节点文献

糖苷合成研究(Ⅶ)──1-O-β-D-芳酰基-2,3,4-三-O-乙酰基葡萄糖醛酸甲酯的合成及其生物学活性

STUDIES ON THE SYNTHESIS OF GLYCOSIDES (Ⅶ )-THE SYNTHESIS OF METHYL 1-O-ARYLCARBONYL -2, 3, 4-TRI-O-ACETYL-β-D-GLUCOPYRANURONATE AND THEIR ANTTUMOR ACTIVITIES

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 孙昌俊王义贵李洪祥戚聿新陈再成薛鹏

【Author】 Sun Changjun ;Wang Yigui;Li Hongxiang ;Qi Yuxin;Chen Zaicheng(Dept.of Chem .,Shandong Univ.,Jinan)Xue Peng(Dept.of Chem .,Wuhan Univ .,Wuhan)

【机构】 武汉大学化学系

【摘要】 以相转移催化法使2,3,4-三-O-乙酰基-1-溴-1-脱氧-α-D-葡萄糖醛酸甲酯与取代呋喃甲酸,取代苯甲酸反应,合成了八个糖酯类化合物,其中六个未见文献报道,所有产物的结构经IR,1HNMR,元素分析等所证实,并初步测定了其抗肿瘤活性.

【Abstract】 A series of compounds:methyl 1-O-arylcarbonyl-2, 3, 4-tri-O-acetyl-β-D-glucopyranuronate 3a ̄3c,5a ̄5e had been synthesized by the reaction of furancarboxylic acid 1a ̄ 1c,substitutied benzoic acid 4a ̄4d,pyrimidin carboxylic acid 4e and methyl 2, 3, 4-tri-O-acetyl-1-bromo-ldeoxy-α -D-glupyranuronate 2 under phase transfer catalysis. 3a ̄3c and 5a ̄5c are new compounds. Their structures were confirmed by IR,1HNMRand elementary analysis. Preliminary results of the in vitro tests on HL-60 tumor cellsshowed that the inhibitory ratio of 3a was 50. 8%, 3b was 47. 0% and sc was 32. 5 %.

  • 【文献出处】 山东大学学报(自然科学版) ,JOURNAL OF SHANDONG UNIVERSITY(NATURAL SCIENCE EDITION) , 编辑部邮箱 ,1996年03期
  • 【分类号】O621.3
  • 【被引频次】15
  • 【下载频次】245
节点文献中: