PE20161443A1 - Compuestos - Google Patents

Compuestos

Info

Publication number
PE20161443A1
PE20161443A1 PE2016001250A PE2016001250A PE20161443A1 PE 20161443 A1 PE20161443 A1 PE 20161443A1 PE 2016001250 A PE2016001250 A PE 2016001250A PE 2016001250 A PE2016001250 A PE 2016001250A PE 20161443 A1 PE20161443 A1 PE 20161443A1
Authority
PE
Peru
Prior art keywords
optionally substituted
alcoxyl
cycloalkyl
disease
methyl
Prior art date
Application number
PE2016001250A
Other languages
English (en)
Spanish (es)
Inventor
Colin Michael Edge
Xiao Ding
Qian Liu
Zehong Wan
Baowei Zhao
Yingxia Sang
Luigi Piero Stasi
Original Assignee
Glaxosmithkline Ip Dev Ltd
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 Glaxosmithkline Ip Dev Ltd filed Critical Glaxosmithkline Ip Dev Ltd
Publication of PE20161443A1 publication Critical patent/PE20161443A1/es

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)
PE2016001250A 2014-01-29 2015-01-28 Compuestos PE20161443A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2014000139 2014-01-29

Publications (1)

Publication Number Publication Date
PE20161443A1 true PE20161443A1 (es) 2017-01-06

Family

ID=53756224

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2016001250A PE20161443A1 (es) 2014-01-29 2015-01-28 Compuestos

Country Status (20)

Country Link
US (2) US10087186B2 (cg-RX-API-DMAC7.html)
EP (1) EP3099695B1 (cg-RX-API-DMAC7.html)
JP (1) JP6422986B2 (cg-RX-API-DMAC7.html)
KR (1) KR20160106622A (cg-RX-API-DMAC7.html)
CN (1) CN105940004B (cg-RX-API-DMAC7.html)
AU (2) AU2015210593A1 (cg-RX-API-DMAC7.html)
CA (1) CA2937431A1 (cg-RX-API-DMAC7.html)
CL (1) CL2016001895A1 (cg-RX-API-DMAC7.html)
CR (1) CR20160348A (cg-RX-API-DMAC7.html)
DO (2) DOP2016000195A (cg-RX-API-DMAC7.html)
EA (1) EA029774B1 (cg-RX-API-DMAC7.html)
ES (1) ES2802174T3 (cg-RX-API-DMAC7.html)
IL (1) IL246579B (cg-RX-API-DMAC7.html)
MA (1) MA39219B1 (cg-RX-API-DMAC7.html)
MX (1) MX367370B (cg-RX-API-DMAC7.html)
PE (1) PE20161443A1 (cg-RX-API-DMAC7.html)
PH (1) PH12016501307B1 (cg-RX-API-DMAC7.html)
SG (1) SG11201605342UA (cg-RX-API-DMAC7.html)
UA (1) UA118369C2 (cg-RX-API-DMAC7.html)
WO (1) WO2015113452A1 (cg-RX-API-DMAC7.html)

