CA2412954A1 - Peptidomimetic inhibitors of cathepsin d and plasmepsins i and ii - Google Patents

Abstract

The present invention relates to the design and synthesis of linear and cyclic inhibitors of cathepsin D
and plasmepsins I and II. The present invention also relates to the uses of these inhibitors for inhibiting invasion and metastasis of cancerous cells. The present invention further relates to the use of cathepsin D and plasmepsin I and II inhibitors for the prevention and treatment of Alzheimer's disease and malaria.

Description

PEPTIDOMIMETIC INHIBITORS OF CATHEPSIN D
AND PLASMEPSINS I AND II
FIELD Ol~ THE INVENTION
The invention relates to linear and cyclic inhibitor compounds of cathepsin D and plasmepsins I and II, and the use of these compounds for the prevention and treatment of diseases, and the like.
BACKGROUND OF THE INVENTION
Human cathepsin D is an intracellular aspartic protease normally found in lysozymes of all cells. The main physiological action of cathepsin D is degradation of cellular and phagocytosed proteins. Cathepsin D has also been implicated in a number of diseases. Elevated levels of cathepsin D have been correlated with poor prognosis in breast cancer. It has also been correlated with increase cell invasion and increased risk of metastasis, as well as shorter relapse-free survival. (See Rochefort, H., ~emin. Canser Biol. 1: 153 (1990) and Tandon, A. K. et al. N. Eng. J. Med.
322, 297 (1990)). The increased level of secretion of cathepsin D in breast cancer cells is due to both overexpression of the gene and altered processing of the protein.
High levels of cathepsin D and other proteases, such as collagenase, produced in the vicinity of the growing tumor may degrade the extracellular matrix and thereby promote the escape of cancer cells to the lymphatic and circulatory systems and enhance the invasion of new tissues. (Liotta L. A., Scientific American Feb:

(1992); and Liotta L. A. and Stetier-Stevenson W.G., Cancer Biol. 1: 99 (1990)).
Most deaths incurred from cancer are due to its metastatic spread to secondary organs, therefore an inhibitor of metastasis would have widespread therapeutic use.
Cathepsin D is also believed to be associated with degenerative brain changes, such as those associated with Alzheimer's disease. Cathepsin D is associated with cleavage of amyloid-(3-protein precursor, (Cataldo, A.M. et al., Proc.
Natl.
A~~d. ci. 87: 3861 ( 1990)) including a mutant precursor that enhances amvloid protein production in transfected cells (Ladror, U.S., et al. J. Biol. Chem.
269: 18422 WO 97/30072 PCTlUS97~2930 (I994)). The amyloid-/3-protein that results from proteolysis of the amyloid-a-protein precursor leads to senile plaque formation in brains and may be responsible for Alzheimer's disease. Recently elevated levels of cathepsin D have been found in cerebrospinal fluid in Alzheimer's patients (Schwager, A.L., et al. J.
Neurochem. 64:
443 (1995).
There is little known about substrate specificity and specific inhibitors for cathepsin D (Agarwal, N.S. and Rich, D.H., J. Med. Chem. 29: 2519 (1986);
Jupp, R.A. et al., Biochem. J. 265: 871 (1990); Scarborough, P.E. et al., Prot in science 2: 264 (1993); Baldwin, E.T. et al., Proc. Natl. Acad. Sci. 90: 6796 ( 1993)).
Accordingly, there is a need for the synthesis of compounds which are specific for the inhibition of the activity of cathepsin D and which may be used in the treatment of metastatic disease and Alzheimer's disease.
A number of cathepsin D inhibitors have been reported (Lin, T. Y. and Williams, H.R., J. Biol. Chem. 25: 11875 (1970)). Agarwal and Rich reported the design and synthesis of cathepsin D inhibitors wherein the scissile dipeptide unit in a substrate sequence was replaced with a statine (Sta) residue or by a phenylstatine (Pst) unit. (Agarwal, N.S. and Rich, D.H., J. Med. Chem. 29: 2519 (1986)). Further, Agarwal and Rich evaluated the inhibition of cathepsin D by various analogues of pepstatin, finding that the fragment spanning P, to P', is necessary for the maximum inhibition of bovine cathepsin D.
U.S. Patent No. 4,746,648 describes peptide derivatives, modeled on the basis of pepstatin, which inhibit renin and acid protease. Tamburini et al., EP 0 569 777 A2 relates to the use of cathepsin D inhibitors for Alzheimer's disease.
Patents relating to cyclic peptide inhibitors of renin include Boger et al., U.S. Patent No. 4.489.099 and Watkins, U.S. Patent No. 4,906,613.
Cyclizing peptidornimetics can increase binding to a target enzyme due to preorganization into the desired conformation. Additionally, such macrocycles offer increased stability against proteolytic cleavage. An area where this approach has been extensively explored is that of renin inhibitors, where various cycles connecting wo 9~r~oo~ rc'r~rs9~roZ93o -- different positions were introduced. The most successful approach was cyclizing from the P, to P', position to generate a series of potent, orally bioavailable renin inhibitors (Weber, A.E. et al. J. Med. Chem. 34: 2692 (1991); Dhanoa, D.S. et al. et. Le t.
33: 1725 (1992); Weber, A.E. et al. J. MediChem. 35: 3755 (1992); Yang, L, et al.
Te . 34: 7035 (1993)). Cyclization of P, to P~ also gave potent renin inhibitors (Sham, H.L. et al. J. Chem. Six. Chem. Commun. 66b (1990); Thaisrivvngs, S. et al. ~ Med. Chem. 34: 1276 (1991)). Some other cycles have been studied (Szewczuk, Z. et al. Int. J. Pelt. Prot. Res. 40: 233 (1992); Sham, H.L. et al. ~
,yied. Chem. 31: 284 (1988); Dutta, A.S. et al. J. Med. Chem. 33: 2552 and ( 1990)), but the only example of which we are aware of a PZ to P~3 bridge in an aspartyl protease inhibitor is a simple disulfide (Boger,1. Peptides 1983, pp.
569-578, Proceedings of the 8th American Peptide Symposium).
The cyclic compounds described herein differ significantly from this prior art. Many of the compounds incorporate a P~ to P ; cycle where the scissile bond isostere is pan of the ring. Since the macrocycle spans a large portion of the binding cleft, activity is retained after truncation to remove the exocyclic backbone extension. This has the dual advantages of decreasing molecular weight and removing the residues most subject to metabolic cleavage.
Modeling studies reveal that the active sites of the aspartic hemoglvbinases (Plasmepsins I and II) from Plasmodium falciparurn are highly homologous with that of human cathepsin D. Goldberg, et al. isolated and characterized plasmepsins I and II, aspartic proteases responsible for the initial cleavage of hemoglobin that occurs inside the protozoan Plasmodium's digestive vacuole (Goldberg, D.E. et al., J.~p. Med. 173: 961 (1991), Hill, J. et al.
FEES
Let rs 352: 155 (1994)). Protozoans of the genus Plasmodium are the causative agents of malaria. The cleavage of hemoglobin by plasmepsins I and II occurs at sites within the hemoglobin sequence that are conserved in human hemoglobins. _ These cleavage events are essential for the conformational breakdown of hemoglobin that enables its subsequent cleavage by a series of other proteolytic enzymes. The digested hemoglobin is a primary nutrition source for the malarial parasite, which cannot grow in the absence of functional hemoglobinases. Goldberg has demonstrated that inhibitors of plasmepsins can kill the parasite in a cell culture of infected human erythrocytes (Goldberg, D.E. et al., EMBO J. 13: 306 (1994), Gluzman, I.Y. et al. J. Clin. Invest. 93: 1602 (1994)).
Therefore, there is a need for cathepsin D inhibitors in the treatment of Alzheimer's disease, cancer, and for aiding in the further elucidation of the roles of cathepsin D in human diseases and a need for plasmepsin inhibitors to treat malaria.
It is an object of an aspect of the present invention to provide cathepsin 1o D and plasmepsin I and II inhibitors for use in the treatment of metastatic disease, for use in the inhibition of cleavage of ~i-amyloid precursors and for the prevention of progressive neurological dysfunction in Alzheimer's disease, as well as for the prevention of the growth of Plasmodium parasites including Plasmodium falciparum, the most deadly cause of malaria.
SUMMARY OF THE INVENTION
The present invention relates to cathepsin D and plasmepsin I and II
inhibitor compounds and their se as pharmaceutically active agents. The 2o present invention further provides for uses of these inhibitors for the prevention and treatment of diseases, such as, for example, cancer, Alzheimer's disease, and malaria.
Specifically, the present invention provides for novel linear compounds as well as branched and cyclic analogs of these compounds which are inhibitors of cathepsin D and which exhibit inhibitory potency against plasmepsins I and II. Further, the present invention relates to novel related cyclic compounds which are cathepsin D and plasmepsin I and II inhibitors.
The present invention also provides for pharmaceutical compositions comprising effective amounts of at least one of the present inhibitors for use in 3o the prevention and treatment of diseases, such as cancer, Alzheimer's disease, and malaria.

Specifically, the present invention provides for pharmaceutical compositions which decrease the levels of activity of cathepsin D present in a subject, thereby inhibiting cancer cell invasion and metastasis.
The present invention also provides for pharmaceutical compositions comprising at least one of the present inhibitors for the treatment and prevention of Alzheimer's disease which decrease the occurrence of cleavage of amyloid-~-protein precursors and senile plaque formation in a subject.
Further, the present invention provides for pharmaceutical compositions which inhibit plasmepsin I or II or both and prevent hemoglobin degradation and are thus useful in the treatment of malaria.
In accordance with one embodiment, the present invention provides a compound of formula (I):
O RZ OH 0 R~- O R6 (I) H H
RNH ~ N N NHR~
H H S
R~ O R3 . O R; O
in which R, R~ = represent hydrogen, alkoxycarbonyl, aralkoxycarbonyl, alkylcarbonyl, cycloalkylcarbonyl, cycloalkylalkoxycarbonyl, cycloalkylalkanoyl, aralkanoyl, aroyl, aryloxycarbonyl, aryloxycarbonylalkyl, aryloxyalkanoyl, heterocyclylcarbonyl, heterocyclyloxycarbonyl, heterocyclylalkanoyl, heterocyclylalkoxycarbonyl, heteroaralkanoyl, heteroaralkoxycarbonyl, heteroaryloxycarbonyl, heteroaroyl, alkyl, alkenyl, cycloalkyl, aryl, aralkyl, aryloxyalkyl, heteroaryloxyalkyl, hydroxyalkyl, aminocarbonyl, aminoalkanoyl, mono- and disubstituted aminocarbonyl and mono- and disubstituted aminoalkyl, alkoxyalkyl, alkylthioalkyl, mono- and disubstituted aminoalkanoyl radicals wherein the substituents are selected from alkyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroaralkyl, heterocycloalkyl, heterocycloalkylalkyl radicals, or where said aminoalkanoyl radical is disubstituted, said substituents along with the nitrogen atom to which they are attached form a heterocycloalkyl or heteroaryl radical;
R~, R2, R4, R5, Rs = optionally substituted lower alkyl, lower cycloalkyl, aryl, 5a aralkyl and heteroaryl;
R3 = optionally substituted lower alkyl, lower alkoxy, lower alkylthio, mono or di-lower alkyl amino, aralkyl, aralkoxy, aralkylthio, aralkylamino, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkylthio, cycloalkylalkylamino;
and wherein R2 and R5 or R~ and R3 are connected by an optionally substituted bridging moiety comprised of a stable combination of C, N, O, or S atoms.
In accordance with a further embodiment, the present invention provides a compound which is selected from the group consisting of (1 Iva-Val-Val-Sta-Val-Leu-Gly-NH2(SEQ. ID. NO.
) 1 );

