2,3,22,23-Tetrahydroxyl-2,6,10,15,19,23-hexamethyl-6,10,14,18-tetracosatetraene, an Acyclic Triterpenoid Isolated from the Seeds of <i>Alpinia katsumadai</i>, Inhibits Acyl-CoA : Cholesterol Acyltransferase Activity-Reference-Cited by-同舟云学术

2,3,22,23-Tetrahydroxyl-2,6,10,15,19,23-hexamethyl-6,10,14,18-tetracosatetraene, an Acyclic Triterpenoid Isolated from the Seeds of Alpinia katsumadai, Inhibits Acyl-CoA : Cholesterol Acyltransferase Activity

Published:2012 Issue:11 Volume:35 Page:2092-2096
ISSN:0918-6158
Container-title:Biological and Pharmaceutical Bulletin
language:en
Short-container-title:Biol. Pharm. Bull.

Author:

Choi Soon-Yong¹,Lee Moon Hee¹,Choi Jung Ho²,Kim Young Kook²

Affiliation:

1. Department of Biological Science and Biotechnology, Hannam University

2. Bio-Therapeutics Research Institute, Korea Research Institute of Bioscience and Biotechnology

Publisher

Pharmaceutical Society of Japan

Subject

Pharmaceutical Science,Pharmacology,General Medicine

Link

https://www.jstage.jst.go.jp/article/bpb/35/11/35_b12-00617/_pdf

Reference20 articles.

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2. LIPOPROTEIN METABOLISM IN THE MACROPHAGE: Implications for Cholesterol Deposition in Atherosclerosis

3. ACYL-COENZYME A:CHOLESTEROL ACYLTRANSFERASE

4. 5) McGovern PG, Pankow JS, Shahar E, Doliszny KM, Folsom AR, Blackburn H, Luepker RV. Recent trends in acute coronary heart disease—mortality, morbidity, medical care, and risk factors. The Minnesota Heart Survey Investigators. N. Engl. J. Med., 334, 884–890 (1996).

5. 6) Sliskovic DR, White AD. Therapeutic potential of ACAT inhibitors as lipid lowering and anti-atherosclerotic agents. Trends Pharmacol. Sci., 12, 194–199 (1991).

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