ligands acting on targets

2′-Bromo-4′,5′-(ethylenedioxy)acetophenone.

2′-Bromo-4′,5′-(ethylenedioxy)acetophenone.

2′-Bromo-4′,5′-(ethylenedioxy)acetophenone.

2′-Bromo-4′-cyanoacetanilide.

2′-Bromo-6′-chloro-2,2,2-trifluoroacetophenone.

2′-Bromo-6′-chloro-2,2,2-trifluoroacetophenone.

2′-C-Methyl 5′-cytidylic acid.

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

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

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

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

2′-chloro-2′-deoxyuridine.