MA28076A1 - Derives de 2,4-di(hetero)-arylamino-pyrimidine comme inhibiteurs des kinases zap-70 et/ou syk - Google Patents

Derives de 2,4-di(hetero)-arylamino-pyrimidine comme inhibiteurs des kinases zap-70 et/ou syk

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Publication number
MA28076A1
MA28076A1 MA28893A MA28893A MA28076A1 MA 28076 A1 MA28076 A1 MA 28076A1 MA 28893 A MA28893 A MA 28893A MA 28893 A MA28893 A MA 28893A MA 28076 A1 MA28076 A1 MA 28076A1
Authority
MA
Morocco
Prior art keywords
zap
arylamino
hetero
inhibitors
pyrimidine derivatives
Prior art date
Application number
MA28893A
Other languages
English (en)
Inventor
Marie Claude Bernhard
Peter Buehlmayer
Nigel Graham Cooke
Rudolf Duthaler
Klaus Hinterding
Gebhard Thoma
Eis Maurice Van
Matt Anette Von
Loius Walliser
Gerhard Zenke
Rolf Baenteli
Original Assignee
Novartis Ag
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 Novartis Ag filed Critical Novartis Ag
Publication of MA28076A1 publication Critical patent/MA28076A1/fr

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    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
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Abstract

L'invention concerne des dérivés de pyrimidine de formule (I), dans laquelle R0, R1, R3 à R9 et Z ont la signification indiquée dans la revendication 1, lesquels dérivés possèdent des activités inhibitrices des kinases ZAP-70 et/ou Syk.
MA28893A 2003-09-16 2006-03-27 Derives de 2,4-di(hetero)-arylamino-pyrimidine comme inhibiteurs des kinases zap-70 et/ou syk MA28076A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0321710.6A GB0321710D0 (en) 2003-09-16 2003-09-16 Organic compounds
GBGB0414440.8A GB0414440D0 (en) 2003-09-16 2004-06-28 Organic compounds

Publications (1)

Publication Number Publication Date
MA28076A1 true MA28076A1 (fr) 2006-08-01

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MA28893A MA28076A1 (fr) 2003-09-16 2006-03-27 Derives de 2,4-di(hetero)-arylamino-pyrimidine comme inhibiteurs des kinases zap-70 et/ou syk

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Country Link
US (2) US7671063B2 (fr)
EP (2) EP2266977B1 (fr)
JP (1) JP4504375B2 (fr)
KR (1) KR100813384B1 (fr)
CN (2) CN102260248A (fr)
AR (1) AR045747A1 (fr)
AT (1) ATE498623T1 (fr)
AU (1) AU2004272283B9 (fr)
BR (1) BRPI0414480A (fr)
CA (1) CA2538909A1 (fr)
DE (1) DE602004031436D1 (fr)
EC (1) ECSP066424A (fr)
ES (2) ES2361412T3 (fr)
GB (2) GB0321710D0 (fr)
IL (1) IL174217A0 (fr)
IS (1) IS8402A (fr)
MA (1) MA28076A1 (fr)
MX (1) MXPA06002966A (fr)
NO (1) NO20061656L (fr)
PE (1) PE20050429A1 (fr)
PL (1) PL1664035T3 (fr)
PT (1) PT1664035E (fr)
RU (1) RU2403251C2 (fr)
SG (1) SG132676A1 (fr)
TN (1) TNSN06083A1 (fr)
TW (1) TW200521118A (fr)
WO (1) WO2005026158A1 (fr)
ZA (1) ZA200601963B (fr)

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TWI329105B (en) 2002-02-01 2010-08-21 Rigel Pharmaceuticals Inc 2,4-pyrimidinediamine compounds and their uses
GB0206215D0 (en) * 2002-03-15 2002-05-01 Novartis Ag Organic compounds
BR0313059B8 (pt) 2002-07-29 2021-07-27 Rigel Pharmaceuticals composto, e, composição farmacêutica
GB0305929D0 (en) * 2003-03-14 2003-04-23 Novartis Ag Organic compounds
CN102358738A (zh) 2003-07-30 2012-02-22 里格尔药品股份有限公司 2,4-嘧啶二胺化合物及其预防和治疗自体免疫疾病的用途
TWI378923B (en) * 2003-08-15 2012-12-11 Novartis Ag Pyrimidine derivatives
GB0321710D0 (en) * 2003-09-16 2003-10-15 Novartis Ag Organic compounds
JP4801096B2 (ja) 2005-01-19 2011-10-26 ライジェル ファーマシューティカルズ, インコーポレイテッド 2,4−ピリミジンジアミン化合物のプロドラッグおよびそれらの使用
AU2006209216A1 (en) * 2005-01-25 2006-08-03 Galenea Corp Substituted arylamine compounds and their use as 5-HT6 modulators
WO2006129100A1 (fr) * 2005-06-03 2006-12-07 Glaxo Group Limited Nouveaux composes
EP1904457B1 (fr) 2005-06-08 2017-09-06 Rigel Pharmaceuticals, Inc. Compositions et procedes d'inhibition de la voie jak
US20070203161A1 (en) 2006-02-24 2007-08-30 Rigel Pharmaceuticals, Inc. Compositions and methods for inhibition of the jak pathway
GB0517329D0 (en) * 2005-08-25 2005-10-05 Merck Sharp & Dohme Stimulation of neurogenesis
US8604042B2 (en) 2005-11-01 2013-12-10 Targegen, Inc. Bi-aryl meta-pyrimidine inhibitors of kinases
US7528143B2 (en) * 2005-11-01 2009-05-05 Targegen, Inc. Bi-aryl meta-pyrimidine inhibitors of kinases
US8133900B2 (en) 2005-11-01 2012-03-13 Targegen, Inc. Use of bi-aryl meta-pyrimidine inhibitors of kinases
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