抗生素
抗菌肽
抗菌剂
抗生素耐药性
化学
抗药性
药品
多重耐药
计算生物学
微生物学
药理学
生物
生物化学
作者
Peng Teng,Haodong Shao,Bo Huang,Junqiu Xie,Sunliang Cui,Kairong Wang,Jianfeng Cai
标识
DOI:10.1021/acs.jmedchem.2c00757
摘要
Clinically, antibiotics are widely used to treat infectious diseases; however, excessive drug abuse and overuse exacerbate the prevalence of drug-resistant bacterial pathogens, making the development of novel antibiotics extremely difficult. Antimicrobial peptide (AMP) is one of the most promising candidates for overcoming bacterial resistance owing to its unique structure and mechanism of action. This study examines the development of small molecular mimetics of AMPs over the past two decades. These mimetics can selectively disrupt membranes, which are the characteristic antibacterial mechanism of AMPs. In addition, the advantages and disadvantages of small AMP mimetics are discussed. The small molecular mimetics of AMPs are anticipated to garner interest and investment in discovering new antibiotics. This Perspective will assist in revitalizing the golden age of antibiotics in the current era of combating bacterial resistance.
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