Synthesis and Structure-Activity Relationships of Side-Chain-Substituted Analogs of the Allylamine Antimycotic Terbinafine Lacking the Central Amino Function
作者:Peter Nussbaumer、Ingrid Leitner、Karin Mraz、Anton Stuetz
DOI:10.1021/jm00010a029
日期:1995.5
Terbinafine is a therapeutically used inhibitor of fungal squalene epoxidase that has prompted extensive derivatization programs for structure-activity relationship studies. In the present study, derivatives of terbinafine were synthesized that lack the central tertiary amino group but have polar substitutents at the tert-butyl residue of the side chain. Evaluation of the antifungal potential revealed
特比萘芬是一种治疗性使用的真菌角鲨烯环氧酶抑制剂,已为结构-活性关系研究提供了广泛的衍生程序。在本研究中,合成了特比萘芬的衍生物,这些衍生物缺乏中心的叔氨基,但在侧链的叔丁基残基上具有极性取代基。对抗真菌潜力的评估表明,这种新型结构类型的代表也可以表现出广泛的抗真菌活性,这表明烯丙胺类抗真菌药的中心氨基功能对于抑制真菌生长不是必需的。效力似乎与引入的官能团的极性相关,而广泛的抗真菌活性似乎仅限于具有碱性取代基的化合物。二甲氨基取代的“碳水化合物类似物”