UA118369C2 - Сполуки, що інгібують активність lrrk2 кінази - Google Patents

Сполуки, що інгібують активність lrrk2 кінази Download PDF

Info

Publication number
UA118369C2
UA118369C2 UAA201609099A UAA201609099A UA118369C2 UA 118369 C2 UA118369 C2 UA 118369C2 UA A201609099 A UAA201609099 A UA A201609099A UA A201609099 A UAA201609099 A UA A201609099A UA 118369 C2 UA118369 C2 UA 118369C2
Authority
UA
Ukraine
Prior art keywords
mmol
rhms
pharmaceutically acceptable
methyl
compound
Prior art date
Application number
UAA201609099A
Other languages
English (en)
Ukrainian (uk)
Inventor
Сяо Дін
Цянь ЛЮ
Інся Сан
Луїджи П'єро Стазі
Цзехун Вань
Баовей Чжао
Колін Майкл Едж
Original Assignee
Глаксосмітклайн Інтеллектьюел Проперті Девелопмент Лімітед
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 Глаксосмітклайн Інтеллектьюел Проперті Девелопмент Лімітед filed Critical Глаксосмітклайн Інтеллектьюел Проперті Девелопмент Лімітед
Publication of UA118369C2 publication Critical patent/UA118369C2/uk

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Epidemiology (AREA)
  • Psychology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
UAA201609099A 2014-01-29 2015-01-28 Сполуки, що інгібують активність lrrk2 кінази UA118369C2 (uk)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN2014000139 2014-01-29
PCT/CN2015/000055 WO2015113452A1 (en) 2014-01-29 2015-01-28 Compounds

Publications (1)

Publication Number Publication Date
UA118369C2 true UA118369C2 (uk) 2019-01-10

Family

ID=53756224

Family Applications (1)

Application Number Title Priority Date Filing Date
UAA201609099A UA118369C2 (uk) 2014-01-29 2015-01-28 Сполуки, що інгібують активність lrrk2 кінази

Country Status (20)

