RS52304B - Substituted indolyl alkyl amino derivatives as novel inhibitors of histone deacetylase - Google Patents

Substituted indolyl alkyl amino derivatives as novel inhibitors of histone deacetylase

Info

Publication number
RS52304B
RS52304B RS20120165A RSP20120165A RS52304B RS 52304 B RS52304 B RS 52304B RS 20120165 A RS20120165 A RS 20120165A RS P20120165 A RSP20120165 A RS P20120165A RS 52304 B RS52304 B RS 52304B
Authority
RS
Serbia
Prior art keywords
alkyl
hydrogen
6alkyl
amino
alkyl amino
Prior art date
Application number
RS20120165A
Other languages
Serbian (sr)
Inventor
Marc Gustaaf C. Verdonck
Patrick René ANGIBAUD
Bruno Roux
Isabelle Noëlle Constance PILATTE
Peter Ten Holte
Janine Arts
Kristof Van Emelen
Original Assignee
Janssen Pharmaceutica Nv
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Priority claimed from PCT/EP2005/053612 external-priority patent/WO2006010750A1/en
Publication of RS52304B publication Critical patent/RS52304B/en

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Jedinjenje formule (I),njegove N-oksid forme, njegove farmaceutski prihvatljive adicijske soli i njegove stereohemijske izomerne forme, naznačeno time dasvaki n je ceo broj s vrednošću 0, 1 ili 2 i kada je n jednako 0 onda je moguća diretna veza;svaki m je ceo broj s vrednošću 1 ili 2;svaki X je neovisno N ili CH;svaki Y je neovisno O, S, ili NR4; gdesvaki R4 je vodonik, C1-6alkil, C1-6alkiloksiC1-6alkil, C3-6cikloalkil,C3-6cikloalkilmetil, fenil-C1-6alkil, -C(=O)-CHR5R6 ili -S(=O)2-N(CH3)2; gde svaki R5i R6 je neovisno vodonik, amino, C1-6alkil ili aminoC1-6alkil; ikada je Y jednako NR4 i R2 je na 7-poziciji indolila onda R2 i R4 zajedno mogu da formiraju dvovaljani radikal-(CH2)2- (a-1), ili-(CH2)3- (a-2);R1 je vodonik, C1-6alkil, hidroksi C1-6alkil, C1-6alkilsulfonil, C1-6alkilkarbonil ili mono- ili di(C1-6alkil)aminosulfonil;R2 je vodonik, hidroksi, amino, halo, C1-6alkil, cijano, C2-6alkenil, polihaloC1-6alkil, nitro, fenil, C1-6alkilkarbonil, hidroksikarbonil, C1-6alkilkarbonilamino, C1-6alkiloksi, ili mono- ili di(C1-6alkil)amino;R3 je vodonik, C1-6alkil, ili C1-6alkiloksi; ikada su R2 i R3 na susednim atomima ugljenika, oba mogu da formiraju dvovaljani radikal -O-CH2-O-.Prijava sadrži još 11 patentnih zahteva.The compound of formula (I), its N-oxide form, its pharmaceutically acceptable addition salts, and its stereochemically isomeric forms, wherein n is an integer having a value of 0, 1 or 2 and when n is 0 then a diuretic bond is possible; m is an integer with value 1 or 2; each X is independently N or CH; each Y is independently O, S, or NR 4; where R4 is hydrogen, C1-6alkyl, C1-6alkyloxyC1-6alkyl, C3-6cycloalkyl, C3-6cycloalkylmethyl, phenyl-C1-6alkyl, -C (= O) -CHR5R6 or -S (= O) 2-N (CH3) 2; wherein each R 5 and R 6 is independently hydrogen, amino, C 1-6 alkyl or aminoC 1-6 alkyl; when Y is NR4 and R2 is at the 7-position of indolyl then R2 and R4 together may form a double-rolled radical- (CH2) 2- (a-1), or- (CH2) 3- (a-2); R1 is hydrogen, C 1-6 alkyl, hydroxy C 1-6 alkyl, C 1-6 alkylsulfonyl, C 1-6 alkylcarbonyl or mono- or di (C 1-6 alkyl) aminosulfonyl; R 2 is hydrogen, hydroxy, amino, halo, C 1-6 alkyl, cyano, C 2-6 alkenyl, polyhaloC 1-6 alkyl, nitro, phenyl, C 1-6 alkylcarbonyl, hydroxycarbonyl, C 1-6 alkylcarbonylamino, C 1-6 alkyloxy, or mono- or di (C 1-6 alkyl) amino; R 3 is hydrogen, C 1-6 alkyl, or C 1-6 alkyloxy; ever R2 and R3 are on adjacent carbon atoms, both of which can form a double-rolled radical -O-CH2-O-.The application contains 11 more claims.

RS20120165A 2004-07-28 2005-07-25 Substituted indolyl alkyl amino derivatives as novel inhibitors of histone deacetylase RS52304B (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP04077172 2004-07-28
US59218204P 2004-07-29 2004-07-29
PCT/EP2005/053612 WO2006010750A1 (en) 2004-07-28 2005-07-25 Substituted indolyl alkyl amino derivatives as novel inhibitors of histone deacetylase

Publications (1)

Publication Number Publication Date
RS52304B true RS52304B (en) 2012-12-31

Family

ID=34928411

Family Applications (1)

Application Number Title Priority Date Filing Date
RS20120165A RS52304B (en) 2004-07-28 2005-07-25 Substituted indolyl alkyl amino derivatives as novel inhibitors of histone deacetylase

Country Status (10)

Country Link
CN (1) CN1993353B (en)
AT (1) ATE542812T1 (en)
DK (1) DK1781639T3 (en)
ES (1) ES2381117T3 (en)
ME (1) ME01444B (en)
PT (1) PT1781639E (en)
RS (1) RS52304B (en)
SI (1) SI1781639T1 (en)
UA (1) UA93352C2 (en)
ZA (1) ZA200700764B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107095871A (en) * 2016-02-22 2017-08-29 中国科学院上海巴斯德研究所 Quisinostat, a kind of new efficient antimalarial agent
CN107721980B (en) * 2017-08-25 2019-07-12 南京医科大学 The weary oxygen targeted prodrug and its application of a kind of fluorouracil and Quisinosta
CN112485233B (en) * 2020-11-03 2022-08-26 山东师范大学 Nano sensor for detecting deacetylase and detection method and application thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2306858T3 (en) * 2002-03-13 2008-11-16 Janssen Pharmaceutica Nv CARBONILAMINE DERIVATIVES AS NEW INHIBITORS OF HISTONADESACETILASAS.

Also Published As

Publication number Publication date
DK1781639T3 (en) 2012-05-14
ME01444B (en) 2013-12-20
CN1993353B (en) 2010-12-01
ATE542812T1 (en) 2012-02-15
ZA200700764B (en) 2008-09-25
SI1781639T1 (en) 2012-06-29
CN1993353A (en) 2007-07-04
PT1781639E (en) 2012-05-02
ES2381117T3 (en) 2012-05-23
UA93352C2 (en) 2011-02-10

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