WO2011056985A3 - Composés hétérocycliques substitués - Google Patents
Composés hétérocycliques substitués Download PDFInfo
- Publication number
- WO2011056985A3 WO2011056985A3 PCT/US2010/055467 US2010055467W WO2011056985A3 WO 2011056985 A3 WO2011056985 A3 WO 2011056985A3 US 2010055467 W US2010055467 W US 2010055467W WO 2011056985 A3 WO2011056985 A3 WO 2011056985A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compounds
- substituted heterocyclic
- heterocyclic compounds
- relates
- diabetes
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/34—Oxygen atoms in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/10—Spiro-condensed systems
Abstract
La présente invention porte sur des composés qui sont des inhibiteurs de canaux sodiques et sur leur utilisation dans le traitement de divers états de maladie, comprenant les maladies cardiovasculaires et le diabète. Dans des modes de réalisation particuliers, la structure des composés est donnée par la Formule (I) telle que décrite en détail présentement. L'invention porte également sur des procédés pour la préparation des composés, et sur des compositions pharmaceutiques contenant de tels composés.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US25813209P | 2009-11-04 | 2009-11-04 | |
US61/258,132 | 2009-11-04 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2011056985A2 WO2011056985A2 (fr) | 2011-05-12 |
WO2011056985A3 true WO2011056985A3 (fr) | 2011-10-27 |
Family
ID=43416386
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2010/055467 WO2011056985A2 (fr) | 2009-11-04 | 2010-11-04 | Composés hétérocycliques substitués |
Country Status (1)
Country | Link |
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WO (1) | WO2011056985A2 (fr) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012049555A1 (fr) | 2010-10-13 | 2012-04-19 | Lupin Limited | Composés spirocycliques en tant que modulateurs de canaux sodiques dépendants du voltage |
TWI510480B (zh) | 2011-05-10 | 2015-12-01 | Gilead Sciences Inc | 充當離子通道調節劑之稠合雜環化合物 |
TW201837023A (zh) | 2011-07-01 | 2018-10-16 | 美商基利科學股份有限公司 | 作為離子通道調節劑之稠合雜環化合物 |
NO3175985T3 (fr) | 2011-07-01 | 2018-04-28 | ||
CN102491979A (zh) * | 2011-12-21 | 2012-06-13 | 天津科技大学 | 一种1-羟乙基-5-取代吲哚酮类衍生物及其制备方法以及应用 |
WO2013112932A1 (fr) | 2012-01-27 | 2013-08-01 | Gilead Sciences, Inc. | Thérapies de combinaison à l'aide de bloqueurs de canaux ioniques au sodium tardifs et de bloqueurs de canaux ioniques au potassium |
AU2015242219A1 (en) | 2014-03-29 | 2016-10-06 | Lupin Limited | Sulfonamide compounds as Voltage gated sodium channel modulators |
AU2016255431B2 (en) | 2015-04-29 | 2020-05-07 | Janssen Pharmaceutica Nv | Imidazopyrazines and pyrazolopyrimidines and their use as AMPA receptor modulators |
WO2016176449A1 (fr) | 2015-04-29 | 2016-11-03 | Janssen Pharmaceutica Nv | Composés de benzimidazolone et de benzothiazolone et leur utilisation comme modulateurs des récepteurs ampa |
CN107835814B (zh) | 2015-04-29 | 2021-07-23 | 詹森药业有限公司 | 氮杂苯并咪唑及其作为ampa受体调节剂的用途 |
CN107750250B (zh) * | 2015-04-29 | 2021-09-07 | 詹森药业有限公司 | 吲哚酮化合物及其作为ampa受体调节剂的用途 |
TW201722938A (zh) | 2015-09-04 | 2017-07-01 | 魯賓有限公司 | 作為電位閘控鈉通道調節子之磺醯胺化合物 |
JP7105797B2 (ja) | 2016-11-28 | 2022-07-25 | プラクシス プレシジョン メディシンズ, インコーポレイテッド | 化合物及びその使用方法 |
US11261188B2 (en) | 2016-11-28 | 2022-03-01 | Praxis Precision Medicines, Inc. | Fused heteroaryl compounds, and methods thereof for treating diseases, disorders, and conditions relating to aberrant function of a sodium channel |
US11492345B2 (en) | 2017-02-13 | 2022-11-08 | Praxis Precision Medicines, Inc. | Compounds and their methods of use |
WO2018163077A1 (fr) | 2017-03-08 | 2018-09-13 | Lupin Limited | Composés indanyle utilisés en tant que modulateurs de canaux sodiques dépendant de la tension |
WO2018187480A1 (fr) | 2017-04-04 | 2018-10-11 | Praxis Precision Medicines, Inc. | Composés et leurs méthodes d'utilisation |
