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- W4309089934 abstract "Chemical modification of old drugs is an important way to obtain new ones, and it has been widely used in developing new aminoglycoside antibiotics. However, many of the previous modifying strategies seem arbitrary for their lack of support from structural biological detail. In this paper, based on the structural information of aminoglycoside and its drug target, we firstly analyzed the reason that some 2′-N-acetylated products of aminoglycosides caused by aminoglycoside-modifying enzyme AAC(2′) can partially retain activity, and then we designed, synthesized, and evaluated a series of 2′-modified kanamycin A derivatives. Bioassay results showed our modifying strategy was feasible. Our study provided valuable structure–activity relationship information, which would help researchers to develop new aminoglycoside antibiotics more effectively." @default.
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- W4309089934 date "2022-11-02" @default.
- W4309089934 modified "2023-10-14" @default.
- W4309089934 title "Design, Synthesis, and Bioassay of 2′-Modified Kanamycin A" @default.
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- W4309089934 doi "https://doi.org/10.3390/molecules27217482" @default.
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