TW200519100A - Biaryl sulfonamides and methods for using same - Google Patents

Biaryl sulfonamides and methods for using same

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Publication number
TW200519100A
TW200519100A TW093100794A TW93100794A TW200519100A TW 200519100 A TW200519100 A TW 200519100A TW 093100794 A TW093100794 A TW 093100794A TW 93100794 A TW93100794 A TW 93100794A TW 200519100 A TW200519100 A TW 200519100A
Authority
TW
Taiwan
Prior art keywords
methods
same
biaryl sulfonamides
biaryl
sulfonamides
Prior art date
Application number
TW093100794A
Other languages
English (en)
Inventor
Jeremy Ian Levin
Iii Thomas Saltmarsh Rush
Frank Lovering
Yong-Han Hu
Jian-Chang Li
Wei Li
Jun Jun Wu
Rajeev Hotchandani
Jason Shaoyun Xiang
Xuemei Du
Derek Cecil Cole
Original Assignee
Wyeth Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Wyeth Corp filed Critical Wyeth Corp
Publication of TW200519100A publication Critical patent/TW200519100A/zh

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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
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US20080119513A1 (en) * 2004-09-06 2008-05-22 Fumihiko Watanabe Sulfonamide Derivative Selectively Inhibiting Mmp-13
EP1912634A4 (en) * 2005-07-29 2010-06-09 Bayer Healthcare Llc PREPARATION AND USE OF BIPHENYL AMINOACIDAL DERIVATIVES TO TREAT OBESITY
US7615363B2 (en) * 2005-08-25 2009-11-10 Wyeth Aggrecanase structure
US7625731B2 (en) * 2005-08-25 2009-12-01 Wyeth Aggrecanase structure
WO2007092153A2 (en) * 2006-02-08 2007-08-16 Wyeth Preparation of 7-alkenyl-3 quinolinecarbonitriles via a palladium mediated coupling reaction
ES2375576T3 (es) 2006-03-31 2012-03-02 Novartis Ag Derivados del �?cido (4-(4-[6-(trifluorometil-piridin-3-ilamino)-heteroarilo con contenido de n]-fenil)-ciclohexil)-acético y sus usos farmacéuticos.
WO2008147763A1 (en) * 2007-05-23 2008-12-04 Array Biopharma Inc. Mmp inhibitors and methods of use thereof
EP2321268A2 (en) * 2008-08-15 2011-05-18 F. Hoffmann-La Roche AG Bi-aryl aminotetralines
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WO2011031628A1 (en) * 2009-09-14 2011-03-17 Schering Corporation Inhibitors of diacylglycerol acyltransferase
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JP5819959B2 (ja) 2010-07-16 2015-11-24 アッヴィ・バハマズ・リミテッド 抗ウイルス性化合物を調製するための方法
US8975443B2 (en) 2010-07-16 2015-03-10 Abbvie Inc. Phosphine ligands for catalytic reactions
EP2681209B1 (en) * 2011-03-02 2018-05-09 Aquilus Pharmaceuticals, Inc Compounds and methods for the treatment of pain and other disorders
AU2013243898A1 (en) 2012-04-05 2014-10-23 Chdi Foundation, Inc. Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof
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EP3049389B1 (en) 2013-09-26 2019-08-07 CHDI Foundation, Inc. Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof
KR20160066490A (ko) * 2014-12-02 2016-06-10 주식회사 씨앤드씨신약연구소 헤테로사이클 유도체 및 그의 용도
WO2017180723A1 (en) 2016-04-12 2017-10-19 Atrin Pharmaceuticals LLC Ataxia telengiectasia and rad3-related (atr) inhibitors and methods of their use
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CN112480020B (zh) * 2020-12-11 2023-10-10 东华理工大学 一种2-取代苯并恶唑化合物
CN113527152B (zh) * 2021-08-09 2023-07-28 西北农林科技大学 一种联苯磺酰胺类化合物及其防治农作物害虫的方法

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