YU47728B - Azaoksindol derivati - Google Patents

Azaoksindol derivati

Info

Publication number
YU47728B
YU47728B YU791A YU791A YU47728B YU 47728 B YU47728 B YU 47728B YU 791 A YU791 A YU 791A YU 791 A YU791 A YU 791A YU 47728 B YU47728 B YU 47728B
Authority
YU
Yugoslavia
Prior art keywords
substituted
phenyl
alkyl
heteroaryl
hydrogen
Prior art date
Application number
YU791A
Other languages
English (en)
Other versions
YU791A (sh
Inventor
R. Robinson
A. Marfat
Original Assignee
Pfizer Inc.
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 Pfizer Inc. filed Critical Pfizer Inc.
Publication of YU791A publication Critical patent/YU791A/sh
Publication of YU47728B publication Critical patent/YU47728B/sh

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

AZAOKSINDOL DERIVATI formule, naznaceno time, u kojoj jedan A, B, D i E je N i drugi su C; X i Y su nezavisno odabrani iz grupe koju sacinjavaju vodonik, OR3, hidroksi (C1-C6)alkil, CF3,COR3, halogen COOR3, CONR3R3, CN, NO", SR3, SOR3, SO2R3R3; R1 je (C1-C6)alkil ili CONHR4; R2 je (C1-C8)alkil, (Ch2)nR5 gde je n 0 ili1, ili NHR6; R3 je (C1-C6) alkil, fenil, benzil, alil ili vodonik, pri cemu pomenuti fenil i fenil ostatak pomenutog benzila moze opciono biti supstituisan sa jednim ili vise supstituenata nezavisno odabrani od fluoro, hloro, bromo, jodo, hidroksi, (C1-C3)alkoksi i CF3 grupe; R4 je vodonik, (C1-C6)alkil, (C2-C6)hidroksialkil, (C3-C8)-cikloalkil, COR3 gde R3 je kao sto je gore definisano, fenil, supstituisani fenil, heteroaril ili supstituisani heteroaril, pri cemu heteroaril ostatak svake od pomenutih heteroaril i supstituisanih heteroaril grupa je odabran od tiofena i furana, i pri cemu svaki pomenuti fenil i supstituisani heteroaril grupa je supstituisan sa jednim ili dva supstituenta nezavisno odabranih od fluoro, hloro, bromo, jodo, hidroksi, (C1-C3)alkil, (C1-C3)alkoksi i CF3; R5 je (C3-C8)cikloalkil, vodonik, fenil, supstituisani fenil, heteroaril i supstituisani heteroaril, pri cemu heteroaril ostatak svake od pomenutih heteroaril i supstituisane heteroaril grupa je odabran od tiofena i furana, i svaki od pomenutih supstituisanih fenil i supstituisanih heteroaril grupa je supstituisan sa jednim ili dva supstituenta nezavisno odabrani od fluoro, hloro, bromo, jodo, hidroksi, (C1-C3) alkil, (C1-C3)alkoksi i trifluorometil grupe; R6 je fenil, tiofen ili furan, pri cemu svaki fenil, tiofen i furan mogu biti opciono supstituisani sa jednim ili vise supstituenata nezavisno odabrani od fluoro, hloro, bromo, jodo, hidroksi, (C1-C3) alkil, (C1-C3)alkoksi i trifluorometil grupe; i W je vodonik, (C2-C10)alkonil, (C5-C7)cikloaliklkarbonil, (C7-C10)fenilakanoilm hlorobenzoil, tenoil, omega-(C2-C4)alkoksikarbonil-(C3-C5)alkanoil, (C2-C10)alkoksikarbonil, fenoksikarbonil, 1/(C1C4)aciloksi/-(C2-C4)alkil;pod uslovom sto (a) kada E je azot, tada najmanje jedan X i Y se razlikuje od vodonika; (b) kada ili R2 je NHR6 ili R1 je (C1-C6)alkil, atada W je vodonik; ili njegova farmaceutski prihvatljiva so. Prijava sadrzi jos 4 zavisna patenta.
YU791A 1990-01-05 1991-01-04 Azaoksindol derivati YU47728B (sh)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US1990/000107 WO1991009598A1 (en) 1990-01-05 1990-01-05 Azaoxindole derivatives

