JP2010265276A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2010265276A5 JP2010265276A5 JP2010142096A JP2010142096A JP2010265276A5 JP 2010265276 A5 JP2010265276 A5 JP 2010265276A5 JP 2010142096 A JP2010142096 A JP 2010142096A JP 2010142096 A JP2010142096 A JP 2010142096A JP 2010265276 A5 JP2010265276 A5 JP 2010265276A5
- Authority
- JP
- Japan
- Prior art keywords
- aryl
- sulfonyl halide
- bis
- compound
- substituted
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38832602P | 2002-06-12 | 2002-06-12 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004513217A Division JP4718172B2 (ja) | 2002-06-12 | 2003-06-11 | ヒトadam−10インヒビター |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010265276A JP2010265276A (ja) | 2010-11-25 |
| JP2010265276A5 true JP2010265276A5 (enExample) | 2011-08-18 |
Family
ID=29736461
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004513217A Expired - Fee Related JP4718172B2 (ja) | 2002-06-12 | 2003-06-11 | ヒトadam−10インヒビター |
| JP2010142096A Pending JP2010265276A (ja) | 2002-06-12 | 2010-06-22 | ヒトadam−10インヒビター |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004513217A Expired - Fee Related JP4718172B2 (ja) | 2002-06-12 | 2003-06-11 | ヒトadam−10インヒビター |
Country Status (7)
| Country | Link |
|---|---|
| US (5) | US7629341B2 (enExample) |
| EP (3) | EP1511488B1 (enExample) |
| JP (2) | JP4718172B2 (enExample) |
| AU (2) | AU2003237532B2 (enExample) |
| CA (1) | CA2485346C (enExample) |
| ES (1) | ES2425013T3 (enExample) |
| WO (1) | WO2003106381A2 (enExample) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7517884B2 (en) * | 1998-03-30 | 2009-04-14 | Kalypsys Inc. | Sulfonyl-substituted bicyclic compounds as modulators of PPAR |
| AU2003237532B2 (en) | 2002-06-12 | 2009-07-30 | Symphony Evolution, Inc. | Human ADAM-10 inhibitors |
| WO2004089294A2 (en) | 2003-04-04 | 2004-10-21 | Incyte Corporation | Compositions, methods and kits relating to her-2 cleavage |
| EP1623995A1 (en) | 2004-08-06 | 2006-02-08 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Inhibitors of L1 and ADAM10 for the treatment of carcinomas |
| US20070190079A1 (en) * | 2004-10-29 | 2007-08-16 | Kalypsys, Inc. | Methods for the selective modulation of ppar |
| RU2384576C2 (ru) * | 2004-10-29 | 2010-03-20 | Калипсис, Инк | Сульфонил-замещенные бициклические соединения в качестве модуляторов ppar |
| EP1896580A2 (en) * | 2005-04-07 | 2008-03-12 | Novartis Vaccines and Diagnostics, Inc. | Adam10 in cancer diagnosis, detection and treatment |
| KR101464767B1 (ko) * | 2005-10-25 | 2014-11-24 | 칼립시스, 인코포레이티드 | Ppar의 조절자의 염 및 대사질환을 치료하는 방법 |
| WO2007084488A2 (en) | 2006-01-13 | 2007-07-26 | Vanderbilt University | Adam10 and its uses related to infection |
| CN100506804C (zh) * | 2006-01-26 | 2009-07-01 | 于学敏 | 羟苯磺酸烷基吡嗪药物及其制备方法和应用 |
| US20070249519A1 (en) * | 2006-04-20 | 2007-10-25 | Kalypsys, Inc. | Methods for the upregulation of glut4 via modulation of ppar delta in adipose tissue and for the treatment of disease |
| AR060937A1 (es) * | 2006-05-16 | 2008-07-23 | Kalypsys Inc | Compuestos biciclicos sustituidos con sulfonilo como moduladores de ppar |