(2) Iva-Gln-Val-Sta-Ala-Leu-Gly-NH2(SEQ. ID. NO.
2);

(3) Iva-Lys-Val-Sta-Ala-Leu-Gly-NH2(SEQ. ID. NO.
3);

(4) Tba-Val-Val-Sta-Ala-Leu-Gly-NH2(SEQ. ID. NO.
4);

(5) Iva-Val-Ile-Sta-Ala-Leu-Gly-NH2(SEQ. ID. NO.
5);

(6) Iva-Val-Leu-Sta-Ala-Leu-Gly-NH2(SEQ. ID. NO.
6);

(7) Tba-Val-Val-Pst-Val-Leu-Gly-NH2(SEQ. ID. NO.
7);

(8) Tba-Val-Cys-Pst-Val-Leu-Gly-NH2(SEQ. ID. NO.
8);

(9) Tba-Val-Glu-Pst-Val-Leu-Gly-NH2(SEQ. ID. NO.
9);

(10)Tba-Val-Asp-Pst-Val-Leu-Gly-NH2(SEQ. ID. NO.
10);

(11 Iva-Val-Val-Sta-Ala-Leu-Gly-NH2(SEQ. ID. NO.
) 11 );

(12)Tba-Val-Cys-Pst-Val-Cys-Gly-NH2(SEQ. ID. N0.12);

NH CO
.,,,~
OH
COVaINH CONH ~COVaINH COGIyNHz (SEQ. ID. NO. 28);

5b CO NH
_, .. ,,, H
COVaiNH CONH COVaINH COGiyNHi s (SEQ. ID. NO. 29);
NH
CO
~/
OH
COVaINH CONH ~~COVaINH COGIyNH~
(SEQ. ID. NO. 30);
NH CO
OH
COVaINH CONH ~ COVaINH COGIyNHi a (SEQ. ID. NO. 3I);

5c ....,''' S'~.'CH2 -CHZ~
S
OH
COVaINH CONH ~COVaINH COGI NH
Y z (SEQ. ID. NO. 32);
S',.. CH=-CHZ-C HZ ~
S
H
COVaINH CONH COVaINH COGIyNH~
(SEQ. ID. NO. 33);
S/.CHZ-CH=-CHZ-CHz ~S
H
COVaINH CONH COVaINH COGIyNH~
(SEQ. ID. NO. 34);

5d ...~~ s s off ~ COVeINH - CONH ~COVaINH COGIyNHZ
(SEQ. ID. IVO. 3S);
.,.aa off CONH ~ COVaINH COVaILeuGIyNH~

CONH
(SEQ. ID. NO. 36);
~,,.~a OH
CONH ~ COVaINH .,,,/~,~~ COVaILeuGIyNHZ
r i CONH
(SEQ. ID. NO. 37).
In accordance with a further embodiment, the present invention provides 5e a compound of formula II:
Rz off o H
N
RNH ~ v -NHR~
II
o Rs in which R, R~ = represent hydrogen, alkoxycarbonyl, aralkoxycarbonyl, alkylcarbonyl, cycloalkylcarbonyl, cycloalkylalkoxycarbonyl, cycloalkylalkanoyl, aralkanoyl, aroyl, aryloxycarbonyl, aryloxycarbonylalkyl, aryloxyalkanoyl, heterocyclylcarbonyl, heterocyclyloxycarbonyl, heterocyclylalkanoyl, heterocyclylalkoxycarbonyl, heteroaralkanoyl, heteroaralkoxycarbonyl, heteroaryloxycarbonyl, heteroaroyl, alkyl, alkenyl, cycloalkyl, aryl, aralkyl, aryloxyalkyl, heteroaryloxyalkyl, hydroxyalkyl, aminocarbonyl, aminoalkanoyl, mono- and disubstituted aminocarbonyl and mono- and disubstituted aminoalkyl, alkoxyalkyl, akylthioalkyl, mono- and disubstituted aminoalkanoyl radicals wherein the substituents are selected from alkyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroaralkyl, heterocycloalkyl, heterocycloalkylalkyl radicals, or where said aminoalkanoyl radical is disubstituted, said substituents along with the nitrogen atom to which they are attached form a heterocycloalkyl or heteroaryl radical;
R2, = optionally substituted lower alkyl, lower cycloalkyl, aryl, aralkyl and heteroaryl;
R3 = optionally substituted lower alkyl, lower alkoxy, lower alkylthio, mono or di-lower alkyl amino, aralkyl, aralkoxy, aralkylthio, aralkylamino, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkylthio, cycloalkylalkylamino;
with the proviso that NHR~ does not comprise or form an alpha-amino acid.
In accordance with a further embodiment, the present invention provides a compound of formula III:

5f OH 0 R, RNH NHR~
N
H III
O R~ O
in which R, R~ = represent hydrogen, alkoxycarbonyl, aralkoxycarbonyl, alkylcarbonyl, cycloalkykarbonyl, cycloalkylalkoxycarbonyl, cycloalkylalkanoyl, aralkanoyl, aroyl, aryloxycarbonyl, aryloxycarbonylalkyi, aryloxyalkanoyl, heterocyclylcarbonyl, heterocyclyloxycarbonyl, heterocyclylalkanoyl, heterocyclylalkoxycarbonyl, heteroaralkanoyl, heteroaralkoxycarbonyl, heteroaryloxycarbonyl, heteroaroyl, alkyl, alkenyl, cycloalkyl, aryl, aralkyl, aryloxyalkyl, heteroaryloxyalkyl, hydroxyalkyl, aminocarbonyl, aminoalkanoyl, hydroxyalkanoyl, alkenoyl, alkoxyalkanoyl, alkylthioalkanoyl, arylthioalkanoyl, alkoxycarbonylalkanoyl, hydroxycarbonylalkanoyl, aryloxycarbonylalkanoyl, heteroaryloxycarbonylalkanoyl, aminocarbonylalkanoyl, mono- and disubstituted aminocarbonylalkanoyl, alkylthioalkoxycarbonyl, arylthioalkoxycarbonyl, cycloalkylthioalkoxycarbonyl, heteroarylthioalkoxycarbonyl, heterocyclylalkylthioalkoxycarbonyl, cycloalkyloxycarbonyl, hydroxyalkoxycarbonyl, alkoxyalkoxycarbonyl, aryloxyalkoxycarbonyl, heteroaryloxyalkoxycarbonyl, cycloalkyloxyalkoxycycarbonyl, heterocyclylalkyloxyalkoxycarbonyl, cycloalkyloxyalkanoyl, heterocyclyloxyalkanoyl, heteroaryloxyalkanoyl, cycloalkylthioalkanoyl, heterocyclylalkylthioalkanoyl, heteroarylthioalkanoyl, aralkenoyl, mono- and disubstituted aminoalkoxycarbonyl, mono-and disubstituted aminocarbonyl and mono- and disubstituted aminoalkyl, alkoxyalkyl, alkylthioalkyl, mono- and disubstituted aminoalkanoyl radicals wherein the substituents are selected from alkyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroaralkyl, heterocycloalkyl, heterocycloalkylalkyl radicals, or where said aminoalkanoyl radical is disubstituted, said substituents along with the nitrogen atom to which they are attached form a heterocycloakyl or heteroaryl radical;

5g R4 = optionally substituted lower alkyl. lower cycloalkyl, aryl, aralkyl and heteroaryl;
R3 = optionally substituted lower alkyl, lower alkoxy, lower alkylthio, mono or di-lower alkyl amino, aralkyl, aralkoxy, aralkylthio, aralkylamino, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkylthio, cycloalkylalkylamino;
with the proviso that R does not comprise an alpha-amino acid.
In accordance with a further embodiment, the present invention provides a compound which is selected from the group consisting of i CONH r :OValNH
OH
(SEQ. ID. NO. 18);
N
COVaINH COAIaLeuNH
N v . 2 H OH
(SEQ. ID. NO. 19);

5h COVaINH ~ ~COAIaLeuNH=
OH
(SEQ. ID. NO. 20);
~N~
COVaINH NHS
OH
(SEQ. ID. NO. 21);
\ \
N COVatNH COAtaLeuNH2 OH
(SEQ. ID. NO. 22);

5i ~N~ COVaINH :OAtaLeuNHz OH
(sEQ. ID. No. 2~);

~COVaiNH t COAIaLtuNHz s OH
ISEQ. ID. NO. 24);
i COVaiYaINH COAIaLeuNHz OH
(SEQ. ID. NO. 25);

