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. 2015 Jun 12;59(7):3899–3905. doi: 10.1128/AAC.00861-15

FIG 2.

FIG 2

Bar graphs showing the relative enzymatic modification initial rates of the listed AACs and APHs with NEO (compound 1) and its dimers 2 to 18. All rates were normalized to that of NEO (compound 1), which was used for the synthesis of the dimers. Graphs are presented for (A) the triazole-linked NEO dimers, (B) the urea-linked NEO dimers, and (C) the thiourea-linked NEO dimers.