Synthesis and biological evaluation of halogenated curcumin analogs as potential nuclear receptor selective agonists
作者:Shane Batie、Jamie H. Lee、Rabia A. Jama、Drew O. Browder、Luis A. Montano、Chanh C. Huynh、Lisa M. Marcus、Dorian G. Tsosie、Zeynab Mohammed、Vu Trang、Pamela A. Marshall、Peter W. Jurutka、Carl E. Wagner
DOI:10.1016/j.bmc.2012.11.033
日期:2013.2
superfamily. Using mammalian-two-hybrid (M2H) and vitaminD responsive element (VDRE) biological assay systems, we tested CM and 11 CM synthetic analogs for their ability to activate VDR signaling. The M2H assay revealed that RXR and VDR association was induced by CM and several of itsanalogs. VDRE-based assays demonstrated that pure curcumin and eight CM analogs activated transcription of a luciferase plasmid