Triterpenoids and Semisynthetic Derivatives with Antimicrobial Activities from the Leaves of Caloncoba glauca (Flacourtiaceae)

J. Mpetga, A. R. N. Donfack, J. Tamokou, Iréne Chinda Kengne, P. Tane, Xiao-jiang Hao, Mathieu Tene
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引用次数: 2

Abstract

Chemical investigation of the MeOH extract from the leaves of C. glauca yielded nine known triterpenoids (1-9) belonging to the cycloartane and friedelane series. Two of these compounds namely glaucartanoic acid A (1) and 3β,21β-dihydroxy-30-nor-(D:A)-friedoolean-20(29)-en-27-oic acid (5) were subjected to chemical derivatizations and afforded five new derivatives: diacetylglaucartanoic acid A (1a), 24-acetylglaucartanoic acid A (1b), glaucartanoic acid A methyl ester (1c), 24-methoxyglaucartanoic acid A methyl ester (1d), and 3β,21β-diacetoxy-30-nor-(D:A)-friedoolean-20(29)-en-27-oic acid (5a). Their structures were assigned based on their NMR and MS data and by comparison with literature values. The MeOH extract, isolated compounds and some new semi-synthetic derivatives were subjected to in vitro antimicrobial assays against a panel of pathogenic microorganisms, including Gram-positive and Gram-negative bacteria, and fungi using broth microdilution method. The MeOH extract displayed activity towards all the tested pathogenic bacterial and fungal strains with good activity (MIC against Staphylococcus aureus ATCC25923 and Shigella flexneri SDINT. Compounds 3 and 5 showed the most potent antimicrobial effect.
海苔叶中的三萜类化合物及具有抗菌活性的半合成衍生物
对C.glauca叶中MeOH提取物的化学研究产生了九种已知的三萜类化合物(1-9),属于环artane和friedelane系列。其中两个化合物,即海蓝酸A(1)和3β,21β-二羟基-30-或-(D:A)-Freedoolean-20(29)-en-27-酸(5,21β-二乙酰氧基-30-或-(D:A)-friedolean-20(29)-烯-27-酸(5a)。基于它们的NMR和MS数据并通过与文献值的比较来确定它们的结构。使用肉汤微量稀释法对甲醇提取物、分离的化合物和一些新的半合成衍生物进行了体外抗菌试验,以对抗一组病原微生物,包括革兰氏阳性菌和革兰氏阴性菌,以及真菌。MeOH提取物对所有测试的具有良好活性的致病细菌和真菌菌株都显示出活性(对金黄色葡萄球菌ATCC25923和福氏志贺菌SDINT的MIC)。化合物3和5显示出最有效的抗菌作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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