ACAT inhibitors CL 283,546 and CL 283,796 reduce LDL cholesterol without affecting cholesterol absorption in African green monkeys.-Reference-Cited by-同舟云学术

ACAT inhibitors CL 283,546 and CL 283,796 reduce LDL cholesterol without affecting cholesterol absorption in African green monkeys.

Published:1995-06 Issue:6 Volume:36 Page:1199-1210
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

Wrenn S.M.,Parks J.S.,Immermann F.W.,Rudel L.L.

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference74 articles.

1. Role of acyl- CoA:cholesterol acyltransferase in cellular cholesterol metabolism;Suckling;J. Lipid Res.,1985

2. Importance of acyl CoA:cholesterol acyltransferase (ACAT) in the esterification of cholesterol by enterocytes;Tso;FASEB J.,1991

3. CL 277,082: a novel inhibitor of ACATcatalyzed cholesterol esterification and cholesterol absorption;Largis;J. Lipid Res.,1989

4. Effects of Bay 0 2752, a hypocholesterolemic agent, on intestinal taurocholate absorption and cholesterol esterification;Harnett;J. Pharmacol. Exp. Ther.,1989

5. Influence of acyl-coenzyme Axholesterol acyltransferase inhibitor octimibate on cholesterol transport in rat mesenteric lymph;Windler;Arzneim. Forsch./Drug Res.,1990

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