=NR80)NR78R79; -(CH2)rS(CH2)mNR78R79;
-(CH2)rS(CH2)mNR77R80;-(CH2)rS(CH2)pC(=NR80)NR78R79; -(CH2)rS(CH2)pC(=NOR50)NR78R79; -(CH2)rS(CH2)pC(=NNR78R79)NR78R79;
-(CH2)rS(CH2)mNR80C(=NR80)NR78R79; -(CH2)rS(CH2)mN=C(NR78R80)NR79R80;
-(CH2)rS(CH2)pC6H4CNR78R79; -(CH2)rS(CH2)pC6H4C(=NR80)NR78R79;
-(CH2)rS(CH2)pC6H4C(=NOR50)NR78R79; -(CH2)rS(CH2)pC6H4C(=NNR78R79)NR78R79; -(CH2)rS(CH2)pC6H4NR80C(=NR80)NR78R79; -(CH2)pNR80COR64; -(CH2)pNR80COR77;
-(CH2)PNR 0CONR78R79; or -(CH2)PC6H4NR80CONR78R79; R75 is lower alkyl; lower alkenyl; or aryl-lower alkyl; R33 and R75 taken together can form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
Figure imgf000106_0001
R75 and R82 taken together can form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; R76 is H; lower alkyl; lower alkenyl; aryl-lower alkyl; -(CH2)0OR72; -(CH2)0SR72;
-(CH2)0NR33R34; -(CH2)0OCONR33R75; -(CH2)oNR20CONR33R82;
-(CH2)0COOR75; -(CH2)0CONR58R59; -(CH2)oPO(OR60)2; -(CH2)pS02R62; or -(CH2)oCOR64;
R77 is -C6R67R68R69R70R76; or a heteroaryl group of one of the formulae
Figure imgf000106_0002
H1 H2 H3 H4 H5
Figure imgf000106_0003
H16 H17 H18 H19 H20
Figure imgf000107_0001
H21 H22 H23 H24 H25
Figure imgf000107_0002
H26 H27 H28 H29
Figure imgf000107_0003
H30 H31 H32 H33
Figure imgf000107_0004
H34 H35 H36 H37
Figure imgf000107_0005
H38 H39 H40 H41
Figure imgf000107_0006
H42 H43 H44 H45
Figure imgf000107_0007
H46 H47 H48 H49 R78 is H; lower alkyl; aryl; or aryl-lower alkyl;
R78 and R82 taken together can form: -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; R79 is H; lower alkyl; aryl; or aryl-lower alkyl; or
R78 and R79, taken together, can be -(CH2)2-7-; -(CH2)20(CH2)2-; or -(CH2)2NR57(CH2)2-;
R80 is H; or lower alkyl;
R81 is H; lower alkyl; or aryl-lower alkyl;
R82 is H; lower alkyl; aryl; heteroaryl; or aryl-lower alkyl; R33 and R82 taken together can form: -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-;
R83 is H; lower alkyl; aryl; or -NR78R79;
R84 is -(CH2)pCONR78R79; -(CH2)PNR80CONR78R79; -(CH2)pC6H4CONR78R79; or - (CH2)pC6H4NR80CONR78R79; R85 is lower alkyl; or lower alkenyl;
R86 is R74; -[(CH2)u-X]r(CH2)vNR78R79; -[(CH2)ll-X],-(CH2)v-C(=NR80)NR78R79; X is -0-, -NR20-
Figure imgf000108_0001
H50 H51 H52 H53 H54
-S-, -OCOO-, u is 1-3, t is 1-6, v is 1-3;
with the proviso that in said chains Z and Z1 of n and , respectively, n' α-amino acid residues
if n is 4 and n' is 6, the amino acid residues in positions 1 to 4 of Z and in positions 1' to 6' of Z1 are:
- PI of type C or of type D or of type E or of type F, or the residue is Pro;
P2 of type E or of type F; P3 of type F, or the residue is Pro; P4 of type E; PI": of type C or of type D or of type E or of type F, or the residue is Gly; P2' of type D or of type C; P3' of type F or the residue is Pro; P4' of type D or of type C; P5' of type E, or of type F or the residue is Pro; and P6': of type E or of type F, or the residue is Pro; or
P3 and P3', taken together, can form a group of type H;
and
if n is 5 and n' is 7, the amino acid residues in positions 1 to 5 of Z and in positions 1' to 7' of Z1 are:
PI of type C or of type D or of type E or of type F, or the residue is Pro; P2 of type E or of type F; P3 of type F, or the residue is Pro; P4 of type F; P5 of type E
PI': of type C or of type D or of type E or of type F, or the residue is Pro;
P2': of type F;
P3': of type D or the residue is Pro;
P4': of type E or of type F;
P5': of type D, or the residue is Pro;
P6': of type E or of type F, or the residue is Pro; and
P7': of type E or of type I, or the residue is Gly; or
P2 and P2' and/or P4 and P4', taken together, can form a group of type H;
at P7' also D-isomers being possible,
and pharmaceutically acceptable salts thereof. Compounds according to claim 1 wherein
Figure imgf000110_0001
is a group of formula (al) or (a2).