US11278535B2 (en) | 2017-08-15 | 2022-03-22 | Praxis Precision Medicines, Inc. | Compounds and their methods of use |
TWI831786B (zh) | 2018-05-30 | 2024-02-11 | 美商普雷西斯精密藥品公司 | 離子通道調節劑 |
US11773099B2 (en) | 2019-05-28 | 2023-10-03 | Praxis Precision Medicines, Inc. | Compounds and their methods of use |
US11505554B2 (en) | 2019-05-31 | 2022-11-22 | Praxis Precision Medicines, Inc. | Substituted pyridines as ion channel modulators |
US11279700B2 (en) | 2019-05-31 | 2022-03-22 | Praxis Precision Medicines, Inc. | Ion channel modulators |
US11767325B2 (en) | 2019-11-26 | 2023-09-26 | Praxis Precision Medicines, Inc. | Substituted [1,2,4]triazolo[4,3-a]pyrazines as ion channel modulators |
CN116813525B (zh) * | 2023-08-28 | 2023-11-21 | 苏州爱玛特生物科技有限公司 | 一种多乙酰基取代的氧化吲哚类化合物的合成方法 |
Citations (10)
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WO2001049288A1 (fr) * | 2000-01-06 | 2001-07-12 | Merck Frosst Canada & Co. | Nouveaux composes et compositions utilises comme inhibiteurs de protease |
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US20020042427A1 (en) * | 2000-02-28 | 2002-04-11 | Tang Peng Cho | 3-(pyrolyllactone)-2-indolinone compounds as kinase inhibitors |
US6462032B1 (en) * | 1999-05-04 | 2002-10-08 | Wyeth | Cyclic regimens utilizing indoline derivatives |
WO2006113864A2 (fr) * | 2005-04-20 | 2006-10-26 | Xenon Pharmaceuticals Inc. | Composes d'oxindole et leurs utilisations comme agents therapeutiques |
EP1820795A1 (fr) * | 2004-12-07 | 2007-08-22 | Toyama Chemical Co., Ltd. | Nouveau derive de l'acide anthranilique ou sel de celui-ci |
EP1860098A1 (fr) * | 2005-03-16 | 2007-11-28 | Toyama Chemical Co., Ltd. | Nouveau dérivé de l'acide anthranilique ou sel de celui-ci |
WO2008138184A1 (fr) * | 2007-05-14 | 2008-11-20 | Shanghai Hengrui Pharmaceutical Co.Ltd. | Dérivés de pyrrolo-azacycles, leur procédé de fabrication et leur utilisation en tant qu'inhibiteurs de protéine kinases |
JP2009023986A (ja) * | 2006-11-08 | 2009-02-05 | Pharma Ip | 抗癌剤としてのビアリール誘導体 |
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2010
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Patent Citations (10)
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US6355648B1 (en) * | 1999-05-04 | 2002-03-12 | American Home Products Corporation | Thio-oxindole derivatives |
US6462032B1 (en) * | 1999-05-04 | 2002-10-08 | Wyeth | Cyclic regimens utilizing indoline derivatives |
WO2001049288A1 (fr) * | 2000-01-06 | 2001-07-12 | Merck Frosst Canada & Co. | Nouveaux composes et compositions utilises comme inhibiteurs de protease |
US20020042427A1 (en) * | 2000-02-28 | 2002-04-11 | Tang Peng Cho | 3-(pyrolyllactone)-2-indolinone compounds as kinase inhibitors |
EP1820795A1 (fr) * | 2004-12-07 | 2007-08-22 | Toyama Chemical Co., Ltd. | Nouveau derive de l'acide anthranilique ou sel de celui-ci |
EP1860098A1 (fr) * | 2005-03-16 | 2007-11-28 | Toyama Chemical Co., Ltd. | Nouveau dérivé de l'acide anthranilique ou sel de celui-ci |
WO2006113864A2 (fr) * | 2005-04-20 | 2006-10-26 | Xenon Pharmaceuticals Inc. | Composes d'oxindole et leurs utilisations comme agents therapeutiques |
JP2009023986A (ja) * | 2006-11-08 | 2009-02-05 | Pharma Ip | 抗癌剤としてのビアリール誘導体 |
WO2008138184A1 (fr) * | 2007-05-14 | 2008-11-20 | Shanghai Hengrui Pharmaceutical Co.Ltd. | Dérivés de pyrrolo-azacycles, leur procédé de fabrication et leur utilisation en tant qu'inhibiteurs de protéine kinases |
WO2009045381A1 (fr) * | 2007-10-04 | 2009-04-09 | Merck & Co., Inc. | Dérivés d'oxindoline n-substituée comme bloqueurs des canaux calciques |
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Also Published As
Publication number | Publication date |
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WO2011056985A2 (fr) | 2011-05-12 |
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