The Journal of Antibiotics · 1996 · 41 citations · 8 references
Life SciencesBiochemistryPharmacologyDrug DiscoveryEnzymologyLipid BiochemistryCholesterol BiosynthesisCholesterol MetabolismFatty Acid BiosynthesisLipid BiosynthesisLipid MetabolismSterol MetabolismAcyl-coa DehydrogenasesAcyltransferase ActivityAcyltransferase EnzymesCholesterol EsterificationPharmacological Inhibition Of Cholesterol Biosynthesis
A novel acyl-CoA : cholesterol acyltransferase (ACAT) inhibitor, designated epi-cochlioquinone A has been isolated from the fermentation broth of Stachybotrys bisbyi SANK 17777. The molecular formula, physicochemical properties, NMR spectroscopic analysis and X-ray crystallographic analysis revealed that this compound was a stereoisomer of cochlioquinone A, which has been previously reported as a nematocidal agent. It inhibited ACAT activity in an enzyme assay using rat liver microsomes with an IC50 value of 1.7 microM. However, it showed about 10-fold less potent inhibitory effect on plasma lecithin cholesterol acyltransferase (LCAT) than on ACAT. In addition, it inhibited in vivo cholesterol absorption in rats by 50% at 75 mg/kg.
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<i>International Tables for X-ray Crystallography</i>
Acta Crystallographica Section B · 1976 · 14.2K citations · Full text
The plasma lecithin:cholesterol acyltransferase reaction
John A. Glomset · Journal of Lipid Research · 1968 · 2.4K citations · Full text