dc.contributor.author | Yurttaş, Leyla | |
dc.contributor.author | Öztürk, Ömer | |
dc.contributor.author | Cantürk, Zerrin | |
dc.date.accessioned | 2019-10-19T14:44:58Z | |
dc.date.available | 2019-10-19T14:44:58Z | |
dc.date.issued | 2019 | |
dc.identifier.issn | 1570-1808 | |
dc.identifier.issn | 1875-628X | |
dc.identifier.uri | https://dx.doi.org/10.2174/1570180815666180926113040 | |
dc.identifier.uri | https://hdl.handle.net/11421/13655 | |
dc.description | WOS: 000468954500005 | en_US |
dc.description.abstract | Background: In this study, novel ortho-hydroxy N-acyl hydrazone moiety including compounds (3a-l) were designed, based on procaspase activating compound (PAC-1) which is a small molecule known with antitumor activity. The antitumor activity was evaluated on A549 (human lung cancer cell line) and CCD 19Lu (human lung normal cell line). Methods: Twelve N'-arylidene-2-[4-(methylsulfonyl) piperazin-1-yl] acetohydrazide derivatives (3a-l) were synthesized starting from ethyl 1-piperazinylacetate. All compounds were tested using MTT method and Xcelligence-Real time cell analysis system (RTCA DP) to determine their antitumor activity. Results: Some physicochemical properties of four active compounds were also predicted using MolSoft, PreADMET and PROTOX software. Four of them, 3h, 3j, 3k and 3l bearing 3-hydroxy, 4-dimethylamino, 2,6-dichloro and 3,4-dichloro substituents in order exhibited selective cytotoxicity. Conclusion: Eligible values were obtained in the specified ranges as to be an oral/intravenous drug considering the physicochemical calculations. | en_US |
dc.description.sponsorship | Anadolu University within the Anadolu University Scientific Research Project, Eskisehir, Turkey [1505S388] | en_US |
dc.description.sponsorship | The authors present their thanks to Anadolu University for financial support within the Anadolu University Scientific Research Project, Eskisehir, Turkey (Project no: 1505S388). | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Bentham Science Publ LTD | en_US |
dc.relation.isversionof | 10.2174/1570180815666180926113040 | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Lung Cancer | en_US |
dc.subject | Hydrazone | en_US |
dc.subject | Procaspase Activating Compound (Pac-1) | en_US |
dc.subject | Real-Time Cell Analysis | en_US |
dc.subject | Physicochemical Properties | en_US |
dc.subject | Antitumor Activity | en_US |
dc.title | New Procaspase Activating Compound (PAC-1) Like Molecules as Potent Antitumoral Agents Against Lung Cancer | en_US |
dc.type | article | en_US |
dc.relation.journal | Letters in Drug Design & Discovery | en_US |
dc.contributor.department | Anadolu Üniversitesi, Eczacılık Fakültesi, Farmasötik Kimya Anabilim Dalı | en_US |
dc.identifier.volume | 16 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.startpage | 645 | en_US |
dc.identifier.endpage | 655 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.contributor.institutionauthor | Yurttaş, Leyla | |
dc.contributor.institutionauthor | Cantürk, Zerrin | |