MA42442B1 - Dérivés d'éthynyle comme modulateurs du récepteur métabotropique au glutamate - Google Patents

Dérivés d'éthynyle comme modulateurs du récepteur métabotropique au glutamate

Info

Publication number
MA42442B1
MA42442B1 MA42442A MA42442A MA42442B1 MA 42442 B1 MA42442 B1 MA 42442B1 MA 42442 A MA42442 A MA 42442A MA 42442 A MA42442 A MA 42442A MA 42442 B1 MA42442 B1 MA 42442B1
Authority
MA
Morocco
Prior art keywords
modulators
glutamate receptor
metabotropic glutamate
compounds
ethynyl derivatives
Prior art date
Application number
MA42442A
Other languages
English (en)
Other versions
MA42442A (fr
Inventor
Daniel Rueher
Eric Vieira
Georg Jaeschke
Lothar Lindemann
Antonio Ricci
Barbara Biemans
Fionn O`Hara
Wolfgang Guba
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MA42442A publication Critical patent/MA42442A/fr
Publication of MA42442B1 publication Critical patent/MA42442B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/10—Spiro-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/527—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim spiro-condensed
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16—Anti-Parkinson drugs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/10—Spiro-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic 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
    • C07D491/02—Heterocyclic 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
    • C07D491/10—Spiro-condensed systems
    • C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic 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
    • C07D491/12—Heterocyclic 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 three hetero rings
    • C07D491/20—Spiro-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Diabetes (AREA)
  • Hospice & Palliative Care (AREA)
  • Otolaryngology (AREA)
  • Psychology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Psychiatry (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Liquid Crystal (AREA)

Abstract

La présente invention concerne des composés de formule i dans laquelle r1 est un alkyle inférieur ; r2 est un phényle ou pyridinyle, l'atome n dans le groupe pyridinyle pouvant être à des positions différentes ; n est 0, 1 ou 2 ; v/u sont indépendamment l'un de l'autre o ou ch2, v et u ne pouvant pas être simultanément o ; et l est un groupe hétéroaryle à cinq ou six chaînons, ou un sel pharmaceutiquement acceptable ou un sel d'addition d'acide, un mélange racémique de ceux-ci, ou un énantiomère et/ou isomère optique et/ou stéréoisomère correspondant. Les composés peuvent être utilisés pour traiter la maladie de parkinson, l'anxiété, les vomissements, les troubles obsessionnels compulsifs, l'autisme, le cancer, la dépression et le diabète de type 2 ainsi que pour la neuroprotection.
MA42442A 2015-07-15 2016-07-11 Dérivés d'éthynyle comme modulateurs du récepteur métabotropique au glutamate MA42442B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP15176854 2015-07-15
PCT/EP2016/066393 WO2017009275A1 (fr) 2015-07-15 2016-07-11 Dérivés d'éthynyle a titre de modulateurs du récepteur métabotropique du glutamate

Publications (2)

Publication Number Publication Date
MA42442A MA42442A (fr) 2018-05-23
MA42442B1 true MA42442B1 (fr) 2019-07-31

Family

ID=53758003

Family Applications (1)

Application Number Title Priority Date Filing Date
MA42442A MA42442B1 (fr) 2015-07-15 2016-07-11 Dérivés d'éthynyle comme modulateurs du récepteur métabotropique au glutamate

Country Status (30)

