PE20050669A1 - Biaril sulfonamidas - Google Patents
Biaril sulfonamidasInfo
- Publication number
- PE20050669A1 PE20050669A1 PE2004001190A PE2004001190A PE20050669A1 PE 20050669 A1 PE20050669 A1 PE 20050669A1 PE 2004001190 A PE2004001190 A PE 2004001190A PE 2004001190 A PE2004001190 A PE 2004001190A PE 20050669 A1 PE20050669 A1 PE 20050669A1
- Authority
- PE
- Peru
- Prior art keywords
- biaryl
- benzofuran
- biphenyl
- amino
- sulphonamides
- Prior art date
Links
- -1 BIARYL SULPHONAMIDES Chemical class 0.000 title abstract 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 abstract 2
- BBVIDBNAYOIXOE-UHFFFAOYSA-N 1,2,4-oxadiazole Chemical compound C=1N=CON=1 BBVIDBNAYOIXOE-UHFFFAOYSA-N 0.000 abstract 1
- 102000017284 Collagenase 3 Human genes 0.000 abstract 1
- 102000013382 Gelatinases Human genes 0.000 abstract 1
- 108010026132 Gelatinases Proteins 0.000 abstract 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 abstract 1
- 108010076503 Matrix Metalloproteinase 13 Proteins 0.000 abstract 1
- 208000011623 Obstructive Lung disease Diseases 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 208000006673 asthma Diseases 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 201000008482 osteoarthritis Diseases 0.000 abstract 1
- 229940124530 sulfonamide Drugs 0.000 abstract 1
Classifications
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- 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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- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
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- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
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- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—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
- 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
- C07D491/06—Peri-condensed systems
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- C—CHEMISTRY; METALLURGY
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- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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Abstract
REFERIDA A UN METODO DE MODULACION (INHIBICION) DE UNA METALOPROTEINA DONDE SE UNE UNA METALOPROTEINASA TAL COMO GELATINASA A, METALOELASTASA DE MACROFAGO, COLAGENASA-3, ENTRE OTRAS; CON UNA CANTIDAD DE BIARIL SULFONAMIDA UNIDA A UN GRUPO HETEROARILO TAL COMO FURANO, 1,2,4-OXADIAZOL, IMIDAZOL, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: N-({4'[1-BENZOFURAN-2-ILCARBONIL)-AMINO]-1,1'-BIFENIL-4-IL}-SULFONIL)-GLICINA, ACIDO L-2-{4'-[(BENZOFURAN-2-CARBONIL)-AMINO]-BIFENIL-4-SULFONILAMINO}-3-METIL-BUTIRICO, ENTRE OTROS. DICHOS COMPUESTOS SON UTILES EN EL TRATAMIENTO DE OSTEOARTRITIS, ASMA, ENFERMEDAD PULMONAR OBSTRUCTIVA, ENTRE OTRAS
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| US52684003P | 2003-12-04 | 2003-12-04 | |
| PCT/US2003/040835 WO2005061477A1 (en) | 2003-12-04 | 2003-12-22 | Biaryl sulfonamides as mmp inhibitors |
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| JP2007525406A (ja) * | 2003-12-04 | 2007-09-06 | ワイス | ビアリールスルホンアミドおよびその使用方法 |
| US20080119513A1 (en) * | 2004-09-06 | 2008-05-22 | Fumihiko Watanabe | Sulfonamide Derivative Selectively Inhibiting Mmp-13 |
| CA2617055A1 (en) * | 2005-07-29 | 2007-02-08 | Bayer Healthcare Llc | Preparation and use of biphenyl amino acid derivatives for the treatment of obesity |
| US7615363B2 (en) * | 2005-08-25 | 2009-11-10 | Wyeth | Aggrecanase structure |
| US7625731B2 (en) * | 2005-08-25 | 2009-12-01 | Wyeth | Aggrecanase structure |
| EP1981505A4 (en) * | 2006-02-08 | 2009-05-13 | Wyeth Corp | PREPARATION OF 7-ALKENYL-3-QUINOLINECARBONITRILES THROUGH PALLADIUM INDUCED COUPLING REACTION |
