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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Caatinga plants: Natural and semi-synthetic compounds potentially active against Trichomonas vaginalis
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Caatinga plants: Natural and semi-synthetic compounds potentially active against Trichomonas vaginalis

机译:Caatinga植物:天然和半合成化合物,可能对阴道毛滴虫具有活性

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摘要

Trichomonas vaginalis causes trichomoniasis; the most common but overlooked non-viral sexually transmitted disease worldwide. The treatment is based at 50-nitroimidazoles, however, failure are related to resistance of T. vaginalis to chemotherapy. Caatinga is a uniquely Brazilian region representing a biome with type desert vegetation and plants present diverse biological activity, however, with few studies. The aim of this study was to investigate the activity against T. vaginalis of different plants from Caatinga and identify the compounds responsible by the activity. A bioguided fractionation of Manilkara rufula was performed and four major compounds were identified: caproate of alpha-amyrin (1b), acetate of beta-amyrin (2a), caproate of b-amyrin (2b), and acetate of lupeol (3a). In addition, six derivatives of alpha-amyrin (1), beta-amyrin (2) and lupeol (3) were synthesized and tested against the parasite. Ursolic acid (5) reduced about 98% of parasite viability after 2 h of incubation and drastic ultrastructural alterations were observed by scanning electron microscopy. Moreover, 5 presented high cytotoxicity to HMVII and HeLa cell line and low cytotoxicity against Vero line at 50 mu M (MIC against the parasite). Metronidazole effect against T. vaginalis resistant isolate was improved when in association with 5. (C) 2016 Elsevier Ltd. All rights reserved.
机译:阴道毛滴虫引起毛滴虫病;世界上最常见但被忽视的非病毒性传播疾病。治疗以50-硝基咪唑为基础,但是失败与阴道锥虫对化学疗法的抵抗力有关。 Caatinga是巴西一个独特的地区,代表着具有群落类型的沙漠植被的生物群落,而植物则具有多种生物活性,但是,很少有研究。这项研究的目的是研究来自Caatinga的不同植物对阴道锥虫的活性,并鉴定引起该活性的化合物。进行了Manilkara rufula的生物引导分馏,并鉴定了四个主要化合物:α-锚蛋白的己酸酯(1b),β-锚蛋白的乙酸酯(2a),b-锚蛋白的己酸酯(2b)和羽扇豆酚的乙酸酯(3a)。另外,合成了六种α-锚蛋白(1),β-锚蛋白(2)和羽扇豆酚(3)衍生物,并测试了该寄生虫的抗性。孵育2小时后,熊果酸(5)降低了约98%的寄生虫生存力,并且通过扫描电子显微镜观察到急剧的超微结构改变。此外,5在50μM时对HMVII和HeLa细胞系表现出高细胞毒性,而对Vero系表现出低细胞毒性(MIC对寄生虫)。与5结合使用时,甲硝唑对阴道弯曲杆菌抗性分离株的作用得到改善。(C)2016 Elsevier Ltd.保留所有权利。

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