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YU151691A - 3-aril-4(3h)hinazolinon cck antagonisti - Google Patents

3-aril-4(3h)hinazolinon cck antagonisti

Info

Publication number
YU151691A
YU151691A YU151691A YU151691A YU151691A YU 151691 A YU151691 A YU 151691A YU 151691 A YU151691 A YU 151691A YU 151691 A YU151691 A YU 151691A YU 151691 A YU151691 A YU 151691A
Authority
YU
Yugoslavia
Prior art keywords
hydrogen
halo
hinazolinon
aril
benzyl
Prior art date
Application number
YU151691A
Other languages
English (en)
Inventor
J.R. Mc Cowan
K.J. Thrasher
Original Assignee
Eli Lilly And Co.
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 Eli Lilly And Co. filed Critical Eli Lilly And Co.
Publication of YU151691A publication Critical patent/YU151691A/sh

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
    • C07D403/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • 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
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Opisano je jedinjenje formule u kome n je 1 ili 2 i m je = ili 1; R je vodonik, C1-C4alkil, benzil, ili fenil; Z je vodonik ili halo; X2,X3,X4 i X5 su vodonik, halo, tri-fluorometil, C1-C6 alkoksi, C1-C5 alkil, C1-C6 alkiltio, i -NR2R3, gde R2 i R3 su nezavisno vodonik, C1-C4 alkil, benzil, ili fenil, ili R2 i R3 uzeti zajedno sa atomom azota za koji su vezani obrazuju 5-ili 6-tročlani prsten; ili Xr i Xr+1, gde r je 2,3, ili 4, uzeti zajedno obrazuju dvovalentnu C -C5 alkilen grupu ili metilendioksi; i Y5 i Y6 su vodonik, C1-C6 alkoksi, halo, i trifluorometil; i farmaceutski prihvatljive soli tog jedinjenja. Takodje su opisani postupci za dobijanje jedinjenja koja su predmet ovog pronalaska biološki aktivnih supstituisanih hinazolinona.
YU151691A 1990-09-13 1991-09-11 3-aril-4(3h)hinazolinon cck antagonisti YU151691A (sh)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US07/581,943 US5075313A (en) 1990-09-13 1990-09-13 3-aryl-4(3H)quinazolinone CCK antagonists and pharmaceutical formulations thereof

Publications (1)

Publication Number Publication Date
YU151691A true YU151691A (sh) 1994-01-20

Family

ID=24327210

Family Applications (1)

Application Number Title Priority Date Filing Date
YU151691A YU151691A (sh) 1990-09-13 1991-09-11 3-aril-4(3h)hinazolinon cck antagonisti

Country Status (20)

