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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)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Psychology (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) PL3194405T3 (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
UY39061A (es) * 2020-01-31 2022-01-31 Oncodesign Sa Inhibidores macrocíclicos de rip2-cinasa
CA3182162A1 (en) 2020-05-06 2021-11-11 Les Laboratoires Servier New macrocyclic lrrk2 kinase inhibitors
TW202304935A (zh) 2021-03-18 2023-02-01 法商施維雅藥廠 新穎的巨環lrrk2激酶抑制劑
US20240417378A1 (en) * 2021-10-11 2024-12-19 Baylor College Of Medicine G-protein-coupled receptor regulators and methods of use thereof
AR127470A1 (es) * 2021-10-27 2024-01-31 H Lundbeck As Inhibidores de lrrk2
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
US11958865B1 (en) 2022-09-15 2024-04-16 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)
AR132486A1 (es) * 2023-04-20 2025-07-02 H Lundbeck As Inhibidores de la cinasa con repeticiones ricas en leucina 2 (lrrk2)
WO2024218296A1 (en) * 2023-04-20 2024-10-24 H. Lundbeck A/S Combination treatments comprising administration of leucine-rich repeat kinase 2 (lrrk2) inhibitors
AR132487A1 (es) * 2023-04-20 2025-07-02 H Lundbeck As Inhibidores de la cinasa con repeticiones ricas en leucina 2 (lrrk2)

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
SG48049A1 (en) 1993-10-01 1998-04-17 Astra Ab Process 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
EA006626B1 (ru) 1996-07-24 2006-02-24 Дюпон Фармасьютикалз Компани Азолопиримидины, фармацевтическая композиция и способ лечения
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
JP3528968B2 (ja) 2000-12-28 2004-05-24 小野薬品工業株式会社 三環式複素環誘導体化合物およびその化合物を有効成分とする医薬
CA2450167A1 (en) * 2001-06-12 2002-12-19 Elan Pharmaceuticals, Inc. Macrocycles useful in the treatment of alzheimer's disease
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
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
PH12012501003B1 (en) 2005-11-16 2018-04-06 Cti Biopharma Corp Oxygen linked pyrimidine derivatives
WO2009127642A2 (en) 2008-04-15 2009-10-22 Cellzome Limited Use of lrrk2 inhibitors for neurodegenerative diseases
WO2011038572A1 (en) 2009-09-29 2011-04-07 Glaxo Group Limited Novel compounds
HUE044025T2 (hu) * 2010-05-20 2019-09-30 Array Biopharma Inc Makrociklusos vegyületek mint TRK-kináz inhibitorok
WO2013001310A1 (en) * 2011-06-30 2013-01-03 Centro Nacional De Investigaciones Oncológicas (Cnio) Macrocyclic compounds and their use as cdk8 inhibitors
UA113186C2 (xx) * 2011-09-30 2016-12-26 Макроциклічні інгібітори lrrk2 кінази
EA025881B1 (ru) * 2011-09-30 2017-02-28 Онкодизайн С.А. Макроциклические ингибиторы flt3-киназы

Also Published As

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

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