3. Compounds according to claim 2 wherein A is a group of one of the formulae Al to
A69;
R1 is hydrogen or lower alkyl;
R2 is H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55 is lower alkyl; or lower alkenyl); -CH2)mSR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; -
(CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)mOCONR33R7S (where R33 is H; lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are
-(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)mNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)oN(R20)COR64(where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl);
(CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; or lower alkyl; or R58 and R59 taken together are -
(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -
(CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R3 is H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55 is lower alkyl; or lower alkenyl);
-(CH2)mSR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mOCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -
(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)n,NR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-;
-(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)oN(R20)COR64 (where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl);
-(CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are - (CH2)2-6-;
-(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy). R4 is H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55 is lower alkyl; or lower alkenyl);
-(CH2)mSR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-;
-(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)m0C0NR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -
(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and
R82 taken together are -(CH2)2.6-;
-(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mN(R20)COR64(where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl);
-(CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; or lower alkyl; or R58 and R59 taken together are -
-(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: isH; or lower alkyl); -(CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
R5 is lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56 is lower alkyl; or lower alkenyl); (CH2)0NR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2-6-; -
Figure imgf000112_0001
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)0OCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are
-(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)0NR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2.6-; -
Figure imgf000112_0002
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)oN(R20)COR64 (where: R20 is H; or lower alkyl; R64 is alkyl; alkenyl; aryl; aryl-lower alkyl; or heteroaryl-lower alkyl); -(CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl);
-(CH2)0CONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; or lower alkyl; or
R58 and R59 taken together are -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or - (CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy):
R6 is H; lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; -
(CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)0OCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are
-(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-; - (CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)oN(R20)COR64 (where R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); - (CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; or lower alkyl; or R58 and R59 taken together are - (CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or - (CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy); R7 is lower alkyl; lower alkenyl; -(CH2)qOR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)qSR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)qNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)qOCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are
-(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)qNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-; - (CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)qN(R20)COR64(where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); - (CH2)rCOOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)qCONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; or lower alkyl; or R58 and R59 taken together are - (CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)rPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)rS02R62 (where R62 is lower alkyl; or lower alkenyl); or - (CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy); R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)oNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2-6-;
-(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)0OCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or - (CH2)2NR57(CH2)2-; where RS7 is H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2.6-;
-(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oN(R20)COR64 (where R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; or lower alkyl; or R58 and R59 taken together are -
-(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R9 is lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2-6-; -
Figure imgf000114_0001
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)0OCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are
-(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-; - (CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)oN(R20)COR64(where R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); - (CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; or lower alkyl; or R58 and R59 taken together are - (CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)0PO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0SO2R62 (where R62 is lower alkyl; or lower alkenyl); or - (CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R10 is lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)0OCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are
-(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57: H is or lower alkyl); -(CH2)oNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-; -
Figure imgf000115_0001
-(CH2)2S(CH2)2-; or -(CH2)2 57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)oN(R20)COR64(where R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); - (CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are -
(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)0PO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or - (CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R11 is H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55 is lower alkyl; or lower alkenyl);
-(CH2)mSR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2-6-;
-(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mOCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or
R33 and R75 taken together ar -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -
(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and
R82 taken together are -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)mN(R20)COR64 (where R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl);
-(CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are -
-(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R12 is H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)mSR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2-6-;
-(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)mOCONR33R75 (where R33is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or
R33 and R75 taken together are -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or - (CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-;
-(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2N 57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mN(R20)COR64 (where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl);
-(CH2)rCOOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)rCONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; or lower alkyl; or R58 and R59 taken together are -
-(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)rPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy):
R13 is lower alkyl; lower alkenyl; -(CH2)qOR55 (where R55 isis lower alkyl; or lower alkenyl);
-(CH2)qSR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)qNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2-6-; -
Figure imgf000116_0001
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)q0C0NR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or
R33 and R75 taken together are -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)qNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-; -
Figure imgf000116_0002
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)qN(R20)COR64 (where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); -
(CH2)rCOOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)qCONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; or lower alkyl; or R58 and R59 taken together are -
(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)rPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)rS02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R14 is H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55 is lower alkyl; or lower alkenyl);
-(CH2)mSR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)mOCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or
R33 and R75 taken together are -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -
(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl is R82: H; or lower alkyl; or R33 and
R82 taken together are -(CH2)2.6-;
-(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)mN(R20)COR64 (where: R20 is H; lower alkyl; R64 is lower alkyl; or lower alkenyl);
-(CH2)oCOOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; or lower alkyl; or R58 and R59 taken together are -
-(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)0PO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R15 is lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl);
-(CH2)0SR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; -
(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)0OCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or
R33 and R75 taken together are
-(CH2)2.5-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-; -
(CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)oN(R20)COR64 (where R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); -
NR20COlower alkyl (R20=H; or lower alkyl); being particularly favoured; -(CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl, or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are -(CH2)2^-; - (CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or (CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R16 is lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)0OCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; J or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)oN(R20)COR64 (where R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); - (CH2)0C00R57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0C0NR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; or lower alkyl; or R58 and R59 taken together are - (CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or - (CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy); and R17 is lower alkyl; lower alkenyl; -(CH2)qOR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)qSR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)qNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; - (CH2)2θ(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)qOCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are
-(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)qNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)qN(R20)COR64(where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); - (CH2)rCOOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)qCONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are - (CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)rPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)rS02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH^ H^8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
4. Compounds according to claim 2 or 3 wherein A is a group of one of the formulae A5
(with R2 being H); A8; A22; A25; A38 (with R2 being H); A42; and A50.
