Abstract |
Design and synthesis of cholesterol-derived anti-apoptotic agents were described. The synthesized cholesterol analogs designed on the structural basis of ginsenoside Rk1 inhibited the undesirable apoptosis of human endothelial cells, which are induced by a vascular injury. In particular, analogue 1 possessing 4,6-di-O-acetyl-2,3-dideoxyhex-2-enopyran linked to hydroxyl group of cholesterol exhibited the most effective anti-apoptotic activities at both 5 and 10 μg/ml.
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Authors | Sujin Lee, Sony Maharjan, Kyeojin Kim, Nam-Jung Kim, Hyun-Jung Choi, Young-Guen Kwon, Young-Ger Suh |
Journal | Bioorganic & medicinal chemistry letters
(Bioorg Med Chem Lett)
Vol. 20
Issue 23
Pg. 7102-5
(Dec 01 2010)
ISSN: 1464-3405 [Electronic] England |
PMID | 20971002
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2010 Elsevier Ltd. All rights reserved. |
Chemical References |
- Ginsenosides
- ginsenoside Rk1
- Cholesterol
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Topics |
- Apoptosis
(drug effects)
- Blood Vessels
(injuries, pathology)
- Cholesterol
(analogs & derivatives, chemistry, pharmacology)
- Dose-Response Relationship, Drug
- Endothelial Cells
(drug effects, pathology)
- Ginsenosides
(chemistry)
- Humans
- Molecular Structure
- Structure-Activity Relationship
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