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MX2017003470A - Inhibidores macrociclicos de cinasa lrrk2. - Google Patents

Inhibidores macrociclicos de cinasa lrrk2.

Info

Publication number
MX2017003470A
MX2017003470A MX2017003470A MX2017003470A MX2017003470A MX 2017003470 A MX2017003470 A MX 2017003470A MX 2017003470 A MX2017003470 A MX 2017003470A MX 2017003470 A MX2017003470 A MX 2017003470A MX 2017003470 A MX2017003470 A MX 2017003470A
Authority
MX
Mexico
Prior art keywords
kinase inhibitors
disease
lrrk2 kinase
compounds
lrrk2
Prior art date
Application number
MX2017003470A
Other languages
English (en)
Inventor
Gomez Sylvie
Lavergne Olivier
Blom Petra
Hoflack Jan
Original Assignee
Oncodesign Sa
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 Oncodesign Sa filed Critical Oncodesign Sa
Publication of MX2017003470A publication Critical patent/MX2017003470A/es

Links

Classifications

    • 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
    • C07D498/22Heterocyclic 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 four or more hetero rings
    • 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
    • C07D487/22Heterocyclic 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 four or more hetero rings
    • 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
    • A61K31/529Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim forming part of bridged ring systems
    • 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
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Psychiatry (AREA)
  • Psychology (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

La presente invención se refiere a nuevos compuestos macrociclicos y a composiciones que contienen dichos compuestos que actúan como inhibidores de cinasa, en particular como inhibidores de LRRK2 (cinasa 2 de repetición rica en leucina). Además, la presente invención proporciona procesos para la preparación de los compuestos expuestos, así como métodos para utilizarlos, por ejemplo como una medicina o agente de diagnóstico, en particular para el tratamiento y/o diagnóstico de enfermedades caracterizadas por la actividad de cinasa LRRK2 tales como los trastornos neurológicos que incluyen enfermedad de Parkinson y enfermedad de Alzheimer.
MX2017003470A 2014-09-17 2015-09-17 Inhibidores macrociclicos de cinasa lrrk2. MX2017003470A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP14290279 2014-09-17
PCT/EP2015/071349 WO2016042089A1 (en) 2014-09-17 2015-09-17 Macrocyclic lrrk2 kinase inhibitors

Publications (1)

Publication Number Publication Date
MX2017003470A true MX2017003470A (es) 2017-08-07

Family

ID=51752058

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2017003470A MX2017003470A (es) 2014-09-17 2015-09-17 Inhibidores macrociclicos de cinasa lrrk2.

Country Status (20)

Country Link
US (1) US10377772B2 (es)
EP (1) EP3194405B1 (es)
JP (1) JP2017529365A (es)
KR (1) KR20170048599A (es)
CN (1) CN107108641A (es)
AU (1) AU2015316801B2 (es)
BR (1) BR112017005299A2 (es)
CA (1) CA2960777A1 (es)
DK (1) DK3194405T3 (es)
EA (1) EA032838B1 (es)
ES (1) ES2717510T3 (es)
HU (1) HUE043972T2 (es)
IL (1) IL251054B (es)
MX (1) MX2017003470A (es)
PL (1) PL3194405T4 (es)
SG (1) SG11201701936WA (es)
TR (1) TR201904514T4 (es)
TW (1) TW201625639A (es)
WO (1) WO2016042089A1 (es)
ZA (1) ZA201701841B (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111221514B (zh) * 2020-01-13 2023-03-03 陕西心像信息科技有限公司 基于OsgEarth的三维可视化组件实现方法及系统
CN115698020B (zh) * 2020-01-31 2025-02-25 昂科迪塞恩精密医药公司(Opm) 大环rip2-激酶抑制剂
CN115996932B (zh) 2020-05-06 2025-08-01 法国施维雅药厂 新的大环lrrk2激酶抑制剂
WO2022194976A1 (en) 2021-03-18 2022-09-22 Les Laboratoires Servier Macrocyclic lrrk2 kinase inhibitors
US20240417378A1 (en) * 2021-10-11 2024-12-19 Baylor College Of Medicine G-protein-coupled receptor regulators and methods of use thereof
TW202330549A (zh) 2021-10-27 2023-08-01 丹麥商H 朗德貝克公司 Lrrk2抑制劑
WO2023222005A1 (zh) * 2022-05-18 2023-11-23 上海翊石医药科技有限公司 一种芳杂环类化合物及其中间体、药物组合物和用途
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
WO2024218288A1 (en) * 2023-04-20 2024-10-24 H. Lundbeck A/S Leucine-rich repeat kinase 2 (lrrk2) inhibitors
AR132488A1 (es) * 2023-04-20 2025-07-02 H Lundbeck As Inhibidores de la cinasa con repeticiones ricas en leucina 2 (lrrk2)
TW202442651A (zh) * 2023-04-20 2024-11-01 丹麥商H 朗德貝克公司 富白胺酸重複激酶2(lrrk2)抑制劑
WO2024218296A1 (en) * 2023-04-20 2024-10-24 H. Lundbeck A/S Combination treatments comprising administration of leucine-rich repeat kinase 2 (lrrk2) inhibitors