5. Compounds according to claim 4 wherein A is a group of formula
Figure imgf000119_0001
A8' wherein R20 is H or lower alkyl; and R64 is alkyl; alkenyl; aryl; aryl-lower alkyl; or heteroaryl- lower alkyl.
6. Compounds according to claim 5 wherein R64 is n-hexyl; n-heptyl; 4-(phenyl)benzyl; diphenylmethyl, 3-amino-propyl; 5-amino-pentyl; methyl; ethyl; isopropyl; isobutyl; n-propyl; cyclohexyl; cyclohexylmethyl; n-butyl; phenyl; benzyl; (3-indolyl)methyl; 2-(3-indolyl)ethyl; (4-phenyl)phenyl; or n-nonyl.
7. Compounds according to claim 2 wherein A is a group of one of the formulae A70 to
A104;
R20 is H; or lower alkyl;
R18 is lower alkyl;
R19 is lower alkyl; lower alkenyl; -(CH2)pOR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)pSR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)pNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; -
(CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)p0C0NR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are
-(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)pNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-; - (CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)PN(R20)COR64 (where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); (CH2)pC00R57 (where R57: lower alkyl; or lower alkenyl); (CH2)pC0NR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; or lower alkyl; or R58 and R59 taken together are - (CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)0PO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)pS02R62 (where R62 is lower alkyl; or lower alkenyl); or (CH2)0C6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R21 is H; lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; -
(CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl) ; -
(CH2)0OCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are
-(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)oNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)oN(R20)COR64 (where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); -
(CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl, or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are -
(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)0PO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -
(CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R22 is lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl);
-(CH2)„SR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)0OCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are
-(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-; - (CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)oN(R20)COR64(where R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); - (CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl, or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are - (CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8 is H; F; Cl; CF; lower alkyl; lower alkenyl; or lower alkoxy);
R23 is H; lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2-6-; -
Figure imgf000121_0001
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)0OCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or
R33 and R75 taken together are
-(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)0NR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-; -
(CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)oN(R20)COR64 (where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); - NR20COlower alkyl (R20=H; or lower alkyl) being particularly favoured; -(CH2)0COOR57
(where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl, or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are -(CH2)2-6-; -
(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -
(CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R24 is lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2-6-; -
Figure imgf000122_0001
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)0OCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)0N(R20)COR64 (where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); - NR20COlower alkyl (R20=H ; or lower alkyl) being particularly favoured; -(CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl, or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are
Figure imgf000122_0002
- (CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)0PO(OR60)2 (where R60 is lower alkyl; or lower alkenyl);
-(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8 is H;' F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R25 is H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -
(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mOCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mN(R20)COR64 (where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); -(CH2)oC00R57 (where R57 is lower alkyl; or lower alkenyl); - (CH2)0CONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or - (CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)0PO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy);
R26 is H; lower alkyl; lower alkenyl; -(CH2)mOR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)mNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or - (CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mOCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)mN(R20)COR64 (where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); - (CH2)0CONR58R59 (where R58 is lower alkyl; or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are -(CH2)2.6-; -(CH2)2θ(CH2)2-; -(CH2)2S(CH2)2-; or - (CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)0PO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)q H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy); or, alternatively, R25 and R26 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR34(CH2)2-; R27 is H; lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)0OCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are
-(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)0NR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)oN(R20)COR64 (where R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); - (CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl, or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are - (CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0SO2R62 (where R62 is lower alkyl; or lower alkenyl); or - (CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy); R28 is lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2-6-; -
Figure imgf000124_0001
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)0OCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are
-(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)oN(R20)COR64(where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); - (CH2)0COOR57 (where R57 is lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl, or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are - (CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl);
-(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy); and
R29 is lower alkyl; lower alkenyl; -(CH2)0OR55 (where R55 is lower alkyl; or lower alkenyl); -(CH2)0SR56 (where R56 is lower alkyl; or lower alkenyl); -(CH2)0NR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2.6-; - (CH2)20(CH2)2-;
-(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)oOCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are -(CH2)2.6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)0NR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-; -
(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); - (CH2)oN(R20)COR64(where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); -
NR20COlower-alkyl (R20=H; or lower alkyl) being particularly favoured; -(CH2)0COOR57
(where R57 is lower alkyl; or lower alkenyl);
-(CH2)0CONR58R59 (where R58 is lower alkyl, or lower alkenyl; and R59 is H; lower alkyl; or
R58 and R59 taken together are -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or - (CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)oPO(OR60)2 (where R60 is lower alkyl; or lower alkenyl);
-(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)qC6H4R8 (where R8 is H;
F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy).
