s0</sub> 值為 8.35±0.66) μmol/L,強于陽性對照藥阿霉素和蘇尼替尼,對L02正常腎細胞具有中等細胞毒性, IC<sub>50</sub> 值為 35.36±2.46) (號 μmol/L 。結論化合物1是1個新的對取代苯的衍生物,化合物3對多種腫瘤細胞具有細胞毒活性。-龍源期刊網(wǎng)" />

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鐮刀菌FusariumoxysporumLHS-P1-3次級代謝產(chǎn)物的分離鑒定及腫瘤細胞毒活性研究

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Isolation, identification and tumor cytotoxic activity study of secondary metabolites from Fusarium oxysporum LHS-P1-3

ShuTing,Sun Jian,WuRongxiang,Wei Caixia,TianJingyuan,WangPei,KongFandong,Wang Cong,and ZhouLiman (KeyLaboratoryofChemistryandEngineeringoforestProducts,StateEthnicAfrsCommision,GuangxiKeyLaboatoyof ChemistryandEngineringofForestProducts,GuangxiCollaborativeInovationCenterforChemistryandEngineringofForest Products, Guangxi Minzu University,Nanning 530006)

AbstractObjective To investigate the secondary metabolites of the endophytic fungus Fusarium oxysporum LHS-P1-3 isolated from ground peanut.MethodsThe fungal secondary metabolites were isolated,purified by normal-phase silica gel column chromatography and high-performance liquid chromatography,etc.The structures were identified by ESI-MS,NMR,and other methods,and the tumor cytotoxicity was evaluated using the CCK8 method.ResultsNine compounds were isolated from the endophytic fungus Fusarium oxysporum LHS-P1-3, including one new compound (stackylineE methyl ester,1).The activityresults showed that compound 3(eiatin J1) had strong tumor cytotoxic activity against HepG2 cells, with an IC50 value of 8.35±0.66 μmol/L , stronger than the positive control drugs doxorubicin and sunitinib,and moderate cytotoxicity against LO2 normal kidney cells. IC50 value of (35.36±2.46 ) μmol/L . ConclusionCompound 1 is a new derivative of the para-substituted benzene, and compound 3 has cytotoxic activity against a variety of tumor cells.

Key wordsFusarium oxysporum LHS-P1-3; Secondary metabolites; Tuomr cytotoxic activity

鐮刀菌屬,隸屬于子囊菌門,其首次記載可追溯至1840年[1]。(剩余13674字)

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