MA49560B1 - Composés cétoniques bicycliques et leurs procédés d'utilisation - Google Patents

Composés cétoniques bicycliques et leurs procédés d'utilisation

Info

Publication number
MA49560B1
MA49560B1 MA49560A MA49560A MA49560B1 MA 49560 B1 MA49560 B1 MA 49560B1 MA 49560 A MA49560 A MA 49560A MA 49560 A MA49560 A MA 49560A MA 49560 B1 MA49560 B1 MA 49560B1
Authority
MA
Morocco
Prior art keywords
methods
ketone compounds
bicyclic ketone
compounds
ring
Prior art date
Application number
MA49560A
Other languages
English (en)
Other versions
MA49560A (fr
Inventor
Huifen Chen
Snahel Patel
Guiling Zhao
Gregory Hamilton
Craig Stivala
Blake Daniels
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 MA49560A publication Critical patent/MA49560A/fr
Publication of MA49560B1 publication Critical patent/MA49560B1/fr

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
    • C07D498/02Heterocyclic 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 two hetero rings
    • C07D498/04Ortho-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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41961,2,4-Triazoles
    • 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
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/12Radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurology (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychology (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Immunology (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

L'invention concerne de nouveaux composés représentés par la formule générale i : (i) dans laquelle r1, le cycle a et le cycle b sont tels que décrits dans la description, ainsi que des compositions pharmaceutiques comprenant lesdits composés et des procédés d'utilisation de ces composés.
MA49560A 2017-07-14 2018-07-12 Composés cétoniques bicycliques et leurs procédés d'utilisation MA49560B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201762532767P 2017-07-14 2017-07-14
PCT/EP2018/068998 WO2019012063A1 (fr) 2017-07-14 2018-07-12 Composés cétoniques bicycliques et leurs procédés d'utilisation

Publications (2)

Publication Number Publication Date
MA49560A MA49560A (fr) 2020-05-20
MA49560B1 true MA49560B1 (fr) 2024-05-31

Family

ID=62916677

Family Applications (1)

Application Number Title Priority Date Filing Date
MA49560A MA49560B1 (fr) 2017-07-14 2018-07-12 Composés cétoniques bicycliques et leurs procédés d'utilisation

Country Status (28)

Country Link
US (2) US11098058B2 (fr)
EP (2) EP4397309A2 (fr)
JP (2) JP7258843B2 (fr)
KR (2) KR102664604B1 (fr)
CN (1) CN110914271A (fr)
AR (1) AR112274A1 (fr)
AU (3) AU2018300043B2 (fr)
BR (1) BR112020000771A2 (fr)
CA (2) CA3067944C (fr)
CL (1) CL2020000101A1 (fr)
CO (1) CO2020000134A2 (fr)
CR (1) CR20200002A (fr)
DK (1) DK3652178T3 (fr)
ES (1) ES2973661T3 (fr)
FI (1) FI3652178T3 (fr)
HR (1) HRP20240354T1 (fr)
IL (2) IL294961A (fr)
LT (1) LT3652178T (fr)
MA (1) MA49560B1 (fr)
PH (1) PH12020500105A1 (fr)
PL (1) PL3652178T3 (fr)
PT (1) PT3652178T (fr)
RS (1) RS65308B1 (fr)
SG (1) SG11202000333UA (fr)
SI (1) SI3652178T1 (fr)
TW (1) TWI805595B (fr)
UA (1) UA125448C2 (fr)
WO (1) WO2019012063A1 (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3548484A1 (fr) 2016-12-02 2019-10-09 H. Hoffnabb-La Roche Ag Composés amide bicycliques et leurs procédés d'utilisation
SG11202000333UA (en) 2017-07-14 2020-02-27 Hoffmann La Roche Bicyclic ketone compounds and methods of use thereof
SG11202002877RA (en) 2017-10-31 2020-04-29 Hoffmann La Roche Bicyclic sulfones and sulfoxides and methods of use thereof
WO2021198981A1 (fr) 2020-04-01 2021-10-07 Janssen Biopharma, Inc. Composés antiviraux et leurs utilisations
TW202206407A (zh) * 2020-04-27 2022-02-16 南韓商奧士擇破利悟股份有限公司 用於ubr盒結構域配體之化合物、組成物以及醫藥組成物
MX2023011482A (es) 2021-04-02 2023-10-03 Genentech Inc Proceso para preparar compuestos de cetona biciclicos.
WO2023039795A1 (fr) * 2021-09-16 2023-03-23 维泰瑞隆(北京)生物科技有限公司 Inhibiteur de la kinase rip1 et son utilisation
US20240025912A1 (en) * 2022-05-19 2024-01-25 Merck Sharp & Dohme Llc Ripk1 inhibitors and methods of use

