EA033198B1 - Оксадиазольные производные, пригодные в качестве ингибиторов hdac - Google Patents

Оксадиазольные производные, пригодные в качестве ингибиторов hdac

Info

Publication number
EA033198B1
EA033198B1 EA201890338A EA201890338A EA033198B1 EA 033198 B1 EA033198 B1 EA 033198B1 EA 201890338 A EA201890338 A EA 201890338A EA 201890338 A EA201890338 A EA 201890338A EA 033198 B1 EA033198 B1 EA 033198B1
Authority
EA
Eurasian Patent Office
Prior art keywords
hdac inhibitors
oxadiazole derivatives
derivatives useful
diseases
compound
Prior art date
Application number
EA201890338A
Other languages
English (en)
Other versions
EA201890338A1 (ru
Inventor
Акира Каиеда
Масаси Тоефуку
Масаки Даини
Хироси Нара
Масато Йосикава
Наоки Исии
Коусуке Хидака
Original Assignee
Такеда Фармасьютикал Компани Лимитед
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Такеда Фармасьютикал Компани Лимитед filed Critical Такеда Фармасьютикал Компани Лимитед
Publication of EA201890338A1 publication Critical patent/EA201890338A1/ru
Publication of EA033198B1 publication Critical patent/EA033198B1/ru

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic 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
    • C07D491/02Heterocyclic 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
    • C07D491/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic 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
    • C07D491/02Heterocyclic 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
    • C07D491/10Spiro-condensed systems
    • C07D491/107Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/08Bridged systems

Abstract

Изобретение относится к гетероциклическому соединению, обладающему ингибирующим HDAC действием и являющемуся пригодным для лечения аутоиммунных заболеваний и/или воспалительных заболеваний, реакции "трансплантат против хозяина", рака, заболеваний центральной нервной системы, включая нейродегенеративные заболевания, болезни Шарко-Мари-Тута и подобных, и фармацевтической композиции, содержащей данное соединение. Настоящее изобретение относится к соединению, представленному формулой (I)где каждый символ представляет собой, как определено в описании, или его соли.
EA201890338A 2015-07-17 2016-07-15 Оксадиазольные производные, пригодные в качестве ингибиторов hdac EA033198B1 (ru)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2015143354 2015-07-17
JP2016029020 2016-02-18
PCT/JP2016/071655 WO2017014321A1 (en) 2015-07-17 2016-07-15 Oxadiazole derivatives useful as hdac inhibitors

Publications (2)

Publication Number Publication Date
EA201890338A1 EA201890338A1 (ru) 2018-07-31
EA033198B1 true EA033198B1 (ru) 2019-09-30

Family

ID=56853775

Family Applications (1)

Application Number Title Priority Date Filing Date
EA201890338A EA033198B1 (ru) 2015-07-17 2016-07-15 Оксадиазольные производные, пригодные в качестве ингибиторов hdac

Country Status (11)