8. Compounds according to claim 7 wherein R23, R24 and R29 are -NR20-CO-lower alkyl where R20 is H; or lower alkyl.
9. Compounds according to claim 7 or 8 wherein A is a group of one of the formulae A74 (with R22 being H); a75; A76; A77 (with R22 being H); A78; and A79.
10. Compounds according to any one of claims 2 to 9 wherein B is a group of formula -NR20CH(R71)- or an enantiomer of one of the groups A5 (with R2 being H); A8; A22; A25; A38 (with R2 being H); A42; A47; and A50.
11. Compounds according to claim 10 wherein B-CO is Asn; Cys; Gin; His; Met; Phe;
Pro; Ser; Thr; Trp; Tyr; Sar; 4AmPhe; 3AmPhe; 2AmPhe; Phe(mC(NH2)=NH;
Phe(pC(NH2)=NH; Phe(mNHC (NH2)=NH; Phe(pNHC (NH2)=NH; Phg; Cha; C4al; C5al; 2-
Nal; 1-Nal; 4C1-Phe; 3C1-Phe; 2C1-Phe; 3,4Cl2Phe; 4F-Phe; 3F-Phe; 2F-Phe; Tic; Thi; Tza;
Mso; Y(Bzl); Bip; S(Bzl); T(Bzl); hCha; hCys; hSer; hPhe; Bpa; Pip; OctG; MePhe; MeNle; MeAla; Melle; MeVal; MeLeu, .
12. Compounds according to claim 10 or 11 wherein B is a group, having (L)- configuration, of formula
Figure imgf000126_0001
A8"
wherein R20 is H; or lower alkyl; and R64 is alkyl; alkenyl; aryl; aryl-lower alkyl; or heteroaryl- lower alkyl.
13. Compounds according to claim 12 wherein R64 is n-hexyl; n-heptyl; 4-(phenyl)benzyl; diphenylmethyl, 3-amino-propyl; 5-amino-pentyl; methyl; ethyl; isopropyl; isobutyl; n-propyl; cyclohexyl; cyclohexylmethyl; n-butyl; phenyl; benzyl; (3-indolyl)methyl; 2-(3-indolyl)ethyl; (4-phenyl)phenyl; or n-nonyl.
14. Compounds according to claim 1 wherein
Figure imgf000126_0002
is a group of formula (a4) or (bl);
Figure imgf000126_0003
is the residue of AMP A;
R1 is H; or lower alkyl;
R20 is H; or lower alkyl;
R30 is H; or methyl;
R31 is H; lower alkyl; lower alkenyl; -(CH2)pOR55 (where R55 is lower alkyl; or lower alkenyl);
-(CH2)PNR33R34 (where R33 is lower alkyl; or lower alkenyl; R34 is H; or lower alkyl; or R33 and R34 taken together are -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or - (CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)pOCONR33R75 (where R33 is H; or lower alkyl; or lower alkenyl; R75 is lower alkyl; or R33 and R75 taken together are -(CH2)2-6-; - (CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or
-(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)PNR20CONR33R82 (where R20 is H; or lower alkyl; R33 is H; or lower alkyl; or lower alkenyl; R82 is H; or lower alkyl; or R33 and R82 taken together are -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl); -(CH2)PN(R20)COR64 (where: R20 is H; or lower alkyl; R64 is lower alkyl; or lower alkenyl); -(CH2)0COOR57 (where R57 is H; lower alkyl; or lower alkenyl); -(CH2)0CONR58R59 (where R58 is lower alkyl, or lower alkenyl; and R59 is H; lower alkyl; or R58 and R59 taken together are -(CH2)2-6-; -(CH2)20(CH2)2-; -(CH2)2S(CH2)2-; or -
(CH2)2NR57(CH2)2-; where R57 is H; or lower alkyl);
-(CH2)0PO(OR60)2 (where R60 is lower alkyl; or lower alkenyl); -(CH2)0S02R62 (where R62 is lower alkyl; or lower alkenyl); or -(CH2)rC6H4R8 (where R8 is H; F; Cl; CF3; lower alkyl; lower alkenyl; or lower alkoxy); most preferably -CH2CONR58R59 (where R58 is H; or lower alkyl; and R59 is lower alkyl; or lower alkenyl); and
R32 is H; or methyl.
15. Compounds according to claim 14 wherein R1 is H; R20 is H; R30 is H; R31 is carboxymethyl; or lower alkoxycarbonylmethyl; and R32 is H.
16. Compounds according to any one of claims 1 to 15 wherein n is 4, n' is 6 and the α- amino acid residues in positions 1 to 4 of the chain Z and l'-6' in chain Z1 are:
PI of type D or of type E or of type F, or the residue is Pro; P2 of type E or of type F; P3 of type F, or the residue is Pro; P4 of type E;
PI': oftype E or of type F, or the residue is Gly;
P2': of type D; - P3': of type F or the residue is Pro;
P4': of type D;
P5': of type E, or of type F or the residue is Pro; and
P6': oftype E or of type F, or the residue is Pro; or P3 and P3', taken together, can form a group of type H
17. Compounds according to any one of claims 1 to 15 wherein n is 5, n' is 7 and the α-amino acid residues in positions 1 to 5 of the chain Z and 1 -7' in chain Z1 are:
PI of type D or of type E or of type F, or the residue is Pro; P2 of type E or of type F; P3 of type F, or the residue is Pro; P4 of type F;
P5 of type E
PI': of type D or of type E or of type F, or the residue is Pro; P2': of type F;
P3': of type D or the residue is Pro; P4': of type F;
P5': of type D, or the residue is Pro; P6': of type E or of type F, or the residue is Pro; and P7': of type E or of type I, or the residue is Gly; or P2 and P2' and/or P4 and P4', taken together, can form a group of type H; at P7'also D-isomers being possible.
