JP2005535594A5 - - Google Patents

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Publication number
JP2005535594A5
JP2005535594A5 JP2004506748A JP2004506748A JP2005535594A5 JP 2005535594 A5 JP2005535594 A5 JP 2005535594A5 JP 2004506748 A JP2004506748 A JP 2004506748A JP 2004506748 A JP2004506748 A JP 2004506748A JP 2005535594 A5 JP2005535594 A5 JP 2005535594A5
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JP
Japan
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heterocycle
aryl
occurrence
alkyl
independently selected
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Pending
Application number
JP2004506748A
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English (en)
Japanese (ja)
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JP2005535594A (ja
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Publication date
Priority claimed from US10/443,263 external-priority patent/US20040034084A1/en
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Publication of JP2005535594A publication Critical patent/JP2005535594A/ja
Publication of JP2005535594A5 publication Critical patent/JP2005535594A5/ja
Pending legal-status Critical Current

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JP2004506748A 2002-05-24 2003-05-23 疾患に関連した消耗を治療または予防するためのjnk阻害剤の使用方法 Pending JP2005535594A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US38320202P 2002-05-24 2002-05-24
US10/443,263 US20040034084A1 (en) 2002-05-24 2003-05-22 Methods for using JNK inhibitors for treating or preventing disease-related wasting
PCT/US2003/016333 WO2003099221A2 (en) 2002-05-24 2003-05-23 Methods for using jnk inhibitors for treating or preventing disease-related wasting

Publications (2)

Publication Number Publication Date
JP2005535594A JP2005535594A (ja) 2005-11-24
JP2005535594A5 true JP2005535594A5 (https=) 2006-03-23

Family

ID=29586989

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004506748A Pending JP2005535594A (ja) 2002-05-24 2003-05-23 疾患に関連した消耗を治療または予防するためのjnk阻害剤の使用方法

Country Status (10)

Country Link
US (1) US20040034084A1 (https=)
EP (1) EP1507528A4 (https=)
JP (1) JP2005535594A (https=)
CN (1) CN1668299A (https=)
AU (1) AU2003256259A1 (https=)
CA (1) CA2487073A1 (https=)
IL (1) IL165359A0 (https=)
MX (1) MXPA04011599A (https=)
NZ (1) NZ537055A (https=)
WO (1) WO2003099221A2 (https=)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4219289B2 (ja) * 2004-03-10 2009-02-04 独立行政法人科学技術振興機構 多環性ケトン化合物及びその製造方法
US20100009928A1 (en) 2004-03-29 2010-01-14 Cheng Jin Q Compositions including triciribine and taxanes and methods of use thereof
US20100009929A1 (en) 2004-03-29 2010-01-14 Cheng Jin Q Compositions including triciribine and bortezomib and derivatives thereof and methods of use thereof
US20100028339A1 (en) * 2004-03-29 2010-02-04 Cheng Jin Q Compositions including triciribine and trastuzumab and methods of use thereof
US20110008327A1 (en) 2004-03-29 2011-01-13 Cheng Jin Q Compositions including triciribine and epidermal growth factor receptor inhibitor compounds or salts thereof and methods of use thereof
US20100173864A1 (en) 2004-03-29 2010-07-08 Cheng Jin Q Compositions including triciribine and one or more platinum compounds and methods of use thereof
AU2005228410A1 (en) 2004-03-29 2005-10-13 University Of South Florida Effective treatment of tumors and cancer with triciribine and related compounds
AR050253A1 (es) * 2004-06-24 2006-10-11 Smithkline Beecham Corp Compuesto derivado de indazol carboxamida, composicion que lo comprende y su uso para la preparacion de un medicamento
AU2005266494B2 (en) * 2004-07-27 2009-09-10 Novartis Ag Inhibitors of Hsp90
MX2007001155A (es) * 2004-07-29 2007-08-14 Creabilis Therapeutics Spa Uso de inhibidores de k-252a y de quinasa para la prevencion o el tratamiento de patologias asociadas con hmgb1.
EP1676574A3 (en) 2004-12-30 2006-07-26 Johnson & Johnson Vision Care, Inc. Methods for promoting survival of transplanted tissues and cells
NZ602832A (en) 2008-07-14 2014-04-30 Gilead Sciences Inc Fused heterocyclic hdac inhibitor compounds
JP5640005B2 (ja) 2008-07-14 2014-12-10 ギリアード サイエンシーズ, インコーポレイテッド Hdacおよび/またはcdk阻害剤としてのイミダゾシルピリジン化合物
WO2010009166A1 (en) 2008-07-14 2010-01-21 Gilead Colorado, Inc. Oxindolyl inhibitor compounds
JP2011529504A (ja) 2008-07-28 2011-12-08 ギリアード サイエンシーズ, インコーポレイテッド シクロアルキリデンヒストン脱アセチル化酵素阻害剤化合物およびヘテロシクロアルキリデンヒストン脱アセチル化酵素阻害剤化合物
WO2010144378A2 (en) 2009-06-08 2010-12-16 Gilead Colorado, Inc. Cycloalkylcarbamate benzamide aniline hdac inhibitor compounds
KR20120031170A (ko) 2009-06-08 2012-03-30 길리애드 사이언시즈, 인코포레이티드 알카노일아미노 벤즈아미드 아닐린 hdac 저해제 화합물
ES2870085T3 (es) * 2013-06-26 2021-10-26 Xigen Inflammation Ltd Inhibidores peptídicos permeables a células de la ruta de transducción de señales de JNK para el tratamiento de la cistitis