| WO2008091863A1 (en) | 2007-01-23 | 2008-07-31 | Kalypsys, Inc. | Sulfonyl-substituted bicyclic compounds as ppar modulators for the treatment of non-alcoholic steatohepatitis |
| WO2009052200A2 (en) * | 2007-10-16 | 2009-04-23 | Symphony Evolution, Inc. | Human adam-10 inhibitors |
| ES2620634T3 (es) | 2008-10-09 | 2017-06-29 | The U.S.A. As Represented By The Secretary, Department Of Health And Human Services | Activadores de piruvato quinasa humana |
| EP2482817A1 (en) * | 2009-10-01 | 2012-08-08 | Symphony Evolution, Inc. | Methods of treating aneurysmal dilatation, blood vessel wall weakness and specifically abdominal aortic and thoracic aneurysm using matrix metalloprotease-2 inhibitors |
| US20130109672A1 (en) | 2010-04-29 | 2013-05-02 | The United States Of America,As Represented By The Secretary, Department Of Health And Human Service | Activators of human pyruvate kinase |
| JP5888667B2 (ja) * | 2010-04-30 | 2016-03-22 | 国立大学法人名古屋大学 | Adam作用阻害物質のスクリーニング方法、仮足の保持方法、仮足保持剤、仮足の制御物質のスクリーニング方法、及びadam作用阻害剤 |
| EP2637679A4 (en) | 2010-11-09 | 2015-09-23 | Univ Chicago | ROLE OF ADAM10 AND ITS RELEVANCE TO DISEASES AND THERAPEUTICS |
| WO2014028334A1 (en) * | 2012-08-11 | 2014-02-20 | Symphony Evolution, Inc. | Selective mmp inhibitors |
| WO2015112842A1 (en) * | 2014-01-24 | 2015-07-30 | Ntercept, Llc | Methods and compositions for immune dis-inhibition |
| CA2962251A1 (en) | 2014-10-03 | 2016-04-07 | Ntercept, Llc | Compositions and methods for inhibiting the biological activity of soluble biomolecules |
| CN108135850A (zh) | 2015-07-29 | 2018-06-08 | 纳米提克斯有限责任公司 | 用于清除可溶性生物分子的模块化组合物及其相关方法 |
| US11065345B2 (en) | 2017-01-04 | 2021-07-20 | Nanotics, Llc | Methods for assembling scavenging particles |
| US20210130430A1 (en) | 2018-05-14 | 2021-05-06 | Werewolf Therapeutics, Inc. | Activatable cytokine polypeptides and methods of use thereof |
| CN108947850B (zh) * | 2018-07-23 | 2021-05-18 | 蚌埠中实化学技术有限公司 | 一种3,4,5-三氟苯胺的制备方法 |
| BR112021022666A2 (pt) | 2019-05-14 | 2022-03-29 | Werewolf Therapeutics Inc | Frações de separação e seus métodos e uso |
| BR112022009110A2 (pt) | 2019-11-14 | 2022-07-26 | Werewolf Therapeutics Inc | Polipeptídeos de citocina ativáveis e métodos de uso destes |
| CN113563235B (zh) * | 2021-07-28 | 2023-04-11 | 上海毕得医药科技股份有限公司 | 一种3-(卤代苯氧基)苯磺酰氯衍生物的合成方法 |
| JP2025507975A (ja) * | 2022-03-08 | 2025-03-21 | ノバ サウスイースタン ユニバーシティー | ディスインテグリンおよびメタロプロテアーゼ10(adam10)の酵素・基質選択的エキソサイト阻害剤を用いた関節リウマチ(ra)の処置方法 |
Family Cites Families (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1016245A (en) | 1962-11-06 | 1966-01-05 | Ici Ltd | Manufacture of polysulphones |
| US4213775A (en) * | 1977-07-28 | 1980-07-22 | Ube Industries, Ltd. | Diphenyl ether derivatives and herbicidal compositions containing the same |
| DE3107700A1 (de) * | 1981-02-28 | 1982-09-16 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von aromatischen sulfohalogeniden |
| WO1991013146A1 (en) | 1990-03-01 | 1991-09-05 | The Upjohn Company | Ruminal bacterium for preventing acute lactic acidosis |
