JP2016513130A5 - - Google Patents

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Publication number
JP2016513130A5
JP2016513130A5 JP2015559501A JP2015559501A JP2016513130A5 JP 2016513130 A5 JP2016513130 A5 JP 2016513130A5 JP 2015559501 A JP2015559501 A JP 2015559501A JP 2015559501 A JP2015559501 A JP 2015559501A JP 2016513130 A5 JP2016513130 A5 JP 2016513130A5
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Japan
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formula
compound
saturated
alkyl
group
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JP2015559501A
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Japanese (ja)
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JP6338601B2 (ja
JP2016513130A (ja
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Priority claimed from PCT/EP2014/053877 external-priority patent/WO2014131855A1/en
Publication of JP2016513130A publication Critical patent/JP2016513130A/ja
Publication of JP2016513130A5 publication Critical patent/JP2016513130A5/ja
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Publication of JP6338601B2 publication Critical patent/JP6338601B2/ja
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JP2015559501A 2013-03-01 2014-02-27 ホスホジエステラーゼとヒストンデアセチラーゼの二重阻害剤としての新規な化合物 Expired - Fee Related JP6338601B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP13382065.4 2013-03-01
EP13382065 2013-03-01
PCT/EP2014/053877 WO2014131855A1 (en) 2013-03-01 2014-02-27 Novel compounds as dual inhibitors of phosphodiesterases and histone deacetylases

Publications (3)

Publication Number Publication Date
JP2016513130A JP2016513130A (ja) 2016-05-12
JP2016513130A5 true JP2016513130A5 (enExample) 2017-03-30
JP6338601B2 JP6338601B2 (ja) 2018-06-06

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ID=47901928

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015559501A Expired - Fee Related JP6338601B2 (ja) 2013-03-01 2014-02-27 ホスホジエステラーゼとヒストンデアセチラーゼの二重阻害剤としての新規な化合物

Country Status (7)

