
Letters in drug design and discovery p. 276 - 281 (2012)
Update date:2022-08-04
Topics:
Murty
Ram, Kesur R.
Rao, Rayudu Venkateswara
Yadav
Rao, Janapala Venkateswara
Pamanji
Velatooru
A series of 3-[3-[4-(Substituted)-1-cyclicamine]propyl]thio-5- substituted[1,2,4]triazoles (8a-j) were synthesized with good yields starting from corresponding carboxylic acids. The cytotoxicity studies of these derivatives were studied against five different human cancer cell lines. Three compounds had shown good anticancer activity. The triazole derivatives, 8i and 8j were most potent particularly against U937 and HL-60 cells. The cytotoxic potency of the compounds varied between the cell lines suggesting that a structural property of these compounds as possible determinants of their biological activity.
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