Cass C E, Tan T H, Selner M
Cancer Res. 1979 May;39(5):1563-9.
The antiproliferative activity of 9-beta-D-arabinofuranosyladenine 5'-monophosphate against a cultured line of mouse leukemia cells (L1210/C2) was enhanced by addition of either 2'-deoxycoformycin or erythro-9-(2-hydroxy-3-nonyl)adenine. The activity of 9-beta-D-arabinofuranosyladenine 5'-monophosphate, alone or in combination with either of the two inhibitors of adenosine deaminase, was comparable to that of 9-beta-D-arabinofuranosyladenine (ara-A), apparently reflecting the rapid conversion of 9-beta-D-arabinofuranosyladenine 5'-monophosphate to ara-A by L1210/C2 cells. Several ara-A analogs were assayed for antiproliferative activity against L1210/C2 cells; of these, only 9-beta-D-arabinofuranosyladenine 5'-O-methylphosphate and 2'-deoxy-2'-amino-9-beta-D-arabinofuraosyladenine were active. Addition of 2'-deoxycoformycin to cell culture fluids enhanced the activity of 9-beta-D-arabinofuranosyladenine 5'-O-methylphosphate suggesting conversion to an adenosine deaminase-sensitive intermediate, presumably ara-A.
通过添加2'-脱氧助间型霉素或赤型-9-(2-羟基-3-壬基)腺嘌呤,9-β-D-阿拉伯呋喃糖基腺嘌呤5'-单磷酸对小鼠白血病细胞系(L1210/C2)的抗增殖活性得到增强。单独的9-β-D-阿拉伯呋喃糖基腺嘌呤5'-单磷酸或与两种腺苷脱氨酶抑制剂之一联合使用时,其活性与9-β-D-阿拉伯呋喃糖基腺嘌呤(ara-A)相当,这显然反映了L1210/C2细胞将9-β-D-阿拉伯呋喃糖基腺嘌呤5'-单磷酸快速转化为ara-A。对几种ara-A类似物进行了针对L1210/C2细胞的抗增殖活性测定;其中,只有9-β-D-阿拉伯呋喃糖基腺嘌呤5'-O-甲基磷酸酯和2'-脱氧-2'-氨基-9-β-D-阿拉伯呋喃糖基腺嘌呤具有活性。向细胞培养液中添加2'-脱氧助间型霉素可增强9-β-D-阿拉伯呋喃糖基腺嘌呤5'-O-甲基磷酸酯的活性,提示其转化为对腺苷脱氨酶敏感的中间体,推测为ara-A。