Literature DB >> 2795605

Potential antiatherosclerotic agents. 6. Hypocholesterolemic trisubstituted urea analogues.

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.

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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


  1 in total

1.  A novel bis-aryl urea compound inhibits tumor proliferation via cathepsin D-associated apoptosis.

Authors:  Jianping Wu; Yao Huang; Qian Xie; Junfeng Zhang; Zhen Zhan
Journal:  Anticancer Drugs       Date:  2020-06       Impact factor: 2.248

  1 in total

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