With S-adenosyl homocysteine formed as a by-product in both steps. Recently, the MCE Chemical 1381289-58-2 flavivirus MTase was also found to catalyze additional 2��-O methylations of internal adenosine of the viral RNA. The first methylation of the viral mRNA cap is an obligate step in the virus life-cycle; and defects in N-7 methylation are lethal to DENV, WNV, YFV, and Kunjin virus replication. Our laboratory recently identified an AdoMet analogue, sinefungin that inhibits the MTase activity and replication among a broad spectrum of flaviviruses. We also observed an additional pocket adjacent to the AdoMet/SIN/AdoHcy binding site; this pocket is specific to and conserved among flavivirus MTase but not found in human MTases. A series of highly selective AdoHcy-based Enasidenib inhibitors of the flavivirus Mtase, that did not inhibit human Mtases, were recently reported to target this pocket, although the antiviral efficacy of the compounds was characterized. To investigate whether more potent and selective inhibitors of the flavivirus MTase could be identified, we designed and synthesized four new AdoHcy derivatives. Unfortunately, these derivatives did not show improved activity towards the viral MTase activity. Upon examination of the intrinsic inhibitory ability of AdoHcy, we unexpectedly found that AdoHcy barely inhibits the N-7 and 2��-O activities of the flavivirus MTase, even at high concentrations. We further observed that AdoHcy also does not inhibit virus growth in cell-culture. Binding studies showed that AdoHcy has a much lower binding affinity than AdoMet and SIN. This result is consistent with computational Molecular Mechanics Poisson-Boltzmann surface Area analysis indicating that SIN has a more favorable binding free energy with the MTase than AdoHcy. Our results indicated that SIN might be a better scaffold to design new inhibitors as compared to AdoHcy. The lack of inhibitory activity in these analogs was quite surprising, particularly because these compounds are very close derivatives of AdoHcy, which showed high potency in inhibition of the MTase activities in a number of studies. These results prompted us to investigate whether AdoHcy is an effective inhibitor for flavivirus MTase.