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首页> 外文期刊>Journal of Pharmacy and Pharmacology >Trypanocidal and antifungal activities of p-hydroxyacetophenone derivatives from Calea uniflora (Heliantheae, Asteraceae).
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Trypanocidal and antifungal activities of p-hydroxyacetophenone derivatives from Calea uniflora (Heliantheae, Asteraceae).

机译:Ca藜(菊科,菊科)的对羟基苯乙酮衍生物的锥虫杀真菌和抗真菌活性。

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摘要

The dichloromethane extract of underground parts of Calea uniflora (Heliantheae, Asteraceae) exhibited trypanocidal and antifungal activities. Four p-hydroxyacetophenone derivatives were isolated as the main compounds: 2-senecioyl-4-(hydroxyethyl)-phenol (1), 2-senecioyl-4-(angeloyloxy-ethyl)-phenol (2), and two new derivatives, 2-senecioyl-4-(methoxyethyl)-phenol (3) and 2-senecioyl-4-(pentadecanoyloxyethyl)-phenol (4). 1 and 4 were active towards Trypanosoma cruzi trypomastigotes, reducing their number by 70 and 71% at 500 microg x mL(-1), whereas 2 and 3 were inactive. All the compounds tested showed antifungal activity with minimal inhibitory concentration values between 500 and 1000 microg x mL(-1) against pathogenic Candida spp. and dermatophytes. The isolation, structure elucidation, NMR spectral assignments and bioactivity results of these compounds are reported.
机译:独生草地下部分(菊科,菊科)的二氯甲烷提取物表现出锥虫杀真菌和抗真菌活性。分离出四种对羟基苯乙酮衍生物作为主要化合物:2-千碳酰-4-(羟乙基)-苯酚(1),2-千碳酰-4-(angelyloxy-ethyl)-苯酚(2)和两种新的衍生物2 -十二碳烯基-4-(甲氧基乙基)-苯酚(3)和2-十二碳烯基-4-(十五烷酰氧基乙基)-苯酚(4)。 1和4对克鲁斯锥虫锥虫有活性,在500微克x mL(-1)下它们的数量分别减少了70%和71%,而2和3无活性。所有测试的化合物均显示出抗真菌活性,并且对致病性念珠菌属的抑制浓度最低,介于500和1000 microg x mL(-1)之间。和皮肤癣菌。报告了这些化合物的分离,结构阐明,NMR光谱分配和生物活性结果。

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