| DE4015834A1 (de) * | 1990-05-17 | 1991-11-21 | Bayer Ag | Phenoxyphenylsulfonylverbindungen |
| US5215549A (en) | 1991-05-08 | 1993-06-01 | Mobil Oil Corporation | Thioester derived hindered phenols and aryl-amines as antioxidant and antiwear additives |
| DE4327026A1 (de) | 1993-08-12 | 1995-02-16 | Bayer Ag | Arylsulfonyloxyphosphonsäurederivate |
| CA2218503C (en) | 1995-04-20 | 2001-07-24 | Pfizer Inc. | Arylsulfonyl hydroxamic acid derivatives |
| JP3837761B2 (ja) * | 1995-08-04 | 2006-10-25 | 住友精化株式会社 | ハロベンゼンスルホニルクロリド類の製造方法 |
| DE19537334A1 (de) | 1995-10-09 | 1997-04-10 | Hoechst Ag | Antiadhäsive Piperidin- und Pyrrolidin-Carbonsäuren |
| US6500948B1 (en) | 1995-12-08 | 2002-12-31 | Agouron Pharmaceuticals, Inc. | Metalloproteinase inhibitors-compositions, uses preparation and intermediates thereof |
| US5753653A (en) * | 1995-12-08 | 1998-05-19 | Agouron Pharmaceuticals, Inc. | Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses |
| EA003294B1 (ru) * | 1995-12-08 | 2003-04-24 | Агурон Фармасьютикалс, Инк. | Ингибиторы металлопротеиназы, фармацевтические композиции, их содержащие, и их фармацевтические применения |
| HUP0000505A3 (en) | 1996-08-28 | 2001-12-28 | Procter & Gamble | Saturated 7-9 membered heterocyclic n-hydroxycarboxamide derivatives and pharmaceutical compositions containing them |
| EP0963432A4 (en) | 1996-08-29 | 2002-11-20 | Univ California | KUZ, NEW FAMILY OF METALLOPROTEASES |
| WO1998027069A1 (en) | 1996-12-17 | 1998-06-25 | Fujisawa Pharmaceutical Co., Ltd. | Piperazine compounds as inhibitors of mmp or tnf |
| JP3563411B2 (ja) * | 1997-01-23 | 2004-09-08 | エフ・ホフマン−ラ ロシュ アーゲー | スルファミド−メタロプロテアーゼ阻害剤 |
| NZ336836A (en) | 1997-02-11 | 2001-02-23 | Pfizer | Arylsulfonyl hydroxamic acid derivatives suitable for a broad range of medicinal treatments |
| EP0973748A1 (en) * | 1997-04-01 | 2000-01-26 | Agouron Pharmaceuticals, Inc. | Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses |
| US5922546A (en) | 1997-08-25 | 1999-07-13 | Smithkline Beecham Corporation | Human disintegrin metalloprotease KUZ gene |
| JP4327915B2 (ja) * | 1998-03-30 | 2009-09-09 | 株式会社デ・ウエスタン・セラピテクス研究所 | スルフォンアミド誘導体 |
| GT199900044A (es) * | 1998-04-10 | 2000-09-14 | Procedimientos para preparar haluros de fenoxifenilsulfonilo. | |
| BR9910678A (pt) | 1998-05-14 | 2001-10-02 | Du Pont Pharm Co | Composto, composição farmacêutica, método para traramento ou prevenção de uma doença inflamatória, método para tratamento de uma condição ou uma doença mediada por mmps, tnf, agrecanase, ou um composto dos mesmos, em um mamìfero, método de redução de nìveis de tnf em pacientes, sem a inibição de mmps, método para tratamento de uma condição ou uma doença e uso de um novo composto |
| WO2000009492A1 (en) | 1998-08-12 | 2000-02-24 | Pfizer Products Inc. | Tace inhibitors |
| US6509337B1 (en) | 1998-09-17 | 2003-01-21 | Pfizer Inc. | Arylsulfonyl Hydroxamic Acid derivatives as MMP and TNF inhibitors |
