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. 2019 Mar 9;8(2):155–170. doi: 10.1007/s40121-019-0239-0

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© The Author(s) 2019

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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Fig. 1 — Structure of plazomicin and modification sites. The hydroxyamino butyric acid (HABA) substituent (green dotted line) at position 1 and the hydroxyethyl compound addition at the 6′-N position, enhancing plazomicin’s activity against various aminoglycoside-modifying enzymes. The 2′-N position remains unblocked to AACs