PE20051004A1 - Compuestos de biaril sulfonamidas como inhibidores de metaloproteinasas - Google Patents
Compuestos de biaril sulfonamidas como inhibidores de metaloproteinasasInfo
- Publication number
- PE20051004A1 PE20051004A1 PE2004001191A PE2004001191A PE20051004A1 PE 20051004 A1 PE20051004 A1 PE 20051004A1 PE 2004001191 A PE2004001191 A PE 2004001191A PE 2004001191 A PE2004001191 A PE 2004001191A PE 20051004 A1 PE20051004 A1 PE 20051004A1
- Authority
- PE
- Peru
- Prior art keywords
- compounds
- methyl
- inhibitors
- metaloproteinases
- iloximethyl
- Prior art date
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/30—Oxygen atoms
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- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4188—1,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
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- A61K31/42—Oxazoles
- A61K31/424—Oxazoles condensed with heterocyclic ring systems, e.g. clavulanic acid
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- A61K31/425—Thiazoles
- A61K31/429—Thiazoles condensed with heterocyclic ring systems
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- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
- C07C311/29—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/45—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups at least one of the singly-bound nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylaminosulfonamides
- C07C311/46—Y being a hydrogen or a carbon atom
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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 to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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 to ring carbon atoms
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
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Abstract
SE REFIERE A COMPUESTO DE FORMULA (I), DONDE R1 ES H, ALQUILO C1-C6; R2 ES H, ALQUILO C1-C6, FENILO, BENCILO, ENTRE OTROS; R3 ES H, HALOGENO, OC(HALOGENO)3, ENTRE OTROS; Z ES ARILO O HETEROARILO; X ES CH2O, OCH2, CH2S(O), ENTRE OTROS; Z ES ARILO O HETROARILO. SON COMPUESTOS PREFERIDOS: ACIDO 3- METIL-2-[4´-(3-METIL-QUINOLIN-2-ILOXIMETIL)-BIFENIL-4-SULFONILAMINO]-BUTIRICO; ACIDO 3-METIL-2-[4´-(5-TRIFLUOROMETIL-PIRIDIN-2-ILOXIMETIL)-BIFENIL-4-SULFONILAMINO]-BUTIRICO; ACIDO 2-[4´-(2,8-BIS-TRIFLUOROMETIL-QUINOLIN-4-ILOXIMETIL)-BIFENIL-4-SULFONILAMINO]-3-METIL-BUTIRICO, ENTRE OTROS. DICHOS COMPUESTOS SON INHIBIDORES DE METALOPROTEINASAS DE MATRIZ (MMPS) UTILES EN EL TRATAMIENTO DE CANCER, OSTEOARTRITIS, ASMA, ATEROSCLEROSIS, ENTRE OTROS
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PCT/US2003/041173 WO2005061459A1 (en) | 2003-12-04 | 2003-12-22 | Biaryl sulfonamides and methods for using same |
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CA2548518A1 (en) * | 2003-12-04 | 2005-07-07 | Wyeth | Biaryl sulfonamides as mmp inhibitors |
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 |
PE20070505A1 (es) * | 2005-07-11 | 2007-05-15 | Wyeth Corp | Inhibidores de glutamato de metaloproteinasas de matriz y agrecanasas |
US7615363B2 (en) * | 2005-08-25 | 2009-11-10 | Wyeth | Aggrecanase structure |
US7625731B2 (en) * | 2005-08-25 | 2009-12-01 | Wyeth | Aggrecanase structure |
GT200600305A (es) | 2005-10-13 | 2007-02-26 | Métodos para preparar derivados de acido glutamico | |
US20090069304A1 (en) | 2006-03-03 | 2009-03-12 | Shionogi & Co., Ltd. | Mmp-13 selective inhibitor |
AR062677A1 (es) * | 2006-09-08 | 2008-11-26 | Novartis Ag | Derivados de biaril-sulfonamida, procesos de produccion y composiciones farmaceuticas que los comprenden |
AU2007309570B2 (en) * | 2006-10-20 | 2012-07-12 | Merck Sharp & Dohme Corp. | Substituted imidazoles as bombesin receptor subtype-3 modulators |
