Synthesis and Anti-Tumor Activities of Ring A Derived Analogues of Oleanolic Acid

doi:10.6023/cjoc201610033

Chin. J. Org. Chem. ›› 2017, Vol. 37 ›› Issue (6): 1417-1425.DOI: 10.6023/cjoc201610033 Previous Articles Next Articles

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齐墩果酸A环衍生的类似物的合成及抗肿瘤活性研究

孟艳秋, 邢雯, 蒯振彧, 张伟晨, 李为

沈阳化工大学制药工程教研室沈阳 110142

收稿日期:2016-10-19 修回日期:2017-01-06 发布日期:2017-02-20
通讯作者: 李为 E-mail:myq@163.com
基金资助:
国家自然科学基金（No.21372156）、辽宁省教育厅高等学校优秀人才支持计划（No.LR2013017）和沈阳市科技计划（No.F16-230-6-00）资助项目.

Synthesis and Anti-Tumor Activities of Ring A Derived Analogues of Oleanolic Acid

Meng Yanqiu, Xing Wen, Kuai Zhenyu, Zhang Weichen, Li Wei

Department of Pharmaceutical Engineering, Shenyang University of Chemical Technology, Shenyang 110142

Received:2016-10-19 Revised:2017-01-06 Published:2017-02-20
Contact: 10.6023/cjoc201610033 E-mail:myq@163.com
Supported by:
Project supported by the National Natural Science Foundation of China (No. 21372156), the Excellent Talents in University of the Department of Education of Liaoning Province (No. LR2013017), and the Scientific Research Project of the Shenyang Science and Technology Board (No.F16-230-6-00).

1. Synthesis and Anti-Tumor Activities of Ring A Derived Analogues of Oleanolic Acid.PDF(843KB)

Abstract

By means of computer aided drug design, simulation of apoptosis inhibiting protein complex glycine receptor kinase C-kit docking with active small molecules. Ten analogues were successfully synthesized by the introduction of nitrogen-containing heterocyclic compounds at ring A and the modification of the esterification and amidation at C(28) position in the natural product oleanolic acid. Their structures were charachterized by ¹H NMR, ¹³C NMR, MS and so forth. Their anti-tumor activities against KB, A549 cells in vitro were evaluated by methyl thiazolyl tetrazolium (MTT) assay. These results indicated that the objective of test compounds of two kinds of tumor cells have good inbitory activity, and 5',6'-dihydro-olean-2-ene-[2,3-b]pyrazin-12-ene-28-acyl-4"-monomethylaniline (I₄) (IC₅₀＝2.67 μmol/L) and olean-2-ene-[2,3-b]pyrimidine-12-ene-28-oic acid n-hextyl ester (II₃) (IC₅₀＝1.03 μmol/L) have especially more potent inbitory activity on A549 tumor cells than 5-fluorouracil (IC₅₀＝7.39 μmol/L), which are worthy to be studied further.

Key words: oleanolic acid analogues, synthesis, anti-tumor activity, molecular docking

Cite this article

Meng Yanqiu, Xing Wen, Kuai Zhenyu, Zhang Weichen, Li Wei. Synthesis and Anti-Tumor Activities of Ring A Derived Analogues of Oleanolic Acid[J]. Chin. J. Org. Chem., 2017, 37(6): 1417-1425.

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齐墩果酸A环衍生的类似物的合成及抗肿瘤活性研究

Synthesis and Anti-Tumor Activities of Ring A Derived Analogues of Oleanolic Acid

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