18. Compounds according to claim 16 wherein the α-amino acid residues in positions 1 to 4 of the chain Z and the α-amino acid residues in positions 1' to 6' chain Z1 are: PI: Tyr, or Arg;
P2: Cit, or Arg;
P3: Cys;
P4: Arg-NH2;
PI': Lys, or Arg;
P2': Tyr;
P3': Cys;
P4': 2-Nal;
P5': Arg; and
P6': Arg.
Cys at pos P3 and P3' form a disulfide bridge
9. Compounds according to claim 17 wherein the α-amino acid residues in positions 1 to of the chain Z and the α-amino acid residues in positions 1' to 7' chain Z1 are: PI: Tyr; - P2: Arg;
P3: Cit; P4: Cys;
P5: Arg, or Arg-NH2; PI': Lys; - P2': Cit;
P3': Tyr; P4': Cys;
P5': 2-Nal, Trp, F(pNH2), or W(6-C1); P6': Arg; and - PT: DArg, Arg, Ac-Arg, iPr-Arg, (EA)G, (PrA)G, (BA)G, (EGU)G,
(PrGU)G, or (BGU)G.
Cys at pos P4 and P4Λ form a disulfide bridge 20. A compound of formula I according to claim 1 wherein the template is LLys- Pro, n is 4, n' is 6 and the amino acid residues in positions 1 to 4 of the chain Z and the amino acid residues in positions 1' to 6' chain Z1 are : PI: Tyr; P2: Cit; P3: Cys; P4: Arg-NH2; - PI': Arg;
P2': Tyr; P3': Cys; P4': 2-Nal; P51: Arg; and - P6': Arg.
Cys at position P4' and P4 are linked by a disulfide bridge
21. A compound of formula I according to claim 1 wherein the template is DPro-LPro, n is 5, n' is 7 and the amino acid residues in positions 1 to 5 of the chain Z and the amino acid residues in positions 1' to 7' chain Z1 are: PI: Tyr; - P2: Arg;
P3: Cit; P4: Cys; P5: Arg-NH2; PI': Lys; - P2': Cit;
P3': Tyr; P4': Cys; P5': 2-Nal; P6': Arg; and - P7': Arg.
Cys at position P4' and P4 form a disulfide bridge
22. A compound of formula I according to claim 1 wherein the template is DPro-LPro, n is 5, n' is 7 and the amino acid residues in positions 1 to 5 of the chain Z and the amino acid residues in positions 1 ' to 7' chain Z1 are:
PI: Tyr;
P2: Arg;
P3: Cit;
P4: Cys; - P5: Arg-NH2;
PI': Lys;
P2': Cit;
P3*: Tyr;
P4': Cys; - P51: 2-Nal;
P6': Arg; and
PT: Ac-Arg. Cys at position P4' and P4 form a disulfide bridge
23. A compound of formula I according to claim 1 wherein the template is DPro-LPro, n is 5, n' is 7 and the amino acid residues in positions 1 to 5 of the chain Z and the amino acid residues in positions 1' to 7' chain Z1 are: Pi: Tyr;
- P2: Arg;
- P3: Cit;
- P4: Cys;
- P5: Arg-NH2;
- PI': Lys;
- P2': Cit;
- P3': Tyr;
- P4': Cys;
- P5': 2-Nal
- P6': Arg; and
- P7': DArg.
Cys at position P4' ; and P4 form a disulfide bridge
24. A compound of formula I according to claim 1 wherein the template is DPro-LPro, n is 5, n' is 7 and the amino acid residues in positions 1 to 5 of the chain Z and the amino acid residues in positions 1 ' to 7' chain Z1 are:
PI: Tyr;
P2: Arg;
P3: Cit;
P4: Cys; - P5: Arg-NH2;
PI': Lys;
P2': Cit;
P3': Tyr;
P4': Cys; - P5': Phe(pNH2);
P6': Arg; and
PT: Arg. Cys at position P4' and P4 form a disulfide bridge
25. A compound of formula I according to claim 1 wherein the template is Pro-LPro, n is 5, n' is 7 and the amino acid residues in positions 1 to 5 of the chain Z and the amino acid residues in positions 1' to 7' chain Z1 are:
PI: Tyr; - P2: Arg;
P3: Cit;
P4: Cys;
P5: Arg-NH2;
PI': Lys; - P2': Cit;
P3': Tyr;
P4': Cys;
P5': 2-Nal;
P6': Arg; and - PT: (PrA)G.
