5,6-Diphenylpyridazine derivatives as acyl-CoA : cholesterol acyltransferase inhibitors

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dc.contributor.authorMaria Palola Giovannoni-
dc.contributor.authorVittorio Dal Piaz-
dc.contributor.authorByoung-Mog Kwon-
dc.contributor.authorMi Kyung Kim-
dc.contributor.authorYoung Kook Kim-
dc.contributor.authorLucio Toma-
dc.contributor.authorDaniela Barlocco-
dc.contributor.authorFranco Bernini-
dc.contributor.authorMonica Canavesi-
dc.date.accessioned2017-04-19T08:58:30Z-
dc.date.available2017-04-19T08:58:30Z-
dc.date.issued2001-
dc.identifier.issn0022-2623-
dc.identifier.uri10.1021/jm010807hko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/5627-
dc.description.abstractAlkyl-5, 6-diphenylpyridazine derivatives combining several main features of ACAT inhibitors, such as a long alkyl side chain linked to a heterocycle and the o-diphenyl system, were synthesized and tested. Moreover, modeling studies on representative terms were performed. Some compounds displayed ACAT inhibition in the micromolar range, both on the enzyme isolated from rat liver microsomes and in cell-free homogenate of murine macrophages.-
dc.publisherAmer Chem Soc-
dc.title5,6-Diphenylpyridazine derivatives as acyl-CoA : cholesterol acyltransferase inhibitors-
dc.title.alternative5,6-Diphenylpyridazine derivatives as acyl-CoA : cholesterol acyltransferase inhibitors-
dc.typeArticle-
dc.citation.titleJournal of Medicinal Chemistry-
dc.citation.number24-
dc.citation.endPage4295-
dc.citation.startPage4292-
dc.citation.volume44-
dc.contributor.affiliatedAuthorByoung-Mog Kwon-
dc.contributor.affiliatedAuthorMi Kyung Kim-
dc.contributor.affiliatedAuthorYoung Kook Kim-
dc.contributor.alternativeNameGiovannoni-
dc.contributor.alternativeNamePiaz-
dc.contributor.alternativeName권병목-
dc.contributor.alternativeName김미경-
dc.contributor.alternativeName김영국-
dc.contributor.alternativeNameToma-
dc.contributor.alternativeNameBarlocco-
dc.contributor.alternativeNameBernini-
dc.contributor.alternativeNameCanavesi-
dc.identifier.bibliographicCitationJournal of Medicinal Chemistry, vol. 44, no. 24, pp. 4292-4295-
dc.identifier.doi10.1021/jm010807h-
dc.description.journalClassY-
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