NO20062645L - Fremgangsmate for behandling av adamts-5-assosiert sykdom - Google Patents
Fremgangsmate for behandling av adamts-5-assosiert sykdomInfo
- Publication number
- NO20062645L NO20062645L NO20062645A NO20062645A NO20062645L NO 20062645 L NO20062645 L NO 20062645L NO 20062645 A NO20062645 A NO 20062645A NO 20062645 A NO20062645 A NO 20062645A NO 20062645 L NO20062645 L NO 20062645L
- Authority
- NO
- Norway
- Prior art keywords
- adamts
- animals
- osteoarthritis
- activity
- treating
- Prior art date
Links
- 201000010099 disease Diseases 0.000 title abstract 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 5
- 238000000034 method Methods 0.000 title abstract 2
- CVYPRDPBCXSVBN-WDZFZDKYSA-N (5z)-5-[[5-[(4-chlorophenyl)methylsulfanyl]-1-methyl-3-(trifluoromethyl)pyrazol-4-yl]methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one Chemical compound C=1C=C(Cl)C=CC=1CSC=1N(C)N=C(C(F)(F)F)C=1\C=C1/SC(=S)NC1=O CVYPRDPBCXSVBN-WDZFZDKYSA-N 0.000 abstract 6
- 102000051389 ADAMTS5 Human genes 0.000 abstract 6
- 108091005663 ADAMTS5 Proteins 0.000 abstract 6
- 241001465754 Metazoa Species 0.000 abstract 6
- 201000008482 osteoarthritis Diseases 0.000 abstract 5
- 239000003795 chemical substances by application Substances 0.000 abstract 4
- 230000000694 effects Effects 0.000 abstract 4
- 230000002401 inhibitory effect Effects 0.000 abstract 2
- 230000009261 transgenic effect Effects 0.000 abstract 2
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 238000010171 animal model Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000012217 deletion Methods 0.000 abstract 1
- 230000037430 deletion Effects 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 230000006698 induction Effects 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- 238000012216 screening Methods 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—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
- 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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- C07C311/22—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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- 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
- C07D213/62—Oxygen or sulfur atoms
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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
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- C07D213/62—Oxygen or sulfur atoms
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Abstract
Foreliggende oppfinnelse angår metoder for behandling av ADAMTS-5-assosierte sykdommer og spesielt osteoartritt omfattende administrering av et middel som er i stand til a modulere ADMATS-5-aktivitet hos et individ rammet av sykdommen. Midlet er fortrinnsvis en biarylsulfonamidforbindelse. Oppfinnelsen er basert, til dels, på oppdagelsen at transgene dyr som ikke uttrykker funksjonell ADAMTS-5 viser en reduksjon i graden av osteoartritt etter fremkalling av osteoartritt sammenlignet med WT-dyr. Videre har ADAMTS-5 transgene dyr redusert aggrekanase-aktivitet i artikulært vev sammenlignet med WT-dyr. Disse dyr er gode modeller for ADAMTS-5-assosierte sykdommer og for screening av medikamenter anvendelige for behandling og/eller forebygging av disse sykdommer. Det er ingen andre dyremodeller hvor delesjon av aktiviteten til et enkelt gen kan avbryte forløpet av osteoartritt. Følgelig viser disse dyr også at osteoartritt kan forhindres og/eller behandles ved administrering til et individ av et ADAMTS-5-hemmende middel og spesielt et middel som er i stand til a hemme aggrekanase-aktiviteten til ADAMTS-5.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US52688303P | 2003-12-04 | 2003-12-04 | |
| PCT/US2004/037169 WO2005060456A2 (en) | 2003-12-04 | 2004-11-08 | Method for treating adamts-5-associate disease |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20062645L true NO20062645L (no) | 2006-08-30 |
Family
ID=33490796
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20062645A NO20062645L (no) | 2003-12-04 | 2006-06-08 | Fremgangsmate for behandling av adamts-5-assosiert sykdom |
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| TW (1) | TW200519089A (no) |
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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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| RU2006123559A (ru) | 2003-12-04 | 2008-01-10 | Уайт (Us) | Биарилсульфонамиды в качестве ммр-ингибиторов |
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