Publication: Synthesis of Diflunisal Thiazolidinones as Anticancer Agents
dc.contributor.author | ŞENER, AZİZE | |
dc.contributor.authors | Senkardes, Sevil; Ozakpinar, Ozlem B.; Ozsavci, Derya; Sener, Azize; Cevik, Ozge; Kucukguzel, S. Guniz | |
dc.date.accessioned | 2022-03-12T20:27:57Z | |
dc.date.available | 2022-03-12T20:27:57Z | |
dc.date.issued | 2016 | |
dc.description.abstract | A series of diflunisal 4-thiazolidinones were synthesized. Some selected compounds were determined at one dose towards the full panel of 60 human cancer cell lines by National Cancer Institute. 2',4'-Difluoro-4-hydroxy-N-[4-oxo-2-(thiophen-2-yl)-1,3-thiazolidin-3-yl]biphenyl-3-carboxamide (4a) demonstrated the most marked effect on K-562 cancer cell line with 58.59 % growth inhibition at 10 mu M. Compound 4a was evaluated in vitro using the MTT colorimetric method against human leukemia cell line K-562 and mouse embryonic fibroblasts cell line NIH-3T3 at different doses for cell viability and growth inhibition. Compound 4a exhibited anticancer activity with IC50 value of 5.2 mu M against K-562 cells and did not display cytotoxicity towards NIH-3T3 cells compared with diflunisal. In addition, this compound could be an interesting prototype as an antiproliferative agent. | |
dc.identifier.doi | 10.2174/1871520615666150831125337 | |
dc.identifier.eissn | 1875-5992 | |
dc.identifier.issn | 1871-5206 | |
dc.identifier.pubmed | 26320814 | |
dc.identifier.uri | https://hdl.handle.net/11424/233815 | |
dc.identifier.wos | WOS:000382267900005 | |
dc.language.iso | eng | |
dc.publisher | BENTHAM SCIENCE PUBL LTD | |
dc.relation.ispartof | ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Annexin-V | |
dc.subject | apoptosis | |
dc.subject | diflunisal | |
dc.subject | K-562 cancer cell line | |
dc.subject | 4-Thiazolidinone | |
dc.subject | NATIONAL-CANCER-INSTITUTE | |
dc.subject | HYDRAZIDE-HYDRAZONES | |
dc.subject | CASPASE ACTIVATION | |
dc.subject | DRUG DISCOVERY | |
dc.subject | APOPTOSIS | |
dc.subject | CYTOTOXICITY | |
dc.subject | DERIVATIVES | |
dc.subject | MECHANISMS | |
dc.subject | SCREEN | |
dc.subject | CELLS | |
dc.title | Synthesis of Diflunisal Thiazolidinones as Anticancer Agents | |
dc.type | article | |
dspace.entity.type | Publication | |
local.avesis.id | 1549f9d9-4925-4599-a1ec-719f82118a8b | |
local.import.package | SS17 | |
local.indexed.at | WOS | |
local.indexed.at | SCOPUS | |
local.indexed.at | PUBMED | |
local.journal.numberofpages | 9 | |
local.journal.quartile | Q2 | |
oaire.citation.endPage | 1274 | |
oaire.citation.issue | 10 | |
oaire.citation.startPage | 1266 | |
oaire.citation.title | ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY | |
oaire.citation.volume | 16 | |
relation.isAuthorOfPublication | fd65174e-4126-41c3-913d-e8bcdce20632 | |
relation.isAuthorOfPublication.latestForDiscovery | fd65174e-4126-41c3-913d-e8bcdce20632 |