US8183275B2 (en) * | 2006-10-20 | 2012-05-22 | Merck Sharp & Dohme Corp. | Substituted imidazoles as bombesin receptor subtype-3 modulators |
EP2083822A2 (en) * | 2006-10-20 | 2009-08-05 | Merck & Co., Inc. | Substituted imidazoles as bombesin receptor subtype-3 modulators |
EP2128134A1 (en) | 2006-11-02 | 2009-12-02 | Shionogi&Co., Ltd. | Sulfonylurea derivative capable of selectively inhibiting mmp-13 |
EP2514767A1 (en) * | 2006-12-19 | 2012-10-24 | Ablynx N.V. | Amino acid sequences directed against a metalloproteinase from the ADAM family and polypeptides comprising the same for the treatment of ADAM-related diseases and disorders |
EP2147684A1 (en) * | 2008-07-22 | 2010-01-27 | Bracco Imaging S.p.A | Diagnostic Agents Selective Against Metalloproteases |
GB0907551D0 (en) * | 2009-05-01 | 2009-06-10 | Univ Dundee | Treatment or prophylaxis of proliferative conditions |
AU2013203591B2 (en) * | 2009-05-01 | 2017-01-19 | University Court Of The University Of Dundee | Treatment or prophylaxis of proliferative conditions |
AR077630A1 (es) * | 2009-07-02 | 2011-09-14 | Glaxo Group Ltd | Polipeptidos y metodo de tratamiento |
US20130336989A1 (en) * | 2011-02-24 | 2013-12-19 | Glaxo Group Limited | Methods of identifying a patient population |
EP2650310B1 (en) * | 2012-04-13 | 2016-06-08 | Rottapharm Biotech S.r.l. | Anti-ADAMTS-5 antibody, derivatives and uses thereof |
GB201312311D0 (en) * | 2013-07-09 | 2013-08-21 | Uni I Oslo | Uses of enzyme inhibitors |
EP3209794A1 (en) * | 2014-10-22 | 2017-08-30 | Katholieke Universiteit Leuven KU Leuven Research & Development | Modulating adipose tissue and adipogenesis |
US10377818B2 (en) | 2015-01-30 | 2019-08-13 | The Board Of Trustees Of The Leland Stanford Junior University | Method of treating glioma |
CN110997717A (zh) | 2017-06-02 | 2020-04-10 | 默克专利股份有限公司 | 结合adamts5、mmp13和聚蛋白聚糖的多肽 |
US11261260B2 (en) * | 2017-06-02 | 2022-03-01 | Merck Patent Gmbh | ADAMTS binding immunoglobulins |
AU2019216531A1 (en) | 2018-02-02 | 2020-09-24 | Maverix Oncology, Inc. | Small molecule drug conjugates of gemcitabine monophosphate |
CN111187289B (zh) * | 2020-02-26 | 2021-03-23 | 湖南中大检测技术集团有限公司 | 一种过氧化氢荧光探针及其制备方法和应用 |
US12043672B2 (en) | 2022-09-07 | 2024-07-23 | Synoa Therapeutics, Llc | Compositions comprising bispecific antibodies to human ADAMTS5 and nerve growth factor |
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CZ298814B6 (cs) * | 1996-01-23 | 2008-02-13 | Shionogi & Co., Ltd. | Sulfonované deriváty aminokyselin a metaloproteasové inhibitory obsahující tyto deriváty |
JP2000511175A (ja) * | 1996-05-17 | 2000-08-29 | ワーナー―ランバート・コンパニー | ビフェニルスルホンアミドマトリックスメタロプロテイナーゼ阻害剤 |
EP0998572A2 (en) | 1997-07-25 | 2000-05-10 | Du Pont Pharmaceuticals Company | Aggrecan degrading metallo proteases |
EP1069110A4 (en) * | 1998-04-03 | 2004-09-01 | Sankyo Co | SULFONAMIDE DERIVATIVES |
US6566381B1 (en) | 1999-03-03 | 2003-05-20 | The Procter & Gamble Company | Hetero-substituted metalloprotease inhibitors |
EP1165500A1 (en) * | 1999-04-02 | 2002-01-02 | Du Pont Pharmaceuticals Company | Amide derivatives as inhibitors of matrix metalloproteinases,tnf-alpha,and aggrecanase |
US6391610B1 (en) * | 1999-08-06 | 2002-05-21 | The Cleveland Clinic Foundation | Nucleic acids encoding zinc metalloproteases |
EP1224171A1 (en) | 1999-10-14 | 2002-07-24 | The Procter & Gamble Company | Beta disubstituted metalloprotease inhibitors |
KR100819680B1 (ko) * | 2000-08-15 | 2008-04-04 | 아크조 노벨 엔.브이. | 트리옥세판 화합물 |
CN1568306A (zh) * | 2001-07-09 | 2005-01-19 | 酶系统产品公司/(Icn-生物医学公司) | 抑制聚集蛋白聚糖酶活性的异羟肟酸血小板凝血酶敏感蛋白肽类似物 |
JP2005516614A (ja) * | 2002-02-05 | 2005-06-09 | ワイス | 切断アグレカナーゼ分子 |
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CA2548518A1 (en) * | 2003-12-04 | 2005-07-07 | Wyeth | Biaryl sulfonamides as mmp inhibitors |
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