In Silico Studies on Fungal Metabolite against Skin Cancer Protein (4,5-Diarylisoxazole HSP90 Chaperone).

ISRN Dermatology Pub Date : 2012-01-01 Epub Date: 2012-09-06 DOI:10.5402/2012/626214
Saravanakumar Kandasamy, Sunil Kumar Sahu, Kathiresan Kandasamy
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引用次数: 20

Abstract

This work was to find out the dominant secondary metabolites derived from the fungus Trichoderma and to test them against skin cancer protein. The metabolites were extracted in 80% methanol from the fungal biomass of Trichoderma isolated from mangrove sediment. The crude methanol extract was purified and analysed for the secondary metabolites by GC-MS. Three predominant compounds (heptadecanoic acid, 16 methyl-, methyl ester; 9,12-octadecadienoic acid; cis-9-octadecenoic acid) identified in the extracts were screened against the skin cancer protein (Hsp90) by in-silico docking method. Of the compounds, heptadecanoic acid, 16 methyl, methyl ester was the most potent having the docking score of -11.4592 Kcal/mol. This value was better than the standard drug "dyclonine". This work recommends the heptadecanoic acid, 16 methyl, methyl ester for further in vitro and in vivo studies towards its development as anticancer drug.

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真菌抗皮肤癌蛋白代谢物(4,5-二芳基异恶唑HSP90伴侣蛋白)的硅片研究
这项工作是为了找出真菌木霉的主要次生代谢物,并测试它们对皮肤癌蛋白的作用。从红树林沉积物中分离的木霉真菌生物量中提取代谢物,用80%甲醇提取。对粗甲醇提取物进行纯化,并采用GC-MS分析其次生代谢产物。三个主要化合物(十六烷酸,16甲基-,甲酯;9日,12-octadecadienoic酸;采用硅对接法对提取液中鉴定的顺式-9-十八烯酸(cis-9- octadecenic acid)抗皮肤癌蛋白(Hsp90)进行筛选。其中,十六甲基十七烷酸甲酯的对接分数最高,为-11.4592 Kcal/mol。该值优于标准药物“代克隆宁”。本工作建议对十六烷酸16甲基甲酯进行进一步的体内外研究,以开发其抗癌药物。
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