JP2004526711A5 - - Google Patents

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Publication number
JP2004526711A5
JP2004526711A5 JP2002565966A JP2002565966A JP2004526711A5 JP 2004526711 A5 JP2004526711 A5 JP 2004526711A5 JP 2002565966 A JP2002565966 A JP 2002565966A JP 2002565966 A JP2002565966 A JP 2002565966A JP 2004526711 A5 JP2004526711 A5 JP 2004526711A5
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JP
Japan
Prior art keywords
formula
compound
substituent
pharmaceutically acceptable
acceptable salt
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.)
Pending
Application number
JP2002565966A
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English (en)
Japanese (ja)
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JP2004526711A (ja
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Publication date
Priority claimed from US10/071,390 external-priority patent/US6987184B2/en
Application filed filed Critical
Publication of JP2004526711A publication Critical patent/JP2004526711A/ja
Publication of JP2004526711A5 publication Critical patent/JP2004526711A5/ja
Pending legal-status Critical Current

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JP2002565966A 2001-02-15 2002-02-13 Jnk阻害剤としてのイソチアゾロアントロン、イソオキサゾロアントロン、イソインドールアントロン及びそれらの誘導体、並びにそれに関連する組成物及び方法 Pending JP2004526711A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US26901301P 2001-02-15 2001-02-15
US10/071,390 US6987184B2 (en) 2001-02-15 2002-02-07 Isothiazoloanthrones, isoxazoloanthrones, isoindolanthrones and derivatives thereof as JNK inhibitors and compositions and methods related
PCT/US2002/004283 WO2002066450A2 (en) 2001-02-15 2002-02-13 Anthrone derivatives and their use as ink inhibitors

Publications (2)

Publication Number Publication Date
JP2004526711A JP2004526711A (ja) 2004-09-02
JP2004526711A5 true JP2004526711A5 (https=) 2005-12-22

Family

ID=26752159

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002565966A Pending JP2004526711A (ja) 2001-02-15 2002-02-13 Jnk阻害剤としてのイソチアゾロアントロン、イソオキサゾロアントロン、イソインドールアントロン及びそれらの誘導体、並びにそれに関連する組成物及び方法

Country Status (6)

Country Link
US (3) US6987184B2 (https=)
EP (1) EP1363891A2 (https=)
JP (1) JP2004526711A (https=)
CA (1) CA2438312A1 (https=)
NZ (1) NZ528034A (https=)
WO (1) WO2002066450A2 (https=)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE465153T1 (de) 2002-02-28 2010-05-15 Eisai R&D Man Co Ltd Neue indazolverbindungen mit kondensiertem ring
WO2003075917A1 (en) 2002-03-08 2003-09-18 Signal Pharmaceuticals, Inc. Combination therapy for treating, preventing or managing proliferative disorders and cancers
JP2005522215A (ja) * 2002-04-12 2005-07-28 セルジーン・コーポレーション 幹細胞及び前駆細胞の分化のモジュレーション、アッセイ、並びにそれらの使用
US20040034084A1 (en) * 2002-05-24 2004-02-19 Celgene Corporation Methods for using JNK inhibitors for treating or preventing disease-related wasting
CN1668733A (zh) * 2002-05-30 2005-09-14 细胞基因公司 利用jnk或mkk抑制剂调节细胞分化并治疗骨髓增生异常和脊髓发育不良综合症的方法
US20040087642A1 (en) * 2002-10-24 2004-05-06 Zeldis Jerome B. Methods of using and compositions comprising a JNK inhibitor for the treatment, prevention, management and/or modification of pain
NZ540546A (en) * 2002-11-18 2008-03-28 Celgene Corp Methods of using and compositions comprising (-)-3-(3,4-dimethoxy-phenyl)-3-(1-oxo-1,3-dihydro-isoindol-2-yl)-propionamide
EP1581205A1 (en) * 2002-11-18 2005-10-05 Celgene Corporation Methods of using and compositions comprising (+)-3-(3,4-dimethoxy-phenyl)-3-(1-oxo-1,3-dihydro-isoindol-2-yl)-propionamide
AU2003298775B2 (en) * 2002-11-26 2008-07-17 Anthrogenesis Corporation Cytotherapeutics, cytotherapeutic units and methods for treatments using them
US20050019366A1 (en) * 2002-12-31 2005-01-27 Zeldis Jerome B. Drug-coated stents and methods of use therefor
WO2004071283A2 (en) * 2003-02-13 2004-08-26 Anthrogenesis Corporation Use of umbilical cord blood to treat individuals having a disease, disorder or condition
KR20060124610A (ko) * 2003-11-06 2006-12-05 셀진 코포레이션 석면-관련된 질환 또는 장애를 치료 및 관리하기 위하여jnk 억제제를 사용하는 방법 및 이 물질을 포함하는조성물
KR20060109979A (ko) * 2003-12-02 2006-10-23 셀진 코포레이션 혈색소병증 및 빈혈의 치료 및 관리를 위한 방법및 조성물
US20050266391A1 (en) * 2004-01-15 2005-12-01 Bennett Brydon L Methods for preserving tissue
WO2005074921A1 (en) * 2004-02-09 2005-08-18 University Of Zurich Treatment of atherosclerosis
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
EP1676574A3 (en) 2004-12-30 2006-07-26 Johnson & Johnson Vision Care, Inc. Methods for promoting survival of transplanted tissues and cells
WO2006090698A1 (ja) * 2005-02-22 2006-08-31 Ono Pharmaceutical Co., Ltd. キナーゼ阻害薬およびその用途
US20060223807A1 (en) * 2005-03-29 2006-10-05 University Of Massachusetts Medical School, A Massachusetts Corporation Therapeutic methods for type I diabetes
DK1957633T3 (en) 2005-10-13 2014-03-17 Anthrogenesis Corp Immunomodulation USING PLACE SPEECH STEM CELLS
CA2633980A1 (en) * 2005-12-29 2007-07-12 Anthrogenesis Corporation Improved composition for collecting and preserving placental stem cells and methods of using the composition
WO2007093873A1 (en) * 2006-02-13 2007-08-23 Council Of Scientific And Industrial Research Bis-pyrr0l0[2,l-c] [1, 4] benzodiazepine- anthraquinone conjugates as antitumour agents and a process for the preparation thereof
EP3763376A1 (en) * 2007-02-12 2021-01-13 Celularity, Inc. Treatment of inflammatory diseases using placental stem cells
US20100239500A1 (en) * 2007-03-30 2010-09-23 Bixby John L Substituted triazine compounds for nerve regeneration
WO2009111264A2 (en) * 2008-02-29 2009-09-11 Alseres Pharmaceuticals, Inc. Systemic purine administration:modulating axonal outgrowth of central nervous system neurons
US8362020B2 (en) 2009-12-30 2013-01-29 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
EP2598864B1 (en) * 2010-07-26 2024-06-12 Parker-Hannifin Corporation Electrode, analyte sensor and method for preparing an electrode
US8969315B2 (en) 2010-12-31 2015-03-03 Anthrogenesis Corporation Enhancement of placental stem cell potency using modulatory RNA molecules
JP6104896B2 (ja) 2011-06-01 2017-03-29 アントフロゲネシス コーポレーション 胎盤幹細胞を使用する疼痛の治療
EP3328819B1 (en) * 2015-07-28 2020-04-01 Beta Cat Pharmaceuticals, Inc. Anthracene-9, 10-dione dioxime compounds prodrugs and their uses