Country Link
US (1) US9573956B2 (enExample)
EP (1) EP2961741B1 (enExample)
JP (1) JP6338601B2 (enExample)
CA (1) CA2908482A1 (enExample)
DK (1) DK2961741T3 (enExample)
ES (1) ES2635016T3 (enExample)
WO (1) WO2014131855A1 (enExample)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9505767B2 (en) * 2013-09-05 2016-11-29 Genentech, Inc. Pyrazolo[1,5-A]pyrimidin-7(4H)-onehistone demethylase inhibitors
EP3085700B1 (en) * 2013-12-20 2018-10-31 Institute of Pharmacology and Toxicology Academy of Military Medical Sciences P.L.A. China Novel piperidine carboxamide compound, preparation method, and usage thereof
CA2987978C (en) * 2014-06-16 2022-08-16 Fundacion Para La Investigacion Medica Aplicada Novel compounds as dual inhibitors of histone methyltransferases and dna methyltransferases
JP2017523204A (ja) * 2014-08-04 2017-08-17 ファンダシオン パラ ラ インベスティガシオン メディカ アプリカダFundacion Para La Investigasion Medica Aplicada 認知向上のために用いる新規化合物
WO2016120432A1 (en) * 2015-01-30 2016-08-04 Fundación Para La Investigación Médica Aplicada Compounds and methods for anticoagulation therapy
CN104610166B (zh) * 2015-03-10 2017-06-13 山东大学 嘧啶苄基异羟肟酸类组蛋白去乙酰化酶抑制剂及制备方法和应用
HK1249104A1 (zh) 2015-03-13 2018-10-26 Forma Therapeutics, Inc. 作为HDAC8抑制剂的α-肉桂酰胺化合物和组合物
KR102457316B1 (ko) * 2015-06-26 2022-10-20 총킹 디캉 에릴 파마 씨오. 엘티디. 새로운 5형포스포디에스테라아제 억제제 및 그 용도
CN110337437B (zh) 2016-12-28 2023-02-03 达特神经科学有限公司 作为pde2抑制剂的取代的吡唑并嘧啶酮化合物
CN107163052B (zh) * 2017-04-18 2020-08-11 华南农业大学 一种针对多种pde-5抑制剂药物的免疫检测方法
WO2019018562A1 (en) 2017-07-19 2019-01-24 Ideaya Biosciences, Inc. AMIDO COMPOUND AS MODULATORS OF AHR
CN108912029B (zh) * 2017-08-25 2021-10-01 广东东阳光药业有限公司 含氮杂环酰胺衍生物及其用途
KR102794907B1 (ko) 2017-11-27 2025-04-14 다트 뉴로사이언스, 엘엘씨 Pde1 억제제로서의 치환된 푸라노피리미딘 화합물
CN110054625B (zh) * 2018-01-18 2022-01-07 山东大学 N-酰基苯磺酰胺异羟肟酸类Bcl-2、HDAC双靶点抑制剂及制备方法和应用
CN108558890A (zh) * 2018-06-28 2018-09-21 重庆康刻尔制药有限公司 一种西地那非中间体合成方法
CN109824516B (zh) * 2019-03-14 2021-07-23 泰州精英化成医药科技有限公司 一种反式-4-羟基环已烷甲酸叔丁酯的制备方法
CN109810108B (zh) * 2019-03-20 2021-08-06 华东理工大学 2,8-二氮杂-螺-[4,5]-癸烷类嘧啶-异羟肟酸化合物及其用途
US11787812B2 (en) 2020-12-11 2023-10-17 Ildong Pharmaceutical Co., Ltd. Substituted pyrazolo[4,3-d]pyrimidines and imidazo[5,1 -f][1,2,4]triazines as androgen receptor and phosphodiesterase dual inhibitors
KR20240124952A (ko) 2021-12-22 2024-08-19 어거스틴 테라퓨틱스 Hdac6 억제제로서의 화합물 및 이의 용도
CN115417877B (zh) * 2022-09-20 2024-05-14 杭州师范大学 组蛋白去乙酰化酶抑制剂及其制备和在制备抗癌症药物上的应用
CN116375714A (zh) * 2023-03-24 2023-07-04 苏州满元生物科技有限公司 卡巴地那非类药物关键中间体的制备方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2003210447B2 (en) * 2002-01-04 2008-02-07 Henry Ford Health System Nitric oxide donors for treatment of disease and injury
CN1548438A (zh) * 2003-05-16 2004-11-24 烟台开发区北方药物研究所 2-取代苯基-6,8-二烃基-3H-咪唑[1,5α][1,3,5]三嗪-4-酮衍生物,其制备方法及其药物用途
DE602005017135D1 (de) * 2004-03-05 2009-11-26 Nycomed Gmbh Neue verwendung von pde5-hemmern
CA2661483A1 (en) * 2006-08-24 2008-02-28 Surface Logix, Inc. Pharmacokinetically improved 2-phenyl-substituted imidazotriazinone derivatives and their use
EP2061772A4 (en) * 2006-09-11 2011-06-29 Curis Inc MULTIFUNCTIONAL SMALL MOLECULES AS PROLIFERATION-ACTIVE ACTIVE SUBSTANCES
JP2010527928A (ja) * 2007-05-18 2010-08-19 ヴィヴァス・インコーポレイテッド ホスホジエステラーゼ−5阻害剤を含む新規の組み合わせおよびそれらの使用
NZ603725A (en) * 2010-08-12 2015-04-24 Boehringer Ingelheim Int 6-cycloalkyl-1,5-dihydro-pyrazolo [3,4-d] pyrimidin-4-one derivatives and their use as pde9a inhibitors
EP2535049A1 (en) * 2011-06-17 2012-12-19 Proyecto de Biomedicina Cima, S.L. Tadalafil for the treatment of dementia

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