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Antitrypanosomal and Cytotoxic Activities of 22-Hydroxyclerosterol, a New Sterol from Allexis cauliflora (Violaceae)

机译:菜青菜(Allexis cauliflora)(堇菜科)的新甾醇22-羟基胆固醇的抗胰蛋白酶和细胞毒活性

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摘要

In the search for new antiparasitic natural compounds from the medicinal plants from Cameroon, the new 22-hydroxyclerosterol, established as such on the basis of detailed chemical and spectroscopic analysis, was isolated from the hexane extract of the stem bark of Allexis cauliflora together with the known clerosterol. 22-Hydroxyclerosterol inhibited the growth of Trypanosoma brucei brucei cells with an ED50 value of 1.56 μM. The compound was also established as an uncompetitive inhibitor of the glycolytic enzyme PGI of T. brucei (Ki’= 3 ± 1 μM), an uncompetitive inhibitor of mammalian rabbit muscles’ enzyme PyK (Ki’= 26 ± 3 μM) and a mixed inhibitor of PyK of Leishmania mexicana (Ki’= 65 ± 10 μM; Ki= 24 ± 5 μM).
机译:在从喀麦隆的药用植物中寻找新的抗寄生虫天然化合物时,从详细的化学和光谱分析的基础上建立了新的22-羟基胆固醇,将其从Allexis花椰菜茎皮的己烷提取物中分离得到。已知的固醇。 22-羟基胆固醇固醇可抑制布氏锥虫布鲁氏菌细胞的生长,ED50值为1.56μM。该化合物还被确定为布鲁氏杆菌糖酵解酶PGI(Ki'= 3±1μM)的非竞争性抑制剂,哺乳动物兔肌肉PyK酶(Ki'= 26±3μM)的非竞争性抑制剂和混合墨西哥利什曼原虫PyK抑制剂(Ki'= 65±10μM; Ki = 24±5μM)。

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