MA32191B1 - Inhibiteurs du recepteur de chimiokine cxcr3 - Google Patents

Inhibiteurs du recepteur de chimiokine cxcr3

Info

Publication number
MA32191B1
MA32191B1 MA33173A MA33173A MA32191B1 MA 32191 B1 MA32191 B1 MA 32191B1 MA 33173 A MA33173 A MA 33173A MA 33173 A MA33173 A MA 33173A MA 32191 B1 MA32191 B1 MA 32191B1
Authority
MA
Morocco
Prior art keywords
chemokine receptor
receptor inhibitors
cxcr3
cxcr3 chemokine
benzsulfonamide
Prior art date
Application number
MA33173A
Other languages
Arabic (ar)
English (en)
Inventor
David S Thorpe
Martin Smrcina
Dagmar D Cabel
Original Assignee
Sanofi Aventis
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 Sanofi Aventis filed Critical Sanofi Aventis
Publication of MA32191B1 publication Critical patent/MA32191B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
    • C07D295/027—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
    • C07D295/033—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring with the ring nitrogen atoms directly attached to carbocyclic rings
    • 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
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/06—Antipsoriatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • 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
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • 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
    • C07D471/12—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 three hetero rings
    • C07D471/20—Spiro-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Dermatology (AREA)
  • Rheumatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Cardiology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Furan Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pyridine Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Cette invention concerne un composé 3-(amido ou sulfamido)-4-(4-azinyle substitué)benzamide ou benzsulfonamide défini ici. Le composé 3-(amido ou sulfamido)-(4-azinyle substitué)benzamide ou benzsulfonamide est utile comme inhibiteur du récepteur de chimiokine cxcr3, et pour la prévention ou le traitement d'une maladie médiée par le récepteur de chimiokine cxcr3 ou d'une affection associée chez un patient le nécessitant.
MA33173A 2008-02-19 2010-09-13 Inhibiteurs du recepteur de chimiokine cxcr3 MA32191B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US2973808P 2008-02-19 2008-02-19
PCT/US2009/034340 WO2009105435A1 (fr) 2008-02-19 2009-02-18 Inhibiteurs du récepteur de chimiokine cxcr3

Publications (1)

Publication Number Publication Date
MA32191B1 true MA32191B1 (fr) 2011-04-01

Family

ID=40527535

Family Applications (1)

Application Number Title Priority Date Filing Date
MA33173A MA32191B1 (fr) 2008-02-19 2010-09-13 Inhibiteurs du recepteur de chimiokine cxcr3

Country Status (25)

Country Link
US (1) US8268828B2 (fr)
EP (1) EP2262784B1 (fr)
JP (1) JP2011512412A (fr)
KR (1) KR20100123835A (fr)
CN (1) CN102007108A (fr)
AR (1) AR070430A1 (fr)
AU (1) AU2009215643A1 (fr)
BR (1) BRPI0908815A2 (fr)
CA (1) CA2715557A1 (fr)
CL (1) CL2009000368A1 (fr)
CO (1) CO6241113A2 (fr)
CR (1) CR11604A (fr)
DO (1) DOP2010000254A (fr)
EC (1) ECSP10010409A (fr)
IL (1) IL207597A0 (fr)
MA (1) MA32191B1 (fr)
MX (1) MX2010008397A (fr)
NI (1) NI201000132A (fr)
NZ (1) NZ587380A (fr)
PE (1) PE20091576A1 (fr)
RU (1) RU2010138577A (fr)
SV (1) SV2010003648A (fr)
TW (1) TW200948791A (fr)
WO (1) WO2009105435A1 (fr)
ZA (1) ZA201005314B (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20091576A1 (es) 2008-02-19 2009-11-05 Sanofi Aventis DERIVADOS DE 3-(AMIDO O SULFAMIDO)-4-(4-AZINIL SUSTITUIDO)BENZAMIDA COMO INHIBIDORES DEL RECEPTOR DE QUIMIOQUINAS CxCR3
EP2424840B1 (fr) 2009-04-27 2014-08-06 Boehringer Ingelheim International GmbH Antagonistes du récepteur cxcr3
US8952004B2 (en) 2010-01-07 2015-02-10 Boehringer Ingelheim International Gmbh CXCR3 receptor antagonists
KR101251788B1 (ko) 2010-12-06 2013-04-08 기아자동차주식회사 차량 연비 정보 단말표시 시스템 및 그 방법
CA2834199C (fr) * 2011-07-18 2020-01-07 Merck Patent Gmbh Benzamides
EP2601950A1 (fr) 2011-12-06 2013-06-12 Sanofi Dérivés de l'acide carboxylique de cycloalcanes en tant qu'antagonistes du recepteur CXCR3
AU2013208082B2 (en) 2012-01-10 2017-07-20 Merck Patent Gmbh Benzamide derivatives as modulators of the follicle stimulating hormone
PL2809668T3 (pl) 2012-02-02 2018-02-28 Idorsia Pharmaceuticals Ltd Związki 4-(benzimidazol-2-ilo)tiazolowowe i pokrewne aza-pochodne
EP2666769A1 (fr) 2012-05-23 2013-11-27 Sanofi Dérivés dýacide B-amino substitués en tant quýantagoniste de récepteur CXCR3
TWI630205B (zh) 2013-07-22 2018-07-21 瑞士商愛杜西亞製藥有限公司 １－（哌－１－基）－２－（［１，２，４］三唑－１－基）－乙酮衍生物
AR099789A1 (es) 2014-03-24 2016-08-17 Actelion Pharmaceuticals Ltd Derivados de 8-(piperazin-1-il)-1,2,3,4-tetrahidro-isoquinolina
JP2017538659A (ja) * 2014-09-10 2017-12-28 エピザイム インコーポレイテッド Ｓｍｙｄ阻害剤
AR103399A1 (es) 2015-01-15 2017-05-10 Actelion Pharmaceuticals Ltd Derivados de (r)-2-metil-piperazina como moduladores del receptor cxcr3
HUE042559T2 (hu) 2015-01-15 2019-07-29 Idorsia Pharmaceuticals Ltd Hidroxialkil-piperazin származékok mint cxcr3 receptor modulátorok
CN110520127B (zh) * 2017-03-26 2023-05-16 武田药品工业株式会社 作为gpr6的调节剂的经哌啶基取代的杂芳族羧酰胺和经哌嗪基取代的杂芳族羧酰胺
CN116410159B (zh) * 2023-06-09 2023-08-22 济南国鼎医药科技有限公司 一种恩曲替尼中间体的制备方法及其应用

