| Literature DB >> 2795605 |
V G DeVries1, J D Bloom, M D Dutia, A S Katocs, E E Largis.
Abstract
The discovery that a series of N,N-dialkyl-N'-arylureas were inhibitors of the ACAT enzyme has led to a structure-activity study involving the systematic modification of three sites of the urea backbone. This study culminated in the selection of N'-(2,4-dimethylphenyl)-N-benzyl-N-n-butylurea (115) for more extensive biological evaluation. ACAT inhibitors are seen as potentially beneficial agents against hypercholesterolemia and atherosclerosis.Entities:
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Year: 1989 PMID: 2795605 DOI: 10.1021/jm00130a016
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446