CA2722582A1 - Inhibiteurs de pde4 biaryle pour traiter une inflammation - Google Patents
Inhibiteurs de pde4 biaryle pour traiter une inflammation Download PDFInfo
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- CA2722582A1 CA2722582A1 CA2722582A CA2722582A CA2722582A1 CA 2722582 A1 CA2722582 A1 CA 2722582A1 CA 2722582 A CA2722582 A CA 2722582A CA 2722582 A CA2722582 A CA 2722582A CA 2722582 A1 CA2722582 A1 CA 2722582A1
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- C07C275/32—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen 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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- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
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- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/04—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
- C07D275/06—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to the ring sulfur atom
-
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- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
-
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- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
- C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
- C07D285/135—Nitrogen atoms
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/18—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one oxygen and one nitrogen atom, e.g. guanine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/40—Heterocyclic compounds containing purine ring systems with halogen atoms or perhalogeno-alkyl radicals directly attached in position 2 or 6
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/05—Isotopically modified compounds, e.g. labelled
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US98955107P | 2007-11-21 | 2007-11-21 | |
US60/989,551 | 2007-11-21 | ||
PCT/US2008/084193 WO2009067600A2 (fr) | 2007-11-21 | 2008-11-20 | Inhibiteurs de pde4 biaryle pour traiter une inflammation |
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CA2722582A1 true CA2722582A1 (fr) | 2009-05-28 |
Family
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CA2722582A Abandoned CA2722582A1 (fr) | 2007-11-21 | 2008-11-20 | Inhibiteurs de pde4 biaryle pour traiter une inflammation |
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EP (1) | EP2222638A2 (fr) |
JP (1) | JP2011505341A (fr) |
CN (1) | CN102089279A (fr) |
AU (1) | AU2008326381B2 (fr) |
CA (1) | CA2722582A1 (fr) |
WO (1) | WO2009067600A2 (fr) |
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CN101490017B (zh) | 2006-02-28 | 2013-01-23 | 海利空医疗公司 | 作为pde4抑制剂的用于治疗的哌嗪类 |
EP2674417A3 (fr) | 2007-11-21 | 2014-04-09 | Decode Genetics EHF | Inhibiteurs de pde4 biaryle pour le traitement de l'inflammation |
WO2010059838A2 (fr) * | 2008-11-20 | 2010-05-27 | Decode Genetics Ehf | Inhibiteurs de pde4 sélectifs pour la forme longue de pde4 pour traiter une inflammation et éviter des effets secondaires |
CN107021951B (zh) | 2010-06-30 | 2020-10-20 | 赛克里翁治疗有限公司 | sGC刺激物 |
US9617197B2 (en) | 2010-08-04 | 2017-04-11 | University Of Virginia Patent Foundation | Compositions and methods for treating inflammatory diseases |
AU2011326241B2 (en) | 2010-11-09 | 2016-11-17 | Ironwood Pharmaceuticals, Inc. | sGC stimulators |
US9540361B2 (en) * | 2010-12-24 | 2017-01-10 | Merck Sharp & Dohme B.V. | N-substituted azetidine derivatives |
CN102617457A (zh) * | 2011-01-28 | 2012-08-01 | 天津药物研究院 | 一种制备罗氟司特的新方法 |
CN103012255B (zh) * | 2011-09-21 | 2014-06-11 | 天津康鸿医药科技发展有限公司 | 罗氟司特晶型化合物、其制备方法、组合物及应用 |
CN102603676B (zh) * | 2012-02-20 | 2014-02-12 | 徐江平 | 一种能避免呕吐反应的磷酸二酯酶4抑制剂 |
US8865723B2 (en) | 2012-10-25 | 2014-10-21 | Tetra Discovery Partners Llc | Selective PDE4 B inhibition and improvement in cognition in subjects with brain injury |
