Synthesis of N′-arylidene-2-(5-aryl-1H-1, 2, 4-triazol-3-ylthio) acetohydrazides as antidepressants

[1] Aouad MR(2015)Synthesis and characterization of some novel 1,2,4-triazoles, 1,3,4-thiadiazoles and Schiff bases incorporating imidazole moiety as potential antimicrobial agents Acta Pharm 65 117-132

[2] Messali M(2005)The tail suspension test as a model for assessing antidepressant activity: review of pharmacological and genetic studies in mice Neurosci Biobehav Rev 29 571-625

[3] Rezki N(2013)Synthesis and anticancer activity of new substituted pyrazoles and their derived 1,2,4-Triazoles and sugar derivatives J Heterocycl Chem 50 344-350

[4] Ali AA(2014)Discovery of potential anti-inflammatory drugs: diaryl-1,2,4-triazoles bearing Org Biomol Chem 12 2114-2117

[5] Lesimple A(2011)-hydroxyurea moiety as dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase Pak J Pharm Sci 24 109-112

[6] Cryan JF(2015)Synthesis and biological evaluation of some schiff bases of [4-(amino)-5-phenyl-4H-1, 2,4-triazole-3-thiol] Cent Nerv Syst Agents Med Chem 15 17-22

[7] Mombereau C(2014)1, 2, 4-triazole derivatives as potential scaffold for anticonvulsant activity Eur J Med Chem 86 75-80

[8] Vassout A(2015)Synthesis of novel 1,2,4-triazoles, triazolothiadiazines and triazolothiadiazoles as potential anticancer agents Bioorg Med Chem Lett 25 3052-3056

[9] Flefel EM(2012)Synthesis and antimicrobial evaluation of 5-aryl-1,2,4-triazole-3-thione derivatives containing a rhodanine moiety Org Med Chem Lett 2 26-30

[10] Tantawy WA(2012)Synthesis and evaluation of antitumor activities of novel chiral 1, 2, 4-triazole Schiff bases bearing γ-butenolide moiety Lett Drug Des Discov 9 687-693

[1] Aouad MR(2015)Synthesis and characterization of some novel 1,2,4-triazoles, 1,3,4-thiadiazoles and Schiff bases incorporating imidazole moiety as potential antimicrobial agents Acta Pharm 65 117-132

[2] Messali M(2005)The tail suspension test as a model for assessing antidepressant activity: review of pharmacological and genetic studies in mice Neurosci Biobehav Rev 29 571-625

[3] Rezki N(2013)Synthesis and anticancer activity of new substituted pyrazoles and their derived 1,2,4-Triazoles and sugar derivatives J Heterocycl Chem 50 344-350

[4] Ali AA(2014)Discovery of potential anti-inflammatory drugs: diaryl-1,2,4-triazoles bearing Org Biomol Chem 12 2114-2117

[5] Lesimple A(2011)-hydroxyurea moiety as dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase Pak J Pharm Sci 24 109-112

[6] Cryan JF(2015)Synthesis and biological evaluation of some schiff bases of [4-(amino)-5-phenyl-4H-1, 2,4-triazole-3-thiol] Cent Nerv Syst Agents Med Chem 15 17-22

[7] Mombereau C(2014)1, 2, 4-triazole derivatives as potential scaffold for anticonvulsant activity Eur J Med Chem 86 75-80

[8] Vassout A(2015)Synthesis of novel 1,2,4-triazoles, triazolothiadiazines and triazolothiadiazoles as potential anticancer agents Bioorg Med Chem Lett 25 3052-3056

[9] Flefel EM(2012)Synthesis and antimicrobial evaluation of 5-aryl-1,2,4-triazole-3-thione derivatives containing a rhodanine moiety Org Med Chem Lett 2 26-30

[10] Tantawy WA(2012)Synthesis and evaluation of antitumor activities of novel chiral 1, 2, 4-triazole Schiff bases bearing γ-butenolide moiety Lett Drug Des Discov 9 687-693