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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)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (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 (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6007417B2 (ja) * 2011-05-31 2016-10-12 レセプトス エルエルシー 新規ｇｌｐ−１受容体安定剤および調節剤
US9260427B2 (en) 2013-06-11 2016-02-16 Receptos, Inc. GLP-1 receptor modulators
JP2017538711A (ja) 2014-12-10 2017-12-28 セルジーン インターナショナル ツー エスエーアールエル Ｇｌｐ−１レセプターモジュレーター
AU2016311426B2 (en) 2015-08-26 2021-05-20 Blueprint Medicines Corporation Compounds and compositions useful for treating disorders related to NTRK
SG10201912607SA (en) * 2015-11-19 2020-02-27 Blueprint Medicines Corp Compounds and compositions useful for treating disorders related to ntrk
WO2017223284A1 (en) 2016-06-23 2017-12-28 University Of Maryland, Baltimore NON-CATALYTIC SUBSTRATE-SELECTIVE P38α-SPECIFIC MAPK INHIBITORS WITH ENDOTHELIAL-STABILIZING AND ANTI-INFLAMMATORY ACTIVITY, AND METHODS OF USE THEREOF
EP3890733A4 (en) 2018-12-07 2022-05-04 University of Maryland, Baltimore NON-ATP/CATALYTIC SITE P38 MITOGENE-ACTIVATED PROTEIN KINASE INHIBITORS
AU2021274475B2 (en) 2020-05-18 2024-03-21 Gen1E Lifesciences Inc. P38alpha mitogen-activated protein kinase inhibitors
EP4313959A1 (en) 2021-03-23 2024-02-07 GEN1E Lifesciences Inc. Substituted naphthyl p38alpha mitogen-activated protein kinase inhibitors

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3907799A (en) 1971-08-16 1975-09-23 Icn Pharmaceuticals Xanthine oxidase inhibitors
JPH05507702A (ja) 1990-05-30 1993-11-04 アメリカン・ホーム・プロダクツ・コーポレイション 置換アリールスルホンアミド類およびベンズアミド類
US5688949A (en) 1991-04-22 1997-11-18 Otsuka Pharmaceutical Factory, Inc. Pyrazolo 1,5-A!pyrimidine derivatives and anti-inflammatory agent 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
WO1995035298A1 (fr) 1994-06-21 1995-12-28 Otsuka Pharmaceutical Factory, Inc. DERIVE DE PYRAZOLO[1,5-a]PYRIMIDINE
GB9716557D0 (en) 1997-08-06 1997-10-08 Glaxo Group Ltd Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity
EP1043998B1 (en) * 1997-12-13 2007-03-07 Bristol-Myers Squibb Company USE OF PYRAZOLO [3,4-b] PYRIDINE AS CYCLIN DEPENDANT KINASE INHIBITORS
US6413974B1 (en) * 1998-02-26 2002-07-02 Aventis Pharmaceuticals Inc. 6,9,-disubstituted 2-[trans-(4-aminocyclohexyl) amino] purines
DE19834047A1 (de) 1998-07-29 2000-02-03 Bayer Ag Substituierte Pyrazolderivate
DK0997474T3 (da) 1998-08-14 2004-02-09 Pfizer Antithrombotiske midler
AU752186B2 (en) 1998-10-30 2002-09-12 Merck & Co., Inc. Thrombin inhibitors
EP1140944B1 (en) 1998-12-22 2003-08-27 Novartis AG Epothilone derivatives and their use as antitumor agents
DE1140938T1 (de) 1999-01-11 2003-01-09 Princeton University, Princeton Kinase-inhibitoren mit hoher affinität zur ziel detektion und ihre verwendung
EP1196411B1 (en) 1999-07-15 2003-09-17 Pharmacopeia, Inc. Bradykinin b1 receptor antagonists
GEP20043367B (en) 2000-07-26 2004-06-10 Bristol Myers Squibb Co N-[5-[[[5-Alkyl-2-Oxazolyl]Methyl]Thio]-2-Thiazolyl Carboxamide Inhibitors of Cyclin Dependent Kinases
DE60122176T2 (de) 2000-09-15 2007-07-05 Vertex Pharmaceuticals Inc., Cambridge Isoxazole und ihre verwendung als erk-inhibitoren
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
AU2509602A (en) * 2000-12-20 2002-07-01 Sod Conseils Rech Applic Cyclin-dependent kinase (CDK) and glycolene synthase kinase-3 (GSK-3) inhibitors
WO2002064211A1 (en) 2001-02-09 2002-08-22 Merck & Co., Inc. Thrombin inhibitors

Also Published As

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

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