| AR035313A1 (es) | 1999-01-27 | 2004-05-12 | Wyeth Corp | Inhibidores de tace acetilenicos de acido hidroxamico de sulfonamida a base de alfa-aminoacidos, composiciones farmaceuticas y el uso de los mismos para la manufactura de medicamentos. |
| US6225311B1 (en) | 1999-01-27 | 2001-05-01 | American Cyanamid Company | Acetylenic α-amino acid-based sulfonamide hydroxamic acid tace inhibitors |
| JP2000247975A (ja) | 1999-02-25 | 2000-09-12 | Nissan Chem Ind Ltd | ヘテロ環縮合ピリミジノン誘導体及びそれらを含む除草剤 |
| US6387901B1 (en) | 1999-07-06 | 2002-05-14 | Pfizer Inc | Alkyne containing metalloproteinase inhibitors |
| EP1081137A1 (en) | 1999-08-12 | 2001-03-07 | Pfizer Products Inc. | Selective inhibitors of aggrecanase in osteoarthritis treatment |
| AU2001233034A1 (en) | 2000-01-27 | 2001-08-07 | American Cyanamid Company | Method for preparing alpha-sulfonyl hydroxamic acid derivatives |
| US6664291B2 (en) * | 2000-03-31 | 2003-12-16 | Pfizer, Inc. | Malonamic acids and derivatives thereof as thyroid receptor ligands |
| JP4635162B2 (ja) * | 2000-04-27 | 2011-02-16 | 独立行政法人理化学研究所 | 芳香族ジアミンの製造方法及び芳香族ジアミン化合物 |
| AU2002255613A1 (en) | 2001-02-27 | 2002-09-12 | Axys Pharmaceuticals, Inc. | Piperazine derivatives as metalloprotease inhibitors |
| CA2357110A1 (en) | 2001-04-11 | 2002-10-11 | American Cyanamid Company | Method for the treatment of polycystic kidney disease |
| JP4365102B2 (ja) | 2001-04-26 | 2009-11-18 | コーロン ライフ サイエンス インク | 新規なスルホンアミド誘導体、その中間体化合物、及びその製造方法、並びにスルホンアミド誘導体を含む薬剤学的組成物 |
| US6399823B1 (en) * | 2001-04-30 | 2002-06-04 | General Electric Company | Method for producing phosgene |
| JP2005507937A (ja) | 2001-11-01 | 2005-03-24 | ワイス・ホールディングズ・コーポレイション | マトリックスメタロプロテイナーゼおよびtace阻害剤としてのアレンアリールスルホンアミドヒドロキサム酸 |
| CN1173960C (zh) | 2001-12-06 | 2004-11-03 | 中国人民解放军军事医学科学院毒物药物研究所 | 取代六元氮杂环类化合物及其作为神经调节剂的用途 |
| WO2003051825A1 (en) * | 2001-12-14 | 2003-06-26 | Exelixis, Inc. | Human adam-10 inhibitors |
| US7504537B2 (en) | 2001-12-27 | 2009-03-17 | Dainippon Sumitomo Pharma Co., Ltd. | Hydroxamic acid derivative and MMP inhibitor containing the same as active ingredient |
| WO2003057214A1 (en) | 2001-12-28 | 2003-07-17 | Somatocor Pharmaceuticals, Inc. | Imidazolidin-2,4-dione derivatives as non-peptide somatostatin receptor ligands |
| US7488754B2 (en) | 2002-04-05 | 2009-02-10 | Wyeth | Method for the treatment of polycystic kidney disease |
| AU2003237532B2 (en) | 2002-06-12 | 2009-07-30 | Symphony Evolution, Inc. | Human ADAM-10 inhibitors |
| MXPA05001603A (es) | 2002-08-13 | 2005-04-25 | Warner Lambert Co | Derivados monociclicos como inhibidores de metaloproteinasa de matriz. |
| EP1400244A1 (en) | 2002-09-17 | 2004-03-24 | Warner-Lambert Company LLC | New spirocondensed quinazolinones and their use as phosphodiesterase inhibitors |
| WO2004071390A2 (en) | 2003-02-14 | 2004-08-26 | Applied Research Systems Ars Holding N.V. | Piperazine-2-carboxamide derivatives |
| JP2006517960A (ja) | 2003-02-18 | 2006-08-03 | ファイザー インコーポレイテッド | C型肝炎ウイルスの阻害剤、それを使用する組成物および治療法 |
| WO2006076442A2 (en) | 2005-01-14 | 2006-07-20 | Janssen Pharmaceutica N.V. | Triazolopyrimidine derivatives |
