AU2011223969B2 - Inhibitors of catechol O-methyl transferase and their use in the treatment of psychotic disorders - Google Patents
Inhibitors of catechol O-methyl transferase and their use in the treatment of psychotic disorders Download PDFInfo
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- AU2011223969B2 AU2011223969B2 AU2011223969A AU2011223969A AU2011223969B2 AU 2011223969 B2 AU2011223969 B2 AU 2011223969B2 AU 2011223969 A AU2011223969 A AU 2011223969A AU 2011223969 A AU2011223969 A AU 2011223969A AU 2011223969 B2 AU2011223969 B2 AU 2011223969B2
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- aryl
- heterocyclyl
- hydroxy
- pyridin
- alkyl
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- C07D213/63—One oxygen atom
- C07D213/68—One oxygen atom attached in position 4
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- 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
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Biomedical Technology (AREA)
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- Chemical Kinetics & Catalysis (AREA)
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- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US31041010P | 2010-03-04 | 2010-03-04 | |
| US61/310,410 | 2010-03-04 | ||
| PCT/US2011/026399 WO2011109254A1 (en) | 2010-03-04 | 2011-02-28 | Inhibitors of catechol o-methyl transferase and their use in the treatment of psychotic disorders |
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| AU2011223969A1 AU2011223969A1 (en) | 2012-08-16 |
| AU2011223969B2 true AU2011223969B2 (en) | 2015-06-11 |
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| EP (1) | EP2542076B1 (enExample) |
| JP (1) | JP5995728B2 (enExample) |
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| CA (1) | CA2789471C (enExample) |
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| MX (1) | MX2012010187A (enExample) |
| RU (1) | RU2586974C2 (enExample) |
| WO (1) | WO2011109254A1 (enExample) |
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|---|---|---|---|---|
| AU2011223969B2 (en) * | 2010-03-04 | 2015-06-11 | Merck Sharp & Dohme Llc | Inhibitors of catechol O-methyl transferase and their use in the treatment of psychotic disorders |
| GB201111704D0 (en) | 2011-07-07 | 2011-08-24 | Takeda Pharmaceutical | Novel compounds |
| GB201111705D0 (en) | 2011-07-07 | 2011-08-24 | Takeda Pharmaceutical | Compounds and their use |
| JO3115B1 (ar) | 2011-08-22 | 2017-09-20 | Takeda Pharmaceuticals Co | مركبات بيريدازينون واستخدامها كمثبطات daao |
| WO2013073577A1 (ja) | 2011-11-15 | 2013-05-23 | アステラス製薬株式会社 | ジヒドロキシ芳香族へテロ環化合物 |
| TWI638802B (zh) * | 2012-05-24 | 2018-10-21 | 芬蘭商奧利安公司 | 兒茶酚o-甲基轉移酶活性抑制化合物 |
| CN103845317B (zh) * | 2012-11-28 | 2018-05-08 | 北京生命科学研究所 | 恩他卡朋在预防或治疗肥胖等代谢综合征中的应用 |
| GB201222711D0 (en) | 2012-12-17 | 2013-01-30 | Takeda Pharmaceutical | Novel compounds |
| KR101685862B1 (ko) * | 2012-12-27 | 2016-12-20 | 에프. 호프만-라 로슈 아게 | Comt 억제제 |
| US9695149B2 (en) | 2013-03-15 | 2017-07-04 | Janssen Pharmaceutica Nv | 1,2,6-substituted benzimidazoles as flap modulators |
| US9067917B2 (en) | 2013-03-15 | 2015-06-30 | Janssen Pharmaceutica Nv | 1,2,5-substituted benzimidazoles as FLAP modulators |
| CN103588702B (zh) * | 2013-10-26 | 2016-01-06 | 浙江大学 | N-取代苯基吡啶-4-酮衍生物及其制备和应用 |
| WO2015099107A1 (ja) | 2013-12-26 | 2015-07-02 | 塩野義製薬株式会社 | 含窒素6員環誘導体およびそれらを含有する医薬組成物 |
| WO2016123576A1 (en) | 2015-01-30 | 2016-08-04 | Lieber Institute For Brain Development | Comt inhibiting methods and compositions |
| BR112017022654A2 (pt) | 2015-04-24 | 2018-07-10 | Shionogi & Co., Ltd. | derivado heterocíclico de 6 membros e composição farmacêutica compreendendo o mesmo |
| ES2928164T3 (es) | 2015-10-19 | 2022-11-15 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