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
WO2017156493A1 (en) 2016-03-11 2017-09-14 Denali Therapeutics Inc. Compounds, compositions, and methods
UA118369C2 (uk) 2014-01-29 2019-01-10 Глаксосмітклайн Інтеллектьюел Проперті Девелопмент Лімітед Сполуки, що інгібують активність lrrk2 кінази
WO2015113451A1 (en) 2014-01-29 2015-08-06 Glaxosmithkline Intellectual Property Development Limited Compounds
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
WO2017087905A1 (en) * 2015-11-20 2017-05-26 Denali Therapeutics Inc. Compound, compositions, and methods
US10023579B2 (en) 2015-12-16 2018-07-17 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
SG10201912632YA (en) 2016-06-16 2020-02-27 Denali Therapeutics Inc Pyrimidin-2-ylamino-1h-pyrazols as lrrk2 inhibitors for use in the treatment of neurodegenerative disorders
EP3573956A4 (en) * 2017-01-25 2020-08-12 GlaxoSmithKline Intellectual Property Management Limited LINKS
KR20180097162A (ko) 2017-02-22 2018-08-30 국립암센터 피롤로-피리미딘 유도체 화합물, 이의 제조방법 및 이를 유효성분으로 함유하는 단백질 키나아제 관련 질환의 예방 또는 치료용 약학적 조성물
RU2730849C1 (ru) 2017-03-23 2020-08-26 Даегу-Гиеонгбук Медикал Инновейшн Фаундейшн Производное пирроло-пиридинового соединения, способ его получения и фармацевтическая композиция, содержащая его в качестве активного ингредиента, для профилактики и лечения заболеваний, связанных с протеинкиназой
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
TWI850262B (zh) * 2018-09-25 2024-08-01 美商卡都瑞恩醫藥公司 胺基嘧啶化合物
KR20200090637A (ko) 2019-01-18 2020-07-29 보로노이바이오 주식회사 피롤로피리딘 유도체 및 단백질 키나아제 관련 질환의 예방 또는 치료에서의 사용을 위한 이의 용도
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
AU2021371697B2 (en) * 2020-10-29 2024-10-24 Suzhou Yabao Pharmaceutical R&D Co., Ltd. Substituted diarylamine compound, pharmaceutical composition thereof, preparation method therefor, 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
EP4422750A1 (en) 2021-10-27 2024-09-04 H. Lundbeck A/S Lrrk2 inhibitors
WO2023076404A1 (en) 2021-10-27 2023-05-04 Aria Pharmaceuticals, Inc. Methods for treating systemic lupus erythematosus
WO2024056775A1 (en) 2022-09-15 2024-03-21 H. Lundbeck A/S Macrocyclic leucine-rich repeat kinase 2 (lrrk2) inhibitors

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
EP2316927B1 (en) 2004-10-21 2014-11-05 Helmholtz Zentrum München Deutsches Forschungszentrum für Gesundheit und Umwelt (GmbH) Kaspp (lrrk2) gene, its production and use for the detection and treatment of neurodegenerative disorders
WO2006050076A1 (en) 2004-10-29 2006-05-11 Janssen Pharmaceutica, N.V. 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
EP1948658A1 (en) 2005-10-13 2008-07-30 Glaxo Group Limited Pyrrolopyrimidine derivatives as syk inhibitors
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
US20090325964A1 (en) 2008-05-23 2009-12-31 Wyeth Piperazine Metabotropic Glutamate Receptor 5 (MGLUR5) Negative Allosteric Modulators For Anxiety/Depression
KR101705158B1 (ko) 2009-05-05 2017-02-09 다나-파버 캔서 인스티튜트 인크. Egfr 억제제 및 질환 치료방법
BR112012006859A2 (pt) 2009-09-29 2019-09-24 Glaxo Group Ltd compostos
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
CN103298474B (zh) 2010-11-10 2016-06-29 无限药品股份有限公司 杂环化合物及其用途
AU2011328139A1 (en) * 2010-11-10 2013-04-04 F. Hoffmann-La Roche Ag Pyrazole aminopyrimidine derivatives as LRRK2 modulators
JP2014503528A (ja) 2010-12-14 2014-02-13 エレクトロプホレトイクス リミテッド カゼインキナーゼ1δ(CK1δ)阻害剤及びタウオパチーなどの神経変性疾患の治療におけるその使用
AU2012244550C1 (en) 2011-04-21 2017-06-22 Origenis Gmbh Pyrazolo [4, 3-d] pyrimidines useful as kinase inhibitors
ES2575710T3 (es) * 2011-09-22 2016-06-30 Pfizer Inc Derivados de pirrolopirimidina y purina
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
BR112014027117B1 (pt) 2012-05-03 2022-09-06 Genentech, Inc Derivados de pirazol aminopirimidina como moduladores de lrrk2, seus usos, e composição
CN106220615A (zh) 2012-05-03 2016-12-14 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
EP3255049A1 (en) 2012-06-29 2017-12-13 Pfizer Inc Novel 4-(substituted-amino)-7h-pyrrolo[2,3-d]pyrimidines as lrrk2 inhibitors
WO2015113451A1 (en) 2014-01-29 2015-08-06 Glaxosmithkline Intellectual Property Development Limited Compounds
UA118369C2 (uk) 2014-01-29 2019-01-10 Глаксосмітклайн Інтеллектьюел Проперті Девелопмент Лімітед Сполуки, що інгібують активність lrrk2 кінази