Cys at position P4' and P4 form a disulfide bridge
26. A compound of formula I according to claim 1 wherein the template is DPro-LPro, n is 5, n' is 7 and the amino acid residues in positions 1 to 5 of the chain Z and the amino acid residues in positions 1' to 7' chain Z1 are:
PI: Tyr;
P2: Arg;
P3: Cit;
P4: Cys;
P5: Arg;
PI': Lys;
P2': Cit;
P3': Tyr;
P4': Cys;
P5': 2-Nal;
P6': Arg; and
PT: Arg.
Cys at position P4Λ and P4 form a disulfide bridge
27. A compound of formula I according to claim 1 wherein the template is (bl)-l 54, n is 5, n' is 7 and the amino acid residues in positions 1 to 5 of the chain Z and the amino acid residues in positions 1' to 7' chain Z! are: PI: Tyr; - P2: Arg;
P3: Cit; P4: Cys; P5: Arg-NH2; PI': Lys; - P2': Cit;
P3': Tyr; P4': Cys; P5': 2-Nal; P6': Arg; and PT: Arg.
Cys at position P4' and P4 form a disulfide bridge
28. A compound of formula I according to claim 1 wherein the template is AMP A, n is 5, n' is 7 and the amino acid residues in positions 1 to 5 of the chain Z and the amino acid residues in positions 1 ' to 7' chain Z1 are: PI: Tyr; P2: Arg; P3: Cit; P4: Cys; - P5: Arg-NH2;
PI': Lys; P2': Cit; P3': Tyr; P4': Cys; - P5': 2-Nal;
P6': Arg; and PT: Arg. Cys at position P4 and P4 form a disulfide bridge
29. Enantiomers of the compounds of formulae I as defined in claim 1.
30. Compounds according to any one of claims 1 to 29 for use as therapeutically active substances.
31. Compounds according the claims 29 for use as CXCR4 antagonists.
32. A pharmaceutical composition containing a compound according to any one of claims 1 to 29 and a pharmaceutically inert carrier.
33. Compositions according to claim 32 in a form suitable for oral, topical, transdermal, injection, buccal, transmucosal, pulmonary or inhalation administration.
34. Compositions according to claim 32 or 33 in form of tablets, dragees, capsules, solutions, liquids, gels, plaster, creams, ointments, syrup, slurries, suspensions, spray, nebuliser or suppositories.
35. The use of compounds according to any one of claims 1 to 29 for the manufacture of a medicament for treating or preventing of HIV infections, or for treatment of cancer or for treatment of inflammatory disorders.
36. A process for the manufacture of compounds according to any one of claims 1 -28 which process comprises
(a) coupling an appropriately functionalized solid support with an appropriately N- protected derivative of that amino acid which in the desired end-product is in position 4 of Z if n is 4 or in position 5 of Z if n is 5, any functional group which may be present in said N- protected amino acid derivative being likewise appropriately protected;
(b) removing the N-protecting group from the product thus obtained;
(c) coupling the product thus obtained with an appropriately N-protected derivative of that amino acid which in Z of the desired end-product is one position nearer the N-terminal amino acid residue, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected;
(d) removing the N-protecting group from the product thus obtained; (e) repeating steps (c) and (d) until the N-terminal amino acid residue of Z has been introduced;
(f) coupling the product thus obtained with a compound of the general formula
Figure imgf000135_0001
II wherein
Figure imgf000135_0002
is as defined in claim 1 and X is an N-protecting group or, if
Figure imgf000135_0003
is to be group (al), or (a2), above, alternatively
(fa) coupling the product obtained in step (e) with an appropriately N-protected derivative of an amino acid of the general formula HOOC-B-H III or HOOC-A-H IV wherein B and A are as defined in claim 1, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected;
(fb) removing the N-protecting group from the product thus obtained; and
(fc) coupling the product thus obtained with an appropriately N-protected derivative of an amino acid of the above general formula IV and, respectively, III, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected; or if
Figure imgf000136_0001
is to be group (a3), above, alternatively (fa') coupling the product obtained in step (e) with an appropriately N-protected derivative of an amino acid of the above general formula III, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected;
(fb') removing the N-protecting group from the product thus obtained; and (fc') coupling the product thus obtained with an appropriately N-protected derivative of an amino acid of the above general formula III, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected; (g) removing the N-protecting group from the product obtained in step (f) or (fc) or (fc'); (h) coupling the product thus obtained with an appropriately N-protected derivative of that amino acid which in the desired end-product is in position 1 of Z1, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected;
(i) removing the N-protecting group from the product thus obtained; (j) coupling the product thus obtained with an appropriately N-protected derivative of that amino acid which in the desired end-product is one position farther away from position 1 of Z1, any functional group which may be present in said N-protected amino acid derivative being likewise appropriately protected;
(k) removing the N-protecting group from the product thus obtained; (1) repeating steps (j) and (k) until all amino acid residues of Z1 have been introduced;
(m) if desired, selectively deprotecting one or several protected functional group(s) present in the molecule and appropriately substituting the reactive group(s) thus liberated; (n) if desired, forming one or two interstrand linkage(s) between side-chains of appropriate amino acid residues at opposite positions of the β-strand region; (o) detaching the product thus obtained from the solid support and removing any protecting groups present on functional groups of any members of the chain of amino acid residues and, if desired, any protecting group(s) which may in addition be present in the molecule; and (p) if desired, converting the product thus obtained into a pharmaceutically acceptable salt or converting a pharmaceutically acceptable, or unacceptable, salt thus obtained into the corresponding free compound of formula I or into a different, pharmaceutically acceptable, salt..
