Larwood David J, Stevens David A
Department of Pharmaceutical Chemistry, University of California-San Francisco, San Francisco, CA 94158, USA.
California Institute for Medical Research, San Jose, CA 95128, USA.
Antibiotics (Basel). 2024 Apr 28;13(5):405. doi: 10.3390/antibiotics13050405.
Natural host defensins, also sometimes termed antimicrobial peptides, are evolutionarily conserved. They have been studied as antimicrobials, but some pharmaceutical properties, undesirable for clinical use, have led to the development of synthetic molecules with constructed peptide arrangements and/or peptides not found in nature. The leading development currently is synthetic small-molecule nonpeptide mimetics, whose physical properties capture the characteristics of the natural molecules and share their biological attributes. We studied brilacidin, an arylamide of this type, for its activity in vitro against fungi (40 clinical isolates, 20 species) that the World Health Organization has highlighted as problem human pathogens. We found antifungal activity at low concentrations for many pathogens, which indicates that further screening for activity, particularly in vivo, is justified to evaluate this compound, and other mimetics, as attractive leads for the development of effective antifungal agents.
天然宿主防御素,有时也被称为抗菌肽,在进化过程中是保守的。它们已作为抗菌剂进行研究,但一些不利于临床使用的药物特性促使人们开发具有特定肽排列结构的合成分子和/或自然界中不存在的肽。目前主要的进展是合成小分子非肽模拟物,其物理性质兼具天然分子的特征并具备相同的生物学属性。我们研究了这类芳基酰胺类药物布立西丁对世界卫生组织列为人类致病性难题的真菌(40株临床分离株,20个菌种)的体外活性。我们发现,许多病原体在低浓度下就表现出抗真菌活性,这表明进一步筛选其活性,尤其是体内活性,对于评估该化合物以及其他模拟物作为有效抗真菌药物开发的有吸引力的先导物是合理的。