5j l w ~ COVatVaINH COAIaLeuNHz a ON
(SEQ. ID. NO. 26);
~0 COVatVatNH ;OVaILeuNH ~'~./N~"/
OH
(SfiQ. ID. NO. 2~.
In accordance with a further embodiment, the present invention provides a compound of formula II:
RZ H OH O
N
RNH ~ ~ -NHA~
B
O R~
in which R, R~ = represent hydrogen, alkoxycarbonyl, aralkoxycarbonyl, alkylcarbonyl, cycloalkylcarbonyl, cycloalkylalkoxycarbonyl, cycloalkylalkanoyl, aralkanoyl, aroyl, aryloxycarbonyl, aryloxycarbonylalkyl, aryloxyalkanoyl, heterocyclylcarbonyl, heterocyclyloxycarbonyl, heterocyclylalkanoyl, heterocyclylalkoxycarbonyl, heteroaralkanoyl, 5k heteroaralkoxycarbonyl, heteroaryloxycarbonyl, heteroaroyl, alkyl, alkenyl, cycloalkyl, aryl, aralkyl, aryloxyalkyl, heteroaryloxyalkyl, hydroxyalkyl, aminocarbonyl, aminoalkanoyl, mono- and disubstituted aminocarbonyl and mono- and disubstituted aminoalkyl, alkoxyalkyl, alkylthioalkyl, mono- and disubstituted aminoalkanoyl radicals wherein the substituents are selected from alkyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroaralkyl, heterocycloalkyl, heterocycloalkylalkyl radicals, or where said aminoalkanoyl radical is disubstituted, said substituents along with the nitrogen atom to which they are attached form a heterocycloalkyl or heteroaryl radical;
R2,= optionally substituted lower alkyl, lower cycloalkyl, aryl, aralkyl and heteroaryl;
R3 = optionally substituted lower alkyl, lower alkoxy, lower alkylthio, mono or di-lower alkyl amino, aralkyl, aralkoxy, aralkylthio, aralkylamino, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkylthio, cycloalkylalkylamino;
and wherein R and R3 are connected by an optionally substituted bridging moiety comprised of a stable combination of C, N, O, or S atoms.
These and other features of the invention will be better understood through the following detailed description of the invention. The scope of the invention is limited only through the claims appended hereto.
DETAILED DESCRIPTION OF THE INVENTION
The present invention relates to compounds of formula (I):
O R~ OH 0 R4- O Re RNN _ N _ N NHR~
H ~ v H ~ H
R~ O R3 . O R5 O
in which R, R~ = represent hydrogen, alkoxycarbonyl, aralkoxycarbonyl, alkylcarbonyl, cycloalkylcarbonyl, cycloalkylalkoxycarbonyl, cycloalkylalkanoyl, aralkanoyl, aroyl, aryloxycarbonyl, aryloxycarbonylalkyl, aryloxyalkanoyl, heterocyclylcarbonyl, heterocyclyloxycarbonyl, heterocyclylalkanoyl, heterocyclylalkoxycarbonyl, heteroaralkanoyl, heteroaralkoxycarbonyl, heteroaryloxycarbonyl, heteroaroyl, alkyl, alkenyl, cycloalkyl, aryl, aralkyl, aryloxyalkyl, heteroaryloxyalkyl, hydroxyalkyl, aminocarbonyl, aminoalkanoyl, mono- and disubstituted aminocarbonyl and mono- and di-substituted aminoalkyl, alkoxyalkyl, WO 97!3007Z PCf/US97/02930 , -- - akylthioalkyl, mono- and disubstituted aminoalkanoyl radicals wherein the substituents are selected from alkyl, aryl, aralkyl, cycloalkyi, cycloalkylalkyl, heteroaryl, heteroaralkyl, heterocycloalkyl, heterocycloalkylalkyl radicals, or where said aminoalkanoyl radical is disubstituted, said substituents along with the nitrogen atom to which they are attached form a heterocycloalkyl or heteroaryl radical;
R,, R2, R,, R5, R.6 = the side chain of a residue of an amino acid remaining after formation of a peptide linkage and include optionally substituted lower alkyl, lower cycloalkyl, aryl, aralkyl and heteroaryl;
R3 = optionally substituted lower alkyl, lower alkoxy, lower alkylthio, mono or di-lower alkyl amino, aralkyl, aralkoxy, aralkylthio, aralkylamino, cycloalkylalkyl.
cycloalkylalkoxy, cycloalkylalkylthio, cycloalkylalkylamino. Also encompassed are compounds where RZ and RS or R, and R3 are connected by a bridging moiety having 4-14 atoms comprised of any stable combination of C, N, O, or S. This chain may be optionally substituted by halo, hydroxy, amino, lower alkyl, lower alkoxy, lower alkylthio, mono or di-lower alkyl amino, oxo, thiono, alkylimino, mono- or dialkylmethylidene, COR3. The bridging group may also be unsaturated so as to include the residues of alkenes, imines, alkynes and alienes. Furthermore, any part of the bridging moiety may comprise part of an optionally substituted aromatic, heteroaromatic, or cycloalkyl ring. Amino acids from which the residues containing R, . R,, R,, RS and R6 can be derived include glycine, alanine, valine, leucine, isoleucine, serine, threonine, cysteine, methionine, aspartic acid, asparagine, glutamic acid, glutamine, lysine, hydroxylysine, arginine, phenylalanine, tyrosine, tryptophan, and histidine. Useful substituents and the optional substituted R,, Rz, R,, R5 and R6 moieties include the functional groups which are attached to the above named aminoacids.
The present invention further relates to compounds of the Formula (I1):
p? OH O
H
N NHR~
RNH ~ II
O Rs wherein R, RZ, Rj, R, are defined as in formula I, or of Formula (III):
RZ OH O Ra H
N NHR~ III
RNH
H
O Ra O
in which R. R,, R3, R" R, are defined as in formula I.
The present invention also relates to cyclic compounds of formula tIV):
/" A
IV
R Z
X~
'R
OH
where X = CWNR, CWOR, S(O)nNR, P(O)(Q)NR; W = O, S, NR; n = 0, I. '_':
Q = R, OR, N(R)z Y = NRCW, NRS(O)~, NRP(O)(Q) Z = CRR' , NR
A = a bridging group having 2-15 atoms comprised of any stable combination of C.
N, O, or S. This bridging group may itself be bridged by one or more chains comprised of C, N, O, or S atoms so as to generate additional rings of 3-~
atoms.
The bridging groups may be optionally substituted by OH. NH,, halo, optionally substituted lower alkyl, lower alkoxy, lower alkylthio, mono or di-lower alkyl amino, -oxo, thiono, alkylimino, mono- or dialkylmethylidene, COR3. The bridging moiety may also be unsaturated so as to contain portions which are the residues of alkene.
imine, alkvne and allene groups. Furthermore, any part of the bridging moiety may comprise pan of an optionally substituted aromatic, heteroaromatic, alicvclic.
or heterocyclic ring.
R = is as defined hereinabove ' 'WO 97130072 PCT/US97/02930 -s-- R', RZ = H, halo, optionally substituted lower alkyl, lower alkoxy, lower alkylthto.
mono or di-lower alkyl amino R3 = is as defined hereinabove Also encompassed within the scope of the invention are compounds of formula IVa where IVa has the structure shown for IV and X, Y = NRCW, NRS(O)~, NRP(O)(Q); Z = CRR', NR, O, S and all other definitions are as above.
Additionally contemplated are compounds of the formula I Vb where IVb has the structure shown for IV, where X = OCWNR, SCWNR; Y = NRCW.
NRS(O)n, NRP(O)(Q); Z = CRR', NR and all other definitions are as above.
The present invention also relates to cyclic compounds of formula ( V ):
a-'~

R ~ ' X
R
OH Rs where X = CWNR, S(O)~NR, P(0)(Q)NR; W = O, S, NR; n = 0. 1, '_';
Q = R, OR, N(R)~ -Y = NRCW, NRS(O)~, NRP(O)(Q) Z = CRR'. NR
A = is as defined hereinabove R = is as defined hereinabove.
R', R~ and Ra = H, halo, optionally substituted lower alkyl, lower alkoxy.
lower alkylthio, mono or di-lower alkyl amino;
Also encompassed within the present invention are compounds of formula Va where Va has the structure shown for V and where X, Y = NRCW.
NRS(O)e, NRP(O)(Q); Z = CRR', NR. 0. S and all other dennitions are as above.
Additionally encompassed are compounds of formula Vb where V'b has the structure shown for V and where ~ = OCWNR. SCWNR: ~' - :~RCV~.
NRS(O)n, NRP(O)(Q): Z = CRR'. NR and all other definitions are as above.

' WO 97130072 PCTItTS97/02930 As utilized herein, the term "alkyl", alone or in combination, means a straight-chain or branched-chain alkyl radical containing from 1 to about t8, preferably from 1 to about 10, carbon atoms. Examples of such radicals include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, ten-butyl, amyl.
isoamyl, hexyl, octyl and the Like. The term "alkenyl", alone or in combination, means a straight-chain or branched-chain hydrocarbon radical having one or more double bonds and containing from 2 to about 18 carbon atoms preferably from 2 to about 10 carbon atoms. Examples of suitable alkenyl radicals include ethenvl, propenyl, allyl, 1,3-butadienyl and the like. The term "atkynyl", alone or in combination, means a straight-chain hydrocarbon or branched chain radical having one or more triple bonds and containing from 2 to about 14 carbon atoms. Examples of alkynyl radicals include ethynyl, propynyl, propargyl, butynyl and the like.
The term "alkoxy", alone or in combination, means an alkyl ether radical wherein the term alkyl is as defined above. Examples of suitable alkyl ether radicals include methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, iso-butoxy. sec-butoxy, tert-butoxy and the like. The term "cycloalkyl", alone or in combination, means a saturated or partially saturated monocyclic, bicyclic or tricyciic alkyl radical wherein each cyclic moiety contains from about 3 to about 8 carbon atoms. Examples of such cycloalkyl radicals include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and the like. The term "cycloalkylalkyl" means an alkyl radical as defined above which is substituted by a cycloalkyl radical as defined above. Examples of cycloalkylalkyl radicals include cyclopropylmethyl, cyclopropylethyl, cyclohexylmethyl, cyclohexylethyk and the like.
The term "aryl", alone or in combination, means an aromatic monocycle or bicyclic or tricyclic such as phenyl, naphthyl, or anthracenyl which optionally carries one or more substituents selected from alkyl, alkoxy, halogen, hydroxy, amino, vitro.
cyano, haloalkyl and the like; such as phenyl, p-tolyl, 4-ethoxyphenyl, 4-(tent-butoxy~ phenyl, 4-fiuorophenyl, 4-chlorophenyl, 4-hydroxyphenyl, 1-naphthyl, 2-naphthyl. and the like. The term "aralkyl", alone or in combination, means an alkyl radical as det~ned above in which one hydrogen atom is replaced by an aryl radical as defined above.
such as benzyl, 2-phenylethyl and the like. The term "aryloxy" means a radical of the - - formula aryl-O- in which the term aryl has the significance given above.
The term "alkanoyl", alone or in combination, means an acyl radical derived from an alkanecarboxylic acid, examples of which include acetyl, propionyl, butyryl, valeryl.
4-methylvaleryl, and the like. The heterocyclyl portion of a heterocyclyl-containing group is a saturated or partially unsaturated monocyclic, bicyclic or tricyclic heterocyle which contains one or more hetero atoms selected from nitrogen, oxygen and sulphur, which is optionally substituted on one or more carbon atoms by halogen, alkyl, alkoxy, oxo, and the like, andlor on a secondary nitrogen atom by alkyl.
aralkoxycarbonyl, alkanoyl, aryl or aralkyl or on a tertiary nitrogen atom by oxido and which is attached via a carbon atom. The heteroaryl group is an aromatic monocyclic, bicyclic, or tricyclic heterocycle which contains the hetero atoms and is optionally substituted as defined above with respect to the definition of heterocyclyl.
Examples of such heterocyclyl and heteroaryl groups are pyrrolidinyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl, pyrrolyl, imidazolyl (e.g. imidazol 4-yl, 1-benzyloxycarbonylimidazol-4-yl, etc.), pyrazolyl, pyridyl, pyrazinyl, pyrimidinyl.
furyl, thienyl, triazolyl, oxazolyl, thiazolyl, indolyl (e.g. 2-indolyl), quinolinyl, (e.g., 3-quinolinyl, 2-quinolinyl, etc.), isoquinolinyl (e.g., l,'_',3,4-tetrahydro-1-oxo-isoquinolinyl, etc.), quinoxalinyl, (3-carbolinyl, - benzofuranyl, 1-, 2-, ~-or 5-benzimidazolyl, and the like. The term "aminoalkanoyl" means an acyl group derived from an amino-substituted alkanecarboxylic acid wherein the amino group can be a primary, secondary or tertiary amino group containing substituents selected from hydrogen, alkyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyi radicals and the like. The term "halogen" means fluorine, chlorine, bromine or iodine. The term "haloalkyl"
means an alkyl radical having the significance as defined above wherein one or more hydrogens are replaced with a halogen. Examples of such haloalkyl radicals include chloromethyl, 1-bromoethyl, fluoromethyl, difluoromethyl, trifluoromethyl, 1,1,1-trifluoroethyl and the like.
The possible optional substituents mentioned in the hereinabove generic description include at least one alkyl, cycloalkyl, aryl, aralkyl, alkaryl.
heteroay I.
alkoxy, halogen, hydroxy, amino, vitro, cyano, haloalkyl wherein the optional substituents may also be optionally substituted and the radicals which are optionally substituted may be singly or multiply substituted with the same or different optional substituents.
The compounds provided by the present invention are advantageous as demonstrated by their activity. Furthermore, the structures of the cyclic compounds of the present invention potentially provide protection of the compounds from enzyme degradation. The low molecular weight and few peptide bonds in these analogs may also contribute to improved bioavailability.
Specific, but non-limiting examples of peptides of Formula (I) useful in the present invention include the following:
K, cachepsin D (nbi) (1) Iva-Val-Val-Sta-Val-Leu-Gly-NHZ (SEQ. ID. NO. 1); 0.1 (2) Iva-Gln-Val-Sta-Ala-Leu-Gly-NHZ (SEQ. ID. NO. 2); 0.35 (3) Iva-Lys-Val-Sta-Ala-Leu-Gly-NHZ (SEQ. ID. NO. 3); 3.9 (4) Tba-Val-Val-Sta-Ala-Leu-Gly-NHZ (SEQ. ID. NO. 4); 0.04 (5) Iva-Val-Ile-Sta-Ala-Leu-Gly-NHZ (SEQ. ID. NO. 5); 0.04 (6) Iva-Val-Leu-Sta-Ala-Leu-Gly-NHZ (SEQ. ID. NO. 6); 0.5 (7) Tba-Val-Val-Pst-Val-Leu-Gly-NHZ (SEQ. ID. NO. 7): 0.015 (8) Tba-VaI-Cys-Pst-Val-Leu-Gly-NH, (SEQ. ID. NO. 8); 0.25 (9) Tba-Val-Glu-Pst-Val-Leu-Gly-NH, (SEQ. ID. NO. 9); 1.25 (10) Tba-Val-Asp-Pst-Val-L,eu-Gly-NHZ (SEQ. ID. NO. 10); ~.1 (11) Iva-Val-Val-Sta-Ala-Leu-Gly-NHS (SEQ. ID. NO. 11); 0.03 (12) Tba-Val-Cys-Pst-Val-Cys-Gly-NH,(SEQ.ID.NO.I2). 0.66 which has a PMI K; = 32 nM PMII K; = 1.7 nM.
Iva = isovaleryl Tba = t-butylacetyl Specific, but not limiting examples of peptides of Formula (II_) of the present invention include the following:

