2-C-Methyladenosine is an inhibitor of hepatitis C virus (HCV) replication. 2-C-Methyladenosine inhibits HCV replicon and NS5B-catalyzed RNA synthesis with IC 50 values of 0.3μM and 1.9 μM, respectively. 2-C-Methyladenosine also potently inhibits LRV1 in Leishmania guyanensis (Lgy) and Leishmania braziliensis.
性状
Solid
IC50 & Target[1][2]
IC50: 0.3μM (HCV replicon); 1.9 μM (NS5B)
体内研究(In Vivo)
2-C-Methyladenosine has inhibitory potency for HCV replicon in HB110A cells with an IC 50 values of 0.3μM.
2-C-Methyladenosine inhibits NS5B-catalyzed RNA synthesis with an IC 50 values of 1.9 μM.
2′-C-methyladenosine potently inhibits LRV1 in Leishmania guyanensis (Lgy) and Leishmania braziliensis has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
参考文献
[1]. Steven S Carroll, et al. Inhibition of hepatitis C virus RNA replication by 2-modified nucleoside analogs. J Biol Chem. 2003 Apr 4;278(14):11979-84.[2]. John I Robinson, et al. Concentration of 2C-methyladenosine triphosphate by Leishmania guyanensis enables specific inhibition of Leishmania RNA virus 1 via its RNA polymerase. J Biol Chem. 2018 Apr 27;293(17):6460-6469.
溶解度数据
In Vitro: DMSO : 31.25 mg/mL (111.10 mM; ultrasonic and warming and heat to 60°C)配制储备液