CA2891412A1 (fr) | 2012-11-20 | 2014-05-30 | Vertex Pharmaceuticals Incorporated | Composes utiles comme inhibiteurs de l'indoleamine 2,3-dioxygenase |
CN103012408B (zh) * | 2012-11-28 | 2015-02-04 | 中国科学院广州生物医药与健康研究院 | 依匹斯汀的合成方法 |
ES2769181T3 (es) * | 2013-03-14 | 2020-06-24 | Dart Neuroscience Cayman Ltd | Compuestos de piridina y de pirazina sustituidos como inhibidores de PDE4 |
KR20160132414A (ko) | 2014-03-14 | 2016-11-18 | 욱크하르트 리미티드 | 소듐 (2s, 5r)-6-(벤질옥시)-7-옥소-1,6-다이아자바이사이클로[3.2.1]옥테인-2-카복실레이트의 제조 공정 |
PT3209655T (pt) | 2014-10-24 | 2020-11-13 | Landos Biopharma Inc | Produtos terapêuticos à base da lancl2 |
EP3165224A1 (fr) | 2015-11-09 | 2017-05-10 | Albert-Ludwigs-Universität Freiburg | Utilisation d'inhibiteurs de pde4 pour la prophylaxie et/ou la thérapie de la dyslipoproteinémie et des troubles apparentés |
WO2017089347A1 (fr) | 2015-11-25 | 2017-06-01 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Procédés et compositions pharmaceutiques pour le traitement de mélanomes résistant aux inhibiteurs de braf |
CA3029857C (fr) * | 2016-07-05 | 2023-07-04 | Guangzhou Maxinovel Pharmaceuticals Co., Ltd | Compose d'acetylene aromatique ou d'ethylene aromatique, produit intermediaire, procede de preparation, composition pharmaceutique et leur utilisation |
WO2019108418A1 (fr) | 2017-11-30 | 2019-06-06 | Landos Biopharma, Inc. | Traitements utilisant des ligands de la protéine 2 analogue au composant c de la lanthionine et cellules préparées avec ceux-ci |
US11384048B2 (en) | 2017-12-29 | 2022-07-12 | Guangzhou Maxinovel Pharmaceuticals Co., Ltd. | Aromatic vinyl or aromatic ethyl derivative, preparation method therefor, intermediate, pharmaceutical composition, and application |
CN110041253B (zh) * | 2018-01-17 | 2022-03-29 | 上海翰森生物医药科技有限公司 | 吡啶类n-氧化衍生物及其制备方法和应用 |
JP2022531129A (ja) * | 2019-04-23 | 2022-07-06 | テトラ ディスカバリー パートナーズ インコーポレイテッド | Pde4d阻害剤としての3-ヒドロキシ-2-フェニル-6-(ピラゾール-4-イルメチル)ピリジン誘導体 |
WO2021127472A1 (fr) | 2019-12-20 | 2021-06-24 | Landos Biopharma, Inc. | Ligands de la protéine 2 de type lanthionine c, cellules préparées avec ceux-ci, et thérapies les utilisant |
JP2023542908A (ja) | 2020-09-18 | 2023-10-12 | シャンハイ ファーマシューティカルズ ホールディング カンパニー,リミティド | カルボニル複素環系化合物及びその使用 |
CN112374984A (zh) * | 2020-11-06 | 2021-02-19 | 苏州求索生物科技有限公司 | 一种2-溴-4-羟基苯甲醚的制备工艺 |
KR102514860B1 (ko) * | 2020-12-01 | 2023-03-29 | 한국과학기술연구원 | 5-ht7 세로토닌 수용체 활성 저해용 바이페닐 피롤리딘 및 바이페닐 다이하이드로이미다졸 유도체 및 이를 유효성분으로 포함하는 약학 조성물 |
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CN103980151A (zh) * | 2006-08-09 | 2014-08-13 | 史密丝克莱恩比彻姆公司 | 作为阿片样物质受体的拮抗剂或反向激动剂的新型化合物 |
CN101687850A (zh) * | 2007-03-21 | 2010-03-31 | 艾美罗股份公司 | 作为腺苷受体拮抗剂的取代的嘧啶 |
EP2674417A3 (fr) * | 2007-11-21 | 2014-04-09 | Decode Genetics EHF | Inhibiteurs de pde4 biaryle pour le traitement de l'inflammation |
FR2932180B1 (fr) * | 2008-06-04 | 2012-08-10 | Centre Nat Rech Scient | Dihydro iso ca-4 et analogues : puissants cytotoxiques, inhibiteurs de la polymerisation de la tubuline |
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2008
- 2008-11-20 AU AU2008326381A patent/AU2008326381B2/en not_active Expired - Fee Related
- 2008-11-20 WO PCT/US2008/084193 patent/WO2009067600A2/fr active Application Filing
- 2008-11-20 JP JP2010535064A patent/JP2011505341A/ja active Pending
- 2008-11-20 EP EP08851045A patent/EP2222638A2/fr not_active Withdrawn
- 2008-11-20 CN CN2008801251758A patent/CN102089279A/zh active Pending
- 2008-11-20 CA CA2722582A patent/CA2722582A1/fr not_active Abandoned
Also Published As
Publication number | Publication date |
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JP2011505341A (ja) | 2011-02-24 |
AU2008326381A1 (en) | 2009-05-28 |
CN102089279A (zh) | 2011-06-08 |
WO2009067600A3 (fr) | 2009-07-30 |
WO2009067600A2 (fr) | 2009-05-28 |
AU2008326381B2 (en) | 2014-10-23 |
EP2222638A2 (fr) | 2010-09-01 |
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