The synthesis and 16S A-site rRNA recognition of carbohydrate-free aminoglycosides

The synthesis and 16S A-site rRNA recognition of carbohydrate-free aminoglycosides Novel 2,5-dideoxystreptamine derivatives targeting the ribosomal decoding site RNA Binding of Aminoglycoside Antibiotics with Modified A-site 16S rRNA Construct Containing Non-Nucleotide Linkers Conjugate of neamine and 2-deoxystreptamine mimic connected by an amide bond MICROBIAL SEMI-SYNTHESIS OF AMINOGLYCOSIDIC ANTIBIOTICS BY MUTANTS OF S. RIBOSIDIFICUS AND S. KANAMYCETICUS Study of aminoglycoside–nucleic acid interactions by an HPLC method Toward Overcoming Staphylococcus aureus Aminoglycoside Resistance Mechanisms with a Functionally Designed Neomycin Analogue Structure-Based Design, Synthesis, and A-Site rRNA Cocrystal Complexes of Functionally Novel Aminoglycoside Antibiotics:  C2‘ ‘ Ether Analogues of Paromomycin Enhanced binding of aminoglycoside dimers to a “dimerized” A-site 16S rRNA construct Aminoglycoside antibiotics. 6. Chemical reactions of aminoglycosides with disodium carbenicillin