Also Published As

Publication number Publication date
MX367370B (es) 2019-08-16
CR20160348A (es) 2017-04-28
EP3099695B1 (en) 2020-04-08
MA39219A1 (fr) 2017-09-29
AU2015210593A1 (en) 2016-07-07
AU2018200277B2 (en) 2019-09-26
AU2018200277A1 (en) 2018-02-01
CN105940004A (zh) 2016-09-14
DOP2016000195A (es) 2016-10-31
KR20160106622A (ko) 2016-09-12
DOP2019000010A (es) 2019-03-15
EA201691514A1 (ru) 2016-12-30
CL2016001895A1 (es) 2016-12-09
MA39219B1 (fr) 2018-11-30
WO2015113452A1 (en) 2015-08-06
CA2937431A1 (en) 2015-08-06
IL246579A0 (en) 2016-08-31
JP6422986B2 (ja) 2018-11-14
SG11201605342UA (en) 2016-08-30
IL246579B (en) 2019-05-30
EP3099695A4 (en) 2017-07-12
US20180354956A1 (en) 2018-12-13
JP2017504631A (ja) 2017-02-09
PH12016501307A1 (en) 2016-08-15
EA029774B1 (ru) 2018-05-31
US20170015668A1 (en) 2017-01-19
PH12016501307B1 (en) 2016-08-15
MX2016009893A (es) 2016-10-31
ES2802174T3 (es) 2021-01-15
US10618901B2 (en) 2020-04-14
CN105940004B (zh) 2018-02-02
US10087186B2 (en) 2018-10-02
UA118369C2 (uk) 2019-01-10
EP3099695A1 (en) 2016-12-07

Similar Documents

Publication Publication Date Title
PE20161443A1 (es) Compuestos
NZ732657A (en) Picolinamides with fungicidal activity and other related compounds
PE20191540A1 (es) DERIVADOS DE PIRROLO [1,2-b] PIRIDAZINA
PE20171341A1 (es) Compuestos de pirazina para el tratamiento de enfermedades infecciosas
PE20180024A1 (es) Triazolopirazinonas como inhibidores de pde1
PE20141974A1 (es) Compuestos de heterociclilo
PE20191245A1 (es) Compuestos de tiazolcarboxamidas y piridinacarboxamida utiles como inhibidores de quinasa pim
MX372997B (es) Compuestos de aminopirimidina como inhibidores de jak.
MX2018002402A (es) Compuestos de heteroarilo o arilo biciclicos fusionados como moduladores de la quinasa 4 asociada al receptor de la interleucina 1 (irak4).
PH12016501440A1 (en) Novel heterocyclic compounds
PE20141404A1 (es) Derivados de tieno[3,2-d]pirimidina que tienen actividad inhibidora por las quinasas de las proteinas
PE20181298A1 (es) Inhibidores de bromodominio bivalentes y usos de los mismos
SA518391307B1 (ar) مركبات ومشتقات سبيرو [ إندول -3، 2- بيروليدين h3] أون جديدة على هيئة مثبطات الدقيقة المزدوجة للفأر(1h)2 بي2-53
UY36056A (es) “compuestos de heteroarilo o arilo bicíclicos fusionados “.
PE20170268A1 (es) Compuestos de heteroarilo para la inhibicion de cinasa
PE20171737A1 (es) Derivados de quinazolinona biciclicos
PE20160992A1 (es) Inhibidores de quinasa relacionada con la tropomiosina (trk)
PE20190339A1 (es) 1h-pirazolo[4,3-b] piridinas como inhibidores de pde1
PE20161444A1 (es) 1,2-ciclopentanos sustituidos como antagonistas del receptor de orexina
PE20181074A1 (es) Compuestos heteroaromaticos como inhibidores de btk
MX2016008910A (es) Compuestos de fenil-triazolo-piridina.
CO2019001181A2 (es) Compuestos de heteroarilcarboxamida como inhibidores de ripk2
ECSP18024565A (es) Benzamidas sustituidas con isoxazolinas y análalogos como insecticidas
EA201891768A1 (ru) Кристаллическая форма a агониста tlr7, ее способ получения и использование
PE20161236A1 (es) Compuesto de triazina y su uso para fines medicos