摘要
Curcumin,adietaryphytochemical,exhibitsmultifunctionalnaturalproductwithregulatoryeffectsoninflammation.However,thepoorbioavailabilitylimitsitsclinicalapplications.Thus,wedesignedandsynthesizedanovelmonocarbonylanalogueofcurcuminB7andtheirinhibitionagainstmonocytechemotacticprotein-1(MCP-1)andinterleukin-8(IL-8)releasewasevaluatedinH2O2-stimulatedhumanvascularendothelialcells(ECs)inadose-responsivemanner,whileexhibitingnocytotoxicityinECs.Takentogether,theseinsightsonthenovelcompoundB7mayserveaspotentialagentsforthetreatmentofatherosclerosis.
出版日期
2015年03月13日(中国期刊网平台首次上网日期,不代表论文的发表时间)