Wataya Y, Hiraoka O
Biochem Biophys Res Commun. 1984 Sep 17;123(2):677-83. doi: 10.1016/0006-291x(84)90282-1.
3'-Deoxyinosine is a potent inhibitor for growth of the promastigote form of Leishmania tropica. In culture, EC50 value is 4.43 X 10(-7) M for the promastigote. On the other hand, it is less toxic towards mouse mammary tumor FM3A cells: EC50 value is 1.25 X 10(-4) M. 3'-Deoxyinosine is metabolized by Leishmania promastigote to give 3'-deoxyinosine-5'-monophosphate and 3'-deoxyadenosine(cordycepin)-5'-mono-, di-, and triphosphates. This metabolic conversion provides a mechanism for the parasite-selective toxicity of 3'-deoxyinosine: Leishmania can aminate the 6-position of 3'-deoxyinosine residue, thereby converting a less toxic nucleoside into the cordycepin nucleotides that are known to be highly toxic to cells.
3'-脱氧肌苷是热带利什曼原虫前鞭毛体生长的强效抑制剂。在培养中,前鞭毛体的半数有效浓度(EC50)值为4.43×10⁻⁷M。另一方面,它对小鼠乳腺肿瘤FM3A细胞的毒性较小:EC50值为1.25×10⁻⁴M。3'-脱氧肌苷被利什曼原虫前鞭毛体代谢,生成3'-脱氧肌苷-5'-单磷酸以及3'-脱氧腺苷(虫草素)-5'-单磷酸、二磷酸和三磷酸。这种代谢转化为3'-脱氧肌苷的寄生虫选择性毒性提供了一种机制:利什曼原虫可以使3'-脱氧肌苷残基的6位胺化,从而将毒性较小的核苷转化为已知对细胞具有高毒性的虫草素核苷酸。