Lin T S, Prusoff W H
J Med Chem. 1978 Jan;21(1):109-12.
3',5'-Diamino-3',5'-dideoxythymidine (7) was synthesized via a nine-step synthesis from thymidine in good overall yield. 3'-Amino-3'-deoxythymidine (8) and 5'-amino-5'-deoxythymidine (12) were prepared with a minor modification of the procedure reported by Horwitz and co-workers. Although the 5'-amino analogue 12 had potent antiviral activity relative to the 3'-amino analogue 8, the latter is a potent inhibitor of the replication of both murine sarcoma 180 cells (ED50 = 5 micrometer) and of murine L1210 cells (ED50 = 1 micrometer) in vitro. Most unexpectedly, however, was the finding of complete lack of either antiviral or antineoplastic activity by the 3',5'-diamino analogue 7 which appears to have acquired the undesirable qualities of both the 3'-amino and 5'-amino analogues of thymidine.
3',5'-二氨基-3',5'-二脱氧胸苷(7)以胸苷为原料,经九步合成法制备,总收率良好。3'-氨基-3'-脱氧胸苷(8)和5'-氨基-5'-脱氧胸苷(12)的制备对Horwitz及其同事报道的方法稍作修改。尽管5'-氨基类似物12相对于3'-氨基类似物8具有较强的抗病毒活性,但后者在体外是鼠肉瘤180细胞(半数有效浓度=5微米)和鼠L1210细胞(半数有效浓度=1微米)复制的有效抑制剂。然而,最出乎意料的是,3',5'-二氨基类似物7完全没有抗病毒或抗肿瘤活性,它似乎兼具了胸苷3'-氨基和5'-氨基类似物的不良特性。