A series of novel [1,2,4]triazolo[4,3-a]quinoxalinone derivatives have been synthesized. The structures of the newly synthesized compounds were confirmed by elemental analysis and different spectral techniques. The invitro antimicrobial screening of some selected compounds was carried out using the diffusion agar technique. Compound 14c was found to be the most active antibacterial agent against Escherichia coli using gentamicin as reference drug. All the tested compounds showed no activity against Candida albicans and Pseudomonas aerugeosa.
Ghiaty, A. (2015). DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF NOVEL [1,2,4]TRIAZOLO[4,3-A] QUINOXALINONES. Al-Azhar Journal of Pharmaceutical Sciences, 52(2), 208-218. doi: 10.21608/ajps.2015.12554
MLA
Adel Ghiaty. "DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF NOVEL [1,2,4]TRIAZOLO[4,3-A] QUINOXALINONES", Al-Azhar Journal of Pharmaceutical Sciences, 52, 2, 2015, 208-218. doi: 10.21608/ajps.2015.12554
HARVARD
Ghiaty, A. (2015). 'DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF NOVEL [1,2,4]TRIAZOLO[4,3-A] QUINOXALINONES', Al-Azhar Journal of Pharmaceutical Sciences, 52(2), pp. 208-218. doi: 10.21608/ajps.2015.12554
VANCOUVER
Ghiaty, A. DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF NOVEL [1,2,4]TRIAZOLO[4,3-A] QUINOXALINONES. Al-Azhar Journal of Pharmaceutical Sciences, 2015; 52(2): 208-218. doi: 10.21608/ajps.2015.12554
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