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Detalle de: Synthesis of Ring II/III Fragment of Kanamycin: A New Minimum Structural Motif for Aminoglycoside Recognition

Title Synthesis of Ring II/III Fragment of Kanamycin: A New Minimum Structural Motif for Aminoglycoside Recognition
Abstract

A novel protocol has been established to prepare the kanamycin ring II/III fragment, which has been validated as a minimum structural motif for the development of new aminoglycosides on the basis of its bactericidal activity even against resistant strains. Furthermore, its ability to act as a AAC-(6′) and APH-(3′) binder, and as a poor substrate for the ravenous ANT-(4′), makes it an excellent candidate for the design of inhibitors of these aminoglycoside modifying enzymes.

Apa Reference Zárate, S.G., Bastida, A., Santana, A.G. & Revuelta, J. (2019). Synthesis of Ring II/III Fragment of Kanamycin: A New Minimum Structural Motif for Aminoglycoside Recognition. Antibiotics, 8(3), 109. 10.3390/antibiotics8030109
Doi 10.3390/antibiotics8030109
Publication Date 2 Aug 2019
Publication Type Article
Researcher Agatha Bastida
Ontology Sequence analysis, Drug Discovery and design, Development
Research Groups
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