37. A process according to claim 36 but wherein an amino acid residue of type I is introduced by coupling with a leaving group-containing acetylating agent, followed by nucleophilic displacement with an amine of the formula H2NR86 which, if necessary, is appropriately protected.
38. A process according to claim 37 wherein said leaving group-containing acetylating agent is bromo, chloro or iodo acetic acid.
39. A modification of the process according to any one of claims 36 to 38 for the manufacture of compounds according to claim 29 in which enantiomers of all chiral starting materials are used.
PCT/EP2003/004641 2003-05-02 2003-05-02 Template-fixed peptidomimetics as medicaments against hiv and cancer WO2004096838A1 (en)

Priority Applications (7)

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DE60321053T DE60321053D1 (en) 2003-05-02 2003-05-02 MATRIC FIXED PEPTIDE MIMETICS AS MEDICAMENTS AGAINST HIV AND CANCER
AT03816774T ATE395355T1 (en) 2003-05-02 2003-05-02 MATTRICE-FIXED PEPTIDE MIMETICS AS MEDICATIONS AGAINST HIV AND CANCER
AU2003232254A AU2003232254A1 (en) 2003-05-02 2003-05-02 Template-fixed peptidomimetics as medicaments against hiv and cancer
PCT/EP2003/004641 WO2004096838A1 (en) 2003-05-02 2003-05-02 Template-fixed peptidomimetics as medicaments against hiv and cancer
EP03816774A EP1622930B9 (en) 2003-05-02 2003-05-02 Template-fixed peptidomimetics as medicaments against hiv and cancer
US10/550,778 US7838496B2 (en) 2003-05-02 2003-05-02 Template-fixed peptidomimetics as medicaments against HIV and cancer
ES03816774T ES2306924T3 (en) 2003-05-02 2003-05-02 PEPTIDOMIMETICS FIXED TO A MATRIX AS MEDICATIONS AGAINST HIV AND CANCER.

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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006087001A1 (en) 2005-02-17 2006-08-24 Polyphor Ltd. Template-fixed beta-hairpin peptidomimetics with protease inhibitory activity
EP1773348A2 (en) * 2004-07-12 2007-04-18 Idun Pharmaceuticals, Inc. Tetrapeptide analogs
WO2007049771A1 (en) 2005-10-28 2007-05-03 Ono Pharmaceutical Co., Ltd. Compound containing basic group and use thereof
WO2007058322A1 (en) 2005-11-18 2007-05-24 Ono Pharmaceutical Co., Ltd. Basic group-containing compound and use thereof
WO2007079597A1 (en) * 2006-01-16 2007-07-19 Polyphor Ltd. Template - fixed peptidomimetics with antimicrobial activity
WO2008092281A1 (en) 2007-01-29 2008-08-07 Polyphor Ltd. Template-fixed peptidomimetics
US7709370B2 (en) 2007-09-20 2010-05-04 International Business Machines Corporation Spin-on antireflective coating for integration of patternable dielectric materials and interconnect structures
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JP2015155430A (en) * 2015-04-02 2015-08-27 ポリフォー・アクチェンゲゼルシャフトＰｏｌｙｐｈｏｒ Ａｇ Conformationally constrained, synthetic macrocyclic compounds
CN105111280A (en) * 2005-02-17 2015-12-02 波利弗尔有限公司 Template-fixed beta-hairpin peptidomimetics with protease inhibitory activity

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7964181B2 (en) * 2006-03-30 2011-06-21 Palatin Technologies, Inc. Amino acid surrogates for peptidic constructs
US8114844B2 (en) * 2006-03-30 2012-02-14 Palatin Technologies, Inc. Linear and cyclic melanocortin receptor-specific peptidomimetics
US8580746B2 (en) * 2006-03-30 2013-11-12 Palatin Technologies, Inc. Amide linkage cyclic natriuretic peptide constructs
CN101641372B (en) 2007-02-28 2012-11-28 波利弗尔有限公司 Template-fixed peptidomimetics
CN107529753A (en) * 2015-03-11 2018-01-02 卢莫斯制药公司 The synthesis of circular muscle acid and the like

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001016161A1 (en) * 1999-08-30 2001-03-08 Universität Zürich SYNTHESIS OF TEMPLATE-FIXED β-HAIRPIN LOOP MIMETICS
WO2002070547A1 (en) * 2001-02-23 2002-09-12 Polyphor Ltd. Template-fixed peptidomimetics with antimicrobial activity
WO2003054000A1 (en) * 2001-12-11 2003-07-03 Polyphor Ltd. Template-fixed peptidomimeticsas inhibitors of serine proteases

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001016161A1 (en) * 1999-08-30 2001-03-08 Universität Zürich SYNTHESIS OF TEMPLATE-FIXED β-HAIRPIN LOOP MIMETICS
