JP2017515848A5 - - Google Patents

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Publication number
JP2017515848A5
JP2017515848A5 JP2016567524A JP2016567524A JP2017515848A5 JP 2017515848 A5 JP2017515848 A5 JP 2017515848A5 JP 2016567524 A JP2016567524 A JP 2016567524A JP 2016567524 A JP2016567524 A JP 2016567524A JP 2017515848 A5 JP2017515848 A5 JP 2017515848A5
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JP
Japan
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alkyl
aryl
heteroaryl
cycloalkyl
optionally substituted
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JP2016567524A
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Japanese (ja)
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JP6803235B2 (ja
JP2017515848A (ja
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Priority claimed from PCT/US2015/030842 external-priority patent/WO2015175813A1/en
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Publication of JP2017515848A5 publication Critical patent/JP2017515848A5/ja
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JP2016567524A 2014-05-14 2015-05-14 タンパク質脱アセチル化酵素阻害剤およびタンパク質脱アセチル化酵素−タンパク質キナーゼ二重阻害剤としての複素環式ヒドロキサム酸ならびにその使用方法 Expired - Fee Related JP6803235B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201461996702P 2014-05-14 2014-05-14
US201461996691P 2014-05-14 2014-05-14
US61/996,702 2014-05-14
US61/996,691 2014-05-14
PCT/US2015/030842 WO2015175813A1 (en) 2014-05-14 2015-05-14 Heterocyclic hydroxamic acids as protein deacetylase inhibitors and dual protein deacetylase-protein kinase inhibitors and methods of use thereof

Publications (3)

Publication Number Publication Date
JP2017515848A JP2017515848A (ja) 2017-06-15
JP2017515848A5 true JP2017515848A5 (enExample) 2019-02-14
JP6803235B2 JP6803235B2 (ja) 2020-12-23

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ID=54480695

Family Applications (1)

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JP2016567524A Expired - Fee Related JP6803235B2 (ja) 2014-05-14 2015-05-14 タンパク質脱アセチル化酵素阻害剤およびタンパク質脱アセチル化酵素−タンパク質キナーゼ二重阻害剤としての複素環式ヒドロキサム酸ならびにその使用方法

Country Status (11)

Country Link
US (3) USRE47690E1 (enExample)
EP (1) EP3142652B1 (enExample)
JP (1) JP6803235B2 (enExample)
KR (1) KR20170003688A (enExample)
CN (1) CN106456580B (enExample)
BR (1) BR112016026518A2 (enExample)
CA (1) CA2949163A1 (enExample)
MX (1) MX2016014911A (enExample)
RU (1) RU2016148863A (enExample)
TW (1) TW201625620A (enExample)
WO (1) WO2015175813A1 (enExample)

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US9550770B2 (en) 2013-08-23 2017-01-24 Neupharma, Inc. Substituted quinazolines for inhibiting kinase activity
WO2015175813A1 (en) 2014-05-14 2015-11-19 The Regents Of The University Of Colorado, A Body Corporate Heterocyclic hydroxamic acids as protein deacetylase inhibitors and dual protein deacetylase-protein kinase inhibitors and methods of use thereof
WO2016095881A1 (en) * 2014-12-15 2016-06-23 Univerzita Palackeho V Olomouci Substituted 6-anilino-9-heterocyclylpurine derivatives for inhibition of plant stress
CA2976227C (en) * 2015-02-17 2023-10-24 Neupharma, Inc. Quinazoline derivatives and their use in treatment of cancer
CN106831780A (zh) * 2015-12-03 2017-06-13 南开大学 具有cdk4/6和hdac抑制活性的新型杂环衍生物
EP3497087B1 (en) 2016-08-15 2021-11-10 Neupharma, Inc. Pyrrolo[1,2-c]pyrimidine, imidazo[1,5-c]pyrimidine, quinazoline, purine and imidazo[1,5-a][1,3,5]triazine derivatives as tyrosine kinase inhibitors for the treatment of cancer
US10781215B2 (en) * 2016-10-28 2020-09-22 Bristol-Myers Squibb Company Heterobicyclic compounds useful as modulators of IL-12, IL-23 and/or IFNα responses
IT201700041723A1 (it) * 2017-04-14 2018-10-14 Italfarmaco Spa Nuovi inibitori selettivi di HDAC6
CN107513064B (zh) * 2017-09-27 2019-07-09 南昌大学 一种嘌呤异羟肟酸衍生物及其制备方法和应用
JOP20180094A1 (ar) 2017-10-18 2019-04-18 Hk Inno N Corp مركب حلقي غير متجانس كمثبط بروتين كيناز
KR102195348B1 (ko) 2018-11-15 2020-12-24 에이치케이이노엔 주식회사 단백질 키나제 억제제로서의 신규 화합물 및 이를 포함하는 약제학적 조성물
KR102847312B1 (ko) * 2021-12-30 2025-08-19 한국화학연구원 피라졸로피리미딘 유도체 및 이를 유효성분으로 함유하는 항암용 약학적 조성물
WO2023128708A1 (ko) * 2021-12-30 2023-07-06 한국화학연구원 피라졸로피리미딘 유도체 및 이를 유효성분으로 함유하는 항암용 약학적 조성물
CN114685507B (zh) * 2022-04-06 2024-01-12 山东大学 嘌呤胺衍生物类cdk2抑制剂及其制备方法和应用
KR102792443B1 (ko) * 2022-05-13 2025-04-08 서울대학교산학협력단 Cdk를 저해하는 신규 피롤로피리미디논 카복사미드 화합물, 이의 입체이성질체 또는 이의 약학적으로 허용가능한 염 및 이를 유효성분으로 함유하는 암 치료용 약학적 조성물

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WO1998039315A1 (en) 1997-03-04 1998-09-11 Monsanto Company Aromatic sulfonyl alpha-cycloamino hydroxamic acid compounds
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KR20140118575A (ko) 2013-03-29 2014-10-08 한미약품 주식회사 신규한 하이드록사메이트 유도체
WO2015175813A1 (en) 2014-05-14 2015-11-19 The Regents Of The University Of Colorado, A Body Corporate Heterocyclic hydroxamic acids as protein deacetylase inhibitors and dual protein deacetylase-protein kinase inhibitors and methods of use thereof

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