Country Link
US (1) US10308643B2 (ru)
EP (1) EP3325475B1 (ru)
JP (1) JP6671456B2 (ru)
CN (1) CN108026088B (ru)
AU (1) AU2016297362B2 (ru)
BR (1) BR112018000906A2 (ru)
CA (1) CA2992700A1 (ru)
EA (1) EA033198B1 (ru)
ES (1) ES2793014T3 (ru)
TW (1) TW201713649A (ru)
WO (1) WO2017014321A1 (ru)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3187497A4 (en) 2014-08-26 2018-02-07 Takeda Pharmaceutical Company Limited Heterocyclic compound
EA033198B1 (ru) 2015-07-17 2019-09-30 Такеда Фармасьютикал Компани Лимитед Оксадиазольные производные, пригодные в качестве ингибиторов hdac
JPWO2017014170A1 (ja) 2015-07-17 2018-04-26 武田薬品工業株式会社 複素環化合物
JPWO2017033946A1 (ja) 2015-08-25 2018-06-07 武田薬品工業株式会社 複素環化合物
WO2017110863A1 (ja) * 2015-12-25 2017-06-29 住友化学株式会社 オキサジアゾール化合物及びその用途
WO2018165520A1 (en) 2017-03-10 2018-09-13 Vps-3, Inc. Metalloenzyme inhibitor compounds
CN111032651A (zh) * 2017-07-31 2020-04-17 武田药品工业株式会社 杂环化合物
WO2019148005A1 (en) * 2018-01-26 2019-08-01 Nurix Therapeutics, Inc. Inhibitors of cbl-b and methods of use thereof
BR112020016234A2 (pt) * 2018-02-12 2020-12-15 Bayer Aktiengesellschaft Oxadiazóis fungicidas
KR102316234B1 (ko) 2018-07-26 2021-10-22 주식회사 종근당 히스톤 탈아세틸화효소 6 억제제로서의 1,3,4-옥사다이아졸 유도체 화합물 및 이를 포함하는 약제학적 조성물
CN113412259A (zh) 2018-10-15 2021-09-17 紐力克斯治疗公司 通过泛素蛋白酶体途径降解btk的双官能化合物
CN111057069B (zh) * 2018-10-16 2024-01-26 武汉光谷通用名药物研究院有限公司 一种环状化合物、其应用及组合物
CN109293567A (zh) * 2018-11-23 2019-02-01 上海睿腾医药科技有限公司 一种5-溴-2-甲基烟酸乙酯的合成方法
WO2020158762A1 (ja) 2019-01-30 2020-08-06 武田薬品工業株式会社 複素環化合物
JP2022526025A (ja) 2019-04-09 2022-05-20 ニューリックス セラピューティクス,インコーポレイテッド Cbl-b阻害のための3-置換ピペリジン化合物、並びに癌ワクチン及び/又は腫瘍溶解性ウイルスと組み合わせたCbl-b阻害剤の使用
WO2020236654A1 (en) 2019-05-17 2020-11-26 Nurix Therapeutics, Inc. Cyano cyclobutyl compounds for cbl-b inhibition and uses thereof
KR20220026581A (ko) 2019-06-26 2022-03-04 누릭스 테라퓨틱스 인코포레이티드 Cbl-b 억제를 위한 치환된 벤질-트리아졸 화합물, 및 이의 추가의 용도
CA3148769A1 (en) * 2019-07-30 2021-02-04 Nurix Therapeutics, Inc. Urea, amide, and substituted heteroaryl compounds for cbl-b inhibition
CN110498759A (zh) * 2019-09-12 2019-11-26 天津瑞岭化工有限公司 异吲哚啉酮类化合物的合成方法
TW202126643A (zh) 2019-09-27 2021-07-16 日商武田藥品工業股份有限公司 雜環化合物
EP4046688A4 (en) * 2019-10-18 2023-09-27 Takeda Pharmaceutical Company Limited HETEROCYCLIC COMPOUND
MX2022006672A (es) 2019-12-04 2022-08-08 Nurix Therapeutics Inc Compuestos bifuncionales para la degradacion de btk a traves de la via de proteosomas de ubiquitina.
EP4192830A1 (en) * 2020-08-07 2023-06-14 Italfarmaco SpA 2-(4-((5-(benzo[b]thiophen-3-yl)-1h-tetrazol-1-yl)methyl)phenyl)-5-(difluoromethyl)-1,3,4-oxadiazole derivatives and similar compounds as selective inhibitors of histone deacetylase 6 (hdac6) for use in treating e.g. peripheral neuropathy
CN111961020A (zh) * 2020-08-31 2020-11-20 南通大学 一种四氢吡喃羧酸衍生物及其合成方法
WO2022129196A1 (en) 2020-12-18 2022-06-23 Bayer Aktiengesellschaft Heterobicycle substituted 1,2,4-oxadiazoles as fungicides
WO2023081328A1 (en) * 2021-11-04 2023-05-11 Valo Health, Inc. Histone deacetylase 6 inhibitor compounds and uses thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013066831A1 (en) * 2011-10-31 2013-05-10 Glaxosmithkline Llc Compounds and methods
WO2013080120A1 (en) * 2011-11-28 2013-06-06 Novartis Ag Novel trifluoromethyl-oxadiazole derivatives and their use in the treatment of disease