Country Link
US (3) US10189848B2 (fr)
EP (1) EP3322701B1 (fr)
JP (1) JP6761821B2 (fr)
KR (1) KR20180026438A (fr)
CN (1) CN107580598B (fr)
AR (1) AR105341A1 (fr)
AU (1) AU2016292863B2 (fr)
CA (1) CA2984711C (fr)
CL (1) CL2018000036A1 (fr)
CO (1) CO2017011174A2 (fr)
CR (1) CR20180022A (fr)
DK (1) DK3322701T3 (fr)
ES (1) ES2733468T3 (fr)
HR (1) HRP20191139T1 (fr)
HU (1) HUE045145T2 (fr)
IL (1) IL255096B (fr)
LT (1) LT3322701T (fr)
MA (1) MA42442B1 (fr)
MX (1) MX374409B (fr)
PE (1) PE20180356A1 (fr)
PH (1) PH12018500106A1 (fr)
PL (1) PL3322701T3 (fr)
PT (1) PT3322701T (fr)
RS (1) RS58929B1 (fr)
RU (1) RU2721776C9 (fr)
SI (1) SI3322701T1 (fr)
TR (1) TR201909160T4 (fr)
TW (1) TWI612962B (fr)
UA (1) UA120463C2 (fr)
WO (1) WO2017009275A1 (fr)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
LT3495367T (lt) 2012-06-13 2021-02-25 Incyte Holdings Corporation Pakeistieji tricikliniai junginiai, kaip fgfr inhibitoriai
LT2986610T (lt) 2013-04-19 2018-04-10 Incyte Holdings Corporation Bicikliniai heterociklai, kaip fgfr inhibitoriai
US10851105B2 (en) 2014-10-22 2020-12-01 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
MA41551A (fr) 2015-02-20 2017-12-26 Incyte Corp Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
SG11201706287PA (en) 2015-02-20 2017-09-28 Incyte Corp Bicyclic heterocycles as fgfr inhibitors
ES2733468T3 (es) 2015-07-15 2019-11-29 Hoffmann La Roche Derivados de etinilo como moduladores de los receptores metabotrópicos de glutamato
SI3484889T1 (sl) 2016-07-18 2020-11-30 F. Hoffmann-La Roche Ag Derivati etinila
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
ES3061844T3 (en) 2018-05-04 2026-04-07 Incyte Corp Salts of an fgfr inhibitor
MX2020011718A (es) 2018-05-04 2021-02-15 Incyte Corp Formas solidas de un inhibidor de receptores del factor de crecimiento de fibroblastos (fgfr) y procesos para prepararlas.
CA3102326A1 (fr) 2018-07-26 2020-01-30 Domain Therapeutics Derives de quinazolinone substitues et leur utilisation en tant que modulateurs allosteriques positifs de mglur4
US11628162B2 (en) 2019-03-08 2023-04-18 Incyte Corporation Methods of treating cancer with an FGFR inhibitor
US11591329B2 (en) 2019-07-09 2023-02-28 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
US12122767B2 (en) 2019-10-01 2024-10-22 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
TWI891666B (zh) 2019-10-14 2025-08-01 美商英塞特公司 作為fgfr抑制劑之雙環雜環
US11566028B2 (en) 2019-10-16 2023-01-31 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
CA3163875A1 (fr) 2019-12-04 2021-06-10 Incyte Corporation Heterocycles tricycliques en tant qu'inhibiteurs de fgfr
WO2021113462A1 (fr) 2019-12-04 2021-06-10 Incyte Corporation Dérivés d'un inhibiteur de fgfr
US12012409B2 (en) 2020-01-15 2024-06-18 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
TW202304459A (zh) 2021-04-12 2023-02-01 美商英塞特公司 包含fgfr抑制劑及nectin-4靶向劑之組合療法
EP4352060A1 (fr) 2021-06-09 2024-04-17 Incyte Corporation Hétérocycles tricycliques utiles en tant qu'inhibiteurs de fgfr
JP2024522189A (ja) 2021-06-09 2024-06-11 インサイト・コーポレイション Fgfr阻害剤としての三環式ヘテロ環
KR20250156792A (ko) * 2023-03-10 2025-11-03 브라이트씨드, 인크. 스트레스 조절을 위한 조성물 및 방법 및 이의 용도

