Kamal Ahmed, Khan M Naseer A, Reddy K Srinivasa, Srikanth Y V V, Sridhar B
Chem Biol Drug Des. 2008 Jan;71(1):78-86. doi: 10.1111/j.1747-0285.2007.00609.x. Epub 2007 Dec 18.
Two series of 10-substituted 5,5-dioxo-5,10-dihydro[1,2,4]triazolo[1,5-b][1,2,4]benzothiadiazine 2-methyl/ethyl sulfanyl benzothiazole derivatives (5a-d) and 10-substituted 5,5-dioxo-5,10-dihydro[1,2,4]triazolo[1,5-b][1,2,4] benzothiadiazine 2-phenoxy benzothiazole derivatives (16a-c) were synthesized and their structures confirmed by NMR, MS, IR and X-ray crystallography. These compounds were evaluated for their cytotoxicity against 60 human tumour cell lines. One of the synthesized compounds (5b) exhibited significant inhibitory activity against most of the cell lines and has been further evaluated for the five-dose screening.
合成了两个系列的10-取代的5,5-二氧代-5,10-二氢[1,2,4]三唑并[1,5-b][1,2,4]苯并噻二嗪2-甲基/乙基硫烷基苯并噻唑衍生物(5a-d)和10-取代的5,5-二氧代-5,10-二氢[1,2,4]三唑并[1,5-b][1,2,4]苯并噻二嗪2-苯氧基苯并噻唑衍生物(16a-c),并通过核磁共振(NMR)、质谱(MS)、红外光谱(IR)和X射线晶体学对其结构进行了确证。对这些化合物针对60种人类肿瘤细胞系的细胞毒性进行了评估。其中一种合成化合物(5b)对大多数细胞系表现出显著的抑制活性,并已进一步进行五剂量筛选评估。