COVaIVaINH CONH~
OH
which has a K; of 800 nM, (SEQ. ID. NO. 13);
COVatVaiNH
CONH
OH
which has a Ki of 12 nM, (SEQ. ID. N0. 14);
~ COVaiNH CONH
OH
which has a K; of 1600 nM, (SEQ. ID. NO. 15);
COVaIVaINH CONH OH
OH
which has an ICso of 600 nlvi. !SEQ. ID. NO. 16);

WO 97/30072 PCTlUS97/02930 ~O
COVatVsINH CONH~N~
OH
which has a K; of 1834 nM (SEQ.ID.NO. 17);
Additional Examples of Cathepsin D Inhibitors within Formula II are shown below based on the formula:
R O R'HN O
~H O
NH
N
H

WO 97!3007Z PCTIUS97/02930 R R' MW Ki (nM) (CH~)4CH3 (CH~6CH3 503 24 _ (CH~ZSPr (CH~ZSPr 539 75 (CH~ZSCHZPh (CH=)2SCHrPh 635 5 (CHZ)ZSCH2Ph (CHi)3SCHZPh 649 17 (CH~,SCH2Ph (CH~3SCH2Ph 663 4.0 O(CH~3-4-Pyr (CHZ)3SCH,Ph 634 249 (CHZ),SCH,Ph (CHz)6CH, 597 b.2 (CH2)ZSCHIPh (CHZ)6CH3 583 7.7 (CH2)4CH3 (CHZ)3SBn 569 6.1 (CHz)ZCOzH n-C,H,s 505 41 (CHZ)2COzMe n-C,H,S 519 178 (CH2)ZCOIVHZ n-C,H,S 504 479 (CH2)3C02H n-C,H,S 519 22 (CHZ)3CO~Me n-C,H,S S33 112 CHZ-p-Ph-Ph n-C,H,S 599 16 (E)-3- n-C,H,s 579 45 CH =CHbenzodioxolane Ph = phenyl, pyr = pyridyl and Bn = benzyl Specific, but not limiting examples of compounds of Formula (III) include:
CONH COYaINH
~H
which has an K; of 400 nM, (SEQ. ID. NO. 18);

OVaINH COAIaLeuNH

N
H OH
which has an ICso of 500 nM, (SEQ. ID. NO. 19);
COVaINH COAIaLeuNHZ
OH
which has a K; of 8 nM, (SEQ. ID. NO. 20);
~N~
NH LeuNH2 COVaI
OH
which has an ICso of 1000 nM, (~Fn m ntn. 21~:
/
N COVaINH NHZ
OH
which has a K; of 21 nM, (SEQ. ID. NO. 22);
/ COVaINH COAIaLeuNHz N
OH
which has a K; of 20 nM, (SEQ. ID. NO. 23);

WO 97!30072 O
~COVafNH COAIaLeuNHZ
OH
which has an ICS of 20 nM, (SEQ. ID. NO. 24);
COVaiVaINH COAIaLeuNH2 OH
which has a K; of 0.18 nM, (SEQ. ID. NO. 25);
O
~COVaIVaINH COAIaLeuNH2 OH
which has a K; of 0.24 nM, (SEQ. ID. NO. 26):
\ ~O
COVaIVaINH COValteuNH ~./N~
OH
which has a K; of 0.14 nM, (SEQ. ID. NO. 27).
Specific examples of cyclic compounds within the scope of the present invention include: (Formula I:) WO 97r30072 PGT/US97102930 NH CO
,,,'~r OH
COVaINH CONH ~~~ COVaINH COGIyNHz which has a K; of 1.4 nM, (SEQ. ID. NO. 28);
CO NH
,,,,,' OH
COVaINH CONH ~~/~,,.COVaINH COGIyNH2 i which has a K; of 2.3 nM, (SEQ. ID. NO. 29);
NN
CO
OH
COVaINH CONH ~~,~.COVaINH COGIyNHz which has a K; of I2 nM, (SEQ. ID. NO. 30);
NH CO
OH
COVaINH CONH ~~/~COVaINH COGIyNH2 which has a K; value of 100 nM, (SEQ. ID. NO. 31);

WO 97/30072 PGT/US97IOZ930 ' -/.CH2 CHz.,, S S
OH
COVaINH CONH ~~COVaINH COGIyNHZ
i which has a K; value of 1.9 nM, (SEQ. ID. NO. 32);
S~CHZ-CH2-CHz~s ,,,...
OH
COVaINH CONH ~~,/~,COVaiNH COGIyNHz which has a K; value of 1.5 nM, (SEQ. ID. NO. 33);
~CHT-CHI-CHZ-CHZ \
S S
OH
COVaINH CONH ~~,,~COVaINH COGIyNH2 which has a K; value of 0.1 nM, (SEQ. ID. NO. 34);
,~~,,o g S
OH
COVaINH CONH ~~,/~COVaINH COGIyNH2 which has a K; value of 150 nM, (SEQ. ID. NO. 35);

WO 97/30072 PCT/t1S97/02930 .,,,,,. _ OH
CONH ~. COVaINH COVatl.euGlyNH2 CONH
which has a K; value of 0.26 nM, (SEQ. ID. NO. 36);
,~,,.a OH
CONH ~ COVaINH COVaIteuGIyNH2 CONH
which has a K; value of 2.5 nM, (SEQ. ID. NO. 37);
Formula II:
CONH
CO O
NH
S \,.'''' ~CONH'~N~
OH
which has an ICso of 10,000 nM (SEQ.ID.NO. 38);
Formula IV:
~(CH2ly C~O NH
NH CO
..
CONH
OH
which has a K; value of 4 nM; (SEQ.ID.NO. 39);

~(CHz)y C~O NH
NH CO
I ~ ..... I
CONH ~~. \
OH
which has a K; value of 21 nM; (SEQ.ID.NO. 40);
~(CH~~~
CO NH
NH CO
f ..... J ...., '''' CONH ''' OH
which has a K; value of 85 nM; (SEQ.ID.NO. 41);
~(CHZj~~
C~O NH
NH CO
J....
CONH
OH
which has a K; value of 22 nM; (SEQ.ID. NO. 42);
~(CH~i~
C~O NH
NH CO
v..., ~''"~~ ~ CONH
OH
which has a K; value of 10 nM; (SEQ.ID.NO. 43);

WO 97!3007Z PCT/US97102930 ~(CH~~~
C~O NH
NH CO
., .
CONH ~~''' OH
which has a K; value of 20 nM; (SEQ.ID.NO. 44);
~(CH2)~~
C~O \N H
NH CO
_..
CONH
OH
which has a Ki value of 140 nM. (SEQ.ID.NO. 45).
Additional Examples of Cathepsin D Inhibitors within Formula IV are shown below based on the following formula:
A
(CH2~~ OH CH
CONH ~ CONH ( ~,~ ONH
R' R R' m n A Ki I~1 PhCHz D-iPr 11 - - -PhCH2 iBu 11 - - 20 PhCH2 Me 11 - - 46 PhCH2 Et 11 - - 22 PhCH2 3-PyrCH2 11 - - 38 PhCH2 CH3CH(OCHzPh 11 - - 460 )CHZ

PhCH2 CH3CH(OH)CH~ 1I - - 300 PhCH2 tBu 11 - - 18 PhCH2 Ph 11 - - 11 p-(PhCH20)- iPr 11 - - 41 PhCHz p-(OH)PhCHz iPr 11 - - 53, 45, . p- iPr 11 - - 8.3 (OMe)PhCH2 p-(OEt)- iPr I I - _ - 8.1 PhCH2 p-(OiPr)- iPr 11 - - 7.4 PhCH2 p-(3PyrCH20)- iPr 11 - - 81 PhCHz p- iPr 11 - - 13 bie0(CHZ)20-PhCH2 (F5-Ph)CH2 iPr 1I - - 90 (m,p- iPr 11 - -CIzPh)CHZ

