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芥酸乙酯的微型有机合成
  • 期刊名称:广西科学院学报. 22(S):399~400. 获广西分析测试协会2006年度优秀学术论文(不分等级
  • 时间:0
  • 分类:R735.7[医药卫生—肿瘤;医药卫生—临床医学]
  • 作者机构:[1]广西医科大学,南宁530021, [2]广西医科大学天然药物化学教研室, [3]病理生理教研室, [4]广西大学化学化工学院
  • 相关基金:国家自然科学基金资助项目(项目编号:30560186);教育部“春晖计划”项目(项目编号:教外司[2003]593);广西壮族自治区科技厅科学基金项目(编号:桂科自0728128);2007年广西研究生教育创新计划项目
  • 相关项目:板蓝根高级不饱脂肪酸逆转肝癌细胞多药耐药性构效关系与机制的实验研究
中文摘要:

目的探讨合成芥酸乙醇酰胺对人肝癌细胞BEL-7404的抑制作用。方法(1)运用微型有机合成技术,以芥酸、甲醇和乙醇胺为原料、金属钠为催化剂合成芥酸乙醇酰胺,采用硅胶柱层析分离纯化,红外光谱和核磁共振谱确证结构;(2)用芥酸乙醇酰胺作用于BEL3404,用倒置显微镜镜下观察其对BEL-7404细胞的生长状况的影响,MTT法观察其抑制作用。结果合成出了芥酸乙醇酰胺并确证了其结构;芥酸乙醇酰胺浓度在50.0μg/ml以上时,能很明显的抑制BEL-404的增殖,抑制率均高于40%,IC50为101.77588μs/ml。结论采用微型合成法能够快速、方便地合成出芥酸乙醇酰胺;芥酸乙醇酰胺对BEL-7404细胞的增殖有明显的抑制作用。

英文摘要:

Objective To study the synthesis of the N-alcohol erucamide and its activity of anti-tumor in vitro. Methods (1)Through the micro-organic synthesis technology, erucic acid and methanol were coupled with ethanolamine as raw matierals, sodium as catalyst to synthesize the N-alcohol erucamide, isolation and purification a- chieved by silical gel column chromatography, and Its structure was confirmed by infrared spectra and nuclear mag- netic resonance spectrum; (2)BEL-7404 was cultured in media added to the N-ethanol erucamide. The ceils' s growth was observed in inverted microscope. The effect of inhibiting cancer cells was detected with MTT. Results The N-alcohol erucamide was synthesized successfully;Its strong inhibiting effect was recorded beyond 50. 0 μg/ml. The inhibiting rates were all beyond 40%, the inhibitory concentration 50% (IC50) was 101. 77588 μg/ml. Conclusion Through the microscale organic synthesis, N-alcohol erucamide can be synthesized quickly and conveniently. N-alcohol erucamide has obvious inhibiting effcet on BEL-7404 ceils in vitro.

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