EFFECTS OF 32-OXYGENATED LANOSTEROL DERIVATIVES ON 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A REDUCTASE-ACTIVITY AND CHOLESTEROL-BIOSYNTHESIS FROM 24,25-DIHYDROLANOSTEROL
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SONODA, Y
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机构:Kyoritsu College of Pharmacy, Tokyo 105, Shibakoen 1-chome, Minato-ku
SONODA, Y
OBI, N
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机构:Kyoritsu College of Pharmacy, Tokyo 105, Shibakoen 1-chome, Minato-ku
OBI, N
ONODA, M
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机构:Kyoritsu College of Pharmacy, Tokyo 105, Shibakoen 1-chome, Minato-ku
ONODA, M
SAKAKIBARA, Y
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机构:Kyoritsu College of Pharmacy, Tokyo 105, Shibakoen 1-chome, Minato-ku
SAKAKIBARA, Y
SATO, Y
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机构:Kyoritsu College of Pharmacy, Tokyo 105, Shibakoen 1-chome, Minato-ku
SATO, Y
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[1] Kyoritsu College of Pharmacy, Tokyo 105, Shibakoen 1-chome, Minato-ku
The effects of 32-oxygenated lanosterol derivatives on 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase activity and cholesterol biosynthesis from [24,25-H-3]24,25-dihydrolanosterol were studied. Among the derivatives, 3beta-hydroxylanost-7-en-32-oic acid was the most active in depressing HMG-CoA reductase activity (IC50: 0.7 muM) and cholesterol biosynthesis (IC50: 0.4 muM) from 24,25-dihydrolanosterol.