{"title":"Kajian in Silico Daun Sungkai (Peronema canescens) dalam Menghambat Enzim lanosterol 14-α demethylase Jamur Candida albicans","authors":"N. Istiqomah, Safitri Fatikasari","doi":"10.37311/ijpe.v3i1.19135","DOIUrl":null,"url":null,"abstract":"Candida albicans (C. albicans) is a fungus that causes candidiasis. C. albicans has the enzyme Lanosterol 14- α demethylase. Lanosterol 14-α-demethylase has bioactivity in converting lanosterol to ergosterol, a special sterol found in fungal membranes, which mediates membrane permeability and fluidity. One way to treat candidiasis is to use traditional medicinal plants. Sungkai (Peronema canescens) can be used as an anti-fungal medicine. Drug development efforts can be done using the In silico method. Objectives of this study was to determine the interaction between terpenoid, flavonoid, and phenol compounds in Sungkai leaves against Lanosterol 14-α demethylase in Candida albicans. The research design used was a pre-experimental one-shot case study. Toxtree software was used to test the toxicity of compounds. Test for compound potency using the Pass Online webserver. Docking molecular using PyRx software. Visualization of docking results using Discovery Studio 2019 Software. Physicochemical test of compounds using Lipinski Test. The results showed that the compounds that had a low risk of toxicity were butanoic, catechol, guaiacol, hydroquinone, isopropanol, methanoic acid, palmitic acid, and phytol. Compounds that have anti-fungal activity based on Pharma-expert analysis are butanoic acid, genkwanin, guaiacol, hydroquinone, isopropanol, palmitic acid, and phytol. Compounds that have hydrogen bonds and binding affinity value 10 and RMSD value 2 are butanoic acid, catechol, genkwanin, guaiacol, hydroquinone, isopropanol, methanoic acid, palmitic acid, and quinic acid compounds. These compounds are thought to inhibit the Lanosterol 14-alpha demethylase enzyme in C. albicans. Compounds that comply with Lipinski's rules are anthocyanin and genkwanin compounds. The groups of compounds found in Sungkai leaves that have antifungal activity are the terpenoids, flavonoids, and phenols.","PeriodicalId":249696,"journal":{"name":"Indonesian Journal of Pharmaceutical Education","volume":"31 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indonesian Journal of Pharmaceutical Education","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37311/ijpe.v3i1.19135","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
摘要
白色念珠菌(C. albicans)是一种引起念珠菌病的真菌。白色念珠菌具有羊毛甾醇14- α去甲基化酶。羊毛甾醇14-α-去甲基化酶具有将羊毛甾醇转化为麦角甾醇的生物活性,麦角甾醇是一种在真菌膜中发现的特殊甾醇,介导膜的通透性和流动性。治疗念珠菌病的一种方法是使用传统药用植物。Sungkai (Peronema canescens)可以用作抗真菌药。药物开发工作可以使用计算机方法完成。本研究的目的是确定松开叶中萜类、黄酮类和酚类化合物对白色念珠菌羊毛甾醇14-α去甲基化酶的相互作用。使用的研究设计是实验前的一次性案例研究。使用Toxtree软件测试化合物的毒性。使用Pass在线web服务器测试复方效价。利用PyRx软件对接分子。使用Discovery Studio 2019软件可视化对接结果。使用利平斯基试验对化合物进行理化试验。结果表明,毒性风险较低的化合物为丁酸、儿茶酚、愈创木酚、对苯二酚、异丙醇、甲醇酸、棕榈酸和叶绿醇。经药学专家分析,具有抗真菌活性的化合物有丁酸、根宽素、愈创木酚、对苯二酚、异丙醇、棕榈酸和叶绿醇。具有氢键且结合亲和值为10和RMSD值为2的化合物有丁酸、儿茶酚、根宽素、愈创木酚、对苯二酚、异丙醇、甲醇酸、棕榈酸和奎宁酸化合物。这些化合物被认为可以抑制白色念珠菌中的羊毛甾醇14- α去甲基酶。符合利平斯基规则的化合物是花青素和根宽素化合物。在松开叶中发现的具有抗真菌活性的化合物是萜类化合物、黄酮类化合物和酚类化合物。
Kajian in Silico Daun Sungkai (Peronema canescens) dalam Menghambat Enzim lanosterol 14-α demethylase Jamur Candida albicans
Candida albicans (C. albicans) is a fungus that causes candidiasis. C. albicans has the enzyme Lanosterol 14- α demethylase. Lanosterol 14-α-demethylase has bioactivity in converting lanosterol to ergosterol, a special sterol found in fungal membranes, which mediates membrane permeability and fluidity. One way to treat candidiasis is to use traditional medicinal plants. Sungkai (Peronema canescens) can be used as an anti-fungal medicine. Drug development efforts can be done using the In silico method. Objectives of this study was to determine the interaction between terpenoid, flavonoid, and phenol compounds in Sungkai leaves against Lanosterol 14-α demethylase in Candida albicans. The research design used was a pre-experimental one-shot case study. Toxtree software was used to test the toxicity of compounds. Test for compound potency using the Pass Online webserver. Docking molecular using PyRx software. Visualization of docking results using Discovery Studio 2019 Software. Physicochemical test of compounds using Lipinski Test. The results showed that the compounds that had a low risk of toxicity were butanoic, catechol, guaiacol, hydroquinone, isopropanol, methanoic acid, palmitic acid, and phytol. Compounds that have anti-fungal activity based on Pharma-expert analysis are butanoic acid, genkwanin, guaiacol, hydroquinone, isopropanol, palmitic acid, and phytol. Compounds that have hydrogen bonds and binding affinity value 10 and RMSD value 2 are butanoic acid, catechol, genkwanin, guaiacol, hydroquinone, isopropanol, methanoic acid, palmitic acid, and quinic acid compounds. These compounds are thought to inhibit the Lanosterol 14-alpha demethylase enzyme in C. albicans. Compounds that comply with Lipinski's rules are anthocyanin and genkwanin compounds. The groups of compounds found in Sungkai leaves that have antifungal activity are the terpenoids, flavonoids, and phenols.