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7868008B2 (en) 2005-08-12 2011-01-11 Astrazeneca Ab Substituted isoindolones and their use as metabotropic glutamate receptor potentiators
CA2626897A1 (en) 2005-11-03 2007-05-18 Joshua Close Histone deacetylase inhibitors with aryl-pyrazolyl motifs
TWI417100B (zh) 2007-06-07 2013-12-01 Astrazeneca Ab 二唑衍生物及其作為代謝型麩胺酸受體增效劑-842之用途
US8389553B2 (en) 2007-06-27 2013-03-05 Merck Sharp & Dohme Corp. 4-carboxybenzylamino derivatives as histone deacetylase inhibitors
TW201103904A (en) 2009-06-11 2011-02-01 Hoffmann La Roche Janus kinase inhibitor compounds and methods
JP2013517281A (ja) 2010-01-13 2013-05-16 テンペロ、ファーマシューティカルズ、インコーポレイテッド 化合物及び方法
AU2011205283B2 (en) 2010-01-13 2014-07-10 Tempero Pharmaceuticals, Inc. Compounds and methods
WO2012149540A1 (en) 2011-04-28 2012-11-01 The Broad Institute Inc Inhibitors of histone deacetylase
WO2013006408A1 (en) 2011-07-01 2013-01-10 Tempero Pharmaceuticals, Inc. Compounds and methods
US9056843B2 (en) 2011-07-08 2015-06-16 Novartis Ag Trifluoromethyl-oxadiazole derivatives and their use in the treatment of disease
WO2013009830A1 (en) 2011-07-13 2013-01-17 Tempero Pharmaceuticals, Inc. Methods of treatment
WO2013009827A1 (en) 2011-07-13 2013-01-17 Tempero Pharmaceuticals, Inc. Methods of treatment
WO2013009810A1 (en) 2011-07-13 2013-01-17 Tempero Pharmaceuticals, Inc. Methods of treatment
US9512083B2 (en) 2011-07-20 2016-12-06 The General Hospital Corporation Histone deacetylase 6 selective inhibitors for the treatment of bone disease
KR101812237B1 (ko) 2011-09-27 2017-12-27 코오롱인더스트리 주식회사 폴리에틸렌테레프탈레이트 연신사의 제조방법, 폴리에틸렌테레프탈레이트 연신사 및 타이어 코오드
WO2013066838A1 (en) 2011-10-31 2013-05-10 Glaxosmithkline Llc Compounds and methods
WO2013066833A1 (en) 2011-10-31 2013-05-10 Glaxosmithkline Llc Compounds and methods to inhibit histone deacetylase (hdac) enzymes
WO2013066839A2 (en) 2011-10-31 2013-05-10 Glaxosmithkline Llc Compounds and methods
WO2013066835A2 (en) 2011-10-31 2013-05-10 Glaxosmithkline Llc Compounds and methods
EP3187497A4 (en) 2014-08-26 2018-02-07 Takeda Pharmaceutical Company Limited Heterocyclic compound
WO2016039398A1 (ja) 2014-09-09 2016-03-17 国立大学法人大阪大学 含窒素複素環誘導体、神経保護剤及び癌治療用医薬組成物
EA033198B1 (ru) 2015-07-17 2019-09-30 Такеда Фармасьютикал Компани Лимитед Оксадиазольные производные, пригодные в качестве ингибиторов hdac
JPWO2017014170A1 (ja) 2015-07-17 2018-04-26 武田薬品工業株式会社 複素環化合物
JPWO2017033946A1 (ja) 2015-08-25 2018-06-07 武田薬品工業株式会社 複素環化合物
WO2017110863A1 (ja) 2015-12-25 2017-06-29 住友化学株式会社 オキサジアゾール化合物及びその用途
WO2017222950A1 (en) 2016-06-23 2017-12-28 Merck Sharp & Dohme Corp. 3-heterocyclyl substituted 5-trifluoromethyl oxadiazoles as histone deacetylase 6 (hdac6) inhibitors
US11066396B2 (en) 2016-06-23 2021-07-20 Merck Sharp & Dohme Corp. 3-aryl- heteroaryl substituted 5-trifluoromethyl oxadiazoles as histonedeacetylase 6 (HDAC6) inhibitors
WO2017222952A1 (en) 2016-06-23 2017-12-28 Merck Sharp & Dohme Corp. 3- heteroaryl substituted 5-trifluoromethyl oxadiazoles as histone deacetylase 6 (hdac6) inhibitors