| CN101415683B (zh) | 2006-03-31 | 2013-07-17 | 诺瓦提斯公司 | 新化合物 |
| WO2008147763A1 (en) * | 2007-05-23 | 2008-12-04 | Array Biopharma Inc. | Mmp inhibitors and methods of use thereof |
| CN102149677A (zh) * | 2008-08-15 | 2011-08-10 | 霍夫曼-拉罗奇有限公司 | 联芳基氨基四氢化萘类 |
| US8716312B2 (en) * | 2008-11-19 | 2014-05-06 | Merck Sharp & Dohme Corporation | Inhibitors of diacylglycerol acyltransferase |
| WO2011031628A1 (en) * | 2009-09-14 | 2011-03-17 | Schering Corporation | Inhibitors of diacylglycerol acyltransferase |
| US8530453B2 (en) * | 2009-09-28 | 2013-09-10 | Aquilus Pharmaceuticals, Inc. | Compounds and methods for the treatment of pain and other diseases |
| US9255074B2 (en) | 2010-07-16 | 2016-02-09 | Abbvie Inc. | Process for preparing antiviral compounds |
| PH12013500105A1 (en) | 2010-07-16 | 2013-02-25 | Abbvie Bahamas Ltd | Process for preparing antiviral compounds |
| EA030228B1 (ru) | 2010-07-16 | 2018-07-31 | ЭббВи Айэленд Анлимитед Компани | Фосфиновые лиганды для каталитических реакций |
| US8975443B2 (en) | 2010-07-16 | 2015-03-10 | Abbvie Inc. | Phosphine ligands for catalytic reactions |
| JP2014514259A (ja) * | 2011-03-02 | 2014-06-19 | アクイラス ファーマシューティカルズ, インコーポレイテッド | 疼痛および他の障害の処置のための化合物および方法 |
| CN104244939A (zh) | 2012-04-05 | 2014-12-24 | Chdi基金会股份有限公司 | 犬尿氨酸-3-单加氧酶抑制剂、其药物组合物及其使用方法 |
| CN103333144B (zh) * | 2013-06-17 | 2014-12-10 | 温州大学 | 一种2-硫基-3-卤代苯并呋喃化合物及其合成方法和用途 |
| US9938252B2 (en) | 2013-09-26 | 2018-04-10 | Chdi Foundation, Inc. | Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
| US9884853B2 (en) | 2013-09-26 | 2018-02-06 | 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 |
| US10301324B2 (en) | 2016-04-12 | 2019-05-28 | Atrin Pharmaceuticals LLC | Ataxia telengiectasia and rad3-related (ATR) inhibitors and methods of their use |
| CN106905348B (zh) * | 2017-02-13 | 2018-12-04 | 牡丹江医学院 | 一种预防和治疗急性肾损伤的药物及其制备方法和用途 |
| 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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| DE69737605T2 (de) * | 1996-01-23 | 2008-04-03 | Shionogi & Co., Ltd. | Sulfonierte aminosäurederivate und metalloproteinase-inhibitoren, die diese enthalten |
| RU2001126719A (ru) * | 1999-03-03 | 2004-02-20 | Дзе Проктер Энд Гэмбл Компани (US) | Дигетерозамещенные ингибиторы металлопротеазы |
| TR200200977T2 (tr) * | 1999-10-14 | 2002-08-21 | The Procter & Gamble Company | Beta konumunda iki kere sübstitüe edilmiş metaloproteaz engelleyiciler |
| JP2007525406A (ja) * | 2003-12-04 | 2007-09-06 | ワイス | ビアリールスルホンアミドおよびその使用方法 |
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- 2004-12-01 US US11/001,589 patent/US7420001B2/en not_active Expired - Fee Related
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- 2006-06-13 EC EC2006006637A patent/ECSP066637A/es unknown
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Also Published As
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| ECSP066637A (es) | 2006-10-25 |
| BR0318640A (pt) | 2006-11-28 |
| AU2004200247A1 (en) | 2005-06-23 |
| ATE411306T1 (de) | 2008-10-15 |
| WO2005061477A1 (en) | 2005-07-07 |
| CR8418A (es) | 2007-08-28 |
| US20100137298A1 (en) | 2010-06-03 |
| AR046859A1 (es) | 2005-12-28 |
| DE60324208D1 (de) | 2008-11-27 |
| AU2003299789A1 (en) | 2005-07-14 |
| US7420001B2 (en) | 2008-09-02 |
| ZA200604551B (en) | 2008-11-26 |
| JP2007524567A (ja) | 2007-08-30 |
| EP1692124A1 (en) | 2006-08-23 |
| CA2548518A1 (en) | 2005-07-07 |
| IL159679A0 (en) | 2004-06-20 |
| EP1692124B1 (en) | 2008-10-15 |
| CN1623537A (zh) | 2005-06-08 |
| TW200519100A (en) | 2005-06-16 |
| US20050143422A1 (en) | 2005-06-30 |
| RU2006123559A (ru) | 2008-01-10 |
| NO20062649L (no) | 2006-09-01 |
| PA8618901A1 (es) | 2005-11-25 |
| KR20060093735A (ko) | 2006-08-25 |
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