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葡萄糖苯丙苷类化合物的合成及其抗肿瘤活性
引用本文:张斌,LI Qiang,张三奇. 葡萄糖苯丙苷类化合物的合成及其抗肿瘤活性[J]. 中国药物化学杂志, 2008, 18(4): 245-249
作者姓名:张斌  LI Qiang  张三奇
作者单位:西安交通大学,医学院,药物研究所,陕西,西安,710061
摘    要:目的设计合成葡萄糖苯丙苷衍生物,并寻求具有抗肿瘤活性的新化合物。方法四乙酰基溴代葡萄糖与醇经过成苷、脱保护、与苯甲醛缩合3步反应得到目标化合物。以A431(人表皮鳞癌细胞)、A549(人肺腺癌细胞)、7721(人肝癌细胞)3种肿瘤细胞为测试细胞株,采用M1vr法评价了目标化合物的抗肿瘤活性。结果与结论合成了19个糖苷衍生物,其结构均经。H—NMR确证。体外抗肿瘤活性实验表明,4,6-O-亚苄基β-D-吡喃葡萄糖-3-(4-甲氧基苯基)丙苷(1j)显示出较好的抗肿瘤活性。

关 键 词:葡萄糖苷  合成  抗肿瘤活性
收稿时间:2008-02-28
修稿时间:2008-05-20

Synthesis and antitumor activities of 3-phenylpropyl -D-glucopyranosides
ZHANG Bin,LI Qiang,ZHANG San-qi. Synthesis and antitumor activities of 3-phenylpropyl -D-glucopyranosides[J]. Chinese Journal of Medicinal Chemistry, 2008, 18(4): 245-249
Authors:ZHANG Bin  LI Qiang  ZHANG San-qi
Affiliation:(Institute of Pharmaceutical Science, School of Medicine, Xi’an Jiaotong University, Xi’an 710061, China)
Abstract:Abstract : Aim To synthesize 3-phenylpropyl -D-glucopyranosides and evaluate their antitumor activities. Methods The reaction of tetra-O-acetyl-α-D-glucopyranosyl bromide with 3-phenylpropanol produced tetra-O-acetyl-β-D-glucopyranosides, which were then treated by deacetylation, condensation with benzaldehyde to give the target compounds. Results and conclusions Nineteen glycosides were synthesized, and their structures were confirmed by 1H-NMR. Their antitumor activities were evaluated by MTT method in vitro. Some synthesized 3-phenylpropyl -D-glucopyranosides had moderate inhibitory effects on A431 (human epithelial carcinoma cell line), A549 (human lung adenocarcinoma cell line), 7721 (human hepatoma cell line). Among them, 3-(4-methyoxyphenyl)propyl -4,6-O-benzyylidene--D-glucopyranoside showed good antitumor activity.
Keywords:glucopyranosides  synthesis  antitumor activity
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