PL375697A1 - Pirazolipirymidyny jako inhibitory kinazy zależnej od cykliny - Google Patents

Pirazolipirymidyny jako inhibitory kinazy zależnej od cykliny

Info

Publication number
PL375697A1
PL375697A1 PL03375697A PL37569703A PL375697A1 PL 375697 A1 PL375697 A1 PL 375697A1 PL 03375697 A PL03375697 A PL 03375697A PL 37569703 A PL37569703 A PL 37569703A PL 375697 A1 PL375697 A1 PL 375697A1
Authority
PL
Poland
Prior art keywords
compounds
cyclin
pyrazolopyrimidines
kinase inhibitors
dependent kinase
Prior art date
Application number
PL03375697A
Other languages
English (en)
Other versions
PL224879B1 (pl
Inventor
Timothy J. Guzi
Kamil Paruch
Michael P. Dwyer
Ronald J. Doll
Viyyoor Moopil Girijavallabhan
Alan Mallams
Carmen S. Alvarez
Kartik M. Keertikar
Jocelyn Rivera
Tin-Yau Chan
Vincent Madison
Thierry O. Fischmann
Lawrence W. Dillard
Vinh D. Tran
Zhen Min He
Ray Anthony James
Haengsoon Park
Vidyadhar M. Paradkar
Douglas Walsh Hobbs
Original Assignee
Schering Corporation
Pharmacopeia Drug Discovery, 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 Schering Corporation, Pharmacopeia Drug Discovery, Inc. filed Critical Schering Corporation
Publication of PL375697A1 publication Critical patent/PL375697A1/pl
Publication of PL224879B1 publication Critical patent/PL224879B1/pl

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

W wielu wykonaniach niniejszy wynalazek dostarcza nowej klasy pirazolo[1,5-a]pirymidynowych związków jako inhibitorów zależnych od cykliny kinaz, sposobów wytwarzania takich związków, farmaceutycznych kompozycji zawierających jeden lub więcej taki związek, sposobów wytwarzania farmaceutycznych preparatów zawierających jeden lub więcej taki związek i sposobów leczenia, zapobiegania, hamowania lub łagodzenia jednej lub więcej chorób związanych z CDK z użyciem takich związków albo farmaceutycznych kompozycji.
PL375697A 2002-09-04 2003-09-03 Pirazolo [1,5-a] pirymidynowy związek, jego zastosowanie do wytwarzania leku oraz zawierająca go farmaceutyczna kompozycja PL224879B1 (pl)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US40802702P 2002-09-04 2002-09-04
US60/408,027 2002-09-04
US42195902P 2002-10-29 2002-10-29
US60/421,959 2002-10-29

Publications (2)

Publication Number Publication Date
PL375697A1 true PL375697A1 (pl) 2005-12-12
PL224879B1 PL224879B1 (pl) 2017-02-28

Family

ID=31981560

Family Applications (1)

Application Number Title Priority Date Filing Date
PL375697A PL224879B1 (pl) 2002-09-04 2003-09-03 Pirazolo [1,5-a] pirymidynowy związek, jego zastosowanie do wytwarzania leku oraz zawierająca go farmaceutyczna kompozycja

Country Status (12)

Country Link
EP (1) EP2194058B1 (pl)
JP (1) JP2010180234A (pl)
AR (1) AR041137A1 (pl)
CY (1) CY1110666T1 (pl)
DE (1) DE60332846D1 (pl)
EC (2) ECSP055642A (pl)
ES (1) ES2346204T3 (pl)
MY (1) MY138201A (pl)
PL (1) PL224879B1 (pl)
PT (1) PT1537116E (pl)
RU (1) RU2380369C9 (pl)
TW (1) TWI344468B (pl)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9278910B2 (en) 2011-05-31 2016-03-08 Receptos, Inc. GLP-1 receptor stabilizers and modulators
CN105593225B (zh) 2013-06-11 2019-04-16 赛尔基因第二国际有限公司 新型glp-1受体调节剂
MX381977B (es) 2014-12-10 2025-03-13 Receptos Llc Moduladores del receptor de péptido 1 tipo glucagón.
RU2744974C2 (ru) 2015-08-26 2021-03-17 Блюпринт Медсинс Корпорейшн Соединения и композиции, применяемые для лечения расстройств, связанных с ntrk
CA3005741A1 (en) * 2015-11-19 2017-05-26 Blueprint Medicines Corporation Compounds and compositions useful for treating disorders related to ntrk
AU2017281222B2 (en) 2016-06-23 2022-06-16 The Usa As Represented By The Department Of Veterans Affairs; Dept. Of Veterans Affairs Office Of General Counsel - Pag Iv (024) Non-catalytic substrate-selective P38α-specific MAPK inhibitors with endothelial-stabilizing and anti-inflammatory activity, and methods of use thereof
WO2020118194A1 (en) * 2018-12-07 2020-06-11 University Of Maryland, Baltimore NON-ATP/CATALYTIC SITE p38 MITOGEN ACTIVATED PROTEIN KINASE INHIBITORS
CN116406355A (zh) 2020-05-18 2023-07-07 Gen1E生命科学公司 P38α促分裂原活化蛋白激酶抑制剂
US11390581B2 (en) 2020-10-29 2022-07-19 Gen1E Lifesciences Inc. Crystalline 5-(dimethylamino)-n-(4-(morpholinomethyl)phenyl)naphthalene-1-sulfonamide di-hydrochloride di-hydrate
CN117120422A (zh) 2021-03-23 2023-11-24 Gen1E生命科学公司 取代的萘基P38α丝裂原活化的蛋白激酶抑制剂
CN116983313A (zh) * 2023-07-13 2023-11-03 四川大学 Nu6300的新用途