| HUE060680T2 (hu) | 2015-11-19 | 2023-04-28 | Incyte Corp | Heterociklusos vegyületek mint immunmodulátorok |
| ES2893613T3 (es) | 2015-11-25 | 2022-02-09 | Lieber Inst Inc Dba Lieber Inst For Brain Development | Tetrahidro-8H-pirido[1,2-a]pirazin-8-onas como inhibidores de COMT para el tratamiento de trastornos neurodegenerativos |
| CN105481812B (zh) * | 2015-11-30 | 2020-04-21 | 重庆天奕恒化科技有限公司 | 一种5-苄氧基-4-氧代-4h-吡喃-2-羧酸的制备方法 |
| DK3394033T3 (da) | 2015-12-22 | 2021-01-04 | Incyte Corp | Heterocykliske forbindelser som immunmodulatorer |
| MA44860A (fr) | 2016-05-06 | 2019-03-13 | Incyte Holdings Corp | Composés hétérocycliques utilisés comme immunomodulateurs |
| WO2017205464A1 (en) | 2016-05-26 | 2017-11-30 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| SG11201811414TA (en) | 2016-06-20 | 2019-01-30 | Incyte Corp | Heterocyclic compounds as immunomodulators |
| ES2930092T3 (es) | 2016-07-14 | 2022-12-07 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
| EP3504198B1 (en) | 2016-08-29 | 2023-01-25 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| EP3527568A4 (en) | 2016-10-17 | 2020-03-18 | Shionogi & Co., Ltd | BICYCLIC NITROGEN HETEROCYCLIC DERIVATIVE AND PHARMACEUTICAL COMPOSITION COMPRISING SAME |
| CA3047991A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Bicyclic heteroaromatic compounds as immunomodulators |
| MD3558990T2 (ro) | 2016-12-22 | 2023-02-28 | Incyte Corp | Derivați tetrahidro imidazo[4,5-c]piridină ca inductori de internalizare a PD-L1 |
| MA47123A (fr) | 2016-12-22 | 2021-03-17 | Incyte Corp | Dérivés de benzooxazole en tant qu'mmunomodulateurs |
| EP3558989B1 (en) | 2016-12-22 | 2021-04-14 | Incyte Corporation | Triazolo[1,5-a]pyridine derivatives as immunomodulators |
| US20180179179A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| RU2019130519A (ru) | 2017-03-31 | 2021-04-30 | Фуджифилм Корпорэйшн | 4-пиридоновое соединение или его соль, фармацевтическая композиция и содержащий их состав |
| CN108191746B (zh) * | 2018-02-02 | 2020-06-16 | 暨南大学 | 一种羟基吡啶酮类化合物及其制备方法与应用 |
| US10669271B2 (en) | 2018-03-30 | 2020-06-02 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| LT3790877T (lt) | 2018-05-11 | 2023-05-10 | Incyte Corporation | Tetrahidro-imidazo[4,5-c]piridino dariniai kaip pd-l1 imunomoduliatoriai |
| WO2020097398A1 (en) | 2018-11-07 | 2020-05-14 | Dana-Farber Cancer Institute, Inc. | Benzothiazole derivatives and 7-aza-benzothiazole derivatives as janus kinase 2 inhibitors and uses thereof |
| TW202115059A (zh) | 2019-08-09 | 2021-04-16 | 美商英塞特公司 | Pd—1/pd—l1抑制劑之鹽 |
| EP4037773A1 (en) | 2019-09-30 | 2022-08-10 | Incyte Corporation | Pyrido[3,2-d]pyrimidine compounds as immunomodulators |
| PE20230407A1 (es) | 2019-11-11 | 2023-03-07 | Incyte Corp | Sales y formas cristalinas de un inhibidor de pd-1/pd-l1 |
| CN111170936B (zh) * | 2020-01-19 | 2021-01-01 | 杭州泽德医药科技有限公司 | 3,4-二羟基-n-(1’-苄基-2’-羟乙基)-2-甲基吡啶氯化物及制备和应用 |
| CA3181537A1 (en) | 2020-05-06 | 2021-11-11 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors |
| KR102377058B1 (ko) | 2020-11-04 | 2022-03-22 | 경북대학교 산학협력단 | 니아스텔라 코리엔시스에서 유래한 카테콜 o-메틸 트렌스퍼라제 및 이의 변이체 |
| US11780836B2 (en) | 2020-11-06 | 2023-10-10 | Incyte Corporation | Process of preparing a PD-1/PD-L1 inhibitor |
| WO2022099075A1 (en) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Crystalline form of a pd-1/pd-l1 inhibitor |
| WO2022099071A1 (en) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Process for making a pd-1/pd-l1 inhibitor and salts and crystalline forms thereof |
| WO2022140527A1 (en) | 2020-12-23 | 2022-06-30 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors |
| US20250276955A1 (en) * | 2021-07-19 | 2025-09-04 | Baylor College Of Medicine | Coronavirus main protease inhibitors and methods using same |
| TW202325289A (zh) | 2021-11-09 | 2023-07-01 | 美商雅捷可斯治療公司 | Jak2抑制劑之形式及組合物 |
