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dc.contributor.authorHuang, Lin-Chiang Sherlocken_US
dc.contributor.authorChuang, Hongen_US
dc.contributor.authorKapoor, Mohiten_US
dc.contributor.authorHsieh, Cheng-Yingen_US
dc.contributor.authorChou, Shih-Chingen_US
dc.contributor.authorLin, Hui-Hsienen_US
dc.contributor.authorChen, Yi-Weien_US
dc.contributor.authorChang, Chia-Chingen_US
dc.contributor.authorHwu, Jih-Ruen_US
dc.contributor.authorLiang, Yu-Chuanen_US
dc.contributor.authorHsu, Ming-Huaen_US
dc.date.accessioned2019-04-03T06:45:03Z-
dc.date.available2019-04-03T06:45:03Z-
dc.date.issued2015-01-01en_US
dc.identifier.issn2046-2069en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c5ra18827jen_US
dc.identifier.urihttp://hdl.handle.net/11536/129600-
dc.description.abstractIn this research, we designed and synthesized a new series of nordihydroguaiaretic acid (NDGA) derivatives for multidrug resistance (MDR) research. A methylsulfonyl NDGA derivative, ((2R,3S)-2,3-dimethylbutane-1,4-diyl)bis(benzene-4,1,2-triyl) tetramethanesulfonate (5d), was found to inhibit MDR1 gene expression and suppress drug resistantMES-SA/Dx5 cells. Moreover, the combination of 5d and doxorubicin/terameprocol (M4N) showed a profound synergistic effect on inhibition of drug resistant cancer cells, suggesting that 5d is a potential adjuvant applied with doxorubicin or terameprocol in cancer treatment.en_US
dc.language.isoen_USen_US
dc.titleDevelopment of nordihydroguaiaretic acid derivatives as potential multidrug-resistant selective agents for cancer treatmenten_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c5ra18827jen_US
dc.identifier.journalRSC ADVANCESen_US
dc.citation.volume5en_US
dc.citation.issue130en_US
dc.citation.spage107833en_US
dc.citation.epage107838en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000367271700071en_US
dc.citation.woscount1en_US
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