Country Link
US (1) US5075313A (sh)
EP (1) EP0475755B1 (sh)
JP (1) JPH04247080A (sh)
KR (1) KR920006350A (sh)
CN (1) CN1059722A (sh)
AU (1) AU641043B2 (sh)
CA (1) CA2050994A1 (sh)
CZ (1) CZ279774B6 (sh)
DE (1) DE69113379T2 (sh)
ES (1) ES2078455T3 (sh)
FI (1) FI914262L (sh)
HU (1) HUT59128A (sh)
IE (1) IE913217A1 (sh)
IL (1) IL99402A0 (sh)
MX (1) MX9101035A (sh)
NO (1) NO913579L (sh)
NZ (1) NZ239712A (sh)
PT (1) PT98915A (sh)
YU (1) YU151691A (sh)
ZA (1) ZA917149B (sh)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5340801A (en) * 1991-05-08 1994-08-23 Rhone-Poulenc Rorer Pharmaceuticals Inc. Compounds having cholecystokinin and gastrin antagonistic properties
US5204354A (en) * 1992-02-14 1993-04-20 Merck & Co., Inc. Substituted quinazolinones as neurotensin antagonists useful in the treatment of CNS disorders
US6982251B2 (en) 2000-12-20 2006-01-03 Schering Corporation Substituted 2-azetidinones useful as hypocholesterolemic agents
GB0031315D0 (en) * 2000-12-21 2001-02-07 Glaxo Group Ltd Indole derivatives
US7417039B2 (en) 2001-01-26 2008-08-26 Schering Corporation Use of substituted azetidinone compounds for the treatment of sitosterolemia
CN100509058C (zh) 2001-01-26 2009-07-08 先灵公司 过氧化物酶体增殖物激活受体(ppar)活化剂和甾醇吸收抑制剂的组合药以及对于血管适应症的治疗
US7071181B2 (en) 2001-01-26 2006-07-04 Schering Corporation Methods and therapeutic combinations for the treatment of diabetes using sterol absorption inhibitors
US7053080B2 (en) 2001-09-21 2006-05-30 Schering Corporation Methods and therapeutic combinations for the treatment of obesity using sterol absorption inhibitors
US7056906B2 (en) 2001-09-21 2006-06-06 Schering Corporation Combinations of hormone replacement therapy composition(s) and sterol absorption inhibitor(s) and treatments for vascular conditions in post-menopausal women
US7132415B2 (en) 2001-09-21 2006-11-07 Schering Corporation Methods and therapeutic combinations for the treatment of xanthoma using sterol absorption inhibitors
CA2504878A1 (en) 2002-11-06 2004-05-27 Schering Corporation Cholesterol absorption inhibitors for the treatment of demyelination
JP2006519869A (ja) 2003-03-07 2006-08-31 シェーリング コーポレイション 置換アゼチジノン化合物、置換アゼチジノン化合物を調製するためのプロセス、それらの処方物および使用
US7459442B2 (en) 2003-03-07 2008-12-02 Schering Corporation Substituted azetidinone compounds, processes for preparing the same, formulations and uses thereof
JP5137228B2 (ja) 2003-03-07 2013-02-06 メルク・シャープ・アンド・ドーム・コーポレーション 高コレステロール血症の処置のための置換アゼチジノン化合物、置換アゼチジノン処方物およびそれらの使用
MXPA05009501A (es) 2003-03-07 2005-10-18 Schering Corp Compuestos de azetidinona sustituidos, formulaciones y usos de los mismos para el tratamiento de hipercolesterolemia.
BRPI0412684A (pt) 2003-07-17 2006-10-03 Plexxinko Inc compostos ppar-ativos
US7348338B2 (en) * 2003-07-17 2008-03-25 Plexxikon, Inc. PPAR active compounds
GB0319126D0 (en) * 2003-08-14 2003-09-17 Smithkline Beecham Corp Chemical compounds
AU2005311826A1 (en) * 2004-11-30 2006-06-08 Plexxikon, Inc. Indole derivatives for use as PPAR active compounds
AU2005311925A1 (en) * 2004-11-30 2006-06-08 Plexxikon, Inc. Indole derivatives for use as PPAR PPAR active compounds
BRPI0615948A2 (pt) * 2005-09-07 2011-05-31 Plexxikon Inc composto ativo de ppar, sua composição, seu kit e seu uso
JP2009509932A (ja) * 2005-09-07 2009-03-12 プレキシコン,インコーポレーテッド Ppar活性化合物
CA2628441A1 (en) * 2005-11-04 2007-05-18 Hydra Biosciences, Inc. Compounds for modulating trpv3 function
PE20090159A1 (es) * 2007-03-08 2009-02-21 Plexxikon Inc COMPUESTOS DERIVADOS DE ACIDO INDOL-PROPIONICO COMO MODULADORES PPARs
JP2023512664A (ja) 2020-01-29 2023-03-28 カマリ ファーマ リミテッド 皮膚障害の治療に使用するための化合物及び組成物

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ192392A (en) * 1978-12-19 1983-02-15 M Ishikawa 3-(substituted (phenyl or pyridyl)) -3,4-dihydroquinazolin-4-ones
WO1989010355A1 (en) * 1988-04-05 1989-11-02 Abbott Laboratories Derivatives of tryptophan as cck antagonists

Also Published As

Publication number Publication date
DE69113379D1 (de) 1995-11-02
AU641043B2 (en) 1993-09-09
CN1059722A (zh) 1992-03-25
HUT59128A (en) 1992-04-28
CZ279774B6 (cs) 1995-06-14
CS279991A3 (en) 1992-04-15
US5075313A (en) 1991-12-24
FI914262A0 (fi) 1991-09-10
EP0475755B1 (en) 1995-09-27
NO913579L (no) 1992-03-16
PT98915A (pt) 1992-08-31
IE913217A1 (en) 1992-02-25
IL99402A0 (en) 1992-08-18
DE69113379T2 (de) 1996-03-21
ZA917149B (en) 1992-05-27
KR920006350A (ko) 1992-04-27
NZ239712A (en) 1993-06-25
FI914262L (fi) 1992-03-14
JPH04247080A (ja) 1992-09-03
EP0475755A1 (en) 1992-03-18
ES2078455T3 (es) 1995-12-16
CA2050994A1 (en) 1992-03-14
AU8382991A (en) 1992-03-19
NO913579D0 (no) 1991-09-11
MX9101035A (es) 1992-05-04
HU912921D0 (en) 1992-01-28

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