JP2004507540A5 - - Google Patents

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Publication number
JP2004507540A5
JP2004507540A5 JP2002523894A JP2002523894A JP2004507540A5 JP 2004507540 A5 JP2004507540 A5 JP 2004507540A5 JP 2002523894 A JP2002523894 A JP 2002523894A JP 2002523894 A JP2002523894 A JP 2002523894A JP 2004507540 A5 JP2004507540 A5 JP 2004507540A5
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JP
Japan
Prior art keywords
formula
alkyl
compound
contacting
compound according
Prior art date
Legal status (The legal status 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 status listed.)
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Application number
JP2002523894A
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English (en)
Japanese (ja)
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JP2004507540A (ja
JP4146721B2 (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/EP2001/009688 external-priority patent/WO2002018379A2/en
Publication of JP2004507540A publication Critical patent/JP2004507540A/ja
Publication of JP2004507540A5 publication Critical patent/JP2004507540A5/ja
Application granted granted Critical
Publication of JP4146721B2 publication Critical patent/JP4146721B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2002523894A 2000-08-31 2001-08-22 7−オキソ−ピリドピリミジン類 Expired - Fee Related JP4146721B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US22957700P 2000-08-31 2000-08-31
PCT/EP2001/009688 WO2002018379A2 (en) 2000-08-31 2001-08-22 7-oxo pyridopyrimidines

Publications (3)

Publication Number Publication Date
JP2004507540A JP2004507540A (ja) 2004-03-11
JP2004507540A5 true JP2004507540A5 (https=) 2005-03-17
JP4146721B2 JP4146721B2 (ja) 2008-09-10

Family

ID=22861834

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002523894A Expired - Fee Related JP4146721B2 (ja) 2000-08-31 2001-08-22 7−オキソ−ピリドピリミジン類

Country Status (18)

Country Link
EP (1) EP1315727B1 (https=)
JP (1) JP4146721B2 (https=)
KR (1) KR100582325B1 (https=)
CN (2) CN100358892C (https=)
AR (1) AR033996A1 (https=)
AT (1) ATE298751T1 (https=)
AU (2) AU2002212147B2 (https=)
BR (1) BR0113590A (https=)
CA (1) CA2420122A1 (https=)
DE (1) DE60111752T2 (https=)
ES (1) ES2243568T3 (https=)
GT (1) GT200100190A (https=)
MX (1) MXPA03001733A (https=)
PA (1) PA8527401A1 (https=)
PE (1) PE20020524A1 (https=)
UY (1) UY26920A1 (https=)
WO (1) WO2002018379A2 (https=)
ZA (1) ZA200301078B (https=)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20040103972A (ko) * 2002-04-19 2004-12-09 스미스클라인 비참 코포레이션 신규 화합물
AU2003300076C1 (en) 2002-12-30 2010-03-04 Angiotech International Ag Drug delivery from rapid gelling polymer composition
WO2005007193A2 (en) * 2003-07-07 2005-01-27 Vande Woude, George, F. Inhibition of tumor angiogenesis by combination of thrombospondin-1 and inhibitors of vascular endothelial growth factor
WO2005105097A2 (en) * 2004-04-28 2005-11-10 Gpc Biotech Ag Pyridopyrimidines for treating inflammatory and other diseases
CA2569654C (en) * 2004-06-15 2010-12-21 Pfizer Inc. Benzimidazolone carboxylic acid derivatives
US20090306380A1 (en) * 2005-04-25 2009-12-10 Shigeyoshi Nishino Process for preparing 4-amino-2-alkylthio-5-pyrimidinecarbaldehyde
JP2006321749A (ja) * 2005-05-19 2006-11-30 Ube Ind Ltd 2−シアノマロンアルデヒドのアルカリ金属塩の製法
ES2329419T3 (es) 2006-01-31 2009-11-25 F. Hoffmann-La Roche Ag 7h-pirido(3,4-d)pirimidin-8-onas, su preparacion y uso como inhibidores de proteinas cinasas.
WO2008055842A1 (en) * 2006-11-09 2008-05-15 F. Hoffmann-La Roche Ag Substituted 6-phenyl-pyrido [2,3-d] pyrimidin-7-one derivatives as kinase inhibitors and methods for using the same
WO2008151992A2 (en) 2007-06-15 2008-12-18 F. Hoffmann-La Roche Ag A novel process for the preparation of 3-amino-pentan-1,5-diol
US8372970B2 (en) * 2009-10-09 2013-02-12 Afraxis, Inc. 8-ethyl-6-(aryl)pyrido[2,3-D]pyrimidin-7(8H)-ones for the treatment of CNS disorders
US20120184542A1 (en) 2011-01-19 2012-07-19 Kevin Anderson Pyrido pyrimidines
US8877763B2 (en) * 2012-03-22 2014-11-04 Genosco Substituted pyridopyrimidine compounds and their use as FLT3 inhibitors
US9321786B2 (en) 2013-03-15 2016-04-26 Celgene Avilomics Research, Inc. Heteroaryl compounds and uses thereof
EP3943087A1 (en) 2013-03-15 2022-01-26 Celgene CAR LLC Heteroaryl compounds and uses thereof
CN105307657B (zh) 2013-03-15 2020-07-10 西建卡尔有限责任公司 杂芳基化合物和其用途
BR112020006677A2 (pt) 2017-10-05 2020-10-06 Fulcrum Therapeutics, Inc. uso de inibidores p38 para reduzir a expressão de dux4
US10342786B2 (en) 2017-10-05 2019-07-09 Fulcrum Therapeutics, Inc. P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD
US12351576B2 (en) 2018-09-14 2025-07-08 Abbisko Therapeutics Co., Ltd. FGFR inhibitor, preparation method therefor and application thereof
CN115960098B (zh) * 2020-09-11 2026-04-10 上海凌达生物医药有限公司 一类含氮稠环类化合物的制备方法和用途

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6183168A (ja) * 1984-09-28 1986-04-26 Ube Ind Ltd 2−メルカプト−4−アミノ−5−ホルミルピリミジンおよびその製法
IL117923A (en) * 1995-05-03 2000-06-01 Warner Lambert Co Anti-cancer pharmaceutical compositions containing polysubstituted pyrido¬2,3-d¾pyrimidine derivatives and certain such novel compounds
JP2000511533A (ja) * 1996-05-20 2000-09-05 メルク エンド カンパニー インコーポレーテッド ゴナドトロピン放出ホルモン拮抗薬
US5945422A (en) * 1997-02-05 1999-08-31 Warner-Lambert Company N-oxides of amino containing pyrido 2,3-D! pyrimidines
US6184226B1 (en) * 1998-08-28 2001-02-06 Scios Inc. Quinazoline derivatives as inhibitors of P-38 α
CA2420286A1 (en) * 2000-08-31 2002-03-07 F. Hoffmann-La Roche Ag 7-oxo pyridopyrimidines as inhibitors of a cellular proliferation

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