
Journal of Medicinal Chemistry p. 219 - 222 (1976)
Update date:2022-08-11
Topics:
Wyrick
Hall
Piantadosi
Fenske
Aliphatic analogs of 2,8 dibenzylcyclooctanone which included C15-C18 ketones have been investigated for hypocholesterolemic activity in rats. The position of the carbonyl group in the chain for maximum activity appears to be the 2 position. 2 Hexadecanone reduced serum cholesterol levels significantly without altering serum triglyceride levels. This drug was not estrogenic at effective doses which is in contrast to the cyclooctanones which possess this activity.
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