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来自红藻冠叶球藻的新型溴代二萜类化合物。

New bromoditerpenes from the red alga Sphaerococcus coronopifolius.

作者信息

Etahiri S, Bultel-Poncé V, Caux C, Guyot M

机构信息

Laboratoire de Biochimie Marine, Faculté des Sciences, Université Chouaib Doukkali, BP 20, El Jadida, Maroc.

出版信息

J Nat Prod. 2001 Aug;64(8):1024-7. doi: 10.1021/np0002684.

Abstract

The organic extract of the red alga Sphaerococcus coronopifolius, collected along the Atlantic coast of Morocco, was tested for biological activities and exhibited antibiotic and antimalarial activities. Two new bromoditerpenes have been isolated from S. coronopifolius, sphaerolabdadiene-3,14-diol (1) and bromosphaerone (2), along with the known compounds 12S-hydroxybromosphaerodiol (3) and sphaerococcenol A (4). Bromosphaerone and 12S-hydroxybromosphaerodiol showed antibacterial activity against the Gram-positive bacterium species Staphylococcus aureus with a minimum inhibitory concentration of 0.104 and 0.146 microM, respectively. Sphaerococcenol A (4) was responsible for the antimalarial activity of the extract, against the chloroquine resistant Plasmodium falsciparum FCB1 strains with an IC(50) of 1 microM. Their structures have been assigned using 1 and 2 D NMR and HRMS.

摘要

从摩洛哥大西洋沿岸采集的红藻冠叶球石藻的有机提取物进行了生物活性测试,结果显示其具有抗生素和抗疟疾活性。从冠叶球石藻中分离出两种新的溴代二萜,球石藻拉巴二烯 -3,14 -二醇(1)和溴球石酮(2),以及已知化合物12S -羟基溴球石二醇(3)和球石藻烯醇A(4)。溴球石酮和12S -羟基溴球石二醇对革兰氏阳性细菌金黄色葡萄球菌显示出抗菌活性,最低抑菌浓度分别为0.104和0.146微摩尔。球石藻烯醇A(4)是该提取物抗疟疾活性的原因所在,对氯喹耐药的恶性疟原虫FCB1菌株的半数抑制浓度(IC50)为1微摩尔。它们的结构已通过一维和二维核磁共振以及高分辨质谱确定。

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