| CA2620414A1 (en) | 2005-08-26 | 2007-03-01 | Methylgene Inc. | Benzodiazepine and benzopiperazine analog inhibitors of histone deacetylase |
| EP1937632A1 (en) | 2005-10-06 | 2008-07-02 | Astra Zeneca AB | Novel compounds |
-
2003
- 2003-06-11 AU AU2003237532A patent/AU2003237532B2/en not_active Ceased
- 2003-06-11 EP EP03736979.0A patent/EP1511488B1/en not_active Expired - Lifetime
- 2003-06-11 CA CA2485346A patent/CA2485346C/en not_active Expired - Fee Related
- 2003-06-11 US US10/518,110 patent/US7629341B2/en not_active Expired - Fee Related
- 2003-06-11 WO PCT/US2003/018262 patent/WO2003106381A2/en not_active Ceased
- 2003-06-11 ES ES03736979T patent/ES2425013T3/es not_active Expired - Lifetime
- 2003-06-11 JP JP2004513217A patent/JP4718172B2/ja not_active Expired - Fee Related
- 2003-06-11 EP EP11188699A patent/EP2436676A1/en not_active Withdrawn
- 2003-06-11 EP EP11188701A patent/EP2428509A1/en not_active Withdrawn
-
2009
- 2009-10-23 US US12/605,118 patent/US7989661B2/en not_active Expired - Fee Related
- 2009-10-28 AU AU2009230801A patent/AU2009230801A1/en not_active Abandoned
-
2010
- 2010-06-22 JP JP2010142096A patent/JP2010265276A/ja active Pending
-
2011
- 2011-06-23 US US13/167,128 patent/US20120071653A1/en not_active Abandoned
-
2012
- 2012-07-03 US US13/541,503 patent/US20130144056A1/en not_active Abandoned
-
2014
- 2014-03-21 US US14/221,937 patent/US20140206865A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Barata‐Vallejo et al. | Recent advances in trifluoromethylation reactions with electrophilic trifluoromethylating reagents | |
| Kang et al. | Copper-catalyzed trifluoromethylthiolation of aryl and vinyl boronic acids with a shelf-stable electrophilic trifluoromethylthiolating reagent | |
| JP2008523069A5 (enExample) | ||
| RU2015143637A (ru) | Способы получения апоптоз агента | |
| RU2012146189A (ru) | Способ получения производных 3-кетобензофурана | |
| JP2014512451A5 (enExample) | ||
| JP2013505929A5 (enExample) | ||
| JP2014508811A5 (enExample) | ||
| JP2013063963A5 (ja) | 複素環化合物 | |
| Yadav et al. | N-arylation of indoles with aryl halides using copper/glycerol as a mild and highly efficient recyclable catalytic system | |
| JP2016512547A5 (enExample) | ||
| RU2016123144A (ru) | Сложноэфирное хиральное соединение (n-замещенный имидазол)-карбоновой кислоты, содержащее простую эфирную боковую цепь, его получение и применение | |
| Feng et al. | Copper-catalyzed conversion of aryl and heteroaryl bromides into the corresponding chlorides | |
| RU2016135762A (ru) | Способ получения (r)-1,1,3-триметил-4-аминоиндана | |
| JP2016540051A5 (enExample) | ||
| JP2010522214A5 (enExample) | ||
| JP2012508747A5 (enExample) | ||
| JP2015078431A5 (enExample) | ||
| JP2014524464A5 (enExample) | ||
| CN102603735B (zh) | 一种c-2芳基化吲哚嗪化合物的制备方法 | |
| JP2018515468A5 (enExample) | ||
| CN103130810B (zh) | 一种吡唑并[1,5-c]喹唑啉类化合物的合成方法 | |
| Fan et al. | Generation of 1-(trifluoromethyl) isoquinolines via a copper-catalyzed reaction of isoquinoline-N-oxide with Togni reagent | |
| JP2014074021A5 (enExample) | ||
| RU2015113741A (ru) | Способ получения вориконазола и его аналогов |