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Synthesis and Biological Evaluation of Ginsenoside Compound K Derivatives as a Novel Class of LXRα Activator
被引:22
|作者:
Huang, Yan
[1
,2
]
Liu, Hongmei
[1
,2
]
Zhang, Yingxian
[1
,2
]
Li, Jin
[1
,2
]
Wang, Chenping
[1
,2
]
Zhou, Li
[3
,4
]
Jia, Yi
[1
,2
]
Li, Xiaohui
[1
,2
]
机构:
[1] Third Mil Med Univ, Coll Pharm, Inst Mat Med, Chongqing 400038, Peoples R China
[2] Third Mil Med Univ, Coll Pharm, Dept Pharmaceut, Chongqing 400038, Peoples R China
[3] Third Mil Med Univ, Xinqiao Hosp, Dept Pharm, Chongqing 400037, Peoples R China
[4] Third Mil Med Univ, Affiliated Hosp 2, Chongqing 400037, Peoples R China
来源:
MOLECULES
|
2017年
/
22卷
/
07期
关键词:
atherosclerosis;
LXR alpha;
ginsenoside compound K;
derivatives;
reverse cholesterol transport;
SAPONINS ATTENUATE ATHEROSCLEROSIS;
LIVER X-RECEPTORS;
GENE-EXPRESSION;
APOE(-/-) MICE;
IN-VITRO;
METABOLITE;
CANCER;
CELLS;
PROLIFERATION;
DISCOVERY;
D O I:
10.3390/molecules22071232
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Compound K is one of the active metabolites of Panaxnotoginseng saponins, which could attenuate the formation of atherosclerosis in mice modelsvia activating LXR alpha. We synthesized and evaluated a series of ginsenoside compound K derivatives modified with short chain fatty acids. All of the structures of this class of ginsenoside compound K derivative exhibited comparable or better biological activity than ginsenoside compound K. Especially structure 1 exhibited the best potency (cholesteryl ester content: 41.51%; expression of ABCA1 mRNA: 319%) and low cytotoxicity.
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页数:13
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