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. Author manuscript; available in PMC: 2021 Aug 15.
Published in final edited form as: Bioorg Med Chem Lett. 2020 May 30;30(16):127292. doi: 10.1016/j.bmcl.2020.127292

Figure 7.

Figure 7.

Preferential binding of compound 6 to the inactive conformation of ChTS. ChTS activity was measured at varying concentrations of 6. The plot in (A) denotes dose-dependent inhibition when 6 was mixed with ChTS in the absence of dUMP (inactive conformation). The plot in (B) denotes dose-dependent inhibition when 6 was mixed with ChTS in the presence of dUMP (active conformation).