JP2010516662A5 - - Google Patents

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Publication number
JP2010516662A5
JP2010516662A5 JP2009545975A JP2009545975A JP2010516662A5 JP 2010516662 A5 JP2010516662 A5 JP 2010516662A5 JP 2009545975 A JP2009545975 A JP 2009545975A JP 2009545975 A JP2009545975 A JP 2009545975A JP 2010516662 A5 JP2010516662 A5 JP 2010516662A5
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JP
Japan
Prior art keywords
prevention
products
treatment
herpes
bronchoconstriction
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JP2009545975A
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English (en)
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JP5264773B2 (ja
JP2010516662A (ja
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Priority claimed from FR0700357A external-priority patent/FR2911604B1/fr
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Publication of JP2010516662A publication Critical patent/JP2010516662A/ja
Publication of JP2010516662A5 publication Critical patent/JP2010516662A5/ja
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Publication of JP5264773B2 publication Critical patent/JP5264773B2/ja
Expired - Fee Related legal-status Critical Current
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Description

同様に、本発明の生成物は、喘息、咳、COPD(慢性閉塞性肺疾患)、気管支収縮および炎症性障害などの呼吸器障害の予防および/または治療用にも使用され得る。これらの生成物は、乾癬、掻痒、皮膚、眼または粘膜の過敏状態、ヘルペスおよび帯状ヘルペスの予防および/または治療用にも使用され得る。
JP2009545975A 2007-01-19 2008-01-17 N−(ヘテロアリール)−1−ヘテロアリール−1h−インドール−2−カルボキサミドの誘導体、これらの調製およびこれらの治療用途 Expired - Fee Related JP5264773B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR07/00357 2007-01-19
FR0700357A FR2911604B1 (fr) 2007-01-19 2007-01-19 Derives de n-(heteroaryl-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique
PCT/FR2008/000055 WO2008107544A1 (fr) 2007-01-19 2008-01-17 Derives de n-(heteroaryl)-1-heteroaryl-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique

Publications (3)

Publication Number Publication Date
JP2010516662A JP2010516662A (ja) 2010-05-20
JP2010516662A5 true JP2010516662A5 (ja) 2013-05-02
JP5264773B2 JP5264773B2 (ja) 2013-08-14

Family

ID=38283097

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009545975A Expired - Fee Related JP5264773B2 (ja) 2007-01-19 2008-01-17 N−(ヘテロアリール)−1−ヘテロアリール−1h−インドール−2−カルボキサミドの誘導体、これらの調製およびこれらの治療用途

Country Status (11)

Country Link
US (1) US7868024B2 (ja)
EP (1) EP2125787B1 (ja)
JP (1) JP5264773B2 (ja)
AR (1) AR064937A1 (ja)
CL (1) CL2008000127A1 (ja)
ES (1) ES2624795T3 (ja)
FR (1) FR2911604B1 (ja)
PE (1) PE20081689A1 (ja)
TW (1) TW200900058A (ja)
UY (1) UY30874A1 (ja)
WO (1) WO2008107544A1 (ja)