WO2002070547A1 (en) * 2001-02-23 2002-09-12 Polyphor Ltd. Template-fixed peptidomimetics with antimicrobial activity
WO2003054000A1 (en) * 2001-12-11 2003-07-03 Polyphor Ltd. Template-fixed peptidomimeticsas inhibitors of serine proteases

Non-Patent Citations (19)

* Cited by examiner, † Cited by third party
Title
"ESCOM Leiden, The Netherlands", 1990
AHMED ET AL., J. BIOL. CHEM., vol. 250, 1975, pages 8477 - 8482
D OBRECHT ET AL.: "Novel peptidemimetic building blocks and strategies for efficient lead finding", ADVANCES IN MEDICINAL CHEMISTRY, vol. 4, 1999, JAI PRESS,, US, pages 1 - 68, XP002137026 *
D, OBRECHT; M. ALTORFER; J. A. ROBINSON, ADV. MED. CHEM., vol. 4, 1999, pages 1 - 68
H TAMAMURA ET AL.: "Certification of the critical importance of a L-3-(2-naphthyl)alanine at position 3 of a sepcific CXCR4 inhibitor, T140, leads to an exploratory performance of its downsizing study", BIOORGANIC & MEDICINAL CHEMISTRY., vol. 10, no. 5, May 2002 (2002-05-01), ELSEVIER SCIENCE LTD., GB, pages 1417 - 1426, XP002265745, ISSN: 0968-0896 *
H TAMAMURA ET AL.: "Conformational study of a highly specific CXCR4 inhibitor, T140, disclosing the close proximity of its intrinsic pharmacophores associated with strong anti-HIV activity", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. 11, 2001, OXFORD, GB, pages 359 - 362, XP002265744, ISSN: 0960-894X *
H TAMAMURA ET AL.: "Development of specific CXCR4 inhibitors possessing high selectivity indexes as well as complete stability in serum based on an anti-HIV peptide T140", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. 11, 2001, OXFORD, GB, pages 1897 - 1902, XP002265743, ISSN: 0960-894X *
J A ROBINSON: "The design, synthesis and conformation of some new beta-hairpin mimetics: novel reagents for drug and vaccine discovery", SYNLETT, vol. 4, 1999, THIEME VERLAG, STUTTGART., DE, pages 429 - 441, XP001080054, ISSN: 0936-5214 *
J. A. ROBINSON, SYN. LETT., vol. 4, 2000, pages 429 - 441
J. P. TAM ET AL., SYNTHESIS, 1979, pages 955 - 957
K SATO ET AL.: "Solid phase synthesis of human growth hormone-releasing factor analogs containing a bicyclic beta-turn dipeptide", INTERNATIONAL JOURNAL OF PEPTIDE AND PROTEIN RESEARCH., vol. 38, no. 4, April 1991 (1991-04-01), MUNKSGAARD, COPENHAGEN., DK, pages 340 - 345, XP000229209, ISSN: 0367-8377 *
L JIANG ET AL.: "Combinatorial biomimetic chemistry: parallel synthesis of a small library of beta-hairpin mimetics based on loop III from human platelet-derived growth factor B", HELVETICA CHIMICA ACTA., vol. 83, 2000, VERLAG HELVETICA CHIMICA ACTA. BASEL., CH, pages 30097 - 3112, XP002202283, ISSN: 0018-019X *
L. JIANG ET AL., HELV. CHIM. ACTA., vol. 83, 2000, pages 3097 - 3112
M FAVRE ET AL.: "Structural mimicry of canonical conformations in antibody hypervariable loops using cyclic peptides containing a heterochiral diproline template", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY., vol. 121, no. 12, 31 March 1999 (1999-03-31), AMERICAN CHEMICAL SOCIETY, WASHINGTON, DC., US, pages 2679 - 2685, XP002137023, ISSN: 0002-7863 *
N FUIJI & H TAMAMURA: "Peptide-lead CXCR4 antagonists with anti-HIV activity", CURRENT OPINION IN INVESTIGATIONAL DRUGS., vol. 2, no. 9, 2001, CURRENT DRUGS, LONDON., GB, pages 1198 - 1202, XP009019518, ISSN: 0967-8298 *
PENNINGTON ET AL., PEPTIDES, pages 164 - 166
S C SHANKARAMMA ET AL.: "Macrocyclic hairpin mimetics of the cationic antimicrobial peptide protegrin I: a new family of broad-spectrum antibiotics", CHEMBIOCHEM - A EUROPEAN JOURNAL OF CHEMICAL BIOLOGY., vol. 3, 2002, WILEY VCH, WEINHEIM., DE, pages 1126 - 1133, XP002272157, ISSN: 1439-4227 *
S HANESSIAN ET AL.: "Design and synthesis of conformationally constrained amino acids as versatile scaffolds and peptide mimetics", TETRAHEDRON., vol. 53, no. 38, 1997, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM., NL, pages 12789 - 12854, XP004106190, ISSN: 0040-4020 *
STEWART ET AL.: "Solid Phase Peptide Synthesis", vol. III, 1984, PIERCE CHEMICAL COMPANY

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