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首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >IN SILICO MOLECULAR DOCKING STUDIES ON THE PHYTOCONSTITUENTS OF CADABA FRUTICOSA (L.) DRUCE FOR ITS FERTILITY ACTIVITY
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IN SILICO MOLECULAR DOCKING STUDIES ON THE PHYTOCONSTITUENTS OF CADABA FRUTICOSA (L.) DRUCE FOR ITS FERTILITY ACTIVITY

机译:在硅分子对接过程中对CADABA FRUTICOSA(L.)果泥的植物成分进行活性研究

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Objective: To study the effectiveness of phytocomponents from Cadaba fruticosa (L.) Druce against CYP 17 using computational molecular docking studies. The characterization of polycystic ovarian syndrome is hyperinsulinemia, menstural irregularities, long-term metabolic disturbances, and hyperandrogenism. Adrenal and ovarian androgen synthesis are induced by an enzyme, CYP 17 (P450c 17α). Due to increase in the activity of this enzyme, hyperandrogenism mainly occurs. By inhibiting the enzymatic activity, excess androgen synthesis can be prevented in ovarian theca cells. Literature study has reported that the gas chromatography mass spectrometry analysis on the ethanolic extract of the aerial parts of C. fruticosa possesses 20 compounds. Methods: Molecular docking analysis was performed for the reported 20 compounds against CYP 17 using Schrodinger Glide software. These results were compared with the docked score of fertility inducing drug clomiphene citrate. Results: All 20 compounds have exhibited moderate to potent inhibition with a range of ?3.3 to ?7.9. Androstan-3-one, 17-hydroxy-2, 4-dimethyl and 3-Trifluoroacetoxypentadecane have showed potent inhibition with the docking score of ?7.9 and ?6.8, respectively. Conclusion: The results revealed out that the compounds present in C. fruticosa can reduce the activity of CYP 17. This study throws a light on establishing the novel drug for infertility through experimental procedures.
机译:目的:利用计算分子对接研究来研究金叶蝉植物成分对CYP 17的抑制作用。多囊卵巢综合征的特征是高胰岛素血症,月经不调,长期代谢紊乱和雄激素过多。肾上腺和卵巢雄激素的合成是由一种酶CYP 17(P450c17α)诱导的。由于该酶活性的增加,主要发生雄激素过多。通过抑制酶活性,可以防止卵巢囊细胞中过多的雄激素合成。文献研究表明,气相色谱质谱分析金黄色葡萄球菌空中部分的乙醇提取物含有20种化合物。方法:使用Schrodinger Glide软件对报告的20种针对CYP 17的化合物进行了分子对接分析。将这些结果与生育能力诱导药物克罗米芬柠檬酸盐的对接分数进行比较。结果:所有20种化合物均表现出中度至强效抑制,范围在〜3.3至〜7.9。 Androstan-3-one,17-羟基-2、4-二甲基和3-Trifluoroacetoxypentadecane已显示出有效的抑制作用,对接得分分别为7.9和6.8。结论:结果表明,存在于金黄色葡萄球菌中的化合物可降低CYP 17的活性。该研究为通过实验方法建立新型不孕症药物提供了启示。

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