JP2004528311A5 - - Google Patents

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Publication number
JP2004528311A5
JP2004528311A5 JP2002576193A JP2002576193A JP2004528311A5 JP 2004528311 A5 JP2004528311 A5 JP 2004528311A5 JP 2002576193 A JP2002576193 A JP 2002576193A JP 2002576193 A JP2002576193 A JP 2002576193A JP 2004528311 A5 JP2004528311 A5 JP 2004528311A5
Authority
JP
Japan
Prior art keywords
compound
optionally substituted
formula
independently selected
disease
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.)
Withdrawn
Application number
JP2002576193A
Other languages
English (en)
Japanese (ja)
Other versions
JP2004528311A (ja
Filing date
Publication date
Priority claimed from US10/082,802 external-priority patent/US6525091B2/en
Application filed filed Critical
Priority claimed from PCT/US2002/006217 external-priority patent/WO2002076930A2/en
Publication of JP2004528311A publication Critical patent/JP2004528311A/ja
Publication of JP2004528311A5 publication Critical patent/JP2004528311A5/ja
Withdrawn legal-status Critical Current

Links

JP2002576193A 2001-03-07 2002-03-01 Fas媒介アポトーシスの刺激剤としての置換ジアリールウレア Withdrawn JP2004528311A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US27398801P 2001-03-07 2001-03-07
US10/082,802 US6525091B2 (en) 2001-03-07 2002-02-22 Substituted diarylureas as stimulators for Fas-mediated apoptosis
PCT/US2002/006217 WO2002076930A2 (en) 2001-03-07 2002-03-01 Substituted diarylureas as stimulators for fas-mediated apoptosis

Publications (2)

Publication Number Publication Date
JP2004528311A JP2004528311A (ja) 2004-09-16
JP2004528311A5 true JP2004528311A5 (cg-RX-API-DMAC7.html) 2006-01-05

Family

ID=26767870

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002576193A Withdrawn JP2004528311A (ja) 2001-03-07 2002-03-01 Fas媒介アポトーシスの刺激剤としての置換ジアリールウレア

Country Status (8)

Country Link
EP (1) EP1366021B1 (cg-RX-API-DMAC7.html)
JP (1) JP2004528311A (cg-RX-API-DMAC7.html)
AT (1) ATE366720T1 (cg-RX-API-DMAC7.html)
AU (1) AU2002306618B2 (cg-RX-API-DMAC7.html)
CA (1) CA2434020A1 (cg-RX-API-DMAC7.html)
DE (1) DE60221104T2 (cg-RX-API-DMAC7.html)
ES (1) ES2286267T3 (cg-RX-API-DMAC7.html)
WO (1) WO2002076930A2 (cg-RX-API-DMAC7.html)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
EP1158985B1 (en) 1999-01-13 2011-12-28 Bayer HealthCare LLC OMEGA-CARBOXY ARYL SUBSTITUTED DIPHENYL UREAS AS p38 KINASE INHIBITORS
ES2425739T3 (es) 2002-02-11 2013-10-17 Bayer Healthcare Llc Sorafenib-tosilato para el tratamiento de enfermedades caracterizadas por angiogénesis anormal
AU2003259007A1 (en) 2002-10-31 2004-05-25 Amersham Biosciences Ab Use of urea variants as affinity ligands
ES2305808T3 (es) 2003-05-20 2008-11-01 Bayer Healthcare Llc Diarilureas con actividad inhibidora de quinasas.
BRPI0412219B8 (pt) 2003-07-23 2021-07-27 Bayer Healthcare Llc compostos ômega-carboxi aril difenil uréia fluoro substituídos e composições farmacêuticas compreendendo os referidos compostos
WO2020123675A1 (en) * 2018-12-11 2020-06-18 Duke University Compositions and methods for the treatment of cancer

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3214468A (en) * 1959-08-14 1965-10-26 Geigy Ag J R Bis-(trifluoromethyl)-carbanilides
US6093742A (en) * 1997-06-27 2000-07-25 Vertex Pharmaceuticals, Inc. Inhibitors of p38
IL136690A0 (en) * 1997-12-22 2001-06-14 Bayer Ag Inhibition of raf kinase using symmetrical and unsymmetrical substituted diphenyl ureas
EP1042305B1 (en) * 1997-12-22 2005-06-08 Bayer Pharmaceuticals Corp. INHIBITION OF p38 KINASE USING SYMMETRICAL AND UNSYMMETRICAL DIPHENYL UREAS
EP1071658B1 (en) * 1998-04-17 2004-06-16 Parker Hughes Institute Btk inhibitors and methods for their identification and use

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