JP2006524669A5 - - Google Patents

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Publication number
JP2006524669A5
JP2006524669A5 JP2006505808A JP2006505808A JP2006524669A5 JP 2006524669 A5 JP2006524669 A5 JP 2006524669A5 JP 2006505808 A JP2006505808 A JP 2006505808A JP 2006505808 A JP2006505808 A JP 2006505808A JP 2006524669 A5 JP2006524669 A5 JP 2006524669A5
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JP
Japan
Prior art keywords
alk
group
alkyl
formula
compound
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JP2006505808A
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English (en)
Japanese (ja)
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JP2006524669A (ja
JP4839208B2 (ja
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Priority claimed from FR0305213A external-priority patent/FR2854158B1/fr
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Publication of JP2006524669A publication Critical patent/JP2006524669A/ja
Publication of JP2006524669A5 publication Critical patent/JP2006524669A5/ja
Application granted granted Critical
Publication of JP4839208B2 publication Critical patent/JP4839208B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2006505808A 2003-04-25 2004-04-22 2−アシルアミノ−4−フェニルチアゾール誘導体、それらの製造法およびそれらの治療用途 Expired - Fee Related JP4839208B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR0305213A FR2854158B1 (fr) 2003-04-25 2003-04-25 Derives de 2-acylamino-4-phenylethiazole, leur preparation et leur application en therapeutique
FR03/05213 2003-04-25
PCT/FR2004/000981 WO2004096798A2 (fr) 2003-04-25 2004-04-22 Derives de 2-acylamino-4-phenylthiazole, leur preparation et leur application en therapeutique

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2011008854A Division JP2011126891A (ja) 2003-04-25 2011-01-19 2−アシルアミノ−4−フェニルチアゾール誘導体の合成中間体

Publications (3)

Publication Number Publication Date
JP2006524669A JP2006524669A (ja) 2006-11-02
JP2006524669A5 true JP2006524669A5 (enExample) 2007-06-28
JP4839208B2 JP4839208B2 (ja) 2011-12-21

Family

ID=33104460

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2006505808A Expired - Fee Related JP4839208B2 (ja) 2003-04-25 2004-04-22 2−アシルアミノ−4−フェニルチアゾール誘導体、それらの製造法およびそれらの治療用途
JP2011008854A Withdrawn JP2011126891A (ja) 2003-04-25 2011-01-19 2−アシルアミノ−4−フェニルチアゾール誘導体の合成中間体

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2011008854A Withdrawn JP2011126891A (ja) 2003-04-25 2011-01-19 2−アシルアミノ−4−フェニルチアゾール誘導体の合成中間体

Country Status (24)

Country Link
US (2) US7504511B2 (enExample)
EP (1) EP1656373B1 (enExample)
JP (2) JP4839208B2 (enExample)
KR (1) KR20060006935A (enExample)
CN (1) CN1826339A (enExample)
AR (1) AR044070A1 (enExample)
AT (1) ATE541843T1 (enExample)
AU (1) AU2004234101A1 (enExample)
BR (1) BRPI0409716A (enExample)
CA (1) CA2521158A1 (enExample)
CO (1) CO5640106A2 (enExample)
CR (1) CR8037A (enExample)
EC (1) ECSP056111A (enExample)
FR (1) FR2854158B1 (enExample)
MA (1) MA27769A1 (enExample)
MX (1) MXPA05011522A (enExample)
NO (1) NO20054905L (enExample)
OA (1) OA13049A (enExample)
RS (1) RS20050769A (enExample)
RU (1) RU2348630C2 (enExample)
TN (1) TNSN05254A1 (enExample)
TW (1) TW200510325A (enExample)
WO (1) WO2004096798A2 (enExample)
ZA (1) ZA200508608B (enExample)

