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来自螺旋线鳍藻的具有抗菌活性的 dolabellanes。

Dolabellanes with antibacterial activity from the brown alga Dilophus spiralis.

机构信息

Department of Pharmacognosy and Chemistry of Natural Products, School of Pharmacy, University of Athens, Panepistimiopolis Zografou, Athens 15771, Greece.

出版信息

J Nat Prod. 2011 Feb 25;74(2):213-22. doi: 10.1021/np1006586. Epub 2010 Dec 29.

Abstract

Seventeen diterpenes featuring the dolabellane skeleton (1-17) were isolated from the organic extracts of the brown alga Dilophus spiralis. Seven compounds are new natural products (1, 3, 5, 6, 11, 14, 15) and eight are structurally revised (2, 4, 7-10, 12, 13), among which three are reported for the first time from a natural source (4, 9, 10). The structure elucidation and the assignment of the relative configurations of the isolated natural products were based on detailed analyses of their spectroscopic data. The structure of metabolite 10 was confirmed by single-crystal X-ray diffraction analysis, whereas the absolute configurations of compounds 2, 4-10, 12, and 13 were determined using the modified Mosher's method on the semisynthetic product 18 and chemical interconversions. The antibacterial activities of compounds 1-18 were evaluated against six strains of Staphylococcus aureus, including multidrug- and methicillin-resistant variants.

摘要

从棕色海藻螺旋黛蛤藤(Dilophus spiralis)的有机提取物中分离得到了 17 种具有 dolabellane 骨架的二萜类化合物(1-17)。其中 7 种化合物为新的天然产物(1、3、5、6、11、14、15),8 种化合物的结构进行了修订(2、4、7-10、12、13),其中 3 种为首次从天然来源中报道(4、9、10)。根据这些化合物的光谱数据的详细分析,对分离得到的天然产物的结构阐明和相对构型进行了分配。代谢产物 10 的结构通过单晶 X 射线衍射分析得到了确认,而化合物 2、4-10、12 和 13 的绝对构型则是通过半合成产物 18 的改进的 Mosher 法和化学转化来确定的。对 1-18 种化合物进行了针对六种金黄色葡萄球菌菌株(包括耐多药和耐甲氧西林的变体)的抗菌活性评估。

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