Binding of Aminoglycoside Antibiotics with Modified A-site 16S rRNA Construct Containing Non-Nucleotide Linkers

Bioorganic & Medicinal Chemistry Letters
2002.0

Abstract

The design and synthesis of synthetically modified cyclic A-site 16S rRNA construct is reported. The binding characteristics of several members of the aminoglycoside antibiotics with this novel class of synthetically modified A-site 16S rRNA constructs were subsequently investigated.

Knowledge Graph

Similar Paper

Binding of Aminoglycoside Antibiotics with Modified A-site 16S rRNA Construct Containing Non-Nucleotide Linkers
Bioorganic & Medicinal Chemistry Letters 2002.0
Enhanced binding of aminoglycoside dimers to a “dimerized” A-site 16S rRNA construct
Bioorganic & Medicinal Chemistry Letters 2000.0
The synthesis and 16S A-site rRNA recognition of carbohydrate-free aminoglycosides
Bioorganic & Medicinal Chemistry Letters 2005.0
The use of aminoglycoside derivatives to study the mechanism of aminoglycoside 6′-N-acetyltransferase and the role of 6′-NH2 in antibacterial activity
Bioorganic & Medicinal Chemistry 2007.0
Novel synthesis and RNA-Binding properties of aminoglycoside dimers conjugated via a naphthalene diimide-based intercalator
Bioorganic & Medicinal Chemistry Letters 2001.0
Rational design and synthesis of potent aminoglycoside antibiotics against resistant bacterial strains
Bioorganic & Medicinal Chemistry 2011.0
Structural hybridization of three aminoglycoside antibiotics yields a potent broad-spectrum bactericide that eludes bacterial resistance enzymes
MedChemComm 2015.0
Novel 2,5-dideoxystreptamine derivatives targeting the ribosomal decoding site RNA
Bioorganic & Medicinal Chemistry Letters 2002.0
Synthesis and Antimicrobial Evaluation of Amphiphilic Neamine Derivatives
Journal of Medicinal Chemistry 2010.0
Structure