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FR2052541A5 (fr) 1969-06-13 1971-04-09 Takeda Chemical Industries Ltd
US3840556A (en) 1971-05-28 1974-10-08 Lilly Co Eli Penicillin conversion by halogen electrophiles and anti-bacterials derived thereby
US6124319A (en) 1997-01-21 2000-09-26 Merck & Co., Inc. 3,3-disubstituted piperidines as modulators of chemokine receptor activity
US6469002B1 (en) 2001-04-19 2002-10-22 Millennium Pharmaceuticals, Inc. Imidazolidine compounds
US6794379B2 (en) 2001-06-06 2004-09-21 Tularik Inc. CXCR3 antagonists
GB0203994D0 (en) 2002-02-20 2002-04-03 Celltech R&D Ltd Chemical compounds
US20050272936A1 (en) 2002-06-03 2005-12-08 Axten Jeffrey M Imidazolium cxcr3 inhibitors
US6734659B1 (en) 2002-06-13 2004-05-11 Mykrolis Corporation Electronic interface for use with dual electrode capacitance diaphragm gauges
US7417045B2 (en) * 2005-02-16 2008-08-26 Schering Corporation Heterocyclic substituted pyridine or phenyl compounds with CXCR3 antagonist activity
MX2007009946A (es) * 2005-02-16 2007-09-26 Schering Corp Piperazin-piperidinas sustituidas con piridilo y fenilo con actividad antagonista de cxcr3.
CA2598458A1 (fr) 2005-02-16 2006-08-24 Schering Corporation Piperazine-piperidines pyrazinyl substituees a activite antagoniste des cxcr3
US20080312215A1 (en) * 2005-06-28 2008-12-18 Pharmacopeia Drug Discovery, Inc. Substituted [1,4]-diazepanes as CXCR3 antagonists and their use in the treatment of inflammatory disorders
ES2382163T3 (es) 2005-10-11 2012-06-05 Schering Corporation Compuestos heterocíclicos sustituidos con actividad antagonista de CXCR3
WO2007064553A2 (fr) 2005-11-29 2007-06-07 Merck & Co., Inc. Derives de thiazole comme modulateurs de recepteurs cxcr3
KR20080106970A (ko) 2006-03-21 2008-12-09 쉐링 코포레이션 Ｃｘｃｒ３ 길항제 활성을 갖는 헤테로사이클릭 치환된 피리딘 화합물
AU2007272884A1 (en) 2006-07-14 2008-01-17 Pharmacopeia, Inc. Heterocyclic substituted piperazine compounds with CXCR3 antagonist activity
PE20091576A1 (es) 2008-02-19 2009-11-05 Sanofi Aventis DERIVADOS DE 3-(AMIDO O SULFAMIDO)-4-(4-AZINIL SUSTITUIDO)BENZAMIDA COMO INHIBIDORES DEL RECEPTOR DE QUIMIOQUINAS CxCR3

Also Published As

Publication number Publication date
CL2009000368A1 (es) 2009-06-26
AU2009215643A1 (en) 2009-08-27
EP2262784B1 (fr) 2014-04-16
IL207597A0 (en) 2010-12-30
NI201000132A (es) 2011-03-16
BRPI0908815A2 (pt) 2019-09-24
WO2009105435A1 (fr) 2009-08-27
CA2715557A1 (fr) 2009-08-27
ECSP10010409A (es) 2010-09-30
MX2010008397A (es) 2010-08-23
KR20100123835A (ko) 2010-11-25
CO6241113A2 (es) 2011-01-20
DOP2010000254A (es) 2010-08-31
CN102007108A (zh) 2011-04-06
US20100305088A1 (en) 2010-12-02
NZ587380A (en) 2011-09-30
US8268828B2 (en) 2012-09-18
AR070430A1 (es) 2010-04-07
ZA201005314B (en) 2011-03-30
EP2262784A1 (fr) 2010-12-22
SV2010003648A (es) 2011-01-31
RU2010138577A (ru) 2012-03-27
TW200948791A (en) 2009-12-01
PE20091576A1 (es) 2009-11-05
JP2011512412A (ja) 2011-04-21
CR11604A (es) 2010-10-05

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