Synthesis and in vitro antiproliferative activity of new 1,3,4-oxadiazole derivatives possessing sulfonamide moiety

Authors
El-Din, Mahmoud M. GamalEl-Gamal, Mohammed I.Abdel-Maksoud, Mohammed S.Yoo, Kyung HoOh, Chang-Hyun
Issue Date
2015-01-27
Publisher
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
Citation
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, v.90, pp.45 - 52
Abstract
Synthesis of a new series of 1,3,4-oxadiazole derivatives possessing sulfonamide moiety is described. Their in vitro antiproliferative activities against NCI-58 human cancer cell lines of nine different cancer types were tested. Compound 1k with p-methoxybenzenesulfonamido moiety showed the highest mean %inhibition value over the 58 cell line panel at 10 mu M concentration. It showed broad-spectrum antiproliferative activity over many cell lines of different cancer types. For instance, compound 1k inhibited the growth of T-47D breast cancer cell line by 90.47% at 10 mu M. And it inhibited growth of SR leukemia, SK-MEL-5 melanoma, and MDA-MB-468 breast cancer cell lines by more than 80% at the same test concentration. Compound 1k showed superior activity than Paditaxel and Gefitinib against the most sensitive cell lines. (C) 2014 Elsevier Masson SAS. All rights reserved.
Keywords
BIOLOGICAL EVALUATION; ANTICANCER ACTIVITY; BEARING OXADIAZOLE; DESIGN; AGENTS; INHIBITORS; CANCER; NUCLEUS; SERIES; ACID; BIOLOGICAL EVALUATION; ANTICANCER ACTIVITY; BEARING OXADIAZOLE; DESIGN; AGENTS; INHIBITORS; CANCER; NUCLEUS; SERIES; ACID; Antiproliferative activity; 1,3,4-Oxadiazole; Sulfonamide
ISSN
0223-5234
URI
https://pubs.kist.re.kr/handle/201004/125848
DOI
10.1016/j.ejmech.2014.11.011
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KIST Article > 2015
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