Family Cites Families (52)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1620508A1 (de) 1965-07-23 1969-09-18 Thomae Gmbh Dr K Verfahren zur Herstellung neuer 4,5,6,7-Tetrahydrothiazolo-[5,4-c]-pyridine
US3773919A (en) 1969-10-23 1973-11-20 Du Pont Polylactide-drug mixtures
US3948903A (en) 1972-12-15 1976-04-06 Parke, Davis & Company Substituted N-(1,2-dihydro-2-oxonicotinyl)-cephalexins and -cephaloglycins
US4485045A (en) 1981-07-06 1984-11-27 Research Corporation Synthetic phosphatidyl cholines useful in forming liposomes
EP0102324A3 (fr) 1982-07-29 1984-11-07 Ciba-Geigy Ag Lipides et composés tensio-actifs en phase aqueuse
US4544545A (en) 1983-06-20 1985-10-01 Trustees University Of Massachusetts Liposomes containing modified cholesterol for organ targeting
HUT35524A (en) 1983-08-02 1985-07-29 Hoechst Ag Process for preparing pharmaceutical compositions containing regulatory /regulative/ peptides providing for the retarded release of the active substance
GB8610530D0 (en) 1986-04-30 1986-06-04 Fbc Ltd Herbicides
US5004697A (en) 1987-08-17 1991-04-02 Univ. Of Ca Cationized antibodies for delivery through the blood-brain barrier
US5112596A (en) 1990-04-23 1992-05-12 Alkermes, Inc. Method for increasing blood-brain barrier permeability by administering a bradykinin agonist of blood-brain barrier permeability
US5268164A (en) 1990-04-23 1993-12-07 Alkermes, Inc. Increasing blood-brain barrier permeability with permeabilizer peptides
EP0652775B1 (fr) 1992-07-27 2000-04-19 THE GOVERNMENT OF THE UNITED STATES OF AMERICA as represented by the SECRETARY OF THE DEPARTMENT OF HEALTH AND HUMAN SERVICES Ciblage de liposomes sur la barriere hemato-encephalique
US6080772A (en) 1995-06-07 2000-06-27 Sugen, Inc. Thiazole compounds and methods of modulating signal transduction
EP1007042A4 (fr) 1997-06-13 2001-07-04 Sugen Inc Nouveaux composes heteroaryle pour la modulation de la transduction de signaux cellulaires associee aux enzymes proteine tyrosine
CA2399791A1 (fr) * 2000-02-11 2001-08-16 Bristol-Myers Squibb Company Modulateurs de recepteurs aux cannabinoides, leurs procedes de preparation et utilisations de modulateurs de recepteurs aux cannabinoides pour le traitement de maladies respiratoires et non respiratoires
US6514221B2 (en) 2000-07-27 2003-02-04 Brigham And Women's Hospital, Inc. Blood-brain barrier opening
US20020065259A1 (en) 2000-08-30 2002-05-30 Schatzberg Alan F. Glucocorticoid blocking agents for increasing blood-brain barrier permeability
US7034036B2 (en) 2000-10-30 2006-04-25 Pain Therapeutics, Inc. Inhibitors of ABC drug transporters at the blood-brain barrier
DE10121982B4 (de) 2001-05-05 2008-01-24 Lts Lohmann Therapie-Systeme Ag Nanopartikel aus Protein mit gekoppeltem Apolipoprotein E zur Überwindung der Blut-Hirn-Schranke und Verfahren zu ihrer Herstellung
EP2147679B1 (fr) 2001-07-25 2014-06-25 Raptor Pharmaceutical, Inc. Compositions pour le transport de barrière hématoencéphalique
US20030162695A1 (en) 2002-02-27 2003-08-28 Schatzberg Alan F. Glucocorticoid blocking agents for increasing blood-brain barrier permeability
EP1572113B1 (fr) 2002-08-26 2017-05-17 Takeda Pharmaceutical Company Limited Compose modulateur de recepteur de calcium et utilisation associee
KR101111477B1 (ko) 2002-12-03 2012-02-23 블랜체트 록펠러 뉴로사이언시즈 인스티튜트 치료제와 연결된 콜레스테롤을 포함하는 접합체
WO2004098589A1 (fr) 2003-05-02 2004-11-18 Elan Pharmaceuticals, Inc. Derives amides de l'acide carboxylique de 4- bromo - 5 - (2- chloro - benzoylamino) - 1h - pyrazole 3 et composes associes en tant qu'antagonistes de recepteur de b1 de la bradykinine pour le traitement de maladies inflammatoires
