作者:Gabriela Marques、Alice Kunzler、Valeria Bareno、Bruna Drawanz、Hellen Mastelloto、Fabio Leite、Gustavo Nascimento、Patrícia Nascente、Geonir Siqueira、Wilson Cunico
DOI:10.2174/15734064113099990030
日期:2014.4
Thiazolidinones, synthesized from multicomponent reactions of 2-heteroarylmethylamine, arenealdehydes and
mercaptoacetic acid, have been tested against six yeasts, namely Candida albicans, C. parapsilosis, C. guilliermondii,
Cryptococcus laurentii, Trichosporon asahii and Rhodotorula spp. The activities were expressed as minimum inhibitory
concentrations (MIC) and the minimum fungicidal concentrations (MFC). The most affected yeasts were Rhodotorula spp
and T. asahii. The cytotoxicities of the thiazolidinones against the fibroblast 3T3/NIH cell line are also described. The
antifungal results and the low cytotoxicity of the compounds in this work provide good guides for the further development
of active compounds.
噻唑烷酮类化合物,由 2-杂芳基甲胺、芳烃醛和
巯基乙酸,已针对六种酵母进行了测试,即白色念珠菌、近平滑念珠菌、吉里蒙念珠菌、
劳伦隐球菌、asahii 毛孢子菌和红酵母属。活性表示为最小抑制
浓度(MIC)和最低杀菌浓度(MFC)。受影响最严重的酵母是红酵母
和T.asahii。还描述了噻唑烷酮类药物对成纤维细胞 3T3/NIH 细胞系的细胞毒性。这
本工作中化合物的抗真菌效果和低细胞毒性为进一步开发提供了良好的指导
活性化合物。