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
MOLECULES | 2023年 / 28卷 / 12期
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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