DE69106532T2 - N-substituierte lactame als cholecystokinin-antagonisten. - Google Patents

N-substituierte lactame als cholecystokinin-antagonisten.

Info

Publication number
DE69106532T2
DE69106532T2 DE69106532T DE69106532T DE69106532T2 DE 69106532 T2 DE69106532 T2 DE 69106532T2 DE 69106532 T DE69106532 T DE 69106532T DE 69106532 T DE69106532 T DE 69106532T DE 69106532 T2 DE69106532 T2 DE 69106532T2
Authority
DE
Germany
Prior art keywords
substituted
lactame
cholecystokinin antagonists
cholecystokinin
antagonists
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Fee Related
Application number
DE69106532T
Other languages
English (en)
Other versions
DE69106532D1 (de
Inventor
Daniel Becker
Daniel Flynn
Clara Villamil
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
GD Searle LLC
Original Assignee
GD Searle LLC
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 GD Searle LLC filed Critical GD Searle LLC
Publication of DE69106532D1 publication Critical patent/DE69106532D1/de
Application granted granted Critical
Publication of DE69106532T2 publication Critical patent/DE69106532T2/de
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • 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
    • C07D401/12—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 chain containing hetero atoms as chain links
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24—Oxygen or sulfur atoms
    • C07D207/26—2-Pyrrolidones
    • C07D207/273—2-Pyrrolidones with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
    • C07D207/277—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D207/28—2-Pyrrolidone-5- carboxylic acids; Functional derivatives thereof, e.g. esters, nitriles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic 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
    • C07D403/12—Heterocyclic 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

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Pyrrole Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Peptides Or Proteins (AREA)
DE69106532T 1990-12-11 1991-11-25 N-substituierte lactame als cholecystokinin-antagonisten. Expired - Fee Related DE69106532T2 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US07/626,590 US5202344A (en) 1990-12-11 1990-12-11 N-substituted lactams useful as cholecystokinin antagonists
PCT/US1991/008648 WO1992010476A1 (en) 1990-12-11 1991-11-25 N-substituted lactams useful as cholecystokinin antagonists

Publications (2)

Publication Number Publication Date
DE69106532D1 DE69106532D1 (de) 1995-02-16
DE69106532T2 true DE69106532T2 (de) 1995-06-08

Family

ID=24511043

Family Applications (1)

Application Number Title Priority Date Filing Date
DE69106532T Expired - Fee Related DE69106532T2 (de) 1990-12-11 1991-11-25 N-substituierte lactame als cholecystokinin-antagonisten.

Country Status (12)