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IS2334B (is) 1992-09-08 2008-02-15 Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) Aspartyl próteasi hemjari af nýjum flokki súlfonamíða
PT721331E (pt) 1993-10-01 2002-05-31 Astrazeneca Ab Processo i
EP0729758A3 (en) 1995-03-02 1997-10-29 Pfizer Pyrazolopyrimidines and pyrrolopyrimidines for the treatment of neuronal and other diseases
US6043358A (en) 1995-11-01 2000-03-28 Merck & Co., Inc. Hexahydro-5-imino-1,4-heteroazepine derivatives as inhibitors of nitric oxide synthases
PT915880E (pt) 1996-07-24 2007-12-31 Bristol Myers Squibb Pharma Co Azol triazinas e pirimidinas
GB9718913D0 (en) 1997-09-05 1997-11-12 Glaxo Group Ltd Substituted oxindole derivatives
US6194410B1 (en) 1998-03-11 2001-02-27 Hoffman-La Roche Inc. Pyrazolopyrimidine and pyrazolines and process for preparation thereof
US6369087B1 (en) 1999-08-26 2002-04-09 Robert R. Whittle Alkoxy substituted benzimidazole compounds, pharmaceutical preparations containing the same, and methods of using the same
CA2432148C (en) 2000-12-28 2011-01-18 Ono Pharmaceutical Co., Ltd. Tri-heterocyclic compounds and a pharmaceutical comprising them as an active ingredient
US7067507B2 (en) * 2001-06-12 2006-06-27 Pharmacia & Upjohn Company Macrocycles useful in the treatment of Alzheimer's disease
DK1802749T3 (da) 2004-10-21 2012-11-26 Mayo Foundation KASPP (LRRK2)-gen, dets fremstilling og anvendelse til påvisning og behandling af neurodegenerative lidelser
NO323175B1 (no) 2004-12-23 2007-01-15 Jan O Aasly Framgangsmate for a pavise en mutasjon som forarsaker arvelig parkinsonisme
FI123725B (fi) 2005-08-01 2013-10-15 Reijo Viljanen Menetelmä sahalaitteen terän jännittämiseksi ja ohjaamiseksi sekä ohjaus- ja jännityslaitteet
KR101499594B1 (ko) 2005-11-16 2015-03-09 씨티아이 바이오파마 코포레이션 산소가 결합된 피리미딘 유도체
WO2009127642A2 (en) 2008-04-15 2009-10-22 Cellzome Limited Use of lrrk2 inhibitors for neurodegenerative diseases
JP5752691B2 (ja) 2009-09-29 2015-07-22 グラクソ グループ リミテッドGlaxo Group Limited 新規化合物
MX2012013467A (es) * 2010-05-20 2013-04-29 Array Biopharma Inc Compuestos macrociclicos como inhibidores de trk cinasa.
WO2013001310A1 (en) * 2011-06-30 2013-01-03 Centro Nacional De Investigaciones Oncológicas (Cnio) Macrocyclic compounds and their use as cdk8 inhibitors
HUE027318T2 (en) * 2011-09-30 2016-10-28 Oncodesign Sa Macrocyclic FLT3 kinase inhibitors
DK2760453T3 (en) * 2011-09-30 2016-08-15 Ipsen Pharma Sas Macrocyclic LRRK2 kinase inhibitors

Also Published As

Publication number Publication date
KR20170048599A (ko) 2017-05-08
CA2960777A1 (en) 2016-03-24
AU2015316801B2 (en) 2019-03-07
ES2717510T3 (es) 2019-06-21
SG11201701936WA (en) 2017-04-27
TR201904514T4 (tr) 2019-04-22
CN107108641A (zh) 2017-08-29
EA201790626A1 (ru) 2017-07-31
IL251054B (en) 2019-03-31
ZA201701841B (en) 2019-08-28
EP3194405B1 (en) 2018-12-26
DK3194405T3 (en) 2019-04-15
US20170240565A1 (en) 2017-08-24
EA032838B1 (ru) 2019-07-31
EP3194405A1 (en) 2017-07-26
PL3194405T3 (pl) 2019-07-31
US10377772B2 (en) 2019-08-13
HUE043972T2 (hu) 2019-09-30
PL3194405T4 (pl) 2019-07-31
TW201625639A (zh) 2016-07-16
WO2016042089A1 (en) 2016-03-24
AU2015316801A1 (en) 2017-04-27
IL251054A0 (en) 2017-04-30
BR112017005299A2 (pt) 2017-12-12
JP2017529365A (ja) 2017-10-05

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