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苏铁属植物小叶及苏铁叶的植物化学研究:具有中等抗菌活性的双黄酮类化合物。

Phytochemical investigation of Cycas circinalis and Cycas revoluta leaflets: moderately active antibacterial biflavonoids.

机构信息

Department of Pharmacognosy and Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, University, MS, USA.

出版信息

Planta Med. 2010 May;76(8):796-802. doi: 10.1055/s-0029-1240743. Epub 2010 Jan 12.

Abstract

Chemical examination of the methanolic extract of the leaflets of CYCAS CIRCINALIS L. led to the isolation of one new biflavonoid, (2 S, 2'' S)-2,3,2'',3''-tetrahydro-4',4'''-di- O-methylamentoflavone (tetrahydroisoginkgetin; 2), and 15 known compounds, 11 of which are reported for the first time from C. CIRCINALIS. Chromatographic separation of the chloroform extract of C. REVOLUTA Thunb. leaflets afforded 12 compounds, seven of which are reported for the first time from this species. The isolated compounds from both species include 14 biflavonoids, three lignans, three flavan-3-ols, two flavone- C-glucosides, two NOR-isoprenoids, and one flavanone. This is the first report of NMR and CD data of 2,3,2'',3''-tetrahydro-4'- O-methyl- and 2,3-dihydro-4'- O-methyl-amentoflavone ( 6) and ( 7). The effect of O-methylation on the chemical shifts of the neighboring carbons in the (13)C NMR spectra of the dihydro- and tetrahydro-amentoflavone skeletons provides a tool to identify the location of the methoxy groups. Compounds 2, 6, and 18 displayed moderate antibacterial activity against STAPHYLOCOCCUS AUREUS (IC (50) values of 3.9, 9.7, and 8.2 microM, respectively) and methicillin-resistant S. AUREUS (MRSA; IC (50) values of 5.9, 12.5, and 11.5 microM, respectively).

摘要

从苏铁科苏铁属植物的小叶甲醇提取物中分离得到一种新的双黄酮类化合物,(2S,2''S)-2,3,2'',3''-四氢-4',4'''-二甲氧基安替比林(四氢异银杏黄素;2),以及 15 种已知化合物,其中 11 种为苏铁属植物首次报道。从苏铁属植物的氯仿提取物中色谱分离得到 12 种化合物,其中 7 种为该种植物首次报道。从这两个物种中分离得到的化合物包括 14 种双黄酮类化合物、3 种木脂素类化合物、3 种黄烷-3-醇类化合物、2 种黄酮-C-葡萄糖苷类化合物、2 种 NOR-异戊二烯类化合物和 1 种黄烷酮类化合物。这是首次报道 2,3,2'',3''-四氢-4'-O-甲基-和 2,3-二氢-4'-O-甲基-安替比林(6)和(7)的 NMR 和 CD 数据。在二氢和四氢安替比林骨架的(13)C NMR 谱中,O-甲基化对相邻碳原子化学位移的影响为确定甲氧基的位置提供了一种工具。化合物 2、6 和 18 对金黄色葡萄球菌(金黄色葡萄球菌;IC(50)值分别为 3.9、9.7 和 8.2 microM)和耐甲氧西林金黄色葡萄球菌(MRSA;IC(50)值分别为 5.9、12.5 和 11.5 microM)表现出中等的抗菌活性。

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