Nucleosides and nucleotides .150. Enzymatic synthesis of 5'-phosphatidyl derivatives of 1-(2-C-cyano-2-deoxy-beta-D-arabino-pentofuranosyl) (CNDAC) and their notable antitumor effects in mice

被引:12
|
作者
Shuto, S
Awano, H
Shimazaki, N
Hanaoka, K
Matsuda, A
机构
[1] HOKKAIDO UNIV,FAC PHARMACEUT SCI,KITA KU,SAPPORO,HOKKAIDO 060,JAPAN
[2] SANKYO CO LTD,BIOL RES LABS,TOKYO,JAPAN
关键词
D O I
10.1016/0960-894X(96)00162-X
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
1-(2-C-Cyano-2-deoxy-beta-D-arabino-pentofuranosyl)cytosine (CNDAC, 1) is a potent antitumor nucleoside developed by us. A series of 5'-phosphatidyl derivatives of CNDAC bearing various fatty acyl residues, namely dimyristoyl derivative 3a, dipalmitoyl derivative 3b, distearoyl 3c, dioleoyl derivative 3d, and dilinoleoyl derivative 3e, was synthesized by phospholipase D-catalyzed transphosphatidylation. All of these 5'-phosphatidyl-CNDACs (3a-e) administered ip almost perfectly inhibited the growth of sc-implanted M5076 sarcoma in mice, and the effects were clearly superior to that of CNDAC. (C) 1996 Elsevier Science Ltd.
引用
收藏
页码:1021 / 1024
页数:4
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