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EP1314733A1 (en) * 2001-11-22 2003-05-28 Aventis Pharma Deutschland GmbH Indole-2-carboxamides as factor Xa inhibitors
FR2888847B1 (fr) 2005-07-22 2007-08-31 Sanofi Aventis Sa Derives de n-(heteriaryl)-1-heteorarylalkyl-1h-indole-2- carboxamides, leur preparation et application en therapeutique
FR2926554B1 (fr) * 2008-01-22 2010-03-12 Sanofi Aventis Derives de carboxamides azabicycliques, leur preparation et leur application en therapeutique
FR2926556B1 (fr) * 2008-01-22 2010-02-19 Sanofi Aventis Derives de carboxamides n-azabicycliques, leur preparation et leur application en therapeutique
FR2926555B1 (fr) * 2008-01-22 2010-02-19 Sanofi Aventis Derives bicycliques de carboxamides azabicycliques, leur preparation et leur application en therapeutique
US8754114B2 (en) 2010-12-22 2014-06-17 Incyte Corporation Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
ME03300B (me) 2012-06-13 2019-07-20 Incyte Holdings Corp Supsтituisana triciklična jedinjenja као inhibiтori fgfr
WO2014026125A1 (en) 2012-08-10 2014-02-13 Incyte Corporation Pyrazine derivatives as fgfr inhibitors
US9266892B2 (en) 2012-12-19 2016-02-23 Incyte Holdings Corporation Fused pyrazoles as FGFR inhibitors
DK2986610T5 (en) 2013-04-19 2018-12-10 Incyte Holdings Corp BICYCLIC HETEROCYCLES AS FGFR INHIBITORS
US10851105B2 (en) 2014-10-22 2020-12-01 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
MA41551A (fr) 2015-02-20 2017-12-26 Incyte Corp Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
WO2016134294A1 (en) 2015-02-20 2016-08-25 Incyte Corporation Bicyclic heterocycles as fgfr4 inhibitors
EA038045B1 (ru) 2015-02-20 2021-06-28 Инсайт Корпорейшн Бициклические гетероциклы в качестве ингибиторов fgfr
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
EA202092649A1 (ru) 2018-05-04 2021-06-21 Инсайт Корпорейшн Соли ингибитора fgfr
US11466004B2 (en) 2018-05-04 2022-10-11 Incyte Corporation Solid forms of an FGFR inhibitor and processes for preparing the same
US11628162B2 (en) 2019-03-08 2023-04-18 Incyte Corporation Methods of treating cancer with an FGFR inhibitor
US11591329B2 (en) 2019-07-09 2023-02-28 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
IL291901A (en) 2019-10-14 2022-06-01 Incyte Corp Bicyclyl heterocycles as fgr suppressors
WO2021076728A1 (en) 2019-10-16 2021-04-22 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
WO2021113479A1 (en) 2019-12-04 2021-06-10 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors
KR20220131900A (ko) 2019-12-04 2022-09-29 인사이트 코포레이션 Fgfr 억제제의 유도체
AR126102A1 (es) 2021-06-09 2023-09-13 Incyte Corp Heterociclos tricíclicos como inhibidores de fgfr
WO2024026290A1 (en) * 2022-07-25 2024-02-01 Cayman Chemical Company Incorporated NOVEL HETEROCYCLES AS sPLA2-X INHIBITORS

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL156306A0 (en) 2000-12-21 2004-01-04 Glaxo Group Ltd Pyrimidineamines as angiogenesis modulators
PL373484A1 (en) 2001-12-10 2005-09-05 Amgen Inc. Vanilloid receptor ligands and their use in treatments
ES2316777T3 (es) * 2002-02-15 2009-04-16 Glaxo Group Limited Moduladores de receptores vainilloides.
ATE450533T1 (de) * 2003-02-14 2009-12-15 Glaxo Group Ltd Carboxamidderivate
US7544803B2 (en) * 2004-01-23 2009-06-09 Amgen Inc. Vanilloid receptor ligands and their use in treatments
FR2874015B1 (fr) * 2004-08-05 2006-09-15 Sanofi Synthelabo Derives de n-(1h-indolyl)-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique
FR2880625B1 (fr) * 2005-01-07 2007-03-09 Sanofi Aventis Sa Derives de n-(heteroaryl)-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique
FR2888847B1 (fr) * 2005-07-22 2007-08-31 Sanofi Aventis Sa Derives de n-(heteriaryl)-1-heteorarylalkyl-1h-indole-2- carboxamides, leur preparation et application en therapeutique
FR2897061B1 (fr) * 2006-02-03 2010-09-03 Sanofi Aventis Derives de n-heteroaryl-carboxamides tricycliques contenant un motif benzimidazole, leur preparation et leur application en therapeutique.

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