JP2007505142A (ja) 2003-09-10 2007-03-08 セダーズ−シナイ メディカル センター 血液脳関門を通過する薬剤のカリウムチャネル媒介性送達
JP2008539220A (ja) 2005-04-26 2008-11-13 ファイザー・リミテッド バソプレシンアンタゴニストとしてのトリアゾール誘導体
EP2083009A1 (fr) 2008-01-22 2009-07-29 Grünenthal GmbH Composés tétrahydroimidazopyridine substitués et leur utilisation en tant que médicament
US8299077B2 (en) 2009-03-02 2012-10-30 Roche Palo Alto Llc Inhibitors of Bruton's tyrosine kinase
CN101824036A (zh) 2009-03-05 2010-09-08 上海恒瑞医药有限公司 四氢咪唑并[1,5-a]吡嗪衍生物的盐,其制备方法及其在医药上的应用
TWI421252B (zh) 2009-07-09 2014-01-01 Irm Llc 用於治療寄生蟲疾病之化合物及組合物
CA2852964A1 (fr) 2011-11-03 2013-05-10 F. Hoffmann-La Roche Ag Composes piperazines bicycliques
EP2852584B1 (fr) 2012-05-22 2018-02-28 F. Hoffmann-La Roche AG Dipyridylamines substituées et leurs utilisations
CN104918934B (zh) 2013-01-18 2017-12-22 霍夫曼-拉罗奇有限公司 3‑取代的吡唑及其作为dlk抑制剂的用途
TWI648274B (zh) * 2013-02-15 2019-01-21 英商葛蘭素史克智慧財產發展有限公司 作為激酶抑制劑之雜環醯胺類 (二)
EP2991977B1 (fr) 2013-05-01 2020-07-22 F.Hoffmann-La Roche Ag Pyrimidines à substitution hétérocycloalkyle liées à c et leurs utilisations
MX2015015130A (es) 2013-05-01 2016-02-18 Hoffmann La Roche Compuestos de biheteroarilo y usos de los mismos.
MX368728B (es) 2013-07-10 2019-10-14 Vertex Pharma Amidas de piperidina fusionadas como moduladores de canales de iones.
MX2016008110A (es) 2013-12-20 2016-08-19 Hoffmann La Roche Derivados de pirazol como inhibidores de la cinasa de cremallera de leucina dual (dlk) y usos de los mismos.
PE20161223A1 (es) 2014-03-26 2016-11-12 Hoffmann La Roche Compuestos condensados de [1,4]diazepina como inhibidores de la produccion de autotaxina (atx) y acido lisofosfatidico (lpa)
WO2016027253A1 (fr) 2014-08-21 2016-02-25 Glaxosmithkline Intellectual Property Development Limited Amides hétérocycliques utilisés comme inhibiteurs de la rip1 kinase en tant que médicaments
WO2016128908A1 (fr) * 2015-02-12 2016-08-18 Advinus Therapeutics Limited Composés bicycliques, compositions et applications médicinales correspondantes
EP3268373B1 (fr) 2015-03-09 2022-04-27 F. Hoffmann-La Roche AG Tricycliques inhibiteurs de dlk et leur utilisation
ES2930749T3 (es) 2015-07-02 2022-12-21 Hoffmann La Roche Lactamas bicíclicas como inhibidores de la proteína de interacción con el receptor 1 (RIP1) cinasa para tratar, por ejemplo, enfermedades inflamatorias
WO2017096301A1 (fr) 2015-12-04 2017-06-08 Denali Therapeutics Inc. Inhibiteurs dérivés d'isoxazolidine de protéine kinase 1 interagissant avec un récepteur (ripk 1)
WO2017109724A1 (fr) 2015-12-21 2017-06-29 Glaxosmithkline Intellectual Property Development Limited Amides hétérocycliques utilisés en tant qu'inhibiteurs de kinase
MA44007A (fr) 2016-02-05 2018-12-19 Denali Therapeutics Inc Inhibiteurs du récepteur interagissant avec protéine kinase 1
EP3548484A1 (fr) 2016-12-02 2019-10-09 H. Hoffnabb-La Roche Ag Composés amide bicycliques et leurs procédés d'utilisation
US11072607B2 (en) 2016-12-16 2021-07-27 Genentech, Inc. Inhibitors of RIP1 kinase and methods of use thereof
WO2018128908A1 (fr) 2017-01-05 2018-07-12 Microsoft Technology Licensing, Llc Redirection de sortie audio
SG11202000333UA (en) 2017-07-14 2020-02-27 Hoffmann La Roche Bicyclic ketone compounds and methods of use thereof
MA50356A (fr) 2017-10-11 2021-04-21 Hoffmann La Roche Composés bicycliques destinés à être utilisés en tant qu'inhibiteurs de la kinase rip1
SG11202002877RA (en) 2017-10-31 2020-04-29 Hoffmann La Roche Bicyclic sulfones and sulfoxides and methods of use thereof

