拟肽
抗菌剂
效力
代谢稳定性
生物利用度
最小抑制浓度
体外
化学
药理学
抗菌肽
组合化学
医学
计算生物学
肽
生物
生物化学
有机化学
作者
Lauren Hellewell,Nakisa Malek Gilani,Christopher James Stanton,Ludovic Pelligand,Henrik Franzyk,Luca Guardabassi,Liam Good
出处
期刊:Future Medicinal Chemistry
[Newlands Press Ltd]
日期:2022-11-24
卷期号:14 (24): 1899-1921
被引量:1
标识
DOI:10.4155/fmc-2022-0160
摘要
Aims: This systematic review was carried out to determine whether synthetic peptidomimetics exhibit significant advantages over antimicrobial peptides in terms of in vitro potency. Structural features – molecular weight, charge and length – were examined for correlations with activity. Methods: Original research articles reporting minimum inhibitory concentration values against Escherichia coli, indexed until 31 December 2020, were searched in PubMed/ScienceDirect/Google Scholar and evaluated using mixed-effects models. Results: In vitro antimicrobial activity of peptidomimetics resembled that of antimicrobial peptides. Net charge significantly affected minimum inhibitory concentration values (p < 0.001) with a trend of 4.6% decrease for increments in charge by +1. Conclusion: AMPs and antibacterial peptidomimetics exhibit similar potencies, providing an opportunity to exploit the advantageous stability and bioavailability typically associated with peptidomimetics.
科研通智能强力驱动
Strongly Powered by AbleSci AI