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首页> 外文期刊>Journal of natural products >Synthesis, cytotoxicity, and antioxidative activity of minor prenylated chalcones from Humulus lupulus.
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Synthesis, cytotoxicity, and antioxidative activity of minor prenylated chalcones from Humulus lupulus.

机译:Hum草中次要的烯丙基查耳酮的合成,细胞毒性和抗氧化活性。

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The minor hop ( Humulus lupulus) chalcones 3'-geranylchalconaringenin (3), 5'-prenylxanthohumol (4), flavokawin (5), xanthohumol H (8), xanthohumol C (9), and 1'',2''-dihydroxanthohumol C (10) were synthesized. The non-natural chalcones 3'-geranyl-6'-O-methylchalconaringenin (2), 3'-methylflavokawin (6), and 2'-O-methyl-3'-prenylchalconaringenin (7) were also synthesized. Cytotoxicity was investigated in HeLa cells, and these compounds all had IC 50 values comparable to xanthohumol (8.2-19.2 microM). The ORAC-fluorescein assay revealed potent antioxidative activity for 7 and 8 with 5.2 and 4.8 Trolox equivalents, respectively.
机译:次要蛇麻草(Humulus lupulus)chalcones 3'-geranylchalconaringenin(3),5'-异戊烯基黄腐酚(4),flavokawin(5),xanthohumol H(8),xanthohumol C(9)和1'',2''-合成了二氢黄腐酚C(10)。还合成了非天然的查耳酮3'-香叶基-6'-O-甲基查尔孔雀碱(2),3'-甲基黄酮香芹素(6)和2'-O-甲基-3'-异戊基查耳烯宁酮(7)。在HeLa细胞中研究了细胞毒性,所有这些化合物的IC 50值均相当于黄腐酚(8.2-19.2 microM)。 ORAC荧光素测定法分别对7.2和4.8 Trolox当量显示了对7和8的有效抗氧化活性。

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