AR046860A1 - Biaril sulfonamidas con capacidad moduladora de actividad de metaloproteasa. - Google Patents
Biaril sulfonamidas con capacidad moduladora de actividad de metaloproteasa.Info
- Publication number
- AR046860A1 AR046860A1 ARP040104462A ARP040104462A AR046860A1 AR 046860 A1 AR046860 A1 AR 046860A1 AR P040104462 A ARP040104462 A AR P040104462A AR P040104462 A ARP040104462 A AR P040104462A AR 046860 A1 AR046860 A1 AR 046860A1
- Authority
- AR
- Argentina
- Prior art keywords
- biaril
- sulfonamids
- metaloprotease
- activity modulating
- halogen
- Prior art date
Links
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- DBTDEFJAFBUGPP-UHFFFAOYSA-N Methanethial Chemical compound S=C DBTDEFJAFBUGPP-UHFFFAOYSA-N 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 235000019256 formaldehyde Nutrition 0.000 abstract 1
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 1
- 239000003475 metalloproteinase inhibitor Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
Classifications
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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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- A61K31/41—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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Abstract
Estos compuestos presentan actividad como inhibidores de metaloproteinasas. Reivindicación 1: Compuesto de fórmula (1), caracterizado porque: R1 es H o alquilo C1-6; R2 es H, alquilo C1-6, (CH2)nR'2, fenilo o bencilo; n es 0-6; R'2 es arilo, heteroarilo, cicloalquilo, o heterocicloalquilo; R3 es, independientemente en cada una de las ocurrencias, H, halógeno, OC(halógeno)3, C(halógeno)3, alcoxi, o alquilo C1-6; X se escoge entre CH2O, OCH2, C(R3)=C(R3), C(R3)2-C(R3)2, CH2NHC(=O), O(C=O)NH, O, C(=O)CH2, SO2CH2C(=O)NH, SO2NH, OC(=O), CH2S(O), y CH2S(O)2; y Z es al menos un grupo arilo o heteroarilo.
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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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| RU2006123559A (ru) * | 2003-12-04 | 2008-01-10 | Уайт (Us) | Биарилсульфонамиды в качестве ммр-ингибиторов |
| WO2005061459A1 (en) * | 2003-12-04 | 2005-07-07 | Wyeth | Biaryl sulfonamides and methods for using same |
| US20080119513A1 (en) * | 2004-09-06 | 2008-05-22 | Fumihiko Watanabe | Sulfonamide Derivative Selectively Inhibiting Mmp-13 |
| BRPI0613030A2 (pt) | 2005-07-11 | 2012-01-03 | Wyeth Corp | composto de fàrmula i; composto ou sal farmaceuticamente aceitÁvel do composto; mÉtodo para modular a atividade de uma metaloproteinase em animal que dele necessite; composiÇço; mÉtodo para tratamento de um distérbio relacionado a metaloproteinase em animal que dele necessite; mÉtodo de sintetizar um composto; composto de fàrmula ii |
| CN101300345A (zh) * | 2005-08-25 | 2008-11-05 | 惠氏公司 | 聚集蛋白聚糖酶结构 |
| US7615363B2 (en) * | 2005-08-25 | 2009-11-10 | Wyeth | Aggrecanase structure |
| WO2007044100A1 (en) | 2005-10-13 | 2007-04-19 | Wyeth | Methods for preparing glutamic acid derivatives |
| EP1997804A1 (en) | 2006-03-03 | 2008-12-03 | Shionogi & Co., Ltd. | Mmp-13-selective inhibitor |
| CN101511783A (zh) * | 2006-09-08 | 2009-08-19 | 诺瓦提斯公司 | 用于治疗淋巴细胞相互作用介导的疾病的n-联芳(杂)芳基磺酰胺衍生物 |
| CA2664794A1 (en) * | 2006-10-20 | 2008-05-02 | Merck & Co., Inc. | Substituted imidazoles as bombesin receptor subtype-3 modulators |
| US8193228B2 (en) * | 2006-10-20 | 2012-06-05 | Merck Sharp & Dohme Corp. | Substituted imidazole as bombesin receptor subtype-3 modulators |
| AU2007309569A1 (en) * | 2006-10-20 | 2008-05-02 | Merck Sharp & Dohme Corp. | Substituted imidazoles as bombesin receptor subtype-3 modulators |
