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. 2016 Feb 26;60(3):1377–1384. doi: 10.1128/AAC.01768-15

TABLE 2.

Inhibition of VIM variants by selected isoquinoline and pyridine-2-carboxylates

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a IC50 determinations were performed in triplicate over a range of inhibitor concentrations from 0.2 to 2,000 μM. KD app values were determined by 1H CPMG NMR experiments (see Table S5 in the supplemental material).