Potential of Prenylated Flavonoid Derivatives from Jackfruit Roots (Artocarpus heterophyllus Lam.) as Liver Anticancer Candidates: In Silico Study

{"title":"Potential of Prenylated Flavonoid Derivatives from Jackfruit Roots (Artocarpus heterophyllus Lam.) as Liver Anticancer Candidates: In Silico Study","authors":"","doi":"10.14710/jksa.26.2.57-63","DOIUrl":null,"url":null,"abstract":"Hepatocellular carcinoma (HCC), or liver cancer, is the fourth largest cancer in Indonesia, with 21,392 new cases and around 20,920 deaths. One of the standard drugs for liver cancer patients is lenvatinib, but lenvatinib has dangerous side effects such as hypertension. Previous studies reported that jackfruit root extract (Artocarpus heterophyllus Lam.) contains prenylated flavonoid compounds known to have anticancer activity. This study aims to find compounds that have the potential to the anticancer liver from jackfruit root by understanding the interaction between prenylated flavonoid derivative compounds against the VEGFR2 receptor (PDB ID: 3WZE) in silico. The methods include toxicity and pharmacokinetic screening, drug scanning, docking, and molecular dynamics simulation. The toxicity, pharmacokinetic, and drug scans of cycloartocarpesin are better than lenvatinib. The docking cycloartocarpesin compound showed ∆G -8.49 kcal/mol and Ki 0.59967 M lower than lenvatinib by forming the same hydrogen bond at residue Glu885. The molecular dynamics simulation of the cycloartocarpesin compound in the MM-GBSA calculation method resulted in a ∆Gtotal of -56.641 kcal/mol. The cycloartocarpesin compound is predicted to be used as a candidate for liver anticancer drugs because it has better stability and affinity than lenvatinib.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Jurnal Kimia Sains dan Aplikasi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14710/jksa.26.2.57-63","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

Hepatocellular carcinoma (HCC), or liver cancer, is the fourth largest cancer in Indonesia, with 21,392 new cases and around 20,920 deaths. One of the standard drugs for liver cancer patients is lenvatinib, but lenvatinib has dangerous side effects such as hypertension. Previous studies reported that jackfruit root extract (Artocarpus heterophyllus Lam.) contains prenylated flavonoid compounds known to have anticancer activity. This study aims to find compounds that have the potential to the anticancer liver from jackfruit root by understanding the interaction between prenylated flavonoid derivative compounds against the VEGFR2 receptor (PDB ID: 3WZE) in silico. The methods include toxicity and pharmacokinetic screening, drug scanning, docking, and molecular dynamics simulation. The toxicity, pharmacokinetic, and drug scans of cycloartocarpesin are better than lenvatinib. The docking cycloartocarpesin compound showed ∆G -8.49 kcal/mol and Ki 0.59967 M lower than lenvatinib by forming the same hydrogen bond at residue Glu885. The molecular dynamics simulation of the cycloartocarpesin compound in the MM-GBSA calculation method resulted in a ∆Gtotal of -56.641 kcal/mol. The cycloartocarpesin compound is predicted to be used as a candidate for liver anticancer drugs because it has better stability and affinity than lenvatinib.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Jackfruit Roots(Artocarpus heterophyllus Lam.)的Prenylated黄酮衍生物作为肝脏抗癌候选药物的潜力:Silico研究
肝细胞癌(HCC)或癌症是印度尼西亚第四大癌症,新增21392例,死亡约20920例。癌症患者的标准药物之一是乐伐替尼,但乐伐替尼有高血压等危险副作用。先前的研究报道,菠萝蜜根提取物(Artocarpus heterophyllus Lam.)含有已知具有抗癌活性的异戊二烯化类黄酮化合物。本研究旨在通过了解在计算机上丙酰化类黄酮衍生物化合物与VEGFR2受体(PDB ID:3WZE)之间的相互作用,从菠萝蜜根中寻找具有抗癌肝脏潜力的化合物。方法包括毒性和药代动力学筛选、药物扫描、对接和分子动力学模拟。环artocarpesin的毒性、药代动力学和药物扫描优于乐伐替尼。对接环artocarpesin化合物通过在残基Glu885处形成相同的氢键,显示出∆G-8.49 kcal/mol和Ki比乐伐替尼低0.59967M。在MM-GBSA计算方法中对环artocarpesin化合物的分子动力学模拟得出∆Gtotal为-56.641 kcal/mol。环artocarpesin化合物被预测为肝脏抗癌药物的候选药物,因为它比乐伐替尼具有更好的稳定性和亲和力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
36
审稿时长
17 weeks
期刊最新文献
Production of Biodiesel from Candlenut Seed Oil (Aleurites Moluccana Wild) Using a NaOH/CaO/Ca Catalyst with Microwave Heating Synthesis of Molecularly Imprinted Polymers with Magnetite Cores for Ibuprofen Adsorption Impact of Fermentation on Hyptolide and Phytochemical Composition of Hyptis pectinata (L.) Poit Effects of Temperature, Molecular Weight, and Non-Solvent Variation on the Physical Properties of PVDF Membranes Prepared through Immersion Precipitation Isolation of Phenolic Acids from Land Kale (Ipomoea reptans Poir) and Antioxidant Activity
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1