(mp-FZPh)CHZ iPr 11 - - -p-F-PhCH2 iPr 11 - - -HSCHZ iPr I1 - - 410 . ~ WO 97130072 - g g~ m a A Ki (x'17 _ MeSCH2 iPr 11 - - 150, EtSCHZ iPr 11 - _ 84 PrSCH2 iPr 11 - - 90 CH2=CHCHZ iPr 11 - - 140 BuSCHz iPr 11 - - -iBuSCH2 iPr 11 - - -PhCH2SCHz iPr 11 - - 68 PhCH2CH2 iPr 11 - - 1600 2-naph-CH2 iPr 11 - - 1.1 1-naph-CH2 iPr 11 - - 121 4-thiazolyl- iPr 11 - - 186 CHZ

3-indolyl-CHZ iPr 11 -PhCH2 iPr PhCH2 - O
Pr 2 -iPr 2 2 S(CHZ)3S 1900 PhCHZ

iPr 2 2 S(CHZ)4S S73 PhCH2 iPr 2 2 S(CHZ)SS 53 PhCH2 iPr 2 2 S(CHZ)6S 19 PhCH2 iPr 2 2 S(CHZ),S 56 PhCH2 iPr 2 2 SCHZCH =CHCHZS 380 PhCHZ (cis) iPr 2 2 SCHZCH=CHCHZS 320 PhCH2 (traps) iPr 2 2 SCHZCCCHZS 65 PhCHz 2 2 SCHZp-Ph-CHZS 9 ~

PhCHz iPr iPr 2 2 SCHZm-Ph-CHZS

PhCH2 iPr 2 2 SCHZo-Ph-CHZS

PhCH2 WO 9'7/30072 PCT/US97~2930 ~ -R R' m n A Ki I~l PhCHz iPr 2 2 SCHZp-(Cl)4Ph- 0.89 CHZS
PhCH2 iPr 11 - replace amide NH 63 by O
naph. = naphthyl The compounds of the present invention may exist in a free, i.e.
unprotected, or protected form. The protected form herein refers to compounds wherein one or more reactive groups, e.g. amino groups or -OH groups, are substituted by a protecting group. Suitable protecting groups are any of those known in the art, such as acetyl, benzyloxycarbonyl and t-butoxycarbonyl.
The compounds of the present invention, whether they are in a free or protected form, may exist as salts or as complexes. Acid addition salts may be formed with organic acids, polymeric acids, and inorganic acids, for example.
Such acid addition salt forms include inter alia the hydrochlorides and acetates.
Complexes are herein defined as compounds of known type, formed on addition of inorganic substances, such as inorganic salts or hydroxides such as Ca- and Zn- salts, and/or on addition of polymeric organic substances.
The present invention further provides methods and compositions for preventing or treating diseases. Particular non-limiting examples of diseases include cancer including for example breast cancer, Alzheimer's disease, and malaria.
Specifically, this invention provides for the use of the compounds and compositions of the present invention to inhibit the activities of cathepsin D
and piasmepsins I and II for treating and preventing diseases such as cancer, Alzheimer's disease, and malaria. The present invention also provides pharmaceutical compositions comprising the same.
The present invention further provides methods of preventing or treating a disease by the administration of a therapeutically effective amount of a cathepsin D
or plasmepsin I or II inhibitor compound.

wo s~r~oo~rz rc~rrtrs9~ro293o -More particularly, the present invention provides methods of treating cancer by administration of a therapeutically effective amount of at least one cathepsin D inhibitor described herein which, for example, inhibits the invasion and metastasis of cancerous cells.
In addition, the present invention provides methods of treating Alzheimer's disease by administration of a therapeutically effective amount of at least one cathepsin D inhibitor described herein which, for example, inhibits the formation of senile plaques.
In addition, the present invention provides methods of treating malaria by administration of a therapeutically effective amount of a plasmepsin I or II inhibitor described herein which, for example, inhibits the degradation of hemoglobin by the malarial intracellular parasite.
The present invention also provides methods of preventing or treating diseases by the administration of a therapeutically effective amount of at least one compound of the present invention in combination with chemotherapeutic agents, toxins, or irradiation. Examples of chemotherapeutic agents are known to those skilled in the art and include, but are not limited to, bleomycin, mitomycin, cyclophosphamide, doxorubicin, paclitaxel, and cisplatin.
In one embodiment of the invention, the compounds of the present invention are administered in a pharmaceutically acceptable carrier. A
pharmaceutically acceptable carrier encompasses any of the standard pharmaceutical carriers such as sterile solution, tablets, coated tablets and capsules. Such carriers may typically contain excipients such as starch, milk, sugar, certain types of clay, gelatin, stearic acid, talc, vegetable fats or oils, gums, glycols, or other known excipients. Such carriers may also include flavor and color additives and other ingredients. , In the practice of the methods of this invention, the amount of the enzyme inhibitor incorporated in the composition may vary widely. Methods for determining the precise amount depend upon the subject being treated, the specific pharmaceutical carrier, the route of administration being employed, the frequency with wo ~r~oon rc~r~s9~roz93o . -which the compound is to be administered, and whether the composition is administered in conjunction with a chemotherapeutic agent and/or irradiation treatment.
The present invention further provides a method of treating a subject afflicted with a tumor which comprises contacting the tumor with an amount of one of the cathepsin D inhibitors described herein which is administered to the subject previous to, simultaneous to, or subsequent to, administration of a chemotherapeutic agent or to an amount of irradiation effective to treat the tumor. The administration of the composition may be effected by any of the well known methods, including but not limited to, oral, intravenous, intramuscular, and subcutaneous administration.
Plasmepsin I and II are enzymes which are required for specific degradation of hemoglobin by the malarial intracellular parasite. Due to the high active site similarity between cathepsin D and plasmepsins, some of the cathepsin D
inhibitors of the present invention are useful in preventing the growth of Plasmodium ,f'alclparum, a causative agent of malaria. Non-limiting examples of compounds which exhibit plasmepsin I or II (aspartic hemoglobinases from Plasmodium falciparum) inhibitory activity include the following:
(Formula I):
COVaIVaINH COAtat-euGIyNH2 OH
which has a PMI K; = 1.2 nM PMII K; = 0.1 nM (SEQ. ID. NO. 46); .

rcrrt~s9~roz93o -wo 9~r~oon ..,a~'' _ OH
CONH ~ COVaiNH COVaILeuGIyNH2 CONH
which has a PMI K;= 22 nM PMII K; = 0.2 nM (SEQ. ID. NO. 36);
COVaINH CON COAIaLeuGIyNH2 OH
which has a PMI K; = 7 nM PMII K; = 3 nM (SEQ. ID. NO. 47);
(Formula III):
N COVaINH
Ohi which has a PMI K; = 16 nM PMII K; = 0.9 nm (SEQ.ID.NO. 22).

S~1THF~IS:
LINEAR INHIBITORS:
The linear peptide inhibitors of the present invention were synthesized by the solid phase method using the Fmoc group for a-amino protection and acid labile groups for side chain protection of trifunctional amino acids e.g.
[FmocCys(Trt)OH, FmocAsp(OtBu)OH and FmocGlu(OtBu)OH]. The aminomethyl polystyrene resin (Bachem California) was modified with acid labile linker Fmoc-2,4-dimethoxy-4'-(carboxymethoxy)-benzhydrylamine(Bachem Bioscience, Inc.) to a fnal substitution of 0.3-0.5 mmol/g. The Fmoc protected amino acids were coupled as HOBt esters, DIC {diisopropylcarbodiimide) was used for activation, and a 20 %
solution of piperidine in DMF (dimethyl formamide) for deprotection in each step.
The Fmoc protected derivatives of statine and 3-hydroxy-4-amino-5-phenyl pentanoic acid (AHPPA or phenylstatine) were prepared according to the modified described procedure of Jouin, P. et al. J. Chem. Soc. Perl~,.n. Trans. 1, 1177 (1987).
The final cleavage of inhibitors from the resin was accomplished by treating with TFA
{trifluoroacetic acid) containing 5 % of water (and 3 % of triethyl silane in the case of cysteine containing inhibitors). All the inhibitors were purified by reverse phase high performance liquid chromatography (HPLC) (column VYDAC C-.18 2.5 X 25 cm) using water-acetonitrile mixtures containing 0.05 % TFA in a gradient elution.
Purity of all compounds was checked with analytical reverse phase HPLC (column CYDAC
C-18 0.4 X 25 cm). All compounds gave correct molecular peaks in the mass spectrum (SIMS).
CYCLIC ANALOGS:
Preparation of Cyclic Disulfides.
The dibenzylated dithiol ( 100-500 mg) was dissolved in 150 ml of refluxing anhydrous liquid ammonia. Sodium metal was then added in small pieces to the solution until it remained blue. The addition was finished when the blue color persisted for 3 minutes. The mixture was then decolorized with a crystal of NH~CI

' WO 9~I30072 PCT/US97I02930 . - and ammonia was evaporated. The solid residue was suspended in 10% aq.

and the precipitated dithiol was filtered off. Yield is usually close to 100 %
.
The dithiol (30 mg) was dissolved in 30 ml of anhydrous degassed DMF containing 10 eq. of diisopropylethylamine (DIEA). A solution of 1.1 eq.
of a,w-dihaloalkane in 5 ml of DMF was then added dropwise during 12 hours to the above solution. The mixture was left to stand for an additional 12 hours at room temperature. DMF was evaporated under reduced pressure and the obtained solid residue was washed with 5% aq. NaHC03 and ether. Yield 70-90% of crude cyclic inhibitor. The product was purified by preparative HPLC for the purpose of I
determination.
Other Cyclic ~naloes Compounds related to Seq. ID number 42 but lacking the Ile can be prepared by condensing an N-protected statine analog with an w-amino ester, hydrolyzing the ester, removing the N-protecting group of the statine, and cyclizing to form the Iactam. Alternatively an ester of statine can be condensed with an N-protected w-amino acid to provide the N-acylated statine which can be deprotected and cyclized to give the lactam.
Analogs such as in compounds of formula IV where a carboxamide is replaced with a sulfonamide or a phosphonamide may be prepared in an analogous way to the carboxamides, but in place of typical peptide coupling conditions, more vigorous activation of the sulfonic or phosphoric acid such as by preparing the sulfonyl or phosphoryl chloride may be required.
The amides described above can be replaced by hydrazides by using a suitably C-protected w-hydrazino acid and condensing it with a suitably activated carboxylic or related acid derivative.
The oxygen of the carbonyl containing derivatives such as carboxamides may be replaced by sulfur by using such common thionating agents as P,SS or Lawesson's reagent. The resulting thiocarbonyls can be converted into imino WO 97130072 PCT/US97102930 .

