2010
DOI: 10.1007/s00706-010-0276-6
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Design, synthesis, and urease inhibition studies of a series of 4-amino-5-aryl-3H-1,2,4-triazole-3-thiones

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Cited by 31 publications
(17 citation statements)
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“…Hydralazine-based hydrazones [14] and 3-chlorobenzaldehyde-based hydrazones [15] have been evaluated separately for their antibacterial and antifungal activity, and they are found to exhibit excellent activity. But as hydrazones are prone to undergo degradation and bacteria can develop resistance to them, complexation of hydrazones with biocompatible metal ions is useful in this regard for long-term effectiveness [16].…”
Section: Introductionmentioning
confidence: 99%
“…Hydralazine-based hydrazones [14] and 3-chlorobenzaldehyde-based hydrazones [15] have been evaluated separately for their antibacterial and antifungal activity, and they are found to exhibit excellent activity. But as hydrazones are prone to undergo degradation and bacteria can develop resistance to them, complexation of hydrazones with biocompatible metal ions is useful in this regard for long-term effectiveness [16].…”
Section: Introductionmentioning
confidence: 99%
“…Як вихідні речовини обрали 2-бромбензойну кислоту, з якої через низку послідовних стадій отримали 5-(2-бром-феніл)-4-аміно-4Н-1,2,4-тріазол-3-тіон [10][11][12].…”
Section: матеріали і методи дослідженняunclassified
“…The presence of the latter group may enhance the genetic toxicity of the former while any modification of -NCS function leads to a greater reduction of mutagenicity [9]. Hence, we have tried to modify -NCS function for mercapto triazoles, considering the high biological significance of the triazole moiety [10][11][12][13][14][15].…”
Section: Introductionmentioning
confidence: 99%