Also Published As

Publication number Publication date
CN110914271A (zh) 2020-03-24
KR20200030558A (ko) 2020-03-20
RS65308B1 (sr) 2024-04-30
BR112020000771A2 (pt) 2020-07-14
SG11202000333UA (en) 2020-02-27
US11834461B2 (en) 2023-12-05
JP7258843B2 (ja) 2023-04-17
US11098058B2 (en) 2021-08-24
FI3652178T3 (fi) 2024-03-19
EP4397309A2 (fr) 2024-07-10
AU2021204369A1 (en) 2021-07-29
TWI805595B (zh) 2023-06-21
PL3652178T3 (pl) 2024-05-06
LT3652178T (lt) 2024-04-10
IL271981A (en) 2020-02-27
SI3652178T1 (sl) 2024-05-31
KR20240065201A (ko) 2024-05-14
JP2023085449A (ja) 2023-06-20
CA3067944C (fr) 2023-03-14
AU2018300043B2 (en) 2021-04-01
TW201920149A (zh) 2019-06-01
JP2020526549A (ja) 2020-08-31
WO2019012063A1 (fr) 2019-01-17
AR112274A1 (es) 2019-10-09
PH12020500105A1 (en) 2020-11-09
MA49560A (fr) 2020-05-20
RU2020106375A (ru) 2021-08-16
CL2020000101A1 (es) 2020-07-17
AU2023203292A1 (en) 2023-06-22
US20190100530A1 (en) 2019-04-04
CR20200002A (es) 2020-02-10
RU2020106375A3 (fr) 2022-03-25
AU2018300043A1 (en) 2020-01-16
IL271981B (en) 2022-09-01
EP3652178B1 (fr) 2024-01-24
PT3652178T (pt) 2024-03-18
ES2973661T3 (es) 2024-06-21
CO2020000134A2 (es) 2020-01-17
UA125448C2 (uk) 2022-03-09
DK3652178T3 (da) 2024-03-25
CA3185865A1 (fr) 2019-01-17
KR102664604B1 (ko) 2024-05-14
US20210139504A1 (en) 2021-05-13
HRP20240354T1 (hr) 2024-06-07
CA3067944A1 (fr) 2019-01-17
EP3652178A1 (fr) 2020-05-20
IL294961A (en) 2022-09-01

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