NO20061656L - 2,4 di(hetero)-arylamino-pyrimidin derivaer som ZAP-70 og/aller SYK inhibitorer - Google Patents

2,4 di(hetero)-arylamino-pyrimidin derivaer som ZAP-70 og/aller SYK inhibitorer

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Publication number
NO20061656L
NO20061656L NO20061656A NO20061656A NO20061656L NO 20061656 L NO20061656 L NO 20061656L NO 20061656 A NO20061656 A NO 20061656A NO 20061656 A NO20061656 A NO 20061656A NO 20061656 L NO20061656 L NO 20061656L
Authority
NO
Norway
Prior art keywords
zap
arylamino
hetero
pyrimidine derivatives
syk inhibitors
Prior art date
Application number
NO20061656A
Other languages
English (en)
Norwegian (no)
Inventor
Rudolf Duthaler
Gebhard Thoma
Nigel Graham Cooke
Gerhard Zenke
Klaus Hinterding
Anette Von Matt
Rolf Baentell
Marie Claude Bernhard
Peter Buchlmayer
Maurice Van Eis
Louis Walliser
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 NO20061656L publication Critical patent/NO20061656L/no

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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
    • C07D239/48Two nitrogen atoms
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NO20061656A 2003-09-16 2006-04-11 2,4 di(hetero)-arylamino-pyrimidin derivaer som ZAP-70 og/aller SYK inhibitorer NO20061656L (no)

Applications Claiming Priority (3)

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
PCT/EP2004/010348 WO2005026158A1 (en) 2003-09-16 2004-09-15 2,4 di (hetero) -arylamino-pyrimidine derivatives as zap-70 and/or syk inhibitors

Publications (1)

Publication Number Publication Date
NO20061656L true NO20061656L (no) 2006-06-16

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NO20061656A NO20061656L (no) 2003-09-16 2006-04-11 2,4 di(hetero)-arylamino-pyrimidin derivaer som ZAP-70 og/aller SYK inhibitorer

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Country Link
US (2) US7671063B2 (de)
EP (2) EP1664035B1 (de)
JP (1) JP4504375B2 (de)
KR (1) KR100813384B1 (de)
CN (2) CN102260248A (de)
AR (1) AR045747A1 (de)
AT (1) ATE498623T1 (de)
AU (1) AU2004272283B9 (de)
BR (1) BRPI0414480A (de)
CA (1) CA2538909A1 (de)
DE (1) DE602004031436D1 (de)
EC (1) ECSP066424A (de)
ES (2) ES2361412T3 (de)
GB (2) GB0321710D0 (de)
IL (1) IL174217A0 (de)
IS (1) IS8402A (de)
MA (1) MA28076A1 (de)
MX (1) MXPA06002966A (de)
NO (1) NO20061656L (de)
PE (1) PE20050429A1 (de)
PL (1) PL1664035T3 (de)
PT (1) PT1664035E (de)
RU (1) RU2403251C2 (de)
SG (1) SG132676A1 (de)
TN (1) TNSN06083A1 (de)
TW (1) TW200521118A (de)
WO (1) WO2005026158A1 (de)
ZA (1) ZA200601963B (de)

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GB0206215D0 (en) * 2002-03-15 2002-05-01 Novartis Ag Organic compounds
MXPA05001096A (es) 2002-07-29 2005-11-23 Rigel Pharmaceuticals Inc Metodos para tratamiento o prevencion de enfermedades autoinmunes con compuestos de 2,4-diamino-pirimidina.
GB0305929D0 (en) * 2003-03-14 2003-04-23 Novartis Ag Organic compounds
KR20120062863A (ko) 2003-07-30 2012-06-14 리겔 파마슈티칼스, 인크. 자가면역 질환의 치료 또는 예방에 사용하기 위한 2,4-피리미딘디아민 화합물
CA2533320A1 (en) * 2003-08-15 2006-02-24 Novartis Ag 2, 4-pyrimidinediamines useful in the treatment of neoplastic diseases, inflammatory and immune system disorders
GB0321710D0 (en) * 2003-09-16 2003-10-15 Novartis Ag Organic compounds
EP2161275A1 (de) 2005-01-19 2010-03-10 Rigel Pharmaceuticals, Inc. Prodrugs aus 2,4-Pyrimidindiamin-Verbindungen und ihre Verwendungen
EP1856075A1 (de) * 2005-01-25 2007-11-21 Epix Delaware, Inc. Substituierte arylaminverbindungen und ihre verwendung als 5-ht6-modulatoren
WO2006129100A1 (en) * 2005-06-03 2006-12-07 Glaxo Group Limited Novel compounds
WO2006133426A2 (en) 2005-06-08 2006-12-14 Rigel Pharmaceuticals, Inc. Compositions and methods for inhibition of the jak pathway
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
WO2007053452A1 (en) * 2005-11-01 2007-05-10 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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