Publications (2)

Publication Number Publication Date
YU791A YU791A (sh) 1994-01-20
YU47728B true YU47728B (sh) 1996-01-08

Family

ID=22220612

Family Applications (1)

Application Number Title Priority Date Filing Date
YU791A YU47728B (sh) 1990-01-05 1991-01-04 Azaoksindol derivati

Country Status (19)

Country Link
EP (1) EP0436333A3 (sh)
JP (1) JPH0826018B2 (sh)
KR (1) KR930005447B1 (sh)
CN (1) CN1031053C (sh)
AU (1) AU635593B2 (sh)
BR (1) BR9100046A (sh)
CA (1) CA2033531C (sh)
CS (1) CS991A2 (sh)
FI (1) FI922347A0 (sh)
IE (1) IE910022A1 (sh)
IL (1) IL96819A0 (sh)
MY (1) MY109722A (sh)
NO (1) NO922634D0 (sh)
NZ (1) NZ236582A (sh)
PL (2) PL165653B1 (sh)
PT (1) PT96411B (sh)
WO (1) WO1991009598A1 (sh)
YU (1) YU47728B (sh)
ZA (1) ZA9172B (sh)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU1625192A (en) * 1991-05-31 1992-12-03 Zeneca Limited Heterocyclic derivatives
GB9226855D0 (en) * 1992-12-23 1993-02-17 Erba Carlo Spa Vinylene-azaindole derivatives and process for their preparation
FR2722196B1 (fr) * 1994-07-07 1996-08-23 Adir Nouveaux derives amines de 1,3-dihydro-2h-pyrrolo(2,3-b) pyridin-2-ones et oxazolo(4,5-b) pyridin-2 (3h)-ones, leur procede de preparation et les compositions pharmaceutique qui les contiennent
US5618819A (en) * 1994-07-07 1997-04-08 Adir Et Compagnie 1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one and oxazolo[4,5-b]pyridin-2-(3H)-one compounds
FR2722195B1 (fr) * 1994-07-07 1996-08-23 Adir Nouveaux derives de 1,3-dihydro-2h-pyrrolo(2,3-b) pyridin-2-ones et oxazolo(4,5-b) pyridin-2(3h)-ones, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
US5939069A (en) * 1996-08-23 1999-08-17 University Of Florida Materials and methods for detection and treatment of immune system dysfunctions
GB9718913D0 (en) 1997-09-05 1997-11-12 Glaxo Group Ltd Substituted oxindole derivatives
AU770375B2 (en) * 1998-12-17 2004-02-19 F. Hoffmann-La Roche Ag 4-alkenyl (and alkynyl) oxindoles as inhibitors of cyclin-dependent kinases, in particular CDK2
WO2000035921A1 (en) 1998-12-17 2000-06-22 F. Hoffmann-La Roche Ag 4,5-pyrazinoxindoles as protein kinase inhibitors
JP2002532493A (ja) 1998-12-17 2002-10-02 エフ.ホフマン−ラ ロシュ アーゲー Jnkプロテインキナーゼ阻害剤としての4−アリールオキシインドール
US6153634A (en) * 1998-12-17 2000-11-28 Hoffmann-La Roche Inc. 4,5-azolo-oxindoles
US6624171B1 (en) 1999-03-04 2003-09-23 Smithkline Beecham Corporation Substituted aza-oxindole derivatives
GB9904933D0 (en) 1999-03-04 1999-04-28 Glaxo Group Ltd Compounds
US6492398B1 (en) 1999-03-04 2002-12-10 Smithkline Beechman Corporation Thiazoloindolinone compounds
US6313310B1 (en) 1999-12-15 2001-11-06 Hoffmann-La Roche Inc. 4-and 5-alkynyloxindoles and 4-and 5-alkenyloxindoles
CO5271715A1 (es) 1999-12-21 2003-04-30 Sugen Inc 7-aza-indolin-2-onas sustituidas en 4 y su uso como inhibidores de proteiuna quinasa
US6620818B1 (en) 2000-03-01 2003-09-16 Smithkline Beecham Corporation Method for reducing the severity of side effects of chemotherapy and/or radiation therapy
DE10053275A1 (de) * 2000-10-27 2002-05-02 Dresden Arzneimittel Neue 7-Azaindole, deren Verwendung als Inhibitoren der Phosphodiesterase 4 und Verfahren zu deren Herstellung
TWI262920B (en) 2000-10-27 2006-10-01 Elbion Ag New 7-azaindoles, their use as inhibitors of phosphodiesterase 4, and a method for synthesizing them
JP2004529110A (ja) 2001-03-06 2004-09-24 アストラゼネカ アクチボラグ 脈管損傷活性を有するインドール誘導体
KR20050013534A (ko) * 2002-03-28 2005-02-04 에자이 가부시키가이샤 c─Jun N─말단 키나아제 억제용 아자인돌
TW200611695A (en) 2004-06-09 2006-04-16 Glaxo Group Ltd Pyrrolopyridine derivatives
US7906528B2 (en) * 2004-10-05 2011-03-15 Novartis International Pharmaceutical Ltd. Pyrrolo-pyridine, pyrrolo-pyrimidine and related heterocyclic compounds
WO2009147476A1 (en) * 2008-06-02 2009-12-10 Matrix Laboratories Ltd. Novel pde inhibitors, pharmaceutical compositions containing them and processes for their preparation

