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. 2015 Jun 4;9(6):e0003773. doi: 10.1371/journal.pntd.0003773

Fig 6. Chemical structures and in vitro inhibition data of the four most active compounds.

Fig 6

IC50 values have been determined using the same conditions as in the primary assay in the presence of 150 μM TS2. IC50 ± SD (n = 3).