Bui Phuc Loc, Vu Manh Hung, Nguyễn Thi Thuy, Tran Hoang Mai, Le Thi Huong, Do Thi Hong Khanh, Bui Thanh Tung
{"title":"Screening in silico Alkaloid Compounds Inhibiting Estrogen-α Receptors Against Breast Cancer","authors":"Bui Phuc Loc, Vu Manh Hung, Nguyễn Thi Thuy, Tran Hoang Mai, Le Thi Huong, Do Thi Hong Khanh, Bui Thanh Tung","doi":"10.25073/2588-1132/vnumps.4426","DOIUrl":null,"url":null,"abstract":"Abstract: The estrogen-α (ER-α) receptor is an important target in breast cancer therapy. Alkaloids are a class of plant extracts that have the potential to inhibit ER-α receptors. In this study, we evaluated the ability of alkaloids to inhibit ER-α receptors by molecular docking method. Based on previous publications, we collected 52 alkaloid compounds. The results showed that there were 4 compounds with stronger inhibitory effects on ER-α receptors than positive controls, which are co-crystallized ligands with 4-hydroxytamoxifen. Conducting analysis according to Lipinski's 5-criteria rule and predicting pharmacokinetic-toxicological parameters, we obtained one compound with drug-like properties is Pityriacitrin B. Therefore, this compound has the potential to develop into drugs that inhibit ER-α receptors for breast cancer treatment. \nKeywords: Breast cancer, ER-α, molecular docking, alkaloid, Pityriacitrin B.","PeriodicalId":23520,"journal":{"name":"VNU Journal of Science: Medical and Pharmaceutical Sciences","volume":"68 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"VNU Journal of Science: Medical and Pharmaceutical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25073/2588-1132/vnumps.4426","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Abstract: The estrogen-α (ER-α) receptor is an important target in breast cancer therapy. Alkaloids are a class of plant extracts that have the potential to inhibit ER-α receptors. In this study, we evaluated the ability of alkaloids to inhibit ER-α receptors by molecular docking method. Based on previous publications, we collected 52 alkaloid compounds. The results showed that there were 4 compounds with stronger inhibitory effects on ER-α receptors than positive controls, which are co-crystallized ligands with 4-hydroxytamoxifen. Conducting analysis according to Lipinski's 5-criteria rule and predicting pharmacokinetic-toxicological parameters, we obtained one compound with drug-like properties is Pityriacitrin B. Therefore, this compound has the potential to develop into drugs that inhibit ER-α receptors for breast cancer treatment.
Keywords: Breast cancer, ER-α, molecular docking, alkaloid, Pityriacitrin B.
摘要雌激素-α (ER-α)受体是乳腺癌治疗的重要靶点。生物碱是一类具有抑制内质网α受体潜能的植物提取物。在本研究中,我们通过分子对接法评估了生物碱对ER-α受体的抑制能力。根据以往的出版物,我们收集了52种生物碱化合物。结果表明,有4种化合物对ER-α受体的抑制作用强于阳性对照,它们是与4-羟他莫昔芬共结晶的配体。根据Lipinski’s 5-criteria法则进行分析,并预测药代动力学毒理学参数,我们得到了一种具有药物样性质的化合物Pityriacitrin b。因此,该化合物具有开发成抑制ER-α受体的乳腺癌治疗药物的潜力。关键词:乳腺癌,ER-α,分子对接,生物碱,Pityriacitrin B