Country Link
US (2) US10087186B2 (enExample)
EP (1) EP3099695B1 (enExample)
JP (1) JP6422986B2 (enExample)
KR (1) KR20160106622A (enExample)
CN (1) CN105940004B (enExample)
AU (2) AU2015210593A1 (enExample)
CA (1) CA2937431A1 (enExample)
CL (1) CL2016001895A1 (enExample)
CR (1) CR20160348A (enExample)
DO (2) DOP2016000195A (enExample)
EA (1) EA029774B1 (enExample)
ES (1) ES2802174T3 (enExample)
IL (1) IL246579B (enExample)
MA (1) MA39219B1 (enExample)
MX (1) MX367370B (enExample)
PE (1) PE20161443A1 (enExample)
PH (1) PH12016501307A1 (enExample)
SG (1) SG11201605342UA (enExample)
UA (1) UA118369C2 (enExample)
WO (1) WO2015113452A1 (enExample)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10339791B2 (en) 2007-06-12 2019-07-02 Icontrol Networks, Inc. Security network integrated with premise security system
US9815841B2 (en) 2014-01-29 2017-11-14 Glaxosmithkline Intellectual Property Development Limited Compounds
CN105940004B (zh) 2014-01-29 2018-02-02 葛兰素史密斯克莱知识产权发展有限公司 化合物
CN105153131B (zh) * 2015-09-21 2017-10-17 马彦丽 一种在护理上治疗人神经胶质瘤的药物组合物
CN105348270B (zh) * 2015-11-09 2018-01-09 吕显艳 一种防治牙体牙髓感染的药物组合物
US11214565B2 (en) 2015-11-20 2022-01-04 Denali Therapeutics Inc. Compound, compositions, and methods
WO2017106771A1 (en) 2015-12-16 2017-06-22 Southern Research Institute Pyrrolopyrimidine compounds, use as inhibitors of the kinase lrrk2, and methods for preparation thereof
CN105418616B (zh) * 2015-12-26 2018-01-12 山东大学 一种含有 4‑氨基吡唑结构的jak 激酶抑制剂及其制备方法和应用
US11028080B2 (en) 2016-03-11 2021-06-08 Denali Therapeutics Inc. Substituted pyrimidines as LRKK2 inhibitors
JOP20180113B1 (ar) 2016-06-16 2022-03-14 Denali Therapeutics Inc مركبات بيريميدين -2-يل امينو -h1- بيرازول كمثبطات lrrk2 للاستخدام في علاج اضطرابات تنكسية عصبية
CN110446700A (zh) * 2017-01-25 2019-11-12 葛兰素史密斯克莱知识产权发展有限公司 化合物
WO2018155916A2 (ko) * 2017-02-22 2018-08-30 재단법인 대구경북첨단의료산업진흥재단 피롤로-피리미딘 유도체 화합물, 이의 제조방법 및 이를 유효성분으로 함유하는 단백질 키나아제 관련 질환의 예방 또는 치료용 약학적 조성물
CN110662745B (zh) * 2017-03-23 2021-08-03 大邱庆北尖端医疗产业振兴财团 吡咯并吡啶衍生物、其制备方法、和用于预防或治疗蛋白激酶相关疾病的药物组合物
EP3722298B1 (en) * 2017-12-05 2023-08-02 Oscotec Inc. Pyrrolo(pyrazolo)pyrimidine derivative as lrrk2 inhibitor
CN108715834B (zh) * 2018-06-01 2021-09-14 天晴干细胞股份有限公司 一种富含cd41+、cd81+微囊的血小板裂解液制备方法
KR20200020622A (ko) * 2018-08-16 2020-02-26 재단법인 대구경북첨단의료산업진흥재단 치환된 헤테로아릴 유도체, 이의 제조방법 및 이를 유효성분으로 함유하는 단백질 키나아제 관련 질환의 예방 또는 치료용 약학적 조성물
MX2021003516A (es) * 2018-09-25 2021-05-27 Cardurion Pharmaceuticals Llc Compuesto de aminopirimidina.
US12240844B2 (en) 2019-01-18 2025-03-04 Voronoi, Inc. Pyrrolopyridine derivative and use thereof in prevention and treatment of protein kinase-related disease
CZ308800B6 (cs) 2019-02-12 2021-05-26 Univerzita Palackého v Olomouci Heterocyklické dusíkaté deriváty purinu, farmaceutické přípravky obsahující tyto deriváty a jejich použití při neuroprotekci
EP4238975A4 (en) * 2020-10-29 2024-06-12 Suzhou Yabao Pharmaceutical R&D Co., Ltd. SUBSTITUTED DIARYLAMINE COMPOUND, PHARMACEUTICAL COMPOSITION THEREOF, MANUFACTURING PROCESS THEREOF AND USE THEREOF
KR20220081631A (ko) 2020-12-09 2022-06-16 보로노이 주식회사 염증성 질환의 예방 및/또는 치료를 위한 피롤로-피리딘 유도체 화합물의 신규 용도
WO2023076404A1 (en) 2021-10-27 2023-05-04 Aria Pharmaceuticals, Inc. Methods for treating systemic lupus erythematosus
EP4422750A1 (en) 2021-10-27 2024-09-04 H. Lundbeck A/S Lrrk2 inhibitors
TW202412777A (zh) 2022-09-15 2024-04-01 丹麥商H 朗德貝克公司 富白胺酸重複激酶2(lrrk2)抑制劑