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013066831A1 (en) * 2011-10-31 2013-05-10 Glaxosmithkline Llc Compounds and methods
WO2013080120A1 (en) * 2011-11-28 2013-06-06 Novartis Ag Novel trifluoromethyl-oxadiazole derivatives and their use in the treatment of disease

Also Published As

Publication number Publication date
JP6671456B2 (ja) 2020-03-25
WO2017014321A1 (en) 2017-01-26
CA2992700A1 (en) 2017-01-26
AU2016297362A1 (en) 2018-02-22
ES2793014T3 (es) 2020-11-12
CN108026088B (zh) 2021-02-12
EP3325475B1 (en) 2020-03-18
TW201713649A (zh) 2017-04-16
US10308643B2 (en) 2019-06-04
EP3325475A1 (en) 2018-05-30
CN108026088A (zh) 2018-05-11
AU2016297362B2 (en) 2020-04-16
JP2018524378A (ja) 2018-08-30
EA201890338A1 (ru) 2018-07-31
US20170015655A1 (en) 2017-01-19
BR112018000906A2 (pt) 2018-09-11

Similar Documents

Publication Publication Date Title
EA033198B1 (ru) Оксадиазольные производные, пригодные в качестве ингибиторов hdac
MX2020011528A (es) Inhibidores heterociclicos sustituidos de ptpn11.
PH12017501817A1 (en) Heterocyclic compounds as lsd1 inhibitors
MX2016011035A (es) Compuestos arilo, heteroarilo y heterociclicos para el tratamiento de trastornos mediados por complemento.
PH12016502382A1 (en) Substituted indazole compounds as irak4 inhibitors
EA201990833A1 (ru) Соединение пиридина
PH12016501972B1 (en) Bicyclic-fused heteroaryl or aryl compounds and their use as irak4 inhibitors
TN2017000009A1 (en) Spirocycloheptanes as inhibitors of rock.
EA201692079A1 (ru) Ингибиторы лизин-специфической деметилазы-1
MX2018010374A (es) Inhibidores del enlace proteína-proteína de wdr5.
MX2017006266A (es) Compuestos de heteroarilo como inhibidores de cinasas asociadas al receptor de interleucina 1(irak) y sus usos.
EA201690952A1 (ru) Пиразол для лечения аутоиммунных расстройств
EA201790170A1 (ru) Терапевтические соединения-ингибиторы
PH12016501702B1 (en) Pyrazole amide derivative
PH12017501160A1 (en) 5-[(piperazin-1-yl)-3-oxo-propyl]-imidazolidine-2,4-dione derivatives as adamts inhibitors for the treatment of osteoarthritis
MY197698A (en) Oxysterols and methods of use thereof
EA033236B1 (ru) Новые производные пиразола в качестве ингибиторов nik
PH12016501462A1 (en) Neprilysin inhibitors
PH12015502611A1 (en) Heterocyclic compounds as hedgehog signaling pathway inhibitors
MX2018001992A (es) Compuestos triciclicos heterociclicos como inhibidores de fosfoinositol 3-quinasa.
WO2016004404A3 (en) Gls1 inhibitors for treating disease
PH12017500007A1 (en) Quinolizinone derivatives as p13k inhibitors
EA201992306A1 (ru) Ингибиторы ip6k
GEP20207130B (en) Imidazolone compounds as human neutrophil elastase inhibitors
EA201792425A1 (ru) Трициклические соединения и их применение в качестве ингибиторов фосфодиэстераз

Legal Events

Date Code Title Description
MM4A Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s)

Designated state(s): AM AZ BY KZ KG TJ TM