Domínguez J M, Kelly V A, Kinsman O S, Marriott M S, Gómez de las Heras F, Martín J J
Departamento de Investigación, Glaxo Wellcome S.A., 28760-Tres Cantos, Madrid, Spain.
Antimicrob Agents Chemother. 1998 Sep;42(9):2274-8. doi: 10.1128/AAC.42.9.2274.
GR135402, a sordarin derivative, was isolated in an antifungal screening program. GR135402, sordarin, and derivatives of both compounds were evaluated for their ability to inhibit cell-free translational systems from five different pathogenic fungi (Candida albicans, Candida glabrata, Candida krusei, Candida parapsilosis, and Cryptococcus neoformans). The activity profile of GR135402 is extended to other chemical compounds derived from sordarin. Experimental results indicate that sordarin analogs exert their antifungal effects by specifically inhibiting the protein synthesis elongation cycle in yeasts but do not affect protein synthesis machinery in mammalian systems. Intrinsically resistant strains owe their resistance to differences in the molecular target of sordarins in these strains. Preliminary studies performed to elucidate the mode of action of this new class of antifungal agents have shown that the putative target of sordarins is one of the protein synthesis elongation factors.
GR135402是一种梭链孢酸衍生物,在一项抗真菌筛选项目中被分离出来。对GR135402、梭链孢酸以及这两种化合物的衍生物抑制来自五种不同致病真菌(白色念珠菌、光滑念珠菌、克柔念珠菌、近平滑念珠菌和新型隐球菌)的无细胞翻译系统的能力进行了评估。GR135402的活性谱扩展到了其他源自梭链孢酸的化合物。实验结果表明,梭链孢酸类似物通过特异性抑制酵母中的蛋白质合成延伸循环发挥其抗真菌作用,但不影响哺乳动物系统中的蛋白质合成机制。固有抗性菌株的抗性归因于这些菌株中梭链孢酸分子靶点的差异。为阐明这类新型抗真菌剂的作用模式而进行的初步研究表明,梭链孢酸的推定靶点是蛋白质合成延伸因子之一。