NO20073960L - Pyrazolderivater for inhibering av CDK og GSK - Google Patents

Pyrazolderivater for inhibering av CDK og GSK

Info

Publication number
NO20073960L
NO20073960L NO20073960A NO20073960A NO20073960L NO 20073960 L NO20073960 L NO 20073960L NO 20073960 A NO20073960 A NO 20073960A NO 20073960 A NO20073960 A NO 20073960A NO 20073960 L NO20073960 L NO 20073960L
Authority
NO
Norway
Prior art keywords
cdk
gsk
kinases
inhibition
methyl
Prior art date
Application number
NO20073960A
Other languages
English (en)
Inventor
Valerio Berdini
Paul Graham Wyatt
Michael Alistair O'brien
Gary Trewartha
Andrew James Woodhead
Adrian Liam Gill
Eva Figueroa Navarro
Theresa Rachel Phillips
Original Assignee
Astex Therapeutics Ltd
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
Priority claimed from GB0501480A external-priority patent/GB0501480D0/en
Priority claimed from GB0501748A external-priority patent/GB0501748D0/en
Application filed by Astex Therapeutics Ltd filed Critical Astex Therapeutics Ltd
Publication of NO20073960L publication Critical patent/NO20073960L/no

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    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic 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
    • C07D231/14Heterocyclic 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
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    • C07D231/14Heterocyclic 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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  • Health & Medical Sciences (AREA)
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Abstract

Oppfinnelsen tilveiebringer forbindelser med formel (I) eller et salt, tautomer, solvat eller N-oksider derav; hvori R1 er valgt fra (a) 2,6-diklorfenyl; (b) 2,6-difluorfenyl; (c) en 2,3,6-trisubstituert fenylgruppe hvori substituentene er fluor, klor, metyl eller metoksy; og (d) en gruppe Ro, hvori Ro er en 3-12-leddet karbosyklisk eller heterosyklisk gruppe; eller eventuelt substituert C 1-8-hydrokarbyl; R2a og R2b er hver hydrogen eller metyl; og R3 er som definert i kravene. Forbindelsene har aktivitet som inhibitorer av syklinavhengige kinaser (CDK) og glykogensyntasekinaser (GSK) og er anvendelige ved behandlingen eller profylakse av sykdommer eller tilstander mediert av kinasene.
NO20073960A 2005-01-21 2007-07-27 Pyrazolderivater for inhibering av CDK og GSK NO20073960L (no)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US64621705P 2005-01-21 2005-01-21
GB0501480A GB0501480D0 (en) 2005-01-22 2005-01-22 Pharmaceutical compounds
GB0501748A GB0501748D0 (en) 2005-01-27 2005-01-27 Pharmaceutical compounds
US65133905P 2005-02-09 2005-02-09
PCT/GB2006/000196 WO2006077419A1 (en) 2005-01-21 2006-01-20 Pyrazole derivatives for the inhibition of cdk' s and gsk' s

Publications (1)

Publication Number Publication Date
NO20073960L true NO20073960L (no) 2007-09-24

Family

ID=35967182

Family Applications (3)

Application Number Title Priority Date Filing Date
NO20073956A NO20073956L (no) 2005-01-21 2007-07-27 Pyrazolderivater for inhibering av CDK og GSK
NO20073960A NO20073960L (no) 2005-01-21 2007-07-27 Pyrazolderivater for inhibering av CDK og GSK
NO20073955A NO20073955L (no) 2005-01-21 2007-07-27 Pyrazolderivater for inhibering av CDK og GSK

Family Applications Before (1)

Application Number Title Priority Date Filing Date
NO20073956A NO20073956L (no) 2005-01-21 2007-07-27 Pyrazolderivater for inhibering av CDK og GSK

Family Applications After (1)

Application Number Title Priority Date Filing Date
NO20073955A NO20073955L (no) 2005-01-21 2007-07-27 Pyrazolderivater for inhibering av CDK og GSK

Country Status (15)

Country Link
US (2) US20080306069A1 (no)
EP (3) EP1853600A1 (no)
JP (3) JP2008528465A (no)
KR (3) KR20070107049A (no)
AR (3) AR052559A1 (no)
AU (3) AU2006207313A1 (no)
BR (2) BRPI0606317A2 (no)
CA (3) CA2593468A1 (no)
IL (3) IL184499A0 (no)
MA (3) MA29253B1 (no)
MX (3) MX2007008782A (no)
NO (3) NO20073956L (no)
PE (3) PE20060876A1 (no)
TN (3) TNSN07279A1 (no)
WO (3) WO2006077414A1 (no)

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TW200533657A (en) 2004-02-17 2005-10-16 Esteve Labor Dr Substituted pyrazoline compounds, their preparation and use as medicaments
AR052559A1 (es) * 2005-01-21 2007-03-21 Astex Therapeutics Ltd Derivados de pirazol para inhibir cdk's y gsk's
US8404718B2 (en) 2005-01-21 2013-03-26 Astex Therapeutics Limited Combinations of pyrazole kinase inhibitors
US20080139620A1 (en) * 2005-01-21 2008-06-12 Astex Therapeutics Limited Pyrazole Derivatives For The Inhibition Of Cdk's And Gsk's
CN101146533A (zh) * 2005-01-21 2008-03-19 阿斯泰克斯治疗有限公司 吡唑激酶抑制剂和其它抗肿瘤剂的组合
MX2007008781A (es) * 2005-01-21 2007-09-11 Astex Therapeutics Ltd Compuestos farmaceuticos.
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US7897589B2 (en) 2005-07-15 2011-03-01 Laboratorios Del Dr. Esteve, S.A. Substituted pyrazoline compounds, their preparation and use as medicaments
EP1743890A1 (en) 2005-07-15 2007-01-17 Laboratorios Del Dr. Esteve, S.A. 4,5-Dihydro-1H-pyrazole derivatives, their preparation and use as medicaments
EP1743892A1 (en) 2005-07-15 2007-01-17 Laboratorios del Dr. Esteve S.A. Substituted pyrazoline compounds, their preparation and use as medicaments
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US20100021420A1 (en) * 2006-07-14 2010-01-28 Astex Therapeutics Limited Combinations of pyrazole derivatives for the inhibition of cdks and gsk's
EP2049516A2 (en) * 2006-07-14 2009-04-22 Astex Therapeutics Limited Pharmaceutical compounds
EP2046327A1 (en) * 2006-07-21 2009-04-15 Astex Therapeutics Limited Medical use of cyclin dependent kinases inhibitors
CA2665804A1 (en) * 2006-08-23 2008-02-28 Astellas Pharma Inc. Urea compound or salt thereof
WO2008044041A1 (en) 2006-10-12 2008-04-17 Astex Therapeutics Limited Pharmaceutical combinations
CA2667720A1 (en) * 2006-11-09 2008-05-15 Abbott Gmbh & Co. Kg. Pharmaceutical dosage form for oral administration of tyrosine kinase inhibitor
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