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JO2676B1 (en) * 2004-04-06 2012-06-17 جانسين فارماسوتيكا ان. في Derivatives of second-aza-spiro- (5,4) -dikan and their use as antihistamines
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FR2876692B1 (fr) * 2004-10-19 2007-02-23 Sanofi Aventis Sa Derives de 2-amido-4-phenylthiazole, leur preparation et leur application en therapeutique
EP1833807A1 (en) * 2005-01-05 2007-09-19 Rigel Pharmaceuticals, Inc. Ubiquitin ligase inhibitors
WO2006094948A1 (en) 2005-03-08 2006-09-14 Janssen Pharmaceutica N.V. Diaza-spiro-[4.4]-nonane derivatives as neurokinin (nk1) antagonists
KR20080019213A (ko) 2005-05-09 2008-03-03 아칠리온 파르마세우티칼스 인코포레이티드 티아졸 화합물 및 그 사용방법
WO2007053499A2 (en) 2005-11-01 2007-05-10 Millennium Pharmaceuticals, Inc. Compounds useful as antagonists of ccr2
US8067457B2 (en) 2005-11-01 2011-11-29 Millennium Pharmaceuticals, Inc. Compounds useful as antagonists of CCR2
US20100016289A1 (en) * 2005-11-01 2010-01-21 Kevin Sprott Compounds Useful as Antagonists of CCR2
FR2895989B1 (fr) * 2006-01-06 2010-04-30 Sanofi Aventis Derives de 2-carbamide-4-phenylthiazole, leur preparation et leur application en therapeutique
WO2007116313A2 (en) * 2006-04-12 2007-10-18 Pfizer Limited Pyrrolidine derivatives as modulators of chemokine ccr5 receptors
RU2303597C1 (ru) * 2006-05-12 2007-07-27 Иващенко Андрей Александрович Фармацевтическая композиция, способы ее получения и применения
CN101096363B (zh) * 2006-06-27 2011-05-11 中国人民解放军军事医学科学院毒物药物研究所 2,4,5-三取代噻唑类化合物、其制备方法、药物组合物及其制药用途
US20080076120A1 (en) * 2006-09-14 2008-03-27 Millennium Pharmaceuticals, Inc. Methods for the identification, evaluation and treatment of patients having CC-Chemokine receptor 2 (CCR-2) mediated disorders
US8754107B2 (en) 2006-11-17 2014-06-17 Abbvie Inc. Aminopyrrolidines as chemokine receptor antagonists
AU2008214679A1 (en) * 2007-02-13 2008-08-21 Ab Science Process for the synthesis of 2-aminothiazole compounds as kinase inhibitors
WO2008124000A2 (en) * 2007-04-02 2008-10-16 Ligand Pharmaceuticals Incorporated Thiazole derivatives as androgen receptor modulator compounds
CA2687931C (en) 2007-05-31 2016-05-24 Boehringer Ingelheim International Gmbh Ccr2 receptor antagonists and uses thereof
MX2010001082A (es) * 2007-07-31 2010-03-01 Shionogi & Co Composicion farmaceutica que contiene compuesto opticamente activo que tiene actividad agonista del receptor de trombopoyetina y compuesto intermedio para el mismo.
CN102256963B (zh) 2008-12-19 2014-06-11 贝林格尔.英格海姆国际有限公司 作为ccr2受体拮抗剂用于治疗炎症、哮喘和copd的环状嘧啶-4-甲酰胺
MX346393B (es) 2009-12-17 2017-03-17 Centrexion Therapeutics Corp Nuevos antagonistas del receptor ccr2 y usos de los mismo.
MX2012010664A (es) 2010-03-17 2013-02-07 Taivex Therapeutics Inc Moduladores de actividad hec1 y sus metodos.
JP2013526507A (ja) 2010-05-12 2013-06-24 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 新規ccr2受容体アンタゴニスト、その製造方法及び薬物としてのその使用
WO2011141477A1 (en) 2010-05-12 2011-11-17 Boehringer Ingelheim International Gmbh New ccr2 receptor antagonists, method for producing the same, and use thereof as medicaments
WO2011144501A1 (en) * 2010-05-17 2011-11-24 Boehringer Ingelheim International Gmbh Ccr2 antagonists and uses thereof
WO2011147772A1 (en) 2010-05-25 2011-12-01 Boehringer Ingelheim International Gmbh Ccr2 receptor antagonists
US8962656B2 (en) 2010-06-01 2015-02-24 Boehringer Ingelheim International Gmbh CCR2 antagonists
WO2013010839A1 (en) 2011-07-15 2013-01-24 Boehringer Ingelheim International Gmbh Novel and selective ccr2 antagonists
CN103086859B (zh) * 2011-11-08 2015-11-11 清华大学 2,4-二羟基-5,6-取代-1-卤代苯衍生物、其合成方法及其应用
US11071736B2 (en) 2011-11-21 2021-07-27 Taivex Therapeutics Corporation Modulators of HEC1 activity and methods therefor
AU2016287584B2 (en) 2015-07-02 2020-03-26 Centrexion Therapeutics Corporation (4-((3R,4R)-3-methoxytetrahydro-pyran-4-ylamino)piperidin-1-yl)(5-methyl-6-(((2R,6S)-6-(p-tolyl)tetrahydro-2H-pyran-2-yl)methylamino)pyrimidin-4yl)methanone citrate
WO2017019772A1 (en) * 2015-07-27 2017-02-02 Sanford Burnham Prebys Medical Discovery Institute Modulators of myocyte lipid accumulation and insulin resistance and methods of use thereof
WO2019222393A1 (en) * 2018-05-15 2019-11-21 The Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College Neuroprotective compositions and methods of using the same
US20210380546A1 (en) * 2018-10-22 2021-12-09 The Regents Of The University Of California Vaccine adjuvant
CN112004798A (zh) * 2019-01-07 2020-11-27 江苏凯迪恩医药科技有限公司 一种苯甲酰胺类化合物、中间体、制备方法及应用
US12479816B2 (en) 2019-02-08 2025-11-25 University of Pittsburgh—of the Commonwealth System of Higher Education 20-HETE formation inhibitors

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FR2872813B1 (fr) 2004-07-09 2007-01-19 Sanofi Synthelabo Derives de 2-carbamide-4-phenylthiazole, leur preparation et leur application en therapeutique
FR2876692B1 (fr) 2004-10-19 2007-02-23 Sanofi Aventis Sa Derives de 2-amido-4-phenylthiazole, leur preparation et leur application en therapeutique
FR2895989B1 (fr) 2006-01-06 2010-04-30 Sanofi Aventis Derives de 2-carbamide-4-phenylthiazole, leur preparation et leur application en therapeutique

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