IT1265209B1 - DIPHENYLIMIDAZOLES USEFUL IN THE TREATMENT OF DYSLIPIDEMIA, ARTERIOSCLEROSIS AND CORONARY DISEASES PROCEDURE FOR THEIR - Google Patents

DIPHENYLIMIDAZOLES USEFUL IN THE TREATMENT OF DYSLIPIDEMIA, ARTERIOSCLEROSIS AND CORONARY DISEASES PROCEDURE FOR THEIR

Info

Publication number
IT1265209B1
IT1265209B1 IT93MI002468A ITMI932468A IT1265209B1 IT 1265209 B1 IT1265209 B1 IT 1265209B1 IT 93MI002468 A IT93MI002468 A IT 93MI002468A IT MI932468 A ITMI932468 A IT MI932468A IT 1265209 B1 IT1265209 B1 IT 1265209B1
Authority
IT
Italy
Prior art keywords
diphenylimidazoles
dyslipidemia
arteriosclerosis
procedure
useful
Prior art date
Application number
IT93MI002468A
Other languages
Italian (it)
Inventor
Marino Gobetti
Massimiliano Palladino
Ermes Vanotti
Manuela Villa
Massimo Bani
Rita Bormetti
Vincenzo Olgiati
Original Assignee
Pierrel Spa
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 Pierrel Spa filed Critical Pierrel Spa
Priority to IT93MI002468A priority Critical patent/IT1265209B1/en
Publication of ITMI932468A0 publication Critical patent/ITMI932468A0/en
Priority to EP94931591A priority patent/EP0680472A1/en
Priority to CA002154475A priority patent/CA2154475A1/en
Priority to AU80618/94A priority patent/AU8061894A/en
Priority to PCT/EP1994/003684 priority patent/WO1995014673A1/en
Priority to JP7514784A priority patent/JPH08506122A/en
Publication of ITMI932468A1 publication Critical patent/ITMI932468A1/en
Application granted granted Critical
Publication of IT1265209B1 publication Critical patent/IT1265209B1/en

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
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • 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
    • A61P9/08—Vasodilators for multiple indications
    • 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
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
    • C07D233/84—Sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems

Abstract

I difenilimidazoli aventi formula di struttura generale (I) (FORMULA I) dove Z rappresenta 4,5-difenilimidazol-2-tio, 2-piridossi; 3,5-diterbutil,4-idrossi-fenil-1-tio; imidazol 1,2-b pirazol-1-ile anche sostituito, 2,3-diidro-1H-imidazo 1,2-b pirazol-1-ile, oppure (FORMULA II) tiazolidin-2,4-dione-5-ile,hanno attività ACAT inibitoria.Sono anche descritti i metodi per la loro preparazione.The diphenylimidazoles having formula of general structure (I) (FORMULA I) where Z represents 4,5-diphenylimidazol-2-thio, 2-pyridoxy; 3,5-diterbutyl, 4-hydroxy-phenyl-1-thio; imidazol 1,2-b pyrazol-1-ile also substituted, 2,3-dihydro-1H-imidazo 1,2-b pyrazol-1-ile, or (FORMULA II) thiazolidin-2,4-dione-5-ile , have inhibitory ACAT activity.The methods for their preparation are also described.

IT93MI002468A 1993-11-22 1993-11-22 DIPHENYLIMIDAZOLES USEFUL IN THE TREATMENT OF DYSLIPIDEMIA, ARTERIOSCLEROSIS AND CORONARY DISEASES PROCEDURE FOR THEIR IT1265209B1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
IT93MI002468A IT1265209B1 (en) 1993-11-22 1993-11-22 DIPHENYLIMIDAZOLES USEFUL IN THE TREATMENT OF DYSLIPIDEMIA, ARTERIOSCLEROSIS AND CORONARY DISEASES PROCEDURE FOR THEIR
EP94931591A EP0680472A1 (en) 1993-11-22 1994-11-09 4,5-diphenylimidazole derivatives, their preparation and their use as acyl coenzyme a: cholesterol-0-acyl-transferase (acat) inhibitor
CA002154475A CA2154475A1 (en) 1993-11-22 1994-11-09 4,5-diphenylimidazole derivatives, their preparation and their use as acyl coenzyme a: cholesterol-0-acyl-transferase (acat) inhibitor
AU80618/94A AU8061894A (en) 1993-11-22 1994-11-09 4,5-diphenylimidazole derivatives, their preparation and their use as acyl coenzyme A: cholesterol-0-acyl-transferase (ACAT) inhibitor
PCT/EP1994/003684 WO1995014673A1 (en) 1993-11-22 1994-11-09 4,5-diphenylimidazole derivatives, their preparation and their use as acyl coenzyme a: cholesterol-0-acyl-transferase (acat) inhibitor
JP7514784A JPH08506122A (en) 1993-11-22 1994-11-09 Novel diphenylimidazole effective for treatment of dyslipidemia, atherosclerosis and heart disease, method for producing the same, and pharmaceutical composition containing them

