Antimicrobial activity of carvacrol and its derivatives on Mycobacterium spp.: systematic review of preclinical studies.

IF 3.2 4区 医学 Q3 CHEMISTRY, MEDICINAL Future medicinal chemistry Pub Date : 2024-04-01 Epub Date: 2024-02-23 DOI:10.4155/fmc-2023-0249
Thiago H Fermiano, João V Perez de Souza, Letícia S Murase, João P Salvaterra Pasquini, Regiane B de Lima Scodro, Paula A Zanetti Campanerut-Sá, Katiany Rizzieri Caleffi-Ferracioli, Vera L Dias Siqueira, Jean E Meneguello, Jorge J Vieira Teixeira, Rosilene Fressatti Cardoso
{"title":"Antimicrobial activity of carvacrol and its derivatives on <i>Mycobacterium</i> spp.: systematic review of preclinical studies.","authors":"Thiago H Fermiano, João V Perez de Souza, Letícia S Murase, João P Salvaterra Pasquini, Regiane B de Lima Scodro, Paula A Zanetti Campanerut-Sá, Katiany Rizzieri Caleffi-Ferracioli, Vera L Dias Siqueira, Jean E Meneguello, Jorge J Vieira Teixeira, Rosilene Fressatti Cardoso","doi":"10.4155/fmc-2023-0249","DOIUrl":null,"url":null,"abstract":"<p><p><b>Background:</b> The scope of the study was to analyze original preclinical studies on the antimicrobial effects of carvacrol and derivatives on the <i>Mycobacterium</i> genus. <b>Materials & methods:</b> According to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement, four databases (PubMed, Web of Science, SCOPUS and EMBASE) were searched. <b>Results:</b> The search retrieved 392 records, of which 11 papers were selected. Heterogeneity in the techniques and mycobacterial targets was observed. Carvacrol demonstrated synergistic antimycobacterial activity with rifampicin against multidrug-resistant <i>Mycobacterium tuberculosis</i> on membranes and biofilms. <i>In silico</i> approaches showed specific targets in mycobacteria, by inhibition and molecular docking assays, on the enzyme chorismate mutase and the heat shock protein 16.3. <b>Conclusion:</b> Carvacrol has been shown to be a scaffold candidate for future molecules with activity against mycobacteria.</p>","PeriodicalId":12475,"journal":{"name":"Future medicinal chemistry","volume":" ","pages":"679-688"},"PeriodicalIF":3.2000,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Future medicinal chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.4155/fmc-2023-0249","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/2/23 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Background: The scope of the study was to analyze original preclinical studies on the antimicrobial effects of carvacrol and derivatives on the Mycobacterium genus. Materials & methods: According to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement, four databases (PubMed, Web of Science, SCOPUS and EMBASE) were searched. Results: The search retrieved 392 records, of which 11 papers were selected. Heterogeneity in the techniques and mycobacterial targets was observed. Carvacrol demonstrated synergistic antimycobacterial activity with rifampicin against multidrug-resistant Mycobacterium tuberculosis on membranes and biofilms. In silico approaches showed specific targets in mycobacteria, by inhibition and molecular docking assays, on the enzyme chorismate mutase and the heat shock protein 16.3. Conclusion: Carvacrol has been shown to be a scaffold candidate for future molecules with activity against mycobacteria.

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
香芹酚及其衍生物对分枝杆菌属的抗菌活性:临床前研究的系统回顾。
背景:本研究的范围是分析有关香芹酚及其衍生物对分枝杆菌抗菌作用的原始临床前研究。材料与方法:根据《系统综述和荟萃分析首选报告项目》声明,检索了四个数据库(PubMed、Web of Science、SCOPUS 和 EMBASE)。结果:检索到 392 条记录,其中 11 篇论文被选中。观察到了技术和霉菌靶标的异质性。香芹酚与利福平对膜和生物膜上的耐多药结核分枝杆菌具有协同抗分枝杆菌活性。通过抑制和分子对接试验,硅学方法显示了该药物在分枝杆菌中的特异性靶点--胆氨酸突变酶和热休克蛋白 16.3。结论研究表明,香芹酚是未来具有抗分枝杆菌活性分子的候选支架。
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
Future medicinal chemistry
Future medicinal chemistry CHEMISTRY, MEDICINAL-
CiteScore
5.80
自引率
2.40%
发文量
118
审稿时长
4-8 weeks
期刊介绍: Future Medicinal Chemistry offers a forum for the rapid publication of original research and critical reviews of the latest milestones in the field. Strong emphasis is placed on ensuring that the journal stimulates awareness of issues that are anticipated to play an increasingly central role in influencing the future direction of pharmaceutical chemistry. Where relevant, contributions are also actively encouraged on areas as diverse as biotechnology, enzymology, green chemistry, genomics, immunology, materials science, neglected diseases and orphan drugs, pharmacogenomics, proteomics and toxicology.
期刊最新文献
A comprehensive insight into naphthalimides as novel structural skeleton of multitargeting promising antibiotics. A call to develop tramadol enantiomer for overcoming the tramadol crisis by reducing addiction. Advancements in PROTAC-based therapies for neurodegenerative diseases. EGFR molecular degraders: preclinical successes and the road ahead. How does machine learning augment alchemical binding free energy calculations?
×
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