Suppr超能文献

绿色蜂胶中异戊烯基化苯丙素类化合物及其衍生物对口腔细菌抗菌活性的体外和计算机模拟研究

In Vitro and In Silico Studies of the Antimicrobial Activity of Prenylated Phenylpropanoids of Green Propolis and Their Derivatives against Oral Bacteria.

作者信息

Vieira Tatiana M, Barco Julia G, de Souza Sara L, Santos Anna L O, Daoud Ismail, Rahali Seyfeddine, Amdouni Noureddine, Bastos Jairo K, Martins Carlos H G, Ben Said Ridha, Crotti Antônio E M

机构信息

Department of Chemistry, Faculty of Philosophy, Science and Letters at Ribeirão Preto, University of São Paulo, Ribeirão Preto 14040-901, SP, Brazil.

Department of Microbiology, Institute of Biomedical Sciences, Federal University of Uberlândia, Uberlândia 38405320, MG, Brazil.

出版信息

Antibiotics (Basel). 2024 Aug 22;13(8):787. doi: 10.3390/antibiotics13080787.

Abstract

Artepillin C, drupanin, and plicatin B are prenylated phenylpropanoids that naturally occur in Brazilian green propolis. In this study, these compounds and eleven of their derivatives were synthesized and evaluated for their in vitro antimicrobial activity against a representative panel of oral bacteria in terms of their minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values. Plicatin B () and its hydrogenated derivative (2',3',7,8-tetrahydro-plicatin B) were the most active compounds. Plicatin B () displayed strong activity against all the bacteria tested, with an MIC of 31.2 μg/mL against , and On the other hand, compound displayed strong activity against , , , (MIC = 62.5 μg/mL), and (MIC = 31.2 μg/mL), as well as moderate activity against and (MIC = 125 μg/mL). Compounds and displayed bactericidal effects (MBC: MIC ≤ 4) against all the tested bacteria. In silico studies showed that the complexes formed by compounds and with the , , and targets (, , and , respectively) had energy score values similar to those of the native , , and ligands due to the formation of strong hydrogen bonds. Moreover, all the estimated physicochemical parameters satisfied the drug-likeness criteria without violating the Lipinski, Veber, and Egan rules, so these compounds are not expected to cause problems with oral bioavailability and pharmacokinetics. Compounds and also had suitable ADMET parameters, as the online server pkCSM calculates. These results make compounds and good candidates as antibacterial agents against oral bacteria.

摘要

阿替匹林C、德鲁帕宁和普立卡汀B是天然存在于巴西绿蜂胶中的异戊烯基化苯丙素类化合物。在本研究中,合成了这些化合物及其11种衍生物,并根据其最低抑菌浓度(MIC)和最低杀菌浓度(MBC)值,评估了它们对一组代表性口腔细菌的体外抗菌活性。普立卡汀B()及其氢化衍生物(2',3',7,8 - 四氢 - 普立卡汀B)是活性最强的化合物。普立卡汀B()对所有测试细菌均表现出强活性,对的MIC为31.2 μg/mL,对……另一方面,化合物对、、、(MIC = 62.5 μg/mL)和(MIC = 31.2 μg/mL)表现出强活性,对和(MIC = 125 μg/mL)表现出中等活性。化合物和对所有测试细菌均表现出杀菌作用(MBC:MIC≤4)。计算机模拟研究表明,化合物和与、、靶点(分别为、、)形成的复合物由于形成了强氢键,其能量得分值与天然的、和配体相似。此外,所有估计的理化参数均满足类药标准,未违反Lipinski、Veber和Egan规则,因此预计这些化合物不会引起口服生物利用度和药代动力学方面的问题。正如在线服务器pkCSM所计算的,化合物和也具有合适的ADMET参数。这些结果使化合物和成为抗口腔细菌的抗菌剂的良好候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/298e/11352038/4f074be8bc99/antibiotics-13-00787-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验