2009
DOI: 10.1155/2009/419214
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Syntheses, Characterization and Biological Activity of Some 1, 2, 4‐Triazole Derivatives

Abstract: Syntheses of a series of 3-alkyl-4-amino-5-cyanomethyl-4H-1, 2, 4-triazoles with active methylene groups are described. The newly synthesized compounds were characterized by spectral and elemental analyses. Some compounds were screened for their antibacterial activity against S. aureus, E. coli, B. subtilis and P. aeruginosa. All the compounds carrying 1, 2, 4-triazole moiety showed significant biological activity.

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Cited by 7 publications
(3 citation statements)
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“…1, 2, 4-Triazoles and their derivatives represent one of the most biologically active classes of compounds, possessing a wide range of therapeutic properties 4 . In views of these observations and in continuation of our earlier work [5][6][7][8][9][10][11] on the syntheses of some 1,2,4-and 1,2,3-triazole derivatives, we now report the syntheses of some more triazoles derived from 4-amino-3-phenyl-5-p-tolyl-4H-1,2,4-triazole and their antifungal activity.…”
Section: Introductionsupporting
confidence: 57%
“…1, 2, 4-Triazoles and their derivatives represent one of the most biologically active classes of compounds, possessing a wide range of therapeutic properties 4 . In views of these observations and in continuation of our earlier work [5][6][7][8][9][10][11] on the syntheses of some 1,2,4-and 1,2,3-triazole derivatives, we now report the syntheses of some more triazoles derived from 4-amino-3-phenyl-5-p-tolyl-4H-1,2,4-triazole and their antifungal activity.…”
Section: Introductionsupporting
confidence: 57%
“…2,4-Dihydro-4-(4-methylphenyl)-5-(isomeric pyridyl)-3H-1,2,4-triazoles have been obtained by treating 1-(4-methylphenyl)-(isomeric pyridoyl) thiosemicarbazides and 2 M sodium hydroxide solution through the cyclization reaction. In views of these observations and in continuation of our earlier work [4][5][6][7][8] on the syntheses of some 1,2,4-&1,2,3-triazole derivatives, we now report the syntheses of some more triazoles derived from 1-(4-methylphenyl)-(isomeric pyridoyl) thiosemicarbazides and their antibacterial activities.…”
Section: Introductionsupporting
confidence: 53%
“…This include hepatitis C and hepatitis B and yellow fever. Taribavirin is as active against influenza as Ribavirin in animal models, with slight less toxicity, so it may also eventually replace Ribavirin as an anti-influenza agent 38 . Out of the ten compounds tested, compounds 3, 4and 10inhibited the formation of viral plaques by more than 30% at 50 mM after 48 hours postinfection and treatment.…”
mentioning
confidence: 99%