derivatives by treating with amines, in some cases after prior activation of the thiocarbonyl by, for example, alkylation.
~R~~ING GROUPS
It is recognized that the c~-amino acid may have up to 4 of its carbon atoms replaced by heteroatoms such as O, N, or S. These amino acids may be prepared by using methods known to those skilled in the art. For example a shorter chain w-halo acid derivative can be reacted with an N-protected amino alcohol, aminoalkanethiol, or diamine to provide an m-amino acid with an O, S, or N
beta to the amino terminus. Similarly an w-hydroxy acid could be derivatized as, for example, a sulfonate, and a similar displacement reaction run. Alternatively a suitably protected shorter chain w-amino, hydroxy, or sulfhydryl acid could be derivatized, for example, by reaction with a suitably N-protected amino alkyl halide or sulfonate.
Similarly it is recognized that replacing a sulfonate or halide in the above alkylations by an epoxide would allow formation of chains with hydroxyl substituents. It should be noted that chains containing heteroatoms need not be synthesized only by using alkylation type chemistry. Chains containing an amide bond can be synthesized, for example, by reacting an amino acid with another amino acid using standard peptide coupling conditions to generate the w-amino acid required. Furthermore an O-protected c~-amino acid could be reacted with a phosgene equivalent to provide an isocyanate which could then be reacted with an N-protected amino alcohol or diamine to provide a urethane or urea-substituted chain.
It is recognized that the chain need not be built up separately, but may be formed by attaching pieces of the chain to the amino and carboxy ends of the molecule and then connecting them in some way. This approach is exemplified in Seq. ID numbers 32-34, where the two cysteine substituents are connected by a dihalide .to form the desired bridge compounds. Similarly Seq. ID. NO. 28 can be prepared by cyclization of a compound with an amino alkyl substituent at one end and a carboxy alkyl substituent at the other to give the chain containing an amide functionality.

PCTlUS9710Z930 It should be noted that chains where carbon atoms have been replaced by heteroatorns are amenable to further chemistry which can also lead to active compounds. For example sulfides can be converted by peracids to sulfoxides or sulfones. Secondary amines can be alkylated or acylated.
Chains containing oxo or hydroxy substitution can also be elaborated.
For example oxo groups may be condensed with amines, hydrazines, hydroxylamine, alkoxyamines, phosphorous pentasulfide, diethylamino sulfur trifluoride (DAST), alkylidene triphenyl phosphoranes or the like to provide imines, hydrazones, oximes, thiones, difluoromethylenes, alkylidenes and the like. Reduction provides alcohols, or methylenes. Alcohols may be converted into halides for example by phosphorous trihalide, oxidized to oxo compounds, acylated to give esters or alkylated to give ethers.
The chain could also incorporate unsaturation such as one or more double or triple bonds. These can be generated by elaboration of saturated analogs, such as, for example, by elimination of an alcohol derivative such as a xanthate ester, or a halide. Alternatively the unsaturation can be present in one of the precursors for the chain. For example an unsaturated fatty acid could be converted to an w-amino unsaturated acid, for example, via the w-bromo derivative. This material could then be used to form the ring as described for the saturated analogs. It should be noted that compounds containing unsaturation in the ring are amenable to further transformation. Cycloadditions such as Diels-Alder reactions, 1,3-dipolar additions, and 2+2 cycloadditions lead to bridged 6-,5-, and 4-membered ring systems.
Three membered rings can be generated by carbene reactions, epoxidations with, for example, peracids, and aziridinations. Alternatively the ring can be part of the w-amino acid before attachment to the core. Thus, for example, w-aminoalkyl benzoic acids could be utilized to form the chain.
Carbamates, thiocarbamates and ureas at Y may be generated by reacting the C-protected amino acid core with a phosgene equivalent such as trichloroacetyl chloride followed by a mono N-protected w-diamine, w-amino alcohol.

or c.~-amino thiol. Similarly sulfamides can be generated by replacing the phosgene equivalent by sulfuryl chloride, or an equivalent. _ Compounds of formula IVa may be generated by replacing the amino acid core in IV by a diamine or equivalent. One way this can be accomplished is by taking a suitably N-protected amino acid, forming an active ester, displacing by NaN3 to form the acyl azide, and then heating to form the isocyanate. Reaction with mono N-protected c~-diamines, c~-amino alcohols, or m-amino thiols as above provides carbamates, thiocarbamates and areas at X. Alternatively, the isocyanate can be hydrolyzed to give the amine which can be acylated to 'form amide derivatives.
Similarly, sulfonylation can provide sulfonyl analogs.
Compounds of formula IVb replace the amine at X in IVa by oxygen or sulfur. These compounds can be synthesized, for example, by using phenylalaninal as the starting material. Conversion of the aldehyde to the epoxide may be accomplished either directly with an appropriate ylide, or indirectly via Wittig olefination followed by epoxidation, for example, with a peracid. The epoxide can then be reacted with a suitable alcohol or thiol to provide a diol or mercapto alcohol respectively. Acylation of these moieties, with for example a suitable isocyanate provides the X functionality described in IVb. -Compounds of formula V may be prepared in a similar fashion as those for formula IV but using an optionally a-alkylated homostatine core rather than a statine core. Homostatine analogs can be synthesized, for example, by activating the carboxylic acid of a protected statine analog, reacting with diazomethane to generate the diazoketone, and then subjecting it to Wolff rearrangement using thermal, photochemical, or metal-catalyzed conditions. The resulting carboxylic acid can then be elaborated as in formula IV.
Compounds of formula Va have the amide of X in formula V reversed.
Such compounds are available from derivatives of statine. Thus a statinal derivative can be reductively aminated to give the required precursor amine which can then be acylated, sulfonylated, or phosphorylated as for previously described examples.

Alternatively the amine could be synthesized by reduction of a statine amide or reaction of an activated statinol derivative with an amine equivaient. -Sirnilarly, compounds of formula Vb can be derived from statinol analogs by acylation on oxygen with, for example, an isocyanate derivative.
Alternatively, the alcohol can be activated as, for example, a sulfonate derivative and then reacted with a thiol to give the sulfur analogs.
The Examples herein are meant to exemplify the various aspects of carrying out the invention and are not intended to limit the scope of the invention in any way.

The synthesis of this inhibitor is represented in Scheme A below:
tSuOCOt~t COON + ~C~. ~Ctt~y". Co00~ ~. ~t OtEI, t~OCD~fl1 . G01W ~(Ci~i~,r ~ r' Ts~tl. hl0et OtEA
T~Ai~! C~!!!-(C~Sr~~ ~' ~ ~ 01!
QII
tauoeo~ ~ r~ 3 ca~~ ccx~"- ~o~, ""°"
o~
(~lflT ~ _. ~~ Q~ OIIf ON
~tO~O~t C0~1 CO
",J

The various compounds shown in scheme A can be prepared as follows:
12-aminododecanoic acid methylester hydrochloride (11 _ To the suspension of 12-aminododecanoic acid (2. I5 g; 10 mmol) in 2,2-dimethoxypropane (I00 ml) was added 36% aqueous HCl (10 ml) and the mixture was treated in an ultrasonic bath until all solid material was dissolved. The mixture was then left to stand overnight, concentrated to dryness, dissolved in 40 ml of methanol and precipitated with approximately 500 ml of dry ether to give 2.4 g of 1 (90.5 %
yield).
2- ut 'n 1 - inod d i i me h 1e er 2 Boc-Ile-NH-(CHZ)"-COOCH3 Boc (t-butyloxycarbonyl)-Ile(isoleucine)-OH. 1/2H20 (384 mg; 1.6 mmol), HC1.HZN-(CH2)"-COOCH3 (1) (398 mg; 1.5 mmol), HOST (N-hydroxybenzotriazole) (260 mg;
1.7 mmol) and TBTU (2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate)) (546 mg; 1.7 mmol) were dissolved in DMF (5 ml). DIEA
(diisopropylethylamine) (860 ~.1; 5 mmol) was added to the above solution and the mixture was left to stand overnight. Five drops of N-aminoethylmorpholine were then added to the solution. After 30 minutes DMF was removed in vacuo and the solid residue suspended in 10% aqueous KHS04 (20 ml). The precipitate was filtered off, washed with water, 5 % aqueous NaHC03, water again, and then dried in a vacuum desiccator to give 630 mg of 2 (95 °Io yield).
12-l t-Butvloxvcarbo~v~~henvlstatinvl-isoleuc_invil-aminododecanoic acid methvlester Boc-Pst-Ile-NH-(CH,~"-COOCH3 Boc-Ile-(CH2)"-COOCH3 (2) (384 mg; 0.8 mmol) was dissolved in TFA
(trifluoroacetic acid) (3 ml). After 30 minutes of standing at room temperature, the TFA was removed in vacuo, the oily residue was concentrated three more times with ether to remove the remaining TFA, and then dissolved in 5 ml of DMF. Boc-Pst-OH

PCTJUS97/02930 . ' (247 mg; 0.8 mmol), TBTU (289 mg; 0.9 mmol) and DIEA (1030 ~cl; 6 mmol) were added to the above solution and the mixture was left to stand overnight.
Workup as for 2 yielded 492 mg of 3 (97%).
'n 1-i 1 a i 1 oic i 4 Boc-Pst-Ile-NH-(CHZ)"-COON
Boc-Pst-Ile-NH-(CHZ)I,-COOCH3 (3) (380 mg; 0.6 mmol) was dissolved in a mixture of 1,4 dioxane (5 ml) and methanol (1 ml) and combined with 1N aqueous solution of NaOH (I.5 mI). The reaction was complete in approximately two hours. The organic solvents were evaporated and the remaining aqueous slurry was acidified with 10% aqueous KHS04 (10 ml). The precipitate was filtered off, washed with water, and dried in a vacuum desiccator to yield 353 mg of 4 (95 % yield).
C~~cLl2-aminododec~oyl-phenylstatinyl-isoleucinyl (5l -CO-Pst-Ile-NH-(CHZ)"-Boc-Pst-Ile-NH-(CH2)"-COON (4) (248 mg; 0.4 mmol) was deprotected with TFA
as described for 3 and dissolved in DMF (20 ml). This solution was added dropwise to a stirred solution of DPPA {diphenyl phosphorylazide) ( 1.1 g; 4 mmol) and DIEA
(1.38 ml; 8 mmol) in DMF (100 ml) over the course of 17 hours via syringe pump.
The mixture was then stirred for an additional 3 hours, evaporated to dryness and triturated with ether. The precipitated product was filtered off, washed with ether, % aqueous NaHC03, and water and then dried in a vacuum desiccator to provide mg of crude 5 (80% yield). For the purpose of biological testing, the product was purified by RP-HPLC.
SIMS MS M+Na+524 An alternate sequence to a cyclic inhibitor is represented in Scheme B below:
?'eTtJ. N01L OQV
coop ~a ~, DI!
J
rarer. ~oe~. dtA~ ~uoeow~.to~sh~