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4556672A (en) * 1984-03-19 1985-12-03 Pfizer Inc. 3-Substituted 2-oxindole-1-carboxamides as analgesic and anti-inflammatory agents
US4569942A (en) * 1984-05-04 1986-02-11 Pfizer Inc. N,3-Disubstituted 2-oxindole-1-carboxamides as analgesic and antiinflammatory agents
DE3681358D1 (de) * 1985-07-09 1991-10-17 Pfizer Substituierte oxindol-3-carboxamine als entzuendungshemmendes und schmerzstillendes mittel.
WO1989012637A1 (en) * 1988-06-14 1989-12-28 Schering Corporation Heterobicyclic compounds having antiinflammatory activity

Also Published As

Publication number Publication date
AU635593B2 (en) 1993-03-25
BR9100046A (pt) 1991-10-22
JPH04210981A (ja) 1992-08-03
WO1991009598A1 (en) 1991-07-11
MY109722A (en) 1997-05-31
CS991A2 (en) 1991-09-15
EP0436333A3 (en) 1992-05-27
PL165653B1 (pl) 1995-01-31
PT96411A (pt) 1991-10-15
CA2033531C (en) 1998-06-23
KR930005447B1 (ko) 1993-06-22
PL288598A1 (en) 1991-12-02
KR910014375A (ko) 1991-08-31
EP0436333A2 (en) 1991-07-10
AU6860691A (en) 1992-03-05
NO922634L (no) 1992-07-03
NO922634D0 (no) 1992-07-03
CA2033531A1 (en) 1991-07-06
FI922347A (fi) 1992-05-22
JPH0826018B2 (ja) 1996-03-13
CN1031053C (zh) 1996-02-21
YU791A (sh) 1994-01-20
ZA9172B (en) 1992-10-28
CN1053065A (zh) 1991-07-17
NZ236582A (en) 1993-10-26
PT96411B (pt) 1999-04-30
IL96819A0 (en) 1991-09-16
PL166512B1 (pl) 1995-05-31
IE910022A1 (en) 1991-07-17
FI922347A0 (fi) 1992-05-22

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