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作 者:杜娟[1] 张喜全[2] 郭键[1] 顾红梅[2] 徐宏江[2] 李宝林[1]
机构地区:[1]教育部药用植物资源与天然药物化学重点实验室、陕西师范大学化学与材料科学学院,陕西西安710062 [2]江苏正大天晴药业股份有限公司,江苏南京210038
出 处:《化学研究与应用》2009年第1期120-122,共3页Chemical Research and Application
基 金:教育部重点科学研究项目(105153)
摘 要:Two new resveratrol analougues,t-butyl 4-[(E)-2-(3,4,5-trimethoxyphenyl)vinyl]phenoxy i-butyrate and ethyl 4-[(E)-2-(3,4,5-trimethoxyphenyl)vinyl]phenoxy n-butyrate,are synthesized from 3,4,5-trimethoxybenzaldehyde and p-nitrotoluene via mutil-steps including condensation,catalytic reduction,diazotization,hydrolyzation,nucleophilic substitution.The effect of the new compounds on HL-60 and A549 cell proliferation are tested by MTT.The results show that the two new compounds exhibite the activities of anti-tumor proliferation.Two new resveratrol analougues, t-butyl 4- [ ( E ) -2- ( 3,4,5 -trimethoxyphenyl ) vinyl ] phenoxy i-butyrate and ethyl 4- [ ( E)-2-( 3,4,5-trimethoxyphenyl ) vinyl ] phenoxy n-butyrate, are synthesized from 3, 4, 5-trimethoxybenzaldehyde and p- nitrotoluene via mufti-steps including condensation, catalytic reduction, diazotization, hydrolyzation, nucleophilic substitution. The effect of the new compounds on HL-60 and A549 cell proliferation are tested by .MTT. The results show that the two new compounds exhibite the activities of anti-tumor proliferation.
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