IL94082A0 - 3-n-substituted carbamoyl-indole derivatives,their preparation and pharmaceutical compositions containing them - Google Patents

3-n-substituted carbamoyl-indole derivatives,their preparation and pharmaceutical compositions containing them

Info

Publication number
IL94082A0
IL94082A0 IL94082A IL9408290A IL94082A0 IL 94082 A0 IL94082 A0 IL 94082A0 IL 94082 A IL94082 A IL 94082A IL 9408290 A IL9408290 A IL 9408290A IL 94082 A0 IL94082 A0 IL 94082A0
Authority
IL
Israel
Prior art keywords
preparation
pharmaceutical compositions
compositions containing
substituted carbamoyl
indole derivatives
Prior art date
Application number
IL94082A
Other languages
English (en)
Original Assignee
Duphar Int Res
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 Duphar Int Res filed Critical Duphar Int Res
Publication of IL94082A0 publication Critical patent/IL94082A0/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • 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
    • C07D471/06Peri-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
    • C07D487/06Peri-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/06Peri-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)
IL94082A 1989-04-18 1990-04-13 3-n-substituted carbamoyl-indole derivatives,their preparation and pharmaceutical compositions containing them IL94082A0 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL8900963 1989-04-18

Publications (1)

Publication Number Publication Date
IL94082A0 true IL94082A0 (en) 1991-01-31

Family

ID=19854496

Family Applications (1)

Application Number Title Priority Date Filing Date
IL94082A IL94082A0 (en) 1989-04-18 1990-04-13 3-n-substituted carbamoyl-indole derivatives,their preparation and pharmaceutical compositions containing them

Country Status (8)

Country Link
US (1) US5102901A (fr)
EP (1) EP0393766A3 (fr)
JP (1) JPH02292281A (fr)
AU (1) AU634534B2 (fr)
CA (1) CA2014641A1 (fr)
IL (1) IL94082A0 (fr)
NZ (1) NZ233285A (fr)
ZA (1) ZA902794B (fr)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8814277D0 (en) * 1988-06-16 1988-07-20 Glaxo Group Ltd Chemical compounds
EP0375045A1 (fr) * 1988-12-22 1990-06-27 Duphar International Research B.V Dérivés d'indoles annelés
US4916129A (en) * 1989-01-19 1990-04-10 E. I. Du Pont De Nemours And Company Combination β-blocking/angiotensin II blocking antihypertensives
GB8913646D0 (en) * 1989-06-14 1989-08-02 Glaxo Group Ltd Chemical compounds
HU211081B (en) * 1990-12-18 1995-10-30 Sandoz Ag Process for producing indole derivatives as serotonin antagonists and pharmaceutical compositions containing the same
US6069162A (en) * 1996-05-27 2000-05-30 Fujisawa Pharmaceutical Co., Ltd. Indolyl and benzofuranyl carboxamides as inhibitors of nitric oxide production
WO2002041889A2 (fr) * 2000-11-24 2002-05-30 Smithkline Beecham P.L.C. Composes utiles pour le traitement de troubles du snc
BR0212676A (pt) * 2001-09-21 2006-05-23 Upjohn Co compostos terapêuticos ligantes de 5-ht, composições farmacêuticas compreendendo tais compostos e seus usos
WO2005058327A1 (fr) 2003-12-17 2005-06-30 Akzo Nobel N.V. Derives tricycliques de piperazine 1-[(3-indol-3-yl)carbonyl] utiles en tant qu’agonistes du recepteur cannabinoide cb1
DE102004025000A1 (de) * 2004-05-21 2005-12-08 Bayer Technology Services Gmbh Verfahren zur Herstellung von chemischen und pharmazeutischen Produkten mit integrierter Mehrsäulen-Chromatographie
CN101460458A (zh) 2006-02-15 2009-06-17 阿勒根公司 具有1-磷酸-鞘氨醇(s1p)受体拮抗剂生物活性的带芳基或者杂芳基基团的吲哚-3-羧酸的酰胺、酯、硫代酰胺和硫羟酸酯化合物
US8097644B2 (en) * 2006-03-28 2012-01-17 Allergan, Inc. Indole compounds having sphingosine-1-phosphate (S1P) receptor antagonist
US8524917B2 (en) * 2007-01-11 2013-09-03 Allergan, Inc. 6-substituted indole-3-carboxylic acid amide compounds having sphingosine-1-phosphate (S1P) receptor antagonist biological activity
MX2009007334A (es) 2007-01-11 2009-07-15 Allergan Inc Compuestos de amida del acido indol-3-carboxilico 6-substituido que tienen actividad antagonista biologica del receptor esfingosina-1-fosfato (s1p).
BRPI0817397A2 (pt) * 2007-09-24 2015-04-07 Allergan Inc Compostos indol contendo grupos arila ou heteroarila com atividade biológica do receptor de esfingosina-1-fosfato (sip)
US8143291B2 (en) 2008-05-09 2012-03-27 Allergan, Inc. Indole compounds bearing aryl or heteroaryl groups having sphingosine-1-phosphate (S1P) receptor biological activity
EP2328863A1 (fr) * 2008-08-12 2011-06-08 Allergan, Inc. Antagonistes des récepteurs de la sphingosine-1-phosphate (s1p) et leurs procédés d'utilisation
WO2011008475A1 (fr) 2009-06-30 2011-01-20 Allergan, Inc. Composés de 2-(arylméthyl, aryloxy ou arylthio)-n-pyridin-2-yl-arylacétamide ou de 2,2-bis(aryl)-n-pyridin-2-yl-acétamide éventuellement substitués comme médicaments pour le traitement de maladies des yeux
US8168795B2 (en) 2009-08-11 2012-05-01 Allergan, Inc. Selective sphingosine-1-phosphate receptor antagonists
WO2011028927A1 (fr) 2009-09-04 2011-03-10 Allergan, Inc. Antagonistes sélectifs des récepteurs de sphingosine-1-phosphate
CA2775587A1 (fr) 2009-09-29 2011-04-07 Allergan, Inc. Composes pyridines a noyaux condenses comme modulateurs selectifs d'un sous-type des recepteurs de la sphingosine-1-phosphate-2 (s1p2)
US8741875B2 (en) 2009-11-24 2014-06-03 Allergan, Inc. Compounds as receptor modulators with therapeutic utility
MX2012006028A (es) 2009-11-24 2012-06-19 Allergan Inc Compuestos novedosos como moduladores de receptor con utilidad terapeutica.
WO2011082266A2 (fr) 2009-12-30 2011-07-07 Arqule, Inc. Composés hétérocycliques substitués
BR112013012719A2 (pt) 2010-11-22 2019-09-24 Allergan Inc "compostos como moduladores de receptor com utilidade terapêutica".