1. TfA
tauOCOIAI.( !
_. O~PA~ OIEA~Ii~
CD !W
CD

WO 97!30072 PCT/US97102930 -t-,iBu~y~oxycarbonyl- henvlstatinyl valine methylester (61 Boc-Pst-Val-OCH3 Boc-Pst-OH (309 mg; 1 mmol), HC1.H-ValOCH3 {184 mg; 1.1 mmol) and TBTU
(385 mg; 1.2 mmol) were dissolved in 5 ml of DMF and DIEA (688 ~cl; 4 mmol) was addexi to the solution. The mixture was left to stand overnight and then evaporated to dryness. The oily residue was dissolved in ethylacetate and the ethylacetate solution was washed with 10% aqueous KHSO,, water, 5% aqueous NAHCO3, and water again, dried over MgSO,, and concentrated to give 420 mg of 6.
11-t-ButylcLxyc bony!-aminoundecanoyl-phen !y statin'yl valine methyl ester 7) Boc-NH-(C Hz), o-CO-Pst-V al-OCH3 Boc-Pst-Val-OCH3 (420 mg; 1 mmol) was deprotected with TFA as described for 3.
After addition of ether, a precipitate of TFA.H-Pst-Val-OCH3 (349 mg; 0.8 mmol) was obtained. This was dissolved in 5 ml of DMF together with Boc-NH-(CHZ),o-COOH (241 mg; 0.8 mmol), TBTU (289 mg; 0.9 mmol) and DIEA (516 ~cl; 3 mmol).
After 10 hours of standing at room temperature, DMF was removed in vacuo, the residue dissolved in ethylacetate and worked up as described above for 6 to yield 480 mg of oily 7.
11-t-Butxlox~carbony_l-aminoundecano rLI-,phenylstatinyl valine l8) Boc-NH-(CHz) 1 o-CO-P st-V aIOH
Hydrolysis of crude Boc-NH(CHZ),o-CO-Pst-ValOCH3 (7) (480 mg; 0.8 mmol) as described above for 4 provided 435 mg of oily 8.
Cyclo-11-aminoundecanovl-nhenylstatinxl-valine (91 -CO-Pst-Val-NH-(CHZ),p Boc-NH-(CHZ),o-CO-Pst-VaIOH (8) was deprotected and cyclized using the procedure described for 5. Yield 260 mg (55 % from Boc-Pst-OH used in 6) of crude solid 9.
For the purpose of biological testing the product 9 was purified by RP-HPLC.
SIMS
MS h4H+474 Example 3 Solid phase synthesis of a cyclic inhibitor.

F~ COC
w t) Pf~rtdn~
Z)~n~. OIC. H09t f 'L,%

~H coo NQ~
1I PIpI~IdIM I
=1 le~C~t-0CQ0 ~~"~~tt 000 ?~A
C0~1 COOEI
i a~~, au 10 /"'_ ~~ n HN
CO
H
_I J
cowl ow (SEQ. ID. N0.48) Solid ~hgs_e Synthesis of TFA.H?N-ICH~" ~~Ol stV~l-OH l10) FmocVal-WANG-resin (1g, 0.37 mmol) was swollen in DMF, washed with DMF (3x2 min), deprotected with 20% piperidine in DMF (1x2 min; 1x20 min) and washed ~ again with DMF (Sx2 min). FmocPstOH (319 mg, 0.74 mmol) was then coupled using DIC (diisopropylcarbodiimide) ( 101 mg, 0. 8 mmol) and HOBt ( 122 mg, 0.8 mmol) for activation. The resulting resin was then deprotected and washed as described above. The solution of BocNH-(CHZ)"-COO-pC6H,-NOZ (452 mg, 1 mmol) and DIEA (190 ~cl, 1.1 mmol) in 5 ml of DMF was added and the mixture was shaken overnight. The resin was washed with DMF (5x2 min), 20% piperidine in DMF (2x2 min), DMF (3x2 min), pyridine-DCM (1:1) (3x2 min) and DCM (dichloromethane) (5x2 min). The product was then cleaved off the resin with 95 % TFA (2x30 min) and the resin was washed with DCM (5x2 min). The combined solutions were evaporated to dryness. The oily residue (200 mg) was used directly for the next reaction.
Synthesis of ( 11 ) lcvclization) TFA.HZN-(CHZ)1,-OCOPstVal-OH(10)was cyclized using theprocedure described for 5. Yield 40 mg (21.5 % based on the resin substitution) of crude 11.
For the purpose of biological testing the product was purified by RP-HPLC.
Product was characterized by SIMS-MS, M+H+ = 504, M+Na+ = 526.
Compound 11 has a K; against cathepsin D of 3.6 nM.

Example 4 Synthesis of a cyclic urea.
Synthesis of Inhibitor 15 _ ;OOH DPP4. Dle~
90~100°C
QtEA
t8u ~ TF~H~N CONH ~ (Cf~y~~~ COOCH~
t8u0 CONH - (Ctl~t,~ COOCH~ NCH. M~OH

CONH ~ (Cii~~~ COOH
t8tt0 Z DPPI~, OtEJI.DMF

(CH~~~
CO ~HN
NN CO
'.
NhICONH
OH 1~
(SEQ.ID.N0.49) Svnth~sis of 13 Boc-Pst(acetonide)OH (850 mg, 2.44 mmol) was dissolved in 13 ml of toluene and approx. 2-3 ml of toluene was distilled off to dry the solution.
DPPA (I
g, 3.66 mmol) and DIEA (0.84 ml, 4.88 mmol) were added and the mixture was heated to 90-100°C for 2 hours. A solution of TFA.H-VaINH-(CHZ)"-COOMe prepared from I.2 g (2.8 mmol) Boc-VaINH(CH~"C02Me and DIEA (1.46 ml, 8.5 mmol) in 3 ml of dry toluene was added to the reaction mixture, the mixture was heated for an additional 30 min and then left to stand overnight .at room temperature.
The toluene was removed in vacuo, the residue dissolved in ethyl acetate and washed subsequently with 10% aq. KHSO,, brine, 5 % NaHC03, brine, and finally dried with MgS04. The ethyl acetate was then removed in vacuo and the oily residue purified by flash chromatography in hexane-ethyl acetate (3:2). Yield 873 mg, 53 % of 13.
Product was characterized by SIMS-MS, M+H* = 675.
Synthesis of I4 13 (850 mg, 1.26 mmol) was hydrolyzed with NaOH according to the procedure described above for 4. Yield 850 mg (- 100%) of oily 14, that was used directly for the next reaction.
Synthesis of 15 ~Cycli~ation~
This compound was prepared using the procedure described above for S. Yield 438 mg (69% calculated from 13). Product was characterized by SIMS-MS, M+H* = 503. ' Compound 1S has a K; against cathepsin D of 45 nM.
Inhibition Assays Kinetic measurements. Fluorogenic substrates Ac-Glu-Glu(EDANS)-Lys-Pro-Iie-Cys-Phe-Phe-Arg-Leu-GIy-Lys(DABCYL)-Glu-NH2 and Ac-Glu-Glu(EDANS)-Lys-Pro-Ile-Cys-Phe-Leu-Arg-Leu-Gly-Lys(DABCYL)-Giu-NH2 were used for measuring the activity of cathepsin D and plasmepsin 2 correspondingly. Typically, 485 ~cl of ~,~ 97~~p7Z PCT/US97/02930 -- 50 mM Gly-HC 1 buffer, pH 3.5 (in the case of cathepsin D), or 100 mM sodium acetate buffer, pH 5.0 (in the case of plasmepsin 2), was mixed with 5 ~cI of DMSO
and 5 ~.1 of titrated protease (final concentration 0.2-10 nM) and incubated 3 min at 37°C. The reaction was initiated by the addition of 5 ~.1 of substrate stock solution in DMSO. Increase in fluorescence intensity at the emission maximum of 487 nm (excitation wavelength was 349 nm) was monitored as a function of time using an Aminco Bowman-2 luminescence spectrometer (SLM Instruments, Inc.).
Plasmepsin 1 assays were run similarly to plasmepsin 2, using the fluorogenic substrate DABCYL-Gaba-Glu-Arg-Met-Phe-Leu-Ser-Pro-Gaba-Glu(EDANS)-NH2.
The initial rate of hydrolysis was calculated by a second degree polynomial fit using SLM AB2 2.0 operating software. Kinetic parameters were determined by nonlinear regression fitting of initial rate versus substrate concentration data to the Michaelis-Menten equation using the program Enzfitter version 1.05 (Leatherbarrow, R.J. 1987. Enzfitter, a program for non-linear regression analysis.
Elsevier Scientific, New York).
For inhibition studies inhibitors were prepared as stock solutions at different concentrations in DMSO. In a typical experiment 485 ~d of the appropriate buffer was mixed with 5 ~1 of inhibitor stock solution and S ~.1 of titrated protease (final concentration 0.2-10 nM) and preincubated 3 min at 37°C. The reaction was initiated by the addition of 5 ~1 of substrate stock solution in DMSO. For data analysis the mathematical model for tight-binding inhibitors (Williams, J.W., and Morrison, J.F. Methods~nz, mil. 63: 437 (1979)) was used. The data were fitted _ by nonlinear regression analysis to the equation V =Vd2Et({[K;( 1 +S/K"~ +hF~,]z+4K;( 1 +S/K"~E,} "z-[K;( 1 +S!K"~ +I,-~l) with the program Enzfitter (version 1.05), where V and Vo are initial velocities with and without inhibitor, K~, is a Michaelis-Menten constant and S, E, and I, are the concentrations of substrate, active enzyme and inhibitor respectively.

WO 97!30072 PCTIUS97I02930 -Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it will be obvious to those skilled in the art that certain changes and modifications may be practiced without departing from the spirit and scope thereof as described in the specification and as defined in the appended claims.

