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Three New Benzophenone Derivatives from Selaginella tamariscina
被引:2
|作者:
Long, Jiayin
[1
]
Mao, Qingqing
[1
]
Peng, Yujie
[1
]
Liu, Lei
[1
]
Hong, Yin
[1
]
Xiang, Honglin
[1
]
Ma, Ming
[2
]
Zou, Hui
[1
]
Kuang, Junwei
[2
]
机构:
[1] Hunan Normal Univ, Sch Med, Key Lab Study & Discovery Small Targeted Mol Hunan, Changsha 410013, Peoples R China
[2] Hunan Normal Univ, Coll Chem & Chem Engn, Key Lab Phytochem R&D Hunan Prov, Key Lab Chem Biol & Tradit Chinese Med Res,Minist, Changsha 410081, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
Selaginella;
Selaginella tamariscina;
benzophenone;
selagibenzophenones D-F;
cytotoxicity;
NO inhibitory effects;
CANCER CELLS;
IN-VITRO;
GROWTH;
D O I:
10.3390/molecules28124582
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:
Six compounds including three new benzophenones, selagibenzophenones D-F (1-3), two known selaginellins (4-5) and one known flavonoid (6), were isolated from Selaginella tamariscina. The structures of new compounds were established by 1D-, 2D-NMR and HR-ESI-MS spectral analyses. Compound 1 represents the second example of diarylbenzophenone from natural sources. Compound 2 possesses an unusual biphenyl-bisbenzophenone structure. Their cytotoxicity against human hepatocellular carcinoma HepG2 and SMCC-7721 cells and inhibitory activities on lipopolysaccharide-induced nitric oxide (NO) production in RAW264.7 cells were evaluated. Compound 2 showed moderate inhibitory activity against HepG2 and SMCC-7721 cells, and compounds 4 and 5 showed moderate inhibitory activity to HepG2 cells. Compounds 2 and 5 also exhibited inhibitory activities on lipopolysaccharide-induced nitric oxide (NO) production.
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页数:10
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