Waisser K, Kubicová L, Gregor J, Budová J, Andrlová A, Drsata J, Odlerová Z
Katedra anorganické a organické chemie Farmaceutické fakulty Univerzity Karlovy, Hradec.
Ceska Slov Farm. 1998 Mar;47(2):84-6.
On the basis of a preliminary study of antimycobacterial activity of thiobenzanilides a series of eight thiosalicylanilides have been prepared. Synthetized compounds have been examined in vitro against Mycobacterium tuberculosis, Mycobacterium kansasii, Mycobacterium avium and Mycobacterium fortuitum. All compounds have been found very active. The values of minimal inhibitory concentrations are summarized in Table 1. 3',4'-Salicylanilide was selected for the following research. The compound have been found inactive in vivo (on experimental murine tuberculosis).
基于对硫代苯甲酰苯胺抗分枝杆菌活性的初步研究,已制备了一系列八种硫代水杨酰苯胺。对合成的化合物进行了体外抗结核分枝杆菌、堪萨斯分枝杆菌、鸟分枝杆菌和偶然分枝杆菌的检测。发现所有化合物都具有很高的活性。最低抑菌浓度值总结在表1中。选择3',4'-水杨酰苯胺进行后续研究。已发现该化合物在体内(对实验性小鼠结核病)无活性。