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. 2014 Mar;58(3):1646–1651. doi: 10.1128/AAC.02296-13

TABLE 2.

Inhibition of B. pseudomallei FabI1 by substituted diphenyl ethersa

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a

Structure-activity relationship studies performed show that A-ring substitutions are critical in determining the type of inhibition and binding affinity for both E-NAD+ (K1) and E-NADH (K2).