A series of 64 derivatives of substituted heterocyclic analogues of salicylanilides was synthesized. The compounds were evaluated for in vitro antimycobacterial activity against Mycobacterium tuberculosis, Mycobacterium avium and two strains of Mycobacterium kansasii. For the QSAR study, the combination of Free-Wilson approach with Hansch approach was used. The molecules were separated on the heterocyclic
合成了一系列64个
水杨酰苯胺取代杂环类似物的衍
生物。评价了化合物对结核分枝杆菌,鸟分枝杆菌和两种堪萨斯分枝杆菌菌株的体外抗分枝杆菌活性。对于Q
SAR研究,将Free-Wilson方法与Hansch方法结合使用。分子在杂环和
水杨基部分上分离,并且还研究了电子和疏
水性质的影响。这些化合物是一组潜在的抗结核药。