NO327708B1 - Pyrazolforbindelser nyttige som proteinkinaseinhibitorer - Google Patents

Pyrazolforbindelser nyttige som proteinkinaseinhibitorer Download PDF

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Publication number
NO327708B1
NO327708B1 NO20031191A NO20031191A NO327708B1 NO 327708 B1 NO327708 B1 NO 327708B1 NO 20031191 A NO20031191 A NO 20031191A NO 20031191 A NO20031191 A NO 20031191A NO 327708 B1 NO327708 B1 NO 327708B1
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Norway
Prior art keywords
ring
alkyl
phenyl
optionally substituted
halo
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NO20031191A
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English (en)
Norwegian (no)
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NO20031191D0 (no
NO20031191L (no
Inventor
Marion W Wannamaker
Cornelia J Forster
David Kay
Ronald Knegtel
David Bebbington
Pan Li
Robert J Davies
Albert Pierce
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Vertex Pharma
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27398347&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO327708(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Vertex Pharma filed Critical Vertex Pharma
Publication of NO20031191D0 publication Critical patent/NO20031191D0/no
Publication of NO20031191L publication Critical patent/NO20031191L/no
Publication of NO327708B1 publication Critical patent/NO327708B1/no

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    • C—CHEMISTRY; METALLURGY
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    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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    • A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
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    • A—HUMAN NECESSITIES
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D471/02—Heterocyclic 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
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    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
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    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems

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  • Organic Chemistry (AREA)
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  • Chemical Kinetics & Catalysis (AREA)
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  • Diabetes (AREA)
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  • Endocrinology (AREA)
  • Hematology (AREA)
  • Biomedical Technology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pulmonology (AREA)
  • Obesity (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Oncology (AREA)
  • Emergency Medicine (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Vascular Medicine (AREA)
  • Virology (AREA)
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NO20031191A 2000-09-15 2003-03-14 Pyrazolforbindelser nyttige som proteinkinaseinhibitorer NO327708B1 (no)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US23279500P 2000-09-15 2000-09-15
US25788700P 2000-12-21 2000-12-21
US28694901P 2001-04-27 2001-04-27
PCT/US2001/028940 WO2002022607A1 (en) 2000-09-15 2001-09-14 Pyrazole compounds useful as protein kinase inhibitors

Publications (3)

Publication Number Publication Date
NO20031191D0 NO20031191D0 (no) 2003-03-14
NO20031191L NO20031191L (no) 2003-05-13
NO327708B1 true NO327708B1 (no) 2009-09-14

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ID=27398347

Family Applications (4)

Application Number Title Priority Date Filing Date
NO20031191A NO327708B1 (no) 2000-09-15 2003-03-14 Pyrazolforbindelser nyttige som proteinkinaseinhibitorer
NO20031189A NO326850B1 (no) 2000-09-15 2003-03-14 Pyrazolforbindelser nyttige som proteinkinaseinhibitorer
NO20031188A NO20031188L (no) 2000-09-15 2003-03-14 Pyrazolforbindelser nyttige som proteinkinaseinhibitorer
NO20031190A NO20031190L (no) 2000-09-15 2003-03-14 Pyrazolforbindelser nyttige som proteinkinaseinhibitorer

Family Applications After (3)

Application Number Title Priority Date Filing Date
NO20031189A NO326850B1 (no) 2000-09-15 2003-03-14 Pyrazolforbindelser nyttige som proteinkinaseinhibitorer
NO20031188A NO20031188L (no) 2000-09-15 2003-03-14 Pyrazolforbindelser nyttige som proteinkinaseinhibitorer
NO20031190A NO20031190L (no) 2000-09-15 2003-03-14 Pyrazolforbindelser nyttige som proteinkinaseinhibitorer

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US (7) US6638926B2 (enExample)
EP (8) EP1317452B1 (enExample)
JP (9) JP4922539B2 (enExample)
KR (4) KR100876069B1 (enExample)
CN (3) CN100355750C (enExample)
AP (1) AP2003002762A0 (enExample)
AT (8) ATE363284T1 (enExample)
AU (9) AU2001294558A1 (enExample)
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CA (8) CA2422378C (enExample)
DE (8) DE60124744T2 (enExample)
DK (1) DK1318997T3 (enExample)
ES (3) ES2266259T3 (enExample)
HU (4) HUP0302173A2 (enExample)
IL (6) IL154786A0 (enExample)
MX (8) MXPA03002299A (enExample)
NO (4) NO327708B1 (enExample)
NZ (4) NZ525008A (enExample)
PE (1) PE20020451A1 (enExample)
PL (1) PL361676A1 (enExample)
PT (2) PT1317448E (enExample)
TW (1) TWI303636B (enExample)
WO (8) WO2002022603A1 (enExample)

Families Citing this family (411)

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EP1679668B1 (en) * 1996-09-04 2010-01-27 Intertrust Technologies Corp. Trusted infrastructure support systems, methods and techniques for secure electronic commerce, electronic transactions, commerce process control and automation, distributed computing, and rights management
US6184226B1 (en) * 1998-08-28 2001-02-06 Scios Inc. Quinazoline derivatives as inhibitors of P-38 α
US6982260B1 (en) 1999-11-22 2006-01-03 Warner-Lambert Company Quinazolines and their use for inhibiting cyclin-dependent kinase enzymes
WO2001047922A2 (en) 1999-12-24 2001-07-05 Aventis Pharma Limited Azaindoles
DK1318997T3 (da) * 2000-09-15 2006-09-25 Vertex Pharma Pyrazolforbindelser der er nyttige som proteinkinase-inhibitorer
US6660731B2 (en) * 2000-09-15 2003-12-09 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
US7473691B2 (en) * 2000-09-15 2009-01-06 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
US7105532B2 (en) * 2000-12-19 2006-09-12 Smithkline Beecham Corporation Pyrazolo[3,4-c]pyridines as gsk-3 inhibitors
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