| Literature DB >> 3701793 |
G E Stokker, A W Alberts, J L Gilfillan, J W Huff, R L Smith.
Abstract
A limited study was conducted to determine the biological consequences of rendering the phenyl rings of the previously reported 7-(3,5-disubstituted [1,1'-biphenyl]-2-yl)-3,5-dihydroxy-6-heptenoic acids coplanar. Such constraint substantially diminished intrinsic HMG-CoA reductase inhibitory activity.Entities:
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Year: 1986 PMID: 3701793 DOI: 10.1021/jm00155a041
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446