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US3907799A (en) 1971-08-16 1975-09-23 Icn Pharmaceuticals Xanthine oxidase inhibitors
WO1991018904A1 (en) 1990-05-30 1991-12-12 American Home Products Corporation Substituted arylsulfonamides and benzamides
WO1992018504A1 (en) 1991-04-22 1992-10-29 Otsuka Pharmaceutical Factory, Inc. PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVE AND ANTI-INFLAMMATORY CONTAINING THE SAME
US5571813A (en) 1993-06-10 1996-11-05 Beiersdorf-Lilly Gmbh Fused pyrimidine compounds and their use as pharmaceuticals
EP0628559B1 (en) * 1993-06-10 2002-04-03 Beiersdorf-Lilly GmbH Pyrimidine compounds and their use as pharmaceuticals
PT714898E (pt) 1994-06-21 2002-04-29 Otsuka Pharma Co Ltd Derivado de pirazolo¬1,5-a|pirimidina
GB9716557D0 (en) 1997-08-06 1997-10-08 Glaxo Group Ltd Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity
ES2281941T3 (es) * 1997-12-13 2007-10-01 Bristol-Myers Squibb Company Uso de pirazolo(3,4-b)piridina como inhibidores de quinasa dependiente de ciclina.
US6413974B1 (en) * 1998-02-26 2002-07-02 Aventis Pharmaceuticals Inc. 6,9,-disubstituted 2-[trans-(4-aminocyclohexyl) amino] purines
US6194410B1 (en) * 1998-03-11 2001-02-27 Hoffman-La Roche Inc. Pyrazolopyrimidine and pyrazolines and process for preparation thereof
DE19834047A1 (de) 1998-07-29 2000-02-03 Bayer Ag Substituierte Pyrazolderivate
DE69912379T2 (de) 1998-08-14 2004-05-06 Pfizer Inc. Antithrombosemittel
EP1124823A1 (en) 1998-10-30 2001-08-22 Merck & Co., Inc. Thrombin inhibitors
ES2207983T3 (es) 1998-12-22 2004-06-01 Novartis Ag Derivados de epotilona y su uso como agentes antitumorales.
CA2369895C (en) 1999-01-11 2010-12-21 Princeton University High affinity inhibitors for target validation and uses thereof
AU777735B2 (en) 1999-07-15 2004-10-28 Pharmacopeia, Inc. Bradykinin B1 receptor antagonists
PL365170A1 (pl) 2000-07-26 2004-12-27 Bristol-Myers Squibb Company N-[5-[[[5-alkilo-2-oksazolilo] metylo] tio]-2-tiazolilo] karboksyamidowe inhibitory kinaz zależnychod cyklin
JP4052573B2 (ja) 2000-09-15 2008-02-27 バーテックス ファーマシューティカルズ インコーポレイテッド イソオキサゾールおよびｅｒｋのインヒビターとしてのその使用
PE20020507A1 (es) 2000-10-17 2002-06-25 Schering Corp Compuestos no-imidazoles como antagonistas del receptor histamina h3
US7067520B2 (en) 2000-11-17 2006-06-27 Ishihara Sangyo Kaisha, Ltd. Preventive or therapeutic medicines for diabetes containing fused-heterocyclic compounds or their salts
WO2002050079A1 (fr) 2000-12-20 2002-06-27 Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) Inhibiteurs de kinases dependantes des cylines (cdk) et de la glycogene synthase kinase-3 (gsk-3)
WO2002064211A1 (en) 2001-02-09 2002-08-22 Merck & Co., Inc. Thrombin inhibitors

Also Published As

Publication number Publication date
TW200410973A (en) 2004-07-01
TWI344468B (en) 2011-07-01
RU2380369C9 (ru) 2011-07-10
EP2194058B1 (en) 2013-11-27
DE60332846D1 (de) 2010-07-15
EP2194058A1 (en) 2010-06-09
ECSP11005642A (es) 2011-10-31
JP2010180234A (ja) 2010-08-19
RU2380369C2 (ru) 2010-01-27
AR041137A1 (es) 2005-05-04
PL224879B1 (pl) 2017-02-28
RU2005109543A (ru) 2006-05-10
MY138201A (en) 2009-05-29
CY1110666T1 (el) 2015-06-11
ECSP055642A (es) 2005-05-30
ES2346204T3 (es) 2010-10-13
PT1537116E (pt) 2010-09-03

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