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2733976A (en) * 1956-02-07 Sulfonateds-acylamino
GB355597A (en) 1929-11-12 1931-08-27 Ig Farbenindustrie Ag Manufacture of carboxylic acid derivatives of the anthraquinone series
DE1026315B (de) * 1954-08-17 1958-03-20 Bayer Ag Verfahren zur Herstellung von Acylamino-amino-anthrachinonen
US3095415A (en) * 1958-05-30 1963-06-25 Ciba Ltd Anthraquinone dyestuffs containing a 2-chloro, 4-hydroxy (lower) alkylamino, triazinylamino group
DE1164003B (de) * 1961-08-05 1964-02-27 Bayer Ag Verfahren zur Herstellung von Anthrachinonfarbstoffen
GB960235A (en) * 1961-08-08 1964-06-10 Ici Ltd New disperse dyestuffs of the polycyclic ketone series
CH428043A (fr) * 1965-08-16 1967-01-15 Sandoz Ag Procédé de fabrication de colorants de dispersion isothiazolantroniques
CH538527A (de) 1968-11-07 1973-06-30 Hoechst Ag Verfahren zur Herstellung von faserreaktiven Farbstoffen
DE2200127A1 (de) 1972-01-03 1973-07-12 Basf Ag Verfahren zur herstellung von dichlor1,1'-dianthrachinonylen und deren derivaten
DE2558813C2 (de) * 1975-12-27 1984-10-31 Hoechst Ag, 6230 Frankfurt Lichtempfindliches Gemisch mit synergistischem Initiatorsystem
DE2558812C2 (de) * 1975-12-27 1987-04-30 Hoechst Ag, 6230 Frankfurt Photopolymerisierbares Gemisch
US4198518A (en) 1977-09-02 1980-04-15 Ciba-Geigy Corporation Process for the production of 3-substituted pyrazolanthrones
DE2950876A1 (de) * 1979-12-18 1981-06-25 Bayer Ag, 5090 Leverkusen Verfahren zur herstellung von triazinylamino-anthrachinonen
JPS6028454A (ja) * 1983-07-27 1985-02-13 Mitsubishi Chem Ind Ltd アントロン系化合物及び反応性アントロン系染料
JPH0625311B2 (ja) 1985-07-09 1994-04-06 住友化学工業株式会社 分散型水不溶性染料組成物
JP2001502315A (ja) * 1996-10-10 2001-02-20 プローブ・インターナショナル ウイルス感染を処置するための組成物および方法
US6162613A (en) 1998-02-18 2000-12-19 Vertex Pharmaceuticals, Inc. Methods for designing inhibitors of serine/threonine-kinases and tyrosine kinases
DE69900847T2 (de) 1998-04-17 2002-09-12 Tufts College Map kinase-inhibitoren zur behandlung von durch tnf-alpha induzierte lipolyse- verursachte krankheiten
AU3786899A (en) 1998-05-04 1999-11-23 Vertex Pharmaceuticals Incorporated Crystallizable jnk complexes
CN1136217C (zh) 1998-12-17 2004-01-28 霍夫曼-拉罗奇有限公司 作为jnk蛋白质激酶抑制剂的4-芳基羟吲哚
DE60041763D1 (de) 1999-04-23 2009-04-23 Vertex Pharma Inhibitoren von c-jun n-terminal kinasen (jnk)
AU5316900A (en) 1999-06-03 2000-12-28 Vertex Pharmaceuticals Incorporated Inhibitors of c-jun n-terminal kinases (jnk)
BR0013551A (pt) 1999-08-13 2003-06-17 Vertex Pharma Inibidores de cinases n-terminal cjun (jnk) e outras cinases de proteìnas
EP1390052A4 (en) 2001-04-24 2008-10-08 Harvard College INHIBITION OF JUN KINASE

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