| TW202334139A (zh) | 2021-11-09 | 2023-09-01 | 美商雅捷可斯治療公司 | 作為jak2抑制劑之6-雜芳氧基苯并咪唑及氮雜苯并咪唑 |
| CN114716366B (zh) * | 2022-04-13 | 2023-12-26 | 浙江大学 | 3-羟基吡啶-4-酮类衍生物及在抑制肾细胞铁死亡中的应用 |
| CN116947812B (zh) * | 2023-06-30 | 2025-09-02 | 南京红太阳医药研究院有限公司 | 一种艾司奥美拉唑镁降解杂质的制备方法 |
| WO2025257687A1 (en) * | 2024-06-11 | 2025-12-18 | Universidade Do Porto | Hydroxypyridinone compounds as inhibitors of catechol-o-methyltransferase |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070232663A1 (en) * | 2006-03-29 | 2007-10-04 | Pirrung Michael C | Small molecule insulin mimetics absent quinones |
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| GB8811055D0 (en) | 1988-05-10 | 1988-06-15 | Ici Plc | Antibiotic compounds |
| US5336482A (en) * | 1991-12-05 | 1994-08-09 | The Du Pont Merck Pharmaceutical Company | Technetium-99m complexes with N-substituted 3-hydroxy-4-pyridinones |
| FR2687674B1 (fr) * | 1992-02-07 | 1995-05-19 | Roussel Uclaf | Nouveaux derives de la pyridone, leur procede de preparation, les nouveaux intermediaires obtenus, leur application a titre de medicaments et les compositions pharmaceutiques les renfermant. |
| JP2001319486A (ja) * | 2000-05-12 | 2001-11-16 | Mitsubishi Electric Corp | 不揮発性半導体記憶装置 |
| SE0004053D0 (sv) * | 2000-11-06 | 2000-11-06 | Astrazeneca Ab | N-type calcium channel antagonists for the treatment of pain |
| DK1441735T3 (da) | 2001-10-26 | 2006-06-12 | Angeletti P Ist Richerche Bio | N-substituerede hydroxypyrimidinon-carboxamid-inhibitorer af HIV-integrase |
| WO2005047268A2 (en) * | 2003-11-10 | 2005-05-26 | X-Ceptor Therapeutics, Inc. | Substituted pyrimidine compositions and methods of use |
| JP2007126716A (ja) * | 2005-11-04 | 2007-05-24 | Miyazaki Tlo:Kk | カドミウムに対する亜鉛の高選択的抽出剤及び亜鉛の回収 |
| JP2009234959A (ja) * | 2008-03-26 | 2009-10-15 | Pias Arise Kk | 3−ヒドロキシ−2−メチル−1−フェニル−4−ピリジノン又はその誘導体からなる美白剤、並びにその美白剤を含有する美白用皮膚外用剤、化粧料 |
| AU2011223969B2 (en) * | 2010-03-04 | 2015-06-11 | Merck Sharp & Dohme Llc | Inhibitors of catechol O-methyl transferase and their use in the treatment of psychotic disorders |
-
2011
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- 2011-02-28 ES ES11751121T patent/ES2862931T3/es active Active
- 2011-02-28 BR BR112012021652A patent/BR112012021652A2/pt not_active IP Right Cessation
- 2011-02-28 WO PCT/US2011/026399 patent/WO2011109254A1/en not_active Ceased
- 2011-02-28 JP JP2012556121A patent/JP5995728B2/ja not_active Expired - Fee Related
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- 2011-02-28 CN CN201180012426.3A patent/CN102869256B/zh not_active Expired - Fee Related
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2015
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| US20070232663A1 (en) * | 2006-03-29 | 2007-10-04 | Pirrung Michael C | Small molecule insulin mimetics absent quinones |
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| US20130084346A1 (en) | 2013-04-04 |
| KR20130044205A (ko) | 2013-05-02 |
| EP2542076A4 (en) | 2015-01-14 |
| EP2542076A1 (en) | 2013-01-09 |
| ES2862931T3 (es) | 2021-10-08 |
| MX2012010187A (es) | 2012-10-03 |
| KR101720824B1 (ko) | 2017-03-28 |
| JP2013521285A (ja) | 2013-06-10 |
| RU2012142194A (ru) | 2014-04-10 |
| CA2789471C (en) | 2018-01-02 |
| RU2586974C2 (ru) | 2016-06-10 |
| JP5995728B2 (ja) | 2016-09-21 |
| CA2789471A1 (en) | 2011-09-09 |
| WO2011109254A1 (en) | 2011-09-09 |
| AU2011223969A1 (en) | 2012-08-16 |
| CN102869256A (zh) | 2013-01-09 |
| US9024032B2 (en) | 2015-05-05 |
| EP2542076B1 (en) | 2021-01-13 |
| US9399651B2 (en) | 2016-07-26 |
| US20150299227A1 (en) | 2015-10-22 |
| BR112012021652A2 (pt) | 2016-06-21 |
| CN102869256B (zh) | 2016-06-22 |
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| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |