2’-C-Methyladenosine is an inhibitor of hepatitis C virus (HCV) replication (IC = 0.3 µM in Huh-7 human hepatoma cells) that is not cytotoxic at concentrations up to 100 µM. It is converted intracellularly to adenosine triphosphate, which inhibits the RNA-dependent RNA polymerase nonstructural protein 5B (NS5B). It also inhibits growth of L. guyanensis in vitro (EC = 3 µM) and eradicates it when used at a concentration of 10 µM.
2'-C-Methyladenosine is an inhibitor of hepatitis C virus (HCV) replication. 2'-C-Methyladenosine inhibits HCV replicon and NS5B-catalyzed RNA synthesis with IC50 values of 0.3μM and 1.9 μM, respectively. 2'-C-Methyladenosine also potently inhibits LRV1 in Leishmania guyanensis (Lgy) and Leishmania braziliensis.
IC50&Target
IC50: 0.3μM (HCV replicon); 1.9 μM (NS5B)
体外研究
2'-C-Methyladenosine exhibits inhibitory effects on HCV replicons in HB110A cells, with an IC50 value of 0.3 μM.
2'-C-Methyladenosine inhibits RNA synthesis catalyzed by NS5B, with an IC50 value of 1.9 μM.
2'-C-Methyladenosine effectively inhibits LRV1 in *Leishmania guyanensis* (Lgy) and *Leishmania braziliensis*.
分子式
C11H15N5O4
分子量
281.27
CAS号
15397-12-3
中文名称
2'-C-甲基腺苷
运输条件
Room temperature in continental US; may vary elsewhere.