| US20100099676A1 (en) | 2006-11-02 | 2010-04-22 | 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 |
| PE20120554A1 (es) * | 2009-07-02 | 2012-06-08 | 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 |
| PL2650310T3 (pl) * | 2012-04-13 | 2017-01-31 | Rottapharm Biotech S.R.L. | Przeciwciało przeciw-ADAMTS-5, jego pochodne i zastosowania |
| GB201312311D0 (en) * | 2013-07-09 | 2013-08-21 | Uni I Oslo | Uses of enzyme inhibitors |
| AU2015336954A1 (en) * | 2014-10-22 | 2017-06-08 | 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 |
| KR20250011229A (ko) | 2017-06-02 | 2025-01-21 | 메르크 파텐트 게엠베하 | Adamts 결합성 면역글로불린 |
| EP3630817A1 (en) | 2017-06-02 | 2020-04-08 | Merck Patent GmbH | Polypeptides binding adamts5, mmp13 and aggrecan |
| CA3064469A1 (en) | 2017-06-02 | 2018-12-06 | Merck Patent Gmbh | Mmp13 binding immunoglobulins |
| EA202091856A1 (ru) | 2018-02-02 | 2020-12-07 | Маверикс Онколоджи, Инк. | Низкомолекулярные лекарственные коньюгаты гемцитабина монофосфата |
| 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 |
| WO2024054922A1 (en) * | 2022-09-07 | 2024-03-14 | Synoa Therapeutics, Llc | Methods and compositions comprising novel bispecific antibodies |
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| KR100338861B1 (ko) * | 1996-01-23 | 2003-02-20 | 시오노기세이야쿠가부시키가이샤 | 술폰화아미노산유도체및이를함유한메탈로프로테이나제저해제 |
| PL186416B1 (pl) * | 1996-05-17 | 2004-01-30 | Warner Lambert Co | Związek bifenylosulfonamidowy i preparat farmaceutyczny zawierający ten związek |
| JP2001511351A (ja) * | 1997-07-25 | 2001-08-14 | デュポン ファーマシューティカルズ カンパニー | アグリカン分解性メタロプロテアーゼ |
| WO1999051572A1 (en) * | 1998-04-03 | 1999-10-14 | Sankyo Company, Limited | Sulfonamide derivatives |
| TR200102524T2 (tr) | 1999-03-03 | 2002-02-21 | The Procter & Gamble Company | Dihetero sübstitüe edilmiş metaloproteaz inhibitörleri. |
| AU4180900A (en) * | 1999-04-02 | 2000-10-23 | Du Pont Pharmaceuticals Company | Novel 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 |
| SK5082002A3 (en) | 1999-10-14 | 2002-10-08 | Procter & Gamble | Beta disubstituted metalloprotease inhibitors |
| KR100819680B1 (ko) * | 2000-08-15 | 2008-04-04 | 아크조 노벨 엔.브이. | 트리옥세판 화합물 |
| HRP20040131A2 (en) * | 2001-07-09 | 2005-12-31 | Enzyme Systems Prducts Inc./(Icn Biomedicals) | A hydroxamic acid thrombospondin peptide analog that inhibits aggrecanase activity |
| EP1472364A4 (en) * | 2002-02-05 | 2005-12-28 | Wyeth Corp | TRUNK AGGRECANASE MOLECULES |
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- 2004-11-08 BR BRPI0417259-0A patent/BRPI0417259A/pt not_active IP Right Cessation
- 2004-11-08 RU RU2006117022/04A patent/RU2006117022A/ru not_active Application Discontinuation
- 2004-12-01 US US11/000,711 patent/US7268135B2/en not_active Expired - Fee Related
- 2004-12-01 AR ARP040104462A patent/AR046860A1/es unknown
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- 2004-12-03 PE PE2004001191A patent/PE20051004A1/es not_active Application Discontinuation
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2006
- 2006-05-19 CR CR8411A patent/CR8411A/es not_active Application Discontinuation
- 2006-05-22 IL IL175818A patent/IL175818A0/en unknown
- 2006-06-02 CO CO06053408A patent/CO5700714A2/es unknown
- 2006-06-02 EC EC2006006599A patent/ECSP066599A/es unknown
- 2006-06-08 NO NO20062645A patent/NO20062645L/no not_active Application Discontinuation
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2007
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2008
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