Schiff base metal complexes as emerging therapeutics against antimicrobial-resistant skin pathogens.

IF 4.3 Q2 CHEMISTRY, MEDICINAL
ADMET and DMPK Pub Date : 2026-03-06 eCollection Date: 2026-01-01 DOI:10.5599/admet.3214
Parami Sinhapitiya, Samawansha Tennakoon, Isuri A D K Weeraratne
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引用次数: 0

Abstract

Background and purpose: The development of antimicrobial resistance reduces the efficacy of antimicrobial agents and poses a significant challenge to treat skin diseases. Many scientists, researchers, and pharmaceutical companies work diligently to investigate novel antimicrobial agents and discover alternatives to existing ones, aiming to address antimicrobial resistance. Within the broad field of metal complexes, Schiff base complexes occupy a prominent position, with structural versatility and significant biological properties that make them promising candidates for developing alternative drugs to combat the global crisis of antimicrobial resistance.

Experimental approach: This paper reviewed the existing literature on how the structural features of some recently studied Schiff base ligands and their complexes influence the antibacterial and antifungal activities of these compounds against common skin pathogens, including Candida albicans sp., dermophytes, Staphylococcus aureus and Streptococcus pyogenes.

Key results: The structural features, including the azomethine group (C=N), heteroatoms and substituents, in Schiff base compounds have been associated with interference with protein synthesis and the growth of bacterial and fungal cells. Schiff base compounds affect cell wall and cell membrane synthesis and inhibit enzymes essential to cell division and other cellular mechanisms. The chelation theory and the overtone's concept suggest that Schiff base metal complexes exhibit higher antibacterial and antifungal activities compared to Schiff base ligands.

Conclusion: This review focuses on providing an overview of how the structural features of Schiff base compounds influence the antimicrobial properties of these compounds against Candida albicans sp., dermophytes, Staphylococcus aureus and Streptococcus pyogenes.

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希夫贱金属配合物作为抗微生物耐药皮肤病原体的新兴疗法。
背景与目的:抗菌药物耐药性的发展降低了抗菌药物的疗效,对皮肤疾病的治疗提出了重大挑战。许多科学家、研究人员和制药公司孜孜不倦地研究新的抗微生物药物,并发现现有药物的替代品,旨在解决抗微生物药物耐药性问题。在广泛的金属配合物领域中,希夫碱配合物以其结构的多功能性和显著的生物学特性占据着突出的地位,使其成为开发替代药物以对抗全球抗菌素耐药性危机的有希望的候选者。实验方法:本文综述了近年来研究的一些希夫碱配体及其配合物的结构特征对这些化合物对白色念珠菌、皮肤真菌、金黄色葡萄球菌和化脓性链球菌等常见皮肤病原体的抗菌和抗真菌活性的影响。主要结果:希夫碱化合物的结构特征,包括亚甲基(C=N)、杂原子和取代基,与干扰蛋白质合成和细菌和真菌细胞的生长有关。希夫碱化合物影响细胞壁和细胞膜的合成,抑制细胞分裂和其他细胞机制所必需的酶。螯合理论和泛音概念表明,希夫碱金属配合物比希夫碱配体具有更高的抗菌和抗真菌活性。结论:本文综述了希夫碱类化合物的结构特征对其抗白色念珠菌、皮肤真菌、金黄色葡萄球菌和化脓性链球菌抗菌性能的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ADMET and DMPK
ADMET and DMPK Multiple-
CiteScore
4.40
自引率
0.00%
发文量
22
审稿时长
4 weeks
期刊介绍: ADMET and DMPK is an open access journal devoted to the rapid dissemination of new and original scientific results in all areas of absorption, distribution, metabolism, excretion, toxicology and pharmacokinetics of drugs. ADMET and DMPK publishes the following types of contributions: - Original research papers - Feature articles - Review articles - Short communications and Notes - Letters to Editors - Book reviews The scope of the Journal involves, but is not limited to, the following areas: - physico-chemical properties of drugs and methods of their determination - drug permeabilities - drug absorption - drug-drug, drug-protein, drug-membrane and drug-DNA interactions - chemical stability and degradations of drugs - instrumental methods in ADMET - drug metablic processes - routes of administration and excretion of drug - pharmacokinetic/pharmacodynamic study - quantitative structure activity/property relationship - ADME/PK modelling - Toxicology screening - Transporter identification and study
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