Abstract
Novel 3-ureido derivatives of 4-phenylcoumarin and 4-phenyl-2-quinolone were synthesized and evaluated for acyl-CoA: cholesterol acyltransferase (ACAT)-inhibitory activity. These derivatives inhibited rat intestinal ACAT with IC50 values at the 10(-8) to 10(-9) M level and were found to normalize plasma cholesterol levels in cholesterol-fed rats when administered as dietary admixtures.
MeSH terms
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Animals
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Coumarins / chemical synthesis*
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Coumarins / chemistry
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Coumarins / pharmacology
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Hypolipidemic Agents / pharmacology
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In Vitro Techniques
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Magnetic Resonance Spectroscopy
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Male
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Quinolones / chemical synthesis*
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Quinolones / chemistry
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Quinolones / pharmacology
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Rats
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Rats, Sprague-Dawley
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Sterol O-Acyltransferase / antagonists & inhibitors*
Substances
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4-phenylquinolone
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Coumarins
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Hypolipidemic Agents
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Quinolones
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4-phenylcoumarin
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Sterol O-Acyltransferase