Synthesis of some novel 1,2,4-triazole derivatives as potential antimicrobial agents.
European Journal of Chemistry • 2013
Publication Information
Authors
Behalo, M. S.; Aly, A. A.; Wasfy, A. F.; Rizk, M. M.
Keywords
Phthalazin-1-(2H)-One; Acid hydrazide, Isoindol-1,3-dione; Antitumor activity.
Journal
European Journal of Chemistry
Publisher
Scholars Research Library
Volume
4
Issue
2
Pages
92-97
publication.type
International
Paper Link
Not Available
Supplementary Materials
Not Available
Abstract
A novel series of phthalazine derivatives bearing isoindol-1,3-dione moiety were synthesized by treating ethyl{4-[4-
(1,3-dioxo-1,3-dihydroisoindole-2-yl)-phenyl] phthalazin-1-yloxy}acetate (3) and {4-[4-(1,3-Dioxo-1,3-
dihydroisoindol-2-yl)phenyl]phthalazin-1-yloxy} acetic acid hydrazide (7a) with various chemical reagents.The
newly synthesized compounds were characterized on the basis of their spectral (1H NMR, 13C NMR, Ms, IR)
analyses. In vitro, most of the synthesized derivatives were screened for their antitumor activity against MCF-7 cells
using MTT assay. Compounds 16b, 18, 13, 15, 17 showed the most potent cytotoxic effect concluded from their IC50
values 50, 70, 150, 180 and 100 μg/ml respectively.
(1,3-dioxo-1,3-dihydroisoindole-2-yl)-phenyl] phthalazin-1-yloxy}acetate (3) and {4-[4-(1,3-Dioxo-1,3-
dihydroisoindol-2-yl)phenyl]phthalazin-1-yloxy} acetic acid hydrazide (7a) with various chemical reagents.The
newly synthesized compounds were characterized on the basis of their spectral (1H NMR, 13C NMR, Ms, IR)
analyses. In vitro, most of the synthesized derivatives were screened for their antitumor activity against MCF-7 cells
using MTT assay. Compounds 16b, 18, 13, 15, 17 showed the most potent cytotoxic effect concluded from their IC50
values 50, 70, 150, 180 and 100 μg/ml respectively.
Staff Members - Benha University