Novel 4-(4-substituted-thiazol-2-ylamino)-N-(pyridin-2-yl)-benzenesulfonamides as cytotoxic and radiosensitizing agents
dc.Affiliation | October University for modern sciences and Arts (MSA) | |
dc.contributor.author | M Ghorab, Mostafa | |
dc.contributor.author | A Ragab, Fatma | |
dc.contributor.author | I Heiba, Helmy | |
dc.contributor.author | M Agha, Hebaallah | |
dc.contributor.author | M Nissan, Yassin | |
dc.date.accessioned | 2020-02-15T08:59:00Z | |
dc.date.available | 2020-02-15T08:59:00Z | |
dc.date.issued | 2012 | |
dc.description | MSA Google Scholar | en_US |
dc.description.abstract | A series of novel 4-(4-substituted-thiazol-2-ylamino)-N-(pyridin-2-yl) benzene-sulfonamides were synthesized and screened for their cytotoxic activity against human breast cancer cell line (MCF-7). Compounds 6, 7, 9, 10, 11, and 14 displayed significant activity against MCF-7 when compared to doxorubicin, which was used as a reference drug. The synergistic effect of Gamma radiation for the most active derivatives 7, 9, and 11 was also studied and their IC50 values markedly decreased to 11.9 μM, 11.7 μM, and 11.6 μM, respectively | en_US |
dc.description.sponsorship | Springer | en_US |
dc.description.uri | https://www.scimagojr.com/journalsearch.php?q=19958&tip=sid&clean=0 | |
dc.identifier.doi | https://doi.org/10.1007/s12272-012-0106-y | |
dc.identifier.issn | 0253-6269 | |
dc.identifier.other | https://doi.org/10.1007/s12272-012-0106-y | |
dc.identifier.uri | https://cutt.ly/prX5zY7 | |
dc.language.iso | en | en_US |
dc.publisher | SPRINGER | en_US |
dc.relation.ispartofseries | Archives of pharmacal research;VOL : 35 Issue : 1 | |
dc.subject | Sulfonamides | en_US |
dc.subject | Thiazoles | en_US |
dc.subject | Cytotoxic | en_US |
dc.subject | Radiosensetizing activities | en_US |
dc.title | Novel 4-(4-substituted-thiazol-2-ylamino)-N-(pyridin-2-yl)-benzenesulfonamides as cytotoxic and radiosensitizing agents | en_US |
dc.type | Article | en_US |
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