文献索引：DeVries, Vern G.; Bloom, Jonathan D.; Dutia, Minu D.; Katocs, Andrew S.; Largis, Elwood E. Journal of Medicinal Chemistry, 1989 , vol. 32, # 10 p. 2318 - 2325
The discovery that a series of N, N-dialkyl-"-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- Nn-butylurea (1 15) for more extensive biological evaluation. ACAT inhibitors are seen as potentially beneficial agents against hypercholesterolemia and atherosclerosis.