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT93MI002468A IT1265209B1 (en) 1993-11-22 1993-11-22 DIPHENYLIMIDAZOLES USEFUL IN THE TREATMENT OF DYSLIPIDEMIA, ARTERIOSCLEROSIS AND CORONARY DISEASES PROCEDURE FOR THEIR

Publications (3)

Publication Number Publication Date
ITMI932468A0 ITMI932468A0 (en) 1993-11-22
ITMI932468A1 ITMI932468A1 (en) 1995-05-22
IT1265209B1 true IT1265209B1 (en) 1996-10-31

Family

ID=11367238

Family Applications (1)

Application Number Title Priority Date Filing Date
IT93MI002468A IT1265209B1 (en) 1993-11-22 1993-11-22 DIPHENYLIMIDAZOLES USEFUL IN THE TREATMENT OF DYSLIPIDEMIA, ARTERIOSCLEROSIS AND CORONARY DISEASES PROCEDURE FOR THEIR

Country Status (6)

Country Link
EP (1) EP0680472A1 (en)
JP (1) JPH08506122A (en)
AU (1) AU8061894A (en)
CA (1) CA2154475A1 (en)
IT (1) IT1265209B1 (en)
WO (1) WO1995014673A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU1182400A (en) * 1998-11-17 2000-06-05 Fuji Photo Film Co., Ltd. Heteroarylthio compounds and cancer remedies containing the same
JPWO2004007464A1 (en) * 2002-07-10 2005-11-10 住友製薬株式会社 Imidazole derivatives

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4188397A (en) * 1978-09-22 1980-02-12 Smithkline Corporation 2,2-Alkyldiylbis(thio)bis(imidazoles)
US4716175A (en) * 1987-02-24 1987-12-29 Warner-Lambert Company Saturated fatty acid amides as inhibitors of acyl-CoA:cholesterol acyltransferase
IL96619A0 (en) * 1989-12-11 1991-09-16 Rhone Poulenc Sante Imidazole derivatives,process for their preparation and pharmaceutical compositions containing them
WO1991009030A1 (en) * 1989-12-12 1991-06-27 Rhone-Poulenc Sante 2-substituted 4,5-diphenyl-imidazoles
WO1991010662A1 (en) * 1990-01-12 1991-07-25 Rhone-Poulenc Rorer S.A. 2-substituted 4,5-diphenyl-imidazoles
GB9005966D0 (en) * 1990-03-16 1990-05-09 May & Baker Ltd New compositions of matter
PL296945A1 (en) * 1990-07-03 1992-07-13 Yamanouchi Pharma Co Ltd
IT1248528B (en) * 1991-06-21 1995-01-19 Pierrel Spa AROMATIC ETHER AND THIOETHER (HETER) DERIVATIVES HAVING ANTI-HYPERLIPIDEMIC ACTIVITY, PROCEDURE FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM.
GB9115190D0 (en) * 1991-07-12 1991-08-28 Rhone Poulenc Rorer Ltd New compositions of matter
CA2085844A1 (en) * 1991-12-27 1993-06-28 Nobuyuki Hamanaka Fused benzeneoxyacetic acid derivatives
US5364875A (en) * 1992-05-11 1994-11-15 The Du Pont Merck Pharmaceutical Company Imidazoles linked to bicyclic heterocyclic groups for the treatment of atherosclerosis
US5310748A (en) * 1992-05-11 1994-05-10 The Du Pont Merck Pharmaceutical Company Imidazoles for the treatment of atherosclerosis

Also Published As

Publication number Publication date
ITMI932468A1 (en) 1995-05-22
ITMI932468A0 (en) 1993-11-22
AU8061894A (en) 1995-06-13
EP0680472A1 (en) 1995-11-08
CA2154475A1 (en) 1995-06-01
JPH08506122A (en) 1996-07-02
WO1995014673A1 (en) 1995-06-01

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