Family Cites Families (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6875433B2 (en) 2002-08-23 2005-04-05 The United States Of America As Represented By The Secretary Of The Army Monoclonal antibodies and complementarity-determining regions binding to Ebola glycoprotein
KR101333861B1 (ko) * 2005-05-24 2013-11-28 메르크 세로노 에스. 에이. Crth2 조정자로서 삼환계 스피로 유도체
JP2010502617A (ja) 2006-08-31 2010-01-28 シェーリング コーポレイション 抗菌物質として有用なヒダントイン誘導体
NZ581817A (en) 2007-06-03 2012-05-25 Univ Vanderbilt Benzamide mglur5 positive allosteric modulators and methods of making and using same
EP2262832A4 (fr) 2008-02-01 2011-03-09 Ca Minister Health & Welfare Anticorps monoclonaux contre les virus d'ebola et de marburg
ES2400515T3 (es) 2009-01-19 2013-04-10 Fondazione Irccs "Ca' Granda - Ospedale Maggiore Policlinico" Análogos de melanocortina con actividad antimicrobiana
WO2011071574A2 (fr) 2009-09-02 2011-06-16 United States Deparment Of The Army, As Represented By The Secretary Of The Army Anticorps monoclonaux dirigés contre la glycoprotéine du virus ebola souche soudan boniface
CA2773038A1 (fr) 2009-09-04 2011-03-10 P. Jeffrey Conn Potentialisateurs allosteriques mglur4, composition et methodes de traitement de dysfonctionnements neurologiques
US8389536B2 (en) 2009-10-27 2013-03-05 Hoffmann-La Roche Inc. Positive allosteric modulators (PAM)
US8759377B2 (en) 2009-11-23 2014-06-24 Vanderbilt University Substituted dioxopiperidines and dioxopyrrolidines as MGLUR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction
US8586581B2 (en) 2009-12-17 2013-11-19 Hoffmann-La Roche Inc Ethynyl compounds useful for treatment of CNS disorders
US8420661B2 (en) * 2010-04-13 2013-04-16 Hoffmann-La Roche Inc. Arylethynyl derivatives
US8772300B2 (en) 2011-04-19 2014-07-08 Hoffmann-La Roche Inc. Phenyl or pyridinyl-ethynyl derivatives
MY165141A (en) 2011-04-26 2018-02-28 Hoffmann La Roche Pyrazolidin-3-one derivatives
KR101554803B1 (ko) 2011-04-26 2015-09-21 에프. 호프만-라 로슈 아게 Mglur5의 양성 알로스테릭 조절체로서 에틴일 유도체
WO2012162635A1 (fr) 2011-05-26 2012-11-29 Sunovion Pharmaceuticals Inc. Modulateurs des récepteurs 5 métabotropiques du glutamate et leurs procédés d'utilisation
US20130123254A1 (en) 2011-09-30 2013-05-16 Barbara Biemans Pharmaceutically acceptable mglur5 positive allosteric modulators and their methods of identification
UA110995C2 (uk) 2011-10-07 2016-03-10 Ф. Хоффманн-Ля Рош Аг Етинільні похідні як модулятори метаботропного глутаматного рецептора
UA110862C2 (uk) 2011-10-07 2016-02-25 Ф. Хоффманн-Ля Рош Аг Похідні етинілу як алостеричні модулятори метаботропного рецептора глутамату mglur 5
WO2014012851A1 (fr) 2012-07-17 2014-01-23 F. Hoffmann-La Roche Ag Dérivés d'aryléthynyle
AU2013333984B2 (en) 2012-10-18 2017-03-09 F. Hoffmann-La Roche Ag Ethynyl derivatives as modulators of mGluR5 receptor activity
EA026941B1 (ru) 2012-10-18 2017-06-30 Ф. Хоффманн-Ля Рош Аг ПРОИЗВОДНЫЕ ЭТИНИЛА В КАЧЕСТВЕ МОДУЛЯТОРОВ АКТИВНОСТИ РЕЦЕПТОРА mGluR5
CN105121424B (zh) 2013-02-18 2019-01-22 华领医药技术(上海)有限公司 mGluR调节剂
UY35400A (es) 2013-03-15 2014-10-31 Novartis Ag Compuestos y composiciones para el tratamiento de enfermedades parasitarias
JO3368B1 (ar) 2013-06-04 2019-03-13 Janssen Pharmaceutica Nv مركبات 6، 7- ثاني هيدرو بيرازولو [5،1-a] بيرازين- 4 (5 يد)- اون واستخدامها بصفة منظمات تفارغية سلبية لمستقبلات ميجلور 2
CN105579447B (zh) 2013-09-25 2018-11-13 豪夫迈·罗氏有限公司 乙炔基衍生物
TWI649310B (zh) * 2014-01-10 2019-02-01 赫孚孟拉羅股份公司 乙炔基衍生物
EP3107567A4 (fr) 2014-02-19 2017-10-25 Cangene Corporation Procédés de modulation d'une réponse immunitaire
CN104860941B (zh) 2014-02-25 2017-03-22 上海海雁医药科技有限公司 2,4‑二取代苯‑1,5‑二胺衍生物及其应用以及由其制备的药物组合物和药用组合物
UA117855C2 (uk) 2014-02-25 2018-10-10 Ф. Хоффманн-Ля Рош Аг Похідні етинілу
SG10201902924RA (en) 2014-10-03 2019-05-30 Massachusetts Inst Technology Antibodies that bind ebola glycoprotein and uses thereof
WO2016146600A1 (fr) 2015-03-19 2016-09-22 F. Hoffmann-La Roche Ag Dérivés 3-(4-éthynylphényl)hexahydropyrimidine-2,4-dione en tant que modulateurs de mglur4
ES2733468T3 (es) 2015-07-15 2019-11-29 Hoffmann La Roche Derivados de etinilo como moduladores de los receptores metabotrópicos de glutamato
SI3484889T1 (sl) 2016-07-18 2020-11-30 F. Hoffmann-La Roche Ag Derivati etinila