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4691016A (en) * 1981-11-06 1987-09-01 Riker Laboratories, Inc. Intermediates for the preparation of 8,9-dihalobenzo[ij]quinolizine carboxylic acids
US4808581A (en) * 1986-03-17 1989-02-28 Glaxo Group Limited Imidazolyl- indolylpropanones as 5-HT3 receptor antagonists
DE3885357T2 (de) * 1987-06-29 1994-03-24 Duphar Int Res Anellierte Indolderivate.
EP0306323B1 (fr) * 1987-09-03 1994-09-21 Glaxo Group Limited Dérivés de lactames
GB8720693D0 (en) * 1987-09-03 1987-10-07 Glaxo Group Ltd Chemical compounds
GB8723157D0 (en) * 1987-10-02 1987-11-04 Beecham Group Plc Compounds
GB8802127D0 (en) * 1988-02-01 1988-03-02 Glaxo Group Ltd Chemical compounds
GB8814277D0 (en) * 1988-06-16 1988-07-20 Glaxo Group Ltd Chemical compounds
EP0350130A3 (fr) * 1988-07-07 1991-07-10 Duphar International Research B.V 1H-indazoles 1,7-annelés substitués
GB8913646D0 (en) * 1989-06-14 1989-08-02 Glaxo Group Ltd Chemical compounds

Also Published As

Publication number Publication date
US5102901A (en) 1992-04-07
CA2014641A1 (fr) 1990-10-18
ZA902794B (en) 1991-04-24
JPH02292281A (ja) 1990-12-03
EP0393766A3 (fr) 1991-11-06
NZ233285A (en) 1992-06-25
AU5361490A (en) 1990-10-25
AU634534B2 (en) 1993-02-25
EP0393766A2 (fr) 1990-10-24

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