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. 2019 Jan 4;10(2):168–174. doi: 10.1021/acsmedchemlett.8b00535

Figure 2.

Figure 2

Chemical structures of synthesized hit compounds 1 and 2 that were identified as nanomolar noncompetitive inhibitors of the Zika virus NS2B-NS3 protease. Compound cn-716 is a previously published4 covalent active-site inhibitor of the Zika virus NS2B-NS3 protease, which has been used in this study for comparison.