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Beilschmiedia cryptocaryoides 的抗菌和抗疟成分。

Antibacterial and antiplasmodial constituents of Beilschmiedia cryptocaryoides.

机构信息

Institute of Environmental Research (INFU) of the Faculty of Chemistry, Chair of Environmental Chemistry and Analytical Chemistry, TU Dortmund, Otto-Hahn-Strasse 6, D-44221 Dortmund, Germany.

出版信息

J Nat Prod. 2013 Jan 25;76(1):97-102. doi: 10.1021/np300773x. Epub 2013 Jan 15.

Abstract

Four new beilschmiedic acid derivatives, cryptobeilic acids A-D (1-4), and tsangibeilin B (5) have been isolated from the bark of Beilschmiedia cryptocaryoides collected from Madagascar. Their structures were elucidated using detailed spectroscopic and spectrometric methods. Cryptobeilic acid A (1) and tsangibeilin B (5) structures were confirmed by single-crystal X-ray diffraction analysis. Compounds 1-5 displayed moderate antibacterial activity against Escherichia coli 6r3, Acinetobacter calcoaceticus DSM 586, and Pseudonamas stutzeri A1501, with the minimum inhibitory concentrations ranging from 10 to 50 μM, respectively. In addition, the compounds exhibited antiplasmodial activity against erythrocytic stages of chloroquine-resistant Plasmodium falciparum strain NF54 and weak cytotoxicity against L6 cell lines.

摘要

从马达加斯加采集的密花八角树皮中分离得到了 4 种新的密花八角酸衍生物,即隐密花八角酸 A-D(1-4)和樟叶密花八角酸 B(5)。采用详细的光谱和光谱学方法阐明了它们的结构。通过单晶 X 射线衍射分析确定了隐密花八角酸 A(1)和樟叶密花八角酸 B(5)的结构。化合物 1-5 对大肠杆菌 6r3、醋酸钙不动杆菌 DSM 586 和假单胞菌 A1501 显示出中等的抗菌活性,最小抑菌浓度范围分别为 10-50μM。此外,这些化合物对氯喹抗性恶性疟原虫 NF54 红内期具有抗疟原虫活性,对 L6 细胞系显示出较弱的细胞毒性。

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