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2004274403A1 (en) 2003-09-03 2005-03-31 Aventis Pharmaceuticals Inc. 5-aryl-Pyrazolo(4,3-d)pyrimidines, pyridines, and pyrazines and related compounds
GB0420719D0 (en) 2004-09-17 2004-10-20 Addex Pharmaceuticals Sa Novel allosteric modulators
US8029986B2 (en) 2004-10-21 2011-10-04 Helmholtz Zentrum Muenchen Deutsches Forschungszentrum fuer Gesundheit und Umwelt(GmbH) KASPP (LRRK2) gene, its production and use for the detection and treatment of neurodegenerative disorders
US7855205B2 (en) 2004-10-29 2010-12-21 Janssen Pharmaceutica Nv Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders
NO323175B1 (no) 2004-12-23 2007-01-15 Jan O Aasly Framgangsmate for a pavise en mutasjon som forarsaker arvelig parkinsonisme
BRPI0617241A2 (pt) 2005-10-13 2016-11-08 Glaxo Group Ltd composto ou um sal ou solvato do mesmo, composição farmacêutica, método para tratar uma doença ou condição mediada por atividade syk inadequada em um mamífero, e, uso de um composto ou um sal ou solvato farmaceuticamente aceitável do mesmo
CA2651072A1 (en) 2006-05-01 2007-11-08 Pfizer Products Inc. Substituted 2-amino-fused heterocyclic compounds
WO2009036066A1 (en) 2007-09-10 2009-03-19 Curis, Inc. Vegfr inhibitors containing a zinc binding moiety
US9315449B2 (en) 2008-05-15 2016-04-19 Duke University Substituted pyrazoles as heat shock transcription factor activators
WO2009143018A2 (en) 2008-05-19 2009-11-26 Plexxikon, Inc. Compounds and methods for kinase modulation, and indications therefor
WO2009143404A1 (en) 2008-05-23 2009-11-26 Wyeth Piperazine metabotropic glutamate receptor 5 (mglur5) negative allosteric modulators for anxiety/depression
CA2760794C (en) 2009-05-05 2017-07-25 Dana Farber Cancer Institute Egfr inhibitors and methods of treating disorders
EP2483254B1 (en) * 2009-09-29 2014-08-13 Glaxo Group Limited Novel compounds
WO2011153553A2 (en) 2010-06-04 2011-12-08 The Regents Of The University Of California Methods and compositions for kinase inhibition
WO2012009258A2 (en) 2010-07-13 2012-01-19 Edward Roberts Peptidomimetic galanin receptor modulators
WO2012045195A1 (en) 2010-10-09 2012-04-12 Abbott Laboratories Pyrrolopyrimidines as fak and alk inhibiters for treatment of cancers and other diseases
US8901133B2 (en) 2010-11-10 2014-12-02 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
CA3017869C (en) * 2010-11-10 2021-07-27 Genentech, Inc. Pyrazole aminopyrimidine derivatives as lrrk2 modulators
CA2818903C (en) 2010-12-14 2021-03-23 Electrophoretics Limited 5-(1,3-benzoxazol-2-yl)-4-(pyridin-4-yl)pyrimidin-2-amine and its use as a casein kinase 1delta inhibitor
MX363696B (es) 2011-04-21 2019-03-28 Origenis Gmbh Pirazolo[4,3-d]pirimidinas utiles como inhibidores de cinasas.
MD20140023A2 (ro) 2011-09-22 2014-06-30 Pfizer Inc. Derivaţi de pirolpirimidină şi purină
RU2650641C2 (ru) * 2011-11-30 2018-04-16 Дженентек, Инк. Фтор-18 и углерод-11 меченые радиолиганды для томографии с позитронной эмиссией (рет), визуализирующей lrrk2
GB201204985D0 (en) 2012-03-21 2012-05-02 Genentech Inc Compounds
CN106279202A (zh) 2012-05-03 2017-01-04 霍夫曼-拉罗奇有限公司 作为lrrk2调节剂用于治疗帕金森病的吡唑氨基嘧啶衍生物
CN104271569B (zh) 2012-05-03 2016-08-24 霍夫曼-拉罗奇有限公司 作为lrrk2调节剂的吡唑氨基嘧啶衍生物
CA2878054C (en) 2012-06-29 2018-09-11 Pfizer Inc. Novel 4-(substituted-amino)-7h-pyrrolo[2,3-d]pyrimidines as lrrk2 inhibitors
US9815841B2 (en) 2014-01-29 2017-11-14 Glaxosmithkline Intellectual Property Development Limited Compounds
CN105940004B (zh) 2014-01-29 2018-02-02 葛兰素史密斯克莱知识产权发展有限公司 化合物