Country Link
US (2) US5202344A (de)
EP (1) EP0561941B1 (de)
JP (1) JPH06503827A (de)
AT (1) ATE116638T1 (de)
AU (1) AU9057191A (de)
CA (1) CA2097517A1 (de)
DE (1) DE69106532T2 (de)
DK (1) DK0561941T3 (de)
ES (1) ES2067322T3 (de)
IE (1) IE62703B1 (de)
PT (1) PT99739A (de)
WO (1) WO1992010476A1 (de)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IE912285A1 (en) * 1990-07-12 1992-01-15 Black James Foundation Amino acid derivatives
DE4127404A1 (de) * 1991-08-19 1993-02-25 Thomae Gmbh Dr K Cyclische iminoderivate, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung
EP0719253B1 (de) * 1993-09-17 2004-04-28 Pfizer Inc. 3-amino-5-carboxy-substituierte piperidine und 3-amino-4-carboxy-substituierte pyrrolidine als tachykinin-antagonisten
US6083943A (en) * 1993-09-17 2000-07-04 Pfizer Inc Substituted azaheterocyclecarboxylic acid
US5719296A (en) * 1995-10-30 1998-02-17 Merck & Co., Inc. Pseudopeptide lactam inhibitors of peptide binding to MHC class II proteins
AU6659298A (en) 1997-02-18 1998-09-08 Thomas Jefferson University Compositions that bind to pancreatic cancer cells and methods of using the same
PL347591A1 (en) * 1998-11-09 2002-04-08 Gastrin and cholecystokinin receptor ligands
US6207638B1 (en) 2000-02-23 2001-03-27 Pacifichealth Laboratories, Inc. Nutritional intervention composition for enhancing and extending satiety
GB0011095D0 (en) 2000-05-08 2000-06-28 Black James Foundation astrin and cholecystokinin receptor ligands (III)
US6558690B2 (en) 2000-12-15 2003-05-06 Pacific Health Laboratories, Inc. Nutritional composition for improving the efficacy of a lipase inhibitor
US6429190B1 (en) 2000-12-15 2002-08-06 Pacifichealth Laboratories, Inc. Method for extending the satiety of food by adding a nutritional composition designed to stimulate cholecystokinin(CCK)
EP1434577A1 (de) * 2001-10-03 2004-07-07 Ucb, S.A. Pyrrolidinon-derivate
GB0130705D0 (en) * 2001-12-21 2002-02-06 Glaxo Group Ltd Chemical compounds
AU2003263393A1 (en) * 2002-09-04 2004-03-29 Glenmark Pharmaceuticals Limited New heterocyclic amide compounds useful for the treatment of inflammatory and allergic disorders: process for their preparation and pharmaceutical compositions containing them
DE60317918T2 (de) 2002-10-23 2009-01-29 Glenmark Pharmaceuticals Ltd. Tricyclische verbindungen zur behandlung von entzündlichen und allergischen erkrankungen verfahren zu deren herstellung und sie enthaltende pharmazeutische zusammensetzungen
BRPI0409747A (pt) 2003-04-11 2006-05-09 Glenmark Pharmaceuticals Sa novos compostos heterocìclicos úteis para tratamento de distúrbios inflamatórios e alérgicos, processo para sua preparação e composições farmacêuticas contendo estes
GB0314373D0 (en) 2003-06-19 2003-07-23 Glaxo Group Ltd Chemical compounds
AR044805A1 (es) 2003-06-19 2005-10-05 Glaxo Group Ltd Compuesto de (2-oxo-3-pirrolidinil) sulfonamida, composicion farmaceutica que lo comprende, su uso para prepararla, y proceso para preparar dicho compuesto
GB0314299D0 (en) 2003-06-19 2003-07-23 Glaxo Group Ltd Chemical compounds
MX2007004400A (es) 2004-10-13 2007-06-19 Glenmark Pharmaceuticals Sa Procedimiento para la preparacion de n-(3,5-dicloropirid-a-il)-4- ifluorometoxi-8-metanosulfonamido-dibenzo [b,d] difuran-1-carboxamida.
WO2006064355A2 (en) 2004-12-17 2006-06-22 Glenmark Pharmaceuticals S.A. Novel heterocyclic compounds useful for the treatment of inflammatory and allergic disorders
DK1831227T3 (da) 2004-12-17 2013-08-19 Glenmark Pharmaceuticals Sa Hidtil ukendte, heterocykliske forbindelser, der er anvendelige til behandling af inflammatoriske og allergiske forstyrrelser
FR2913888B1 (fr) * 2007-03-21 2010-01-01 Jean Pierre Breda Procede et dispositif d'irradiation par rayonnement d'energie photonique modulee
GB0910003D0 (en) 2009-06-11 2009-07-22 Univ Leuven Kath Novel compounds for the treatment of neurodegenerative diseases
EA027136B1 (ru) * 2012-07-02 2017-06-30 Пнб Веспер Лайф Сайенс Пвт Лимитед Новые лиганды холецистокининовых рецепторов
WO2015079692A1 (ja) * 2013-11-28 2015-06-04 杏林製薬株式会社 ウレア誘導体、またはその薬理学的に許容される塩
PE20210046A1 (es) 2018-03-05 2021-01-08 Bristol Myers Squibb Co Agonistas de fenilpirrolidinona del receptor 2 de formil peptido

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3474093A (en) * 1966-05-03 1969-10-21 American Home Prod Enamine adducts of n-acyloxy-n-acylaminoacetanilide
US4200572A (en) * 1975-09-03 1980-04-29 Smithkline Corporation Substituted azetidinones
US4085100A (en) * 1976-11-01 1978-04-18 Smithkline Corporation Intermediate for dephthaloylation of azetidinone compounds
US4260743A (en) * 1979-12-31 1981-04-07 Gist-Brocades N.V. Preparation of β-lactams and intermediates therefor
US4757068A (en) * 1984-06-26 1988-07-12 Merck & Co., Inc. Lactams and bicyclic lactams useful as cholecystokinin antagonists

Also Published As

Publication number Publication date
JPH06503827A (ja) 1994-04-28
IE62703B1 (en) 1995-02-22
CA2097517A1 (en) 1992-06-12
IE914293A1 (en) 1992-06-17
ATE116638T1 (de) 1995-01-15
EP0561941B1 (de) 1995-01-04
US5202344A (en) 1993-04-13
PT99739A (pt) 1992-11-30
DE69106532D1 (de) 1995-02-16
WO1992010476A1 (en) 1992-06-25
DK0561941T3 (da) 1995-03-06
ES2067322T3 (es) 1995-03-16
AU9057191A (en) 1992-07-08
EP0561941A1 (de) 1993-09-29
US5314886A (en) 1994-05-24

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Legal Events

Date Code Title Description
8364 No opposition during term of opposition
8339 Ceased/non-payment of the annual fee