Mathew V, Keshavayya J, Vaidya V P
Acharya and B.M. Reddy College of Pharmacy, Bangalore, Karnataka, India.
Eur J Med Chem. 2006 Sep;41(9):1048-58. doi: 10.1016/j.ejmech.2006.03.018. Epub 2006 Jul 5.
Several 3,6-disubstituted-1,2,4-triazolo[3,4-b]-1,3,4-thiadizoles were prepared by the condensation of 4-amino-3-aryl/aralkyl substituted-5-mercapto-1,2,4-triazoles 3(a-c) with various substituted aromatic/hetero aromatic acids through a single step reaction. Elemental analysis, IR, 1H NMR and mass spectral data confirmed the structure of the newly synthesized compounds. Synthesized triazolo thiadiazoles investigated for their antibacterial, antifungal, anti-inflammatory and analgesic activities. Some of the tested compounds showed moderate antimicrobial activity against various tested bacterial and fungal strains. None of the synthesized compounds have significant anti-inflammatory and analgesic activities.
通过4-氨基-3-芳基/芳烷基取代的-5-巯基-1,2,4-三唑3(a - c)与各种取代的芳香族/杂芳香族酸的一步反应缩合制备了几种3,6-二取代-1,2,4-三唑并[3,4 - b]-1,3,4-噻二唑。元素分析、红外光谱、1H核磁共振和质谱数据证实了新合成化合物的结构。对合成的三唑并噻二唑进行了抗菌、抗真菌、抗炎和镇痛活性研究。一些测试化合物对各种测试的细菌和真菌菌株显示出中等抗菌活性。所合成的化合物均无显著的抗炎和镇痛活性。