Also Published As

Publication number Publication date
US10618901B2 (en) 2020-04-14
AU2015210593A1 (en) 2016-07-07
US20180354956A1 (en) 2018-12-13
CN105940004A (zh) 2016-09-14
EP3099695B1 (en) 2020-04-08
WO2015113452A1 (en) 2015-08-06
US10087186B2 (en) 2018-10-02
US20170015668A1 (en) 2017-01-19
MA39219B1 (fr) 2018-11-30
PH12016501307B1 (en) 2016-08-15
KR20160106622A (ko) 2016-09-12
DOP2016000195A (es) 2016-10-31
AU2018200277A1 (en) 2018-02-01
JP6422986B2 (ja) 2018-11-14
SG11201605342UA (en) 2016-08-30
CR20160348A (es) 2017-04-28
CA2937431A1 (en) 2015-08-06
DOP2019000010A (es) 2019-03-15
CL2016001895A1 (es) 2016-12-09
MX2016009893A (es) 2016-10-31
EP3099695A1 (en) 2016-12-07
ES2802174T3 (es) 2021-01-15
EA201691514A1 (ru) 2016-12-30
IL246579A0 (en) 2016-08-31
MA39219A1 (fr) 2017-09-29
PH12016501307A1 (en) 2016-08-15
IL246579B (en) 2019-05-30
EP3099695A4 (en) 2017-07-12
PE20161443A1 (es) 2017-01-06
MX367370B (es) 2019-08-16
EA029774B1 (ru) 2018-05-31
AU2018200277B2 (en) 2019-09-26
CN105940004B (zh) 2018-02-02
JP2017504631A (ja) 2017-02-09

Similar Documents

Publication Publication Date Title
UA118369C2 (uk) Сполуки, що інгібують активність lrrk2 кінази
AU2020267169B2 (en) Processes of making and crystalline forms of a MDM2 inhibitor
JP5792279B2 (ja) ジスピロピロリジン誘導体
CA2861150C (en) Morphinan derivative
EP3227297B1 (en) 4,6-substituted-pyrazolo[1,5-a]pyrazines as janus kinase inhibitors
KR102672512B1 (ko) 항바이러스 피리도피라진디온 화합물
UA123689C2 (uk) Імідазопіролопіридинові сполуки як інгібітори кіназ родини jак
UA125824C2 (uk) 6,7,8,9-ТЕТРАГІДРО-3H-ПІРАЗОЛО[4,3-f]ІЗОХІНОЛІНОВІ ПОХІДНІ, ЗАСТОСОВНІ В ЛІКУВАННІ РАКУ
JPWO2009151069A1 (ja) 4,7−ジアザスピロ[2.5]オクタン環構造を有するイミダゾチアゾール誘導体
TW201107325A (en) Nitrogen-containing spiro cyclic compounds and pharmaceutical use thereof
TW201120040A (en) Bruton's tyrosine kinase inhibitors
JP2021519266A (ja) 3−ヒドロキシ−N−(3−(7H−ピロロ[2,3−d]ピリミジン−4−イル)フェニル)ピロリジン−1−カルボキサミド誘導体
EA024171B1 (ru) Ингибиторы вируса гепатита с
JP5520236B2 (ja) プロリン環構造を有するイミダゾチアゾール誘導体
UA119569C2 (uk) Метил- та трифлуорметилзаміщені піролопіридинові модулятори rorc2 та способи їх застосування
JP7417715B2 (ja) 抗ウイルスピラゾロピリジノン化合物
EP3889138A1 (en) Histone acetylase p300 inhibitor and use thereof
CN115087655A (zh) 苯并咪唑衍生物
EP3576743B1 (en) 5-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-5-azaspiro[2 5]octane-8-carboxylic acid derivatives as jak kinase inhibitors
RU2803284C1 (ru) Производные бензимидазола
JP2012036181A (ja) プロリン環構造を有するイミダゾチアゾール誘導体
HK40081050A (en) Benzimidazole derivatives
EA047837B1 (ru) Аналоги бензоазепина в качестве ингибирующих агентов для тирозинкиназы брутона
HK1226052B (en) Crystalline form of a mdm2 inhibitor
HK1238236B (en) 4,6-substituted-pyrazolo[1,5-a]pyrazines as janus kinase inhibitors