JP2003238406A5 - - Google Patents

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Publication number
JP2003238406A5
JP2003238406A5 JP2002356114A JP2002356114A JP2003238406A5 JP 2003238406 A5 JP2003238406 A5 JP 2003238406A5 JP 2002356114 A JP2002356114 A JP 2002356114A JP 2002356114 A JP2002356114 A JP 2002356114A JP 2003238406 A5 JP2003238406 A5 JP 2003238406A5
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JP
Japan
Prior art keywords
group
substituted
pharmaceutical composition
composition according
benzimidazol
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.)
Granted
Application number
JP2002356114A
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English (en)
Japanese (ja)
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JP2003238406A (ja
JP5249484B2 (ja
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Application filed filed Critical
Priority to JP2002356114A priority Critical patent/JP5249484B2/ja
Priority claimed from JP2002356114A external-priority patent/JP5249484B2/ja
Publication of JP2003238406A publication Critical patent/JP2003238406A/ja
Publication of JP2003238406A5 publication Critical patent/JP2003238406A5/ja
Application granted granted Critical
Publication of JP5249484B2 publication Critical patent/JP5249484B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2002356114A 2001-12-11 2002-12-09 医薬組成物 Expired - Fee Related JP5249484B2 (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2002356114A JP5249484B2 (ja) 2001-12-11 2002-12-09 医薬組成物

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2001-376954 2001-12-11
JP2001376954 2001-12-11
JP2001376954 2001-12-11
JP2002356114A JP5249484B2 (ja) 2001-12-11 2002-12-09 医薬組成物

Publications (3)

Publication Number Publication Date
JP2003238406A JP2003238406A (ja) 2003-08-27
JP2003238406A5 true JP2003238406A5 (enExample) 2006-03-30
JP5249484B2 JP5249484B2 (ja) 2013-07-31

Family

ID=27790693

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002356114A Expired - Fee Related JP5249484B2 (ja) 2001-12-11 2002-12-09 医薬組成物

Country Status (1)

Country Link
JP (1) JP5249484B2 (enExample)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101068770B (zh) 2004-09-28 2012-01-04 三共株式会社 制备6-取代的-1-甲基-1-h-苯并咪唑衍生物的方法及其合成中间体
JP4789180B2 (ja) * 2004-09-28 2011-10-12 第一三共株式会社 6−置換−1−メチル−1−h−ベンズイミダゾール誘導体の製造方法及びその製造中間体
WO2007091622A1 (ja) * 2006-02-09 2007-08-16 Daiichi Sankyo Company, Limited 抗癌医薬組成物
TW200838512A (en) * 2007-02-08 2008-10-01 Daiichi Sankyo Co Ltd Crystalline forms of a thiazolidinedione compound and manufacturing methods thereof
JPWO2010013768A1 (ja) * 2008-07-31 2012-01-12 第一三共株式会社 チアゾリジンジオン化合物の結晶及びその製造方法
US20110160462A1 (en) 2008-07-31 2011-06-30 Daiichi Sankyo Company, Limited Crystalline forms of thiazolidinedione compound and its manufacturing method

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CZ282548B6 (cs) * 1992-01-22 1997-08-13 F. Hoffmann-La Roche Ag Farmaceutický přípravek
AU5664294A (en) * 1993-01-11 1995-02-28 Ligand Pharmaceuticals, Inc. Compounds having selective activity for retinoid x receptors, and means for modulation of processes mediated by retinoid x receptors
MX9306629A (es) * 1993-01-11 1994-07-29 Ligand Pharm Inc Compuestos que tienen actividad selectiva para receptores retinoide x, medios para modulacion de procesos mediados pr receptores de retinoide x.
BR9610875A (pt) * 1995-10-06 1999-07-13 Ligand Pharm Inc Modulares rxr seletivos - dimeros e processos para seu uso
EP0948324B1 (en) * 1996-12-11 2003-11-12 Dana-Farber Cancer Institute, Inc. Methods and pharmaceutical compositions for inhibiting tumour cell growth comprising a ppar-gamma agonist and a map kinase inhibitor
AU5811298A (en) * 1996-12-31 1998-07-31 Salk Institute For Biological Studies, The Treatment of disease states which result from neoplastic cell proliferation using ppar-gamma activators and compositions useful therefor
PL334840A1 (en) * 1997-01-24 2000-03-27 Univ California Application of fxr, pparalpha and lxralpha activators in order to restore the barrier function, to stimulate epithelium differentation and to inhibit proliferation
JP3488099B2 (ja) * 1997-10-08 2004-01-19 三共株式会社 置換縮合複素環化合物
KR20020010581A (ko) * 1999-03-11 2002-02-04 사단호진 산교 소죠켄큐쇼 핵수용체 ppar의 신규한 리간드
JP4169450B2 (ja) * 1999-04-07 2008-10-22 第一三共株式会社 インスリン抵抗性改善剤
JP4197387B2 (ja) * 1999-04-07 2008-12-17 第一三共株式会社 アミン誘導体化合物
CA2369910A1 (en) * 1999-04-23 2000-11-02 Bristol-Myers Squibb Company Compositions and methods for treatment of hyperproliferative diseases

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