糖苷
类黄酮
葡萄糖苷
EC50型
合胞体
化学
立体化学
乙醚
传统医学
生物
生物化学
体外
医学
有机化学
抗氧化剂
细胞
病理
替代医学
作者
Vichai Reutrakul,Niwat Ningnuek,Manat Pohmakotr,Chalobon Yoosook,Chanita Napaswad,Jitra Kasisit,Thawatchai Santisuk,Patoomratana Tuchinda
出处
期刊:Planta Medica
[Georg Thieme Verlag KG]
日期:2007-06-01
卷期号:73 (7): 683-688
被引量:55
标识
DOI:10.1055/s-2007-981538
摘要
Bioassay-guided fractionation of the anti-HIV-1 active EtOAc extract from leaves and twigs of Ochna integerrima led to the isolation of five new flavonoid glycosides 1 - 5, five known flavonoids 6 - 10, and two known flavonoid glycosides 11 and 12. Structures were determined based on spectroscopic analyses. 6- gamma, gamma-Dimethylallyldihydrokaempferol 7- O- beta-D-glucoside (1), 6-gamma, gamma-dimethylallylquercetin 7- O- beta- D-glucoside (3), 6-(3-hydroxy-3-methylbutyl)taxifolin 7- O- beta-D-glucoside (4), 6-(3-hydroxy-3-methylbutyl)quercetin 7- O-beta-D-glucoside (5), and 6-gamma, gamma-dimethylallyltaxifolin 7-O-beta-D-glucoside (11) showed anti-HIV-1 activities in the syncytium assay using the (Delta Tat/rev)MC99 virus and the 1A2 cell line system with EC(50) values ranging from 14.0 - 102.4 microg/mL. Furthermore, ochnaflavone 7''-O-methyl ether (7) and 2'', 3''-dihydroochnaflavone 7''-O-methyl ether (8) were very active; they exerted activities in the syncytium assay with EC(50) values of 2.0 and 0.9 microg/mL, respectively, and likewise inhibited HIV-1 reverse transcriptase (RT) with IC(50) values of 2.0 and 2.4 microg/mL, respectively.
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