Invidiata F P, Furnò G, Simoni D, Lampronti I, Musiu C, Milia C, Scintu F, La Colla P
Istituto Farmacochimico dell'Università di Palermo, Italy.
Farmaco. 1997 Apr;52(4):259-61.
A series of novel 3,6-disubstituted 1,2,4-triazolo[3,4-b][1,3,4]thiadiazole derivatives was prepared and tested to evaluate their antimycotic, antibacterial and anti-HIV-1 activities. The reaction of thiocarbohydrazide with carboxylic acids at the melting temperature allows an improved preparation of the 5-substituted 4-amino-3-mercapto-1,2,4-triazole heterocycles which in turn allows an easier preparation of the 1,2,4-triazolo[3,4-b] [1,3,4]thiadiazole ring system. All tested compounds didn't show any significant activity.
制备了一系列新型的3,6-二取代-1,2,4-三唑并[3,4-b][1,3,4]噻二唑衍生物,并对其抗真菌、抗菌和抗HIV-1活性进行了测试。硫代碳酰肼与羧酸在熔点温度下反应,可改进5-取代-4-氨基-3-巯基-1,2,4-三唑杂环的制备,进而更易于制备1,2,4-三唑并[3,4-b][1,3,4]噻二唑环系。所有测试化合物均未显示出任何显著活性。