从多糖中分离的拉丹二萜的抗增殖活性及其分子相互作用研究。

Q3 Pharmacology, Toxicology and Pharmaceutics
Ravi Kumar Ys, Aditya Rao Sj, Usha Bm, B. Verma, Paramesha Mahadevappa
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引用次数: 0

摘要

牛耳藤以其治疗效果而闻名,被南印度和非洲的部落人民广泛用于治疗不孕症、牙痛、炎症、风湿病、发烧和对抗压力。目的研究从金菖蒲茎皮中分离得到的两种活性物质的抗肿瘤活性。Bedd。对番荔枝科植物进行了研究。方法将干燥后的茎皮制成粉末,用甲醇提取,再用石油醚分馏。采用柱状色谱和制备薄层色谱法从石油醚馏分中分离出黄色粘稠油。色谱组分采用气相色谱-质谱法进行表征。采用MTT-细胞毒性试验评价分离化合物对HepG2细胞的抗增殖作用。此外,我们还进行了比较硅对接研究,以预测分离分子的结合模式,以及与α, β -微管蛋白(一种参与微管形成分子机制的关键蛋白)的结合模式。结果通过gc - ms对石油馏分中黄色粘稠油进行质谱分析,证实含有2种labdane二萜,经质谱分析鉴定为12e -3,4- seco -labda-4(18)、8(17)、12,14-四烯-3-oic酸和哈瓦酸甲酯C。mtt细胞毒实验显示其对HepG2细胞的毒作用呈剂量依赖性。比较对接研究表明,分离的化合物与α, β -微管蛋白具有较强的相互作用。结论分离得到的化合物与α、β -微管蛋白有效结合,具有明显的抗增殖作用,可作为重要的抗癌分子加以利用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-proliferative activity of labdane diterpenes isolated from Polyalthia cerasoides and their molecular interaction studies.
BACKGROUND Polyalthia cerasoides is well known for its therapeutic effects and is extensively used by the tribal people of South India and Africa to treat infertility, toothache, inflammation, rheumatism, fever, and to combat stress. OBJECTIVE In the present research, the anti-proliferative potential of two bioactive compounds isolated from the stem bark of P. cerasoides (Roxb.) Bedd. of the Annonaceae family were investigated. METHOD The dried stem bark was powdered and subjected to extraction using methanol and further partitioned using petroleum ether. Yellow viscous oil was isolated from the petroleum ether fraction using column and preparative thin-layer chromatography. The chromatographic fractions were characterized using GC-MS. The anti-proliferative effect of the isolated compounds was assessed against HepG2 Cells using MTT- Cytotoxicity test. Furthermore, comparative in-silico docking studies were performed to predict the binding pattern of isolated molecules individually, as well as simultaneously with α, β -tubulin, a critical protein involved in the molecular mechanism of microtubule formation. RESULTS GC-MS analysis of yellow viscous oil from petroleum fraction confirmed the presence of two labdane diterpenes and were identified as 12E-3,4-Seco-labda-4(18),8(17),12,14-tetraen-3-oic acid , and methyl harvadate C by mass fragmentation analysis. The MTT-Cytotoxicity assay showed the dose-dependent cytotoxic effect on HepG2 Cells. The comparative docking studies of the isolated compounds exhibited strong interactions with the α, β -tubulin protein. CONCLUSION The prominent anti-proliferative effect exhibited by the isolated compounds along with effective binding to α, β -tubulin protein encourages their future utilization as prominent anti-cancer molecules.
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来源期刊
Current drug discovery technologies
Current drug discovery technologies Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
3.70
自引率
0.00%
发文量
48
期刊介绍: Due to the plethora of new approaches being used in modern drug discovery by the pharmaceutical industry, Current Drug Discovery Technologies has been established to provide comprehensive overviews of all the major modern techniques and technologies used in drug design and discovery. The journal is the forum for publishing both original research papers and reviews describing novel approaches and cutting edge technologies used in all stages of drug discovery. The journal addresses the multidimensional challenges of drug discovery science including integration issues of the drug discovery process.
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