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US3994890A (en) * 1974-01-31 1976-11-30 Chugai Seiyaku Kabushiki Kaisha 1-Aminoalkyl, 3-phenyl indazoles
US4198518A (en) * 1977-09-02 1980-04-15 Ciba-Geigy Corporation Process for the production of 3-substituted pyrazolanthrones
JPS57109787A (en) * 1980-12-26 1982-07-08 Chugai Pharmaceut Co Ltd Pyrazoloindazole derivative
US4788195A (en) * 1986-01-13 1988-11-29 American Cyanamid Company 4,5,6-substituted-N-(substituted-phenyl)-2-pyrimidinamines
US4966622A (en) * 1988-04-12 1990-10-30 Ciba-Geigy Corporation N-phenyl-N-pyrimidin-2-ylureas
US4973690A (en) * 1988-04-12 1990-11-27 Ciba-Geigy Corporation Novel ureas
JP2515162B2 (ja) * 1990-02-23 1996-07-10 富士写真フイルム株式会社 メチン化合物
GB9016449D0 (en) * 1990-07-26 1990-09-12 Ici Plc Anionic compounds
DE69230387T2 (de) * 1991-04-22 2000-06-29 Fuji Photo Film Co., Ltd. Photographische Silberhalogenidmaterialien und Verfahren zu ihrer Verarbeitung
JP2692021B2 (ja) * 1991-09-13 1997-12-17 富士写真フイルム株式会社 ハロゲン化銀感光材料
US5516775A (en) * 1992-08-31 1996-05-14 Ciba-Geigy Corporation Further use of pyrimidine derivatives
EP0774967A1 (en) * 1994-08-12 1997-05-28 Takeda Chemical Industries, Ltd. Use of quinone and hydroquinone derivatives for the teatment of cachexia
AP2001002304A0 (en) * 1996-05-03 2001-12-31 Pfizer Substituted indazole derivatives and related compounds
US6162613A (en) * 1998-02-18 2000-12-19 Vertex Pharmaceuticals, Inc. Methods for designing inhibitors of serine/threonine-kinases and tyrosine kinases
US6897231B2 (en) * 2000-07-31 2005-05-24 Signal Pharmaceuticals, Inc. Indazole derivatives as JNK inhibitors and compositions and methods related thereto
US6987184B2 (en) * 2001-02-15 2006-01-17 Signal Pharmaceuticals, Llc Isothiazoloanthrones, isoxazoloanthrones, isoindolanthrones and derivatives thereof as JNK inhibitors and compositions and methods related

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