1224600-56-9Relevant academic research and scientific papers
Synthesis, antimicrobial, and anti-inflammatory activities of novel 5-(1-adamantyl)-4-arylideneamino-3-mercapto-1,2,4-triazoles and related derivatives
Al-Omar, Mohamed A.,Al-Abdullah, Ebtehal S.,Shehata, Ihsan A.,Habib, Elsayed E.,Ibrahim, Tarek M.,El-Emam, Ali A.
, p. 2526 - 2550 (2010)
The reaction of 5-(1-adamantyl)-4-amino-3-mercapto-1,2,4-triazole (5) with various aromatic aldehydes in ethanol or acetic acid yielded the corresponding 4arylideneamino derivatives 6a-v. Treatment of the 4-(2,6-difluoro- and dichlorobenzylideneamino) derivatives 6o and 6q with 1-substituted piperazines, and formaldehyde solution in ethanol afforded good yields of the corresponding 5-(1adamantyl)-4-(2,6-dihalobenzylideneamino-2-(4-substituted-1- piperazinylmethyl)-1,2,4triazoline-3-thiones 7a-p. 5-(1-Adamantyl)-4- arylideneamino-2-(4-ethoxycarbonyl-1piperidylmethyl)-1,2,4-triazoline-3-thiones 8a-n, were similarly prepared via the reaction of the corresponding arylideneamino derivative with ethyl 4-piperidinecarboxylate and formaldehyde solution in ethanol. Compounds 6a-v, 7a-p and 8a-n were tested for in vitro activities against a panel of Gram-positive and Gram-negative bacteria and the yeastlike pathogenic fungus Candida albicans. Several derivatives showed good or moderate activities, particularly against the tested Gram-positive bacteria. In addition, the in vivo anti-inflammatory activity of 21 compounds was determined using the carrageenan-induced paw oedema method in rats. Compounds 7d, 7g, 7i, 7j, 7l, 8c, 8e and 8l showed good or moderate dose-dependent activity in this area. Copyright
