Triazole antifungals. IV. Synthesis and antifungal activities of 3-acylamino-2-aryl-2-butanol derivatives
New triazole compounds were designed and synthesized as potential inhibitors of the fungal cytochrome P-450 14α-demethylase. In testing for antifungal activity against a mouse systemic Candida albicans infection, (2R,3R)3-acylamino-2-aryl-2-butanol deriva
Konosu,Tajima,Takeda,Miyaoka,Kasahara,Yasuda,Oida
p. 2581 - 2589
(2007/10/02)
More Articles about upstream products of 126925-23-3
Get Best Price for126925-23-35-Chloro-thiophene-2-carboxylic acid [(1S,2S)-2-(2,4-difluoro-phenyl)-2-hydroxy-1-methyl-3-[1,2,4]triazol-1-yl-propyl]-amide