WO 9'1130072 PCT/US97/02930 -REFERENCES
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2. Baldwin E.T. et al., Proc. Natl. Acad. Sci. U.S.A. 90, 6796, (1993).
3. Boger, J. Peptides 1983 pp. 569-578, Proceedings of the 8th American Peptide Symposium.
4. Cataldo A.M. et al., Proc. Natl. Acad. Sci. U.S.A. 87, 3861, (1990).
5. Dhanaa, D.S. et al., Tet. Lett. 33: 1725 (1992).
6. Dutta, A.S. et al. J. Med. Chem. 33: 2552 and 2560 (1990).
7. Goldberg D.E. et al., J. Exp. Med. 173, 961, (1991).
8. Goldberg D.E. et al., EMBO J. 13, 306, (1994).
9. Gluzman, I.Y. et al. 1. Clin. invest. 93: 1602 (1994).
10. Hill, J. et al. FEBS Letters 352: 155 (1994).
11. Jouin, P. et al. J. Chem. Soc. Perkin Trans. 1177 (1987).
I2. Jupp, R. A. et al. , Biochem. J. 265, 871, ( 1990).
13. Kenessey A. et aL, Neurosci. Res. 23, 454, (1989).
14. Ladror, U.S. et al. J. Biol. Chem. 269: 18422 (1994).
15. Leatherbarrow, R.H. 1987. Enzfitter, a program for no-linear regression analysis. Elsevier Scientific, New York.
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I7. Liotta L. A., Scientific American Feb., 54, (1992).
18. Liotta L. A. and Stetler-Stevenson W.G., Cancer Biol. 1, 99, (1990).
19. Rochefort, Acta Oncol. 31, 125 (1992).
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Claims (11)

1. A compound of formula (I):
in which R, R7 = represent hydrogen, alkoxycarbonyl, aralkoxycarbonyl, alkylcarbonyl, cycloalkylcarbonyl, cycloalkylalkoxycarbonyl, cycloalkylalkanoyl, aralkanoyl, aroyl, aryloxycarbonyl, aryloxycarbonylalkyl, aryloxyalkanoyl, heterocyclylcarbonyl, heterocyclyloxycarbonyl, heterocyclylalkanoyl, heterocyclylalkoxycarbonyl, heteroaralkanoyl, heteroaralkoxycarbonyl, heteroaryloxycarbonyl, heteroaroyl, alkyl, alkenyl, cycloalkyl, aryl, aralkyl, aryloxyalkyl, heteroaryloxyalkyl, hydroxyalkyl, aminocarbonyl, aminoalkanoyl, mono- and disubstituted aminocarbonyl and mono- and disubstituted aminoalkyl, alkoxyalkyl, alkylthioalkyl, mono- and disubstituted aminoalkanoyl radicals wherein the substituents are selected from alkyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroaralkyl, heterocycloalkyl, heterocycloalkylalkyl radicals, or where said aminoalkanoyl radical is disubstituted, said substituents along with the nitrogen atom to which they are attached form a heterocycloalkyl or heteroaryl radical;
R1, R2, R4, R5, R6 = optionally substituted lower alkyl, lower cycloalkyl, aryl, aralkyl and heteroaryl;
R3 = optionally substituted lower alkyl, lower alkoxy, lower alkylthio, mono or di-lower alkyl amino, aralkyl, aralkoxy, aralkylthio, aralkylamino, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkylthio, cycloalkylalkylamino;
and wherein R2 and R5 or R1 and R3 are connected by an optionally substituted bridging moiety comprised of a stable combination of C, N, O, or S atoms.

2. The compound of claim 1, wherein R1, R2, R4, R5 and R6 represent the side chain or a residue of an amino acid after formation of a peptide linkage.

3. A compound which is selected from the group consisting of (1) Iva-Val-Val-Sta-Val-Leu-Gly-NH2 (SEQ. ID. NO. 1);
(2) Iva-Gln-Val-Sta-Ala-Leu-Gly-NH2 (SEQ. ID. NO. 2);
(3) Iva-Lys-Val-Sta-Ala-Leu-Gly-NH2 (SEQ. ID. NO. 3);
(4) Tba-Val-Val-Sta-Ala-Leu-Gly-NH2 (SEQ. ID. NO. 4);
(5) Iva-Val-Ile-Sta-Ala-Leu-Gly-NH2 (SEQ. ID. NO. 5);
(6) Iva-Val-Leu-Sta-Ala-Leu-Gly-NH2 (SEQ. ID. NO. 6);
(7) Tba-Val-Val-Pst-Val-Leu-Gly-NH2 (SEQ. ID. NO. 7);
(8) Tba-Val-Cys-Pst-Val-Leu-Gly-NH2 (SEQ. ID. NO. 8);
(9) Tba-Val-Glu-Pst-Val-Leu-Gly-NH2 (SEQ. ID. NO. 9);
(10) Tba-Val-Asp-Pst-Val-Leu-Gly-NH2 (SEQ. ID. NO. 10);
(11) Iva-Val-Val-Sta-Ala-Leu-Gly-NH2 (SEQ. ID. NO. 11);
(12) Tba-Val-Cys-Pst-Val-Cys-Gly-NH2 (SEQ. ID. NO. 12);

4. A compound of formula II:
in which R, R7 = represent hydrogen, alkoxycarbonyl, aralkoxycarbonyl, alkylcarbonyl, cycloalkylcarbonyl, cycloalkylalkoxycarbonyl, cycloalkylalkanoyl, aralkanoyl, aroyl, aryloxycarbonyl, aryloxycarbonylalkyl, aryloxyalkanoyl, heterocyclylcarbonyl, heterocyclyloxycarbonyl, heterocyclylalkanoyl, heterocyclylalkoxycarbonyl, heteroaralkanoyl, heteroaralkoxycarbonyl, heteroaryloxycarbonyl, heteroaroyl, alkyl, alkenyl, cycloalkyl, aryl, aralkyl, aryloxyalkyl, heteroaryloxyalkyl, hydroxyalkyl, aminocarbonyl, aminoalkanoyl, mono- and disubstituted aminocarbonyl and mono- and disubstituted aminoalkyl, alkoxyalkyl, akylthioalkyl, mono- and disubstituted aminoalkanoyl radicals wherein the substituents are selected from alkyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroaralkyl, heterocycloalkyl, heterocycloalkylalkyl radicals, or where said aminoalkanoyl radical is disubstituted, said substituents along with the nitrogen atom to which they are attached form a heterocycloalkyl or heteroaryl radical;
R2, = optionally substituted lower alkyl, lower cycloalkyl, aryl, aralkyl and heteroaryl;
R3 = optionally substituted lower alkyl, lower alkoxy, lower alkylthio, mono or di-lower alkyl amino, aralkyl, aralkoxy, aralkylthio, aralkylamino, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkylthio, cycloalkylalkylamino;
with the proviso that NHR7 does not comprise or form an alpha-amino acid.

5. The compound of claim 4, wherein R and R3 are connected by an optionally substituted bridging moiety comprised of a stable combination of C, N, O, or S atoms.

6. The compound of claim 4, wherein R2 represents the side chain of a residue of an amino acid after formation of a peptide linkage.

7. The compound of claim 4, which is selected from the group consisting of

8. A compound of formula III:
in which R, R7 = represent hydrogen, alkoxycarbonyl, aralkoxycarbonyl, alkylcarbonyl, cycloalkykarbonyl, cycloalkylalkoxycarbonyl, cycloalkylalkanoyl, aralkanoyl, aroyl, aryloxycarbonyl, aryloxycarbonylalkyi, aryloxyalkanoyl, heterocyclylcarbonyl, heterocyclyloxycarbonyl, heterocyclylalkanoyl, heterocyclylalkoxycarbonyl, heteroaralkanoyl, heteroaralkoxycarbonyl, heteroaryloxycarbonyl, heteroaroyl, alkyl, alkenyl, cycloalkyl, aryl, aralkyl, aryloxyalkyl, heteroaryloxyalkyl, hydroxyalkyl, aminocarbonyl, aminoalkanoyl, hydroxyalkanoyl, alkenoyl, alkoxyalkanoyl, alkylthioalkanoyl, arylthioalkanoyl, alkoxycarbonylalkanoyl, hydroxycarbonylalkanoyl, aryloxycarbonylalkanoyl, heteroaryloxycarbonylalkanoyl, aminocarbonylalkanoyl, mono- and disubstituted aminocarbonylalkanoyl, alkylthioalkoxycarbonyl, arylthioalkoxycarbonyl, cycloalkylthioalkoxycarbonyl, heteroarylthioalkoxycarbonyl, heterocyclylalkylthioalkoxycarbonyl, cycloalkyloxycarbonyl, hydroxyalkoxycarbonyl, alkoxyalkoxycarbonyl, aryloxyalkoxycarbonyl, heteroaryloxyalkoxycarbonyl, cycloalkyloxyalkoxycycarbonyl, heterocyclylalkyloxyalkoxycarbonyl, cycloalkyloxyalkanoyl, heterocyclyloxyalkanoyl, heteroaryloxyalkanoyl, cycloalkylthioalkanoyl, heterocyclylalkylthioalkanoyl, heteroarylthioalkanoyl, aralkenoyl, mono- and disubstituted aminoalkoxycarbonyl, mono-and disubstituted aminocarbonyl and mono- and disubstituted aminoalkyl, alkoxyalkyl, alkylthioalkyl, mono- and disubstituted aminoalkanoyl radicals wherein the substituents are selected from alkyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroaralkyl, heterocycloalkyl, heterocycloalkylalkyl radicals, or where said aminoalkanoyl radical is disubstituted, said substituents along with the nitrogen atom to which they are attached form a heterocycloakyl or heteroaryl radical;
R4 = optionally substituted lower alkyl, lower cycloalkyl, aryl, aralkyl and heteroaryl;
R3 = optionally substituted lower alkyl, lower alkoxy, lower alkylthio, mono or di-lower alkyl amino, aralkyl, aralkoxy, aralkylthio, aralkylamino, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkylthio, cycloalkylalkylamino;
with the proviso that R does not comprise an alpha-amino acid.

9. The compound of claim 8, wherein R4 represents a side chain of a residue of an amino acid after formation of a peptide linkage.

10. A compound which is selected from the group consisting of

11. A compound of formula II:

in which R, R7 = represent hydrogen, alkoxycarbonyl, aralkoxycarbonyl, alkylcarbonyl, cycloalkylcarbonyl, cycloalkylalkoxycarbonyl, cycloalkylalkanoyl, aralkanoyl, aroyl, aryloxycarbonyl, aryloxycarbonylalkyl, aryloxyalkanoyl, heterocyclylcarbonyl, heterocyclyloxycarbonyl, heterocyclylalkanoyl, heterocyclylalkoxycarbonyl, heteroaralkanoyl, heteroaralkoxycarbonyl, heteroaryloxycarbonyl, heteroaroyl, alkyl, alkenyl, cycloalkyl, aryl, aralkyl, aryloxyalkyl, heteroaryloxyalkyl, hydroxyalkyl, aminocarbonyl, aminoalkanoyl, mono- and disubstituted aminocarbonyl and mono- and disubstituted aminoalkyl, alkoxyalkyl, alkylthioalkyl, mono- and disubstituted aminoalkanoyl radicals wherein the substituents are selected from alkyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroaralkyl, heterocycloalkyl, heterocycloalkylalkyl radicals, or where said aminoalkanoyl radical is disubstituted, said substituents along with the nitrogen atom to which they are attached form a heterocycloalkyl or heteroaryl radical;
R2,= optionally substituted lower alkyl, lower cycloalkyl, aryl, aralkyl and heteroaryl;
R3 = optionally substituted lower alkyl, lower alkoxy, lower alkylthio, mono or di-lower alkyl amino, aralkyl, aralkoxy, aralkylthio, aralkylamino, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkylthio, cycloalkylalkylamino;
and wherein R and R3 are connected by an optionally substituted bridging moiety comprised of a stable combination of C, N, O, or S atoms.