Also Published As

Publication number Publication date
CA2984711A1 (fr) 2017-01-19
DK3322701T3 (da) 2019-07-08
JP2018524305A (ja) 2018-08-30
CR20180022A (es) 2018-02-26
MX374409B (es) 2025-03-04
PE20180356A1 (es) 2018-02-21
EP3322701B1 (fr) 2019-05-01
WO2017009275A1 (fr) 2017-01-19
US10189848B2 (en) 2019-01-29
US20180134721A1 (en) 2018-05-17
PL3322701T3 (pl) 2019-09-30
AR105341A1 (es) 2017-09-27
RU2721776C2 (ru) 2020-05-22
EP3322701A1 (fr) 2018-05-23
TW201707705A (zh) 2017-03-01
IL255096B (en) 2020-01-30
JP6761821B2 (ja) 2020-09-30
MA42442A (fr) 2018-05-23
RU2018103944A (ru) 2019-08-16
AU2016292863B2 (en) 2020-03-05
CA2984711C (fr) 2023-08-29
AU2016292863A1 (en) 2017-11-02
IL255096A0 (en) 2017-12-31
US20190119290A1 (en) 2019-04-25
CN107580598A (zh) 2018-01-12
RU2018103944A3 (fr) 2019-12-13
MX2018000592A (es) 2018-04-24
RU2721776C9 (ru) 2020-10-22
CL2018000036A1 (es) 2018-06-29
HUE045145T2 (hu) 2019-12-30
BR112017023084A2 (pt) 2018-07-10
CO2017011174A2 (es) 2018-01-31
UA120463C2 (uk) 2019-12-10
SI3322701T1 (sl) 2019-08-30
LT3322701T (lt) 2019-07-10
US11034699B2 (en) 2021-06-15
TR201909160T4 (tr) 2019-07-22
KR20180026438A (ko) 2018-03-12
TWI612962B (zh) 2018-02-01
RS58929B1 (sr) 2019-08-30
US12006323B2 (en) 2024-06-11
PT3322701T (pt) 2019-06-28
CN107580598B (zh) 2020-11-13
PH12018500106A1 (en) 2018-07-23
HRP20191139T1 (hr) 2019-09-20
ES2733468T3 (es) 2019-11-29
US20210269452A1 (en) 2021-09-02

Similar Documents

Publication Publication Date Title
MA42442A (fr) Dérivés d'éthynyle comme modulateurs du récepteur métabotropique au glutamate
MA35133B1 (fr) Dérivés d'éthynyle comme modulateurs allostériques positifs de mglur5
MA38272A1 (fr) Peptides en tant qu'agonistes de l'oxytocine
MA31865B1 (fr) Dérivés isoxazolo-pyridine
MA38012B1 (fr) Dérivés d'éthynyle comme modulateurs de l'activité des récepteurs mglur5
MA53668B1 (fr) Traitement de la drépanocytose avec un composé activant la pyruvate kinase r
MA35062B1 (fr) Dérivés d'amines hétérocycliques
MA34361B1 (fr) Dérivés de tétrahydro-pyrido-pyrimidine
MA38325A2 (fr) Dérivés de benzothiophène et compositions correspondantes en tant qu'agents de dégradation sélectifs des récepteurs des œstrogènes
PE20040164A1 (es) Mimeticos de glucocorticoides, procedimientos para su preparacion y composiciones farmaceuticas
WO2019007696A1 (fr) Nouveaux composés et compositions pharmaceutiques de ceux-ci destinés au traitement de la fibrose
MA35113B1 (fr) 5-(phényl/pyridinyl-éthinyl)-2-pyridine/2 pyrimidine-carboxamides comme modulateur de mglur5
MA35192B1 (fr) Derives de pyrazole
MA38885A1 (fr) Dérivés d'éthynyle modulateurs allosteriques positifs (pam) du recepteur metabotropique du glutamate 4 (mglu4)
MA54447B1 (fr) Dérivés de 7-phénoxy-n-(3-azabicyclo[3.2.1]octan-8-yl)-6,7-dihydro-5h-pyrrolo[1,2-b][1,2,4]triazol-2-amine et composés similaires en tant que modulateurs de la secretase gamma pour le traitement de la maladie d'alzheimer
PH12016501100B1 (en) Ethynyl-imidazolin-2,4-dione derivatives as mglur4 modulators
MX2016000895A (es) Derivados de 1,7-naftiridina.
MA31742B1 (fr) Derives de l'indol-2-one disubstitues en 3, leur preparation et leur application en therapeutique
MA29809B1 (fr) N-[1,3,4]-thiadiazol-2-yl-benzenesulfonamides,procedes pour leur preparation et leur utilisation en tant que produits pharmaceutiques
MA38659B1 (fr) Dérivés éthynyle comme antagonistes du récepteur métabotrope du glutamate
MA38011B1 (fr) Dérivés d'éthynyle comme modulateurs de l'activité du récepteur mglur5
MX2020008523A (es) Compuesto que tiene actividad agonista del receptor esfingosina-1-fosfato [(2s,3r,4e)-2-amino-3-hidroxioctadec-4-enil- 1-fosfato (s1p5).
MA45665B1 (fr) Dérivés d'éthynyle
MA29806B1 (fr) Derives de 2-aminothiazoles et 2- aminooxazoles,procedes pour leur preparation et leur utilisation en tant que produits pharmaceutiques
TH1701007595A (th) อนุพันธ์เอไทนิลในฐานะโมดูเลเตอร์ของเมทาโบโทรปิกกลูตาเมตรีเซปเตอร์