Synthesis and bioassay of a new class of disubstituted 1,3,4-oxadiazoles, 1,3,4-thiadiazoles and 1,2,4-triazoles

[1] Abdel-Megeed AM(2009)Design, synthesis and molecular modeling study of acylated 1,2,4-triazole-3-acetates with potential anti- inflammatory activity Eur J Med Chem 44 117-123

[2] Abdel-Rahman HM(2010)Antioxidant and antibacterial activities of novel N’-arylmethylidene2-(3,4-dimethyl-5,5-dioxidopyrazolo [4,3 Eur J Med Chem 45 698-704

[3] Alkaramany GS(2010)][1,2]benzothiazin-2(4 Biomed Pharmacother 64 287-290

[4] Ahmad M(2015))yl)acetohydrazides Eur J Med Chem 105 194-207

[5] Siddiqui HL(2015)Relationship between structure and antibacterial activity of lipophilic N-acyldiamines Eur J Med Chem 97 124-141

[6] Zia-ur-Rehman M(2016)A click chemistry approach for the synthesis of mono and bis aryloxy linked coumarinyl triazoles as anti-tubercular agents Tetrahedron Lett 57 4056-4060

[7] Parvez M(2008)1,3,4-Oxadiazoles: an emerging scaffold to target growth factors, enzymes and kinases as anticancer agents Eur J Med Chem 43 456-463

[8] Almeida de CG(1953)Rapid, microwave accelerated synthesis of [1,2,4]triazole [3,4-b][1,3,4]oxadiazolesfrom 4-acylamino-1,2,4-triazoles Chem Abstr 47 4373-323

[9] Garbois GD(2014)Synthesis and biological evaluation of some thiazolyl and thiadiazolyl derivatives of Eur J Med Chem 71 316-103

[10] Amaral LM(2016)-pyrazole as anti-inflammatory, antimicrobial agents Eur J Med Chem 108 89-503

[1] Abdel-Megeed AM(2009)Design, synthesis and molecular modeling study of acylated 1,2,4-triazole-3-acetates with potential anti- inflammatory activity Eur J Med Chem 44 117-123

[2] Abdel-Rahman HM(2010)Antioxidant and antibacterial activities of novel N’-arylmethylidene2-(3,4-dimethyl-5,5-dioxidopyrazolo [4,3 Eur J Med Chem 45 698-704

[3] Alkaramany GS(2010)][1,2]benzothiazin-2(4 Biomed Pharmacother 64 287-290

[4] Ahmad M(2015))yl)acetohydrazides Eur J Med Chem 105 194-207

[5] Siddiqui HL(2015)Relationship between structure and antibacterial activity of lipophilic N-acyldiamines Eur J Med Chem 97 124-141

[6] Zia-ur-Rehman M(2016)A click chemistry approach for the synthesis of mono and bis aryloxy linked coumarinyl triazoles as anti-tubercular agents Tetrahedron Lett 57 4056-4060

[7] Parvez M(2008)1,3,4-Oxadiazoles: an emerging scaffold to target growth factors, enzymes and kinases as anticancer agents Eur J Med Chem 43 456-463

[8] Almeida de CG(1953)Rapid, microwave accelerated synthesis of [1,2,4]triazole [3,4-b][1,3,4]oxadiazolesfrom 4-acylamino-1,2,4-triazoles Chem Abstr 47 4373-323

[9] Garbois GD(2014)Synthesis and biological evaluation of some thiazolyl and thiadiazolyl derivatives of Eur J Med Chem 71 316-103

[10] Amaral LM(2016)-pyrazole as anti-inflammatory, antimicrobial agents Eur J Med Chem 108 89-503