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首页> 外文期刊>International Journal of Molecular Sciences >In Vitro Antiprotozoal Activity of Abietane Diterpenoids Isolated from Plectranthus barbatus Andr.
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In Vitro Antiprotozoal Activity of Abietane Diterpenoids Isolated from Plectranthus barbatus Andr.

机译:从凤尾兰Andr。分离的Abietane二萜类化合物的体外原虫活性。

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Chromatographic separation of the n-hexane extract of the aerial part of Plectranthus barbatus led to the isolation of five abietane-type diterpenes: dehydroabietane (1); 5,6-didehydro-7-hydroxy-taxodone (2); taxodione (3); 20-deoxocarnosol (4) and 6α,11,12,-trihydroxy-7β,20-epoxy-8,11,13-abietatriene (5). The structures were determined using spectroscopic methods including one- and two-dimensional NMR methods. Compounds (1)–(3) and (5) are isolated here for the first time from the genus Plectranthus. The isolated abietane-type diterpenes tested in vitro for their antiprotozoal activity against erythrocytic schizonts of Plasmodium falciparum, intracellular amastigotes of Leishmania infantum and Trypanosoma cruzi and free trypomastigotes of T. brucei. Cytotoxicity was determined against fibroblast cell line MRC-5. Compound (2) 5,6-didehydro-7-hydroxy-taxodone showed remarkable activity with acceptable selectivity against P. falciparum (IC50 9.2 μM, SI 10.4) and T. brucei (IC50 1.9 μM, SI 50.5). Compounds (3)–(5) exhibited non-specific antiprotozoal activity due to high cytotoxicity. Compound (1) dehydroabietane showed no antiprotozoal potential.
机译:分离苦苣菜(Plectranthus barbatus)空中部分的正己烷提取物,进行色谱分离,从而分离出五种枞豆型二萜:脱氢松香烷(1); 5,6-二氢-7-羟基紫杉烷酮(2);紫杉二酮(3); 20-脱氧杂恶酚(4)和6α,11,12,-三羟基-7β,20-环氧-8,11,13-松香三烯(5)。使用包括一维和二维NMR法的光谱法确定结构。在这里,化合物(1)-(3)和(5)首次从忍冬属中分离出来。分离出的abietanee型二萜体外测试了其对恶性疟原虫,婴儿利什曼原虫和锥虫锥虫的胞内变形虫和布鲁氏锥虫的游离锥虫的抗原生动物活性的原生动物活性。测定了针对成纤维细胞系MRC-5的细胞毒性。化合物(2)5,6-二氢-7-羟基紫杉烷酮对恶性疟原虫(IC 50 9.2μM,SI 10.4)和布鲁氏杆菌(IC 50 1.9μM,SI 50.5)。化合物(3)–(5)由于具有高细胞毒性,因此表现出非特异性的抗原生动物活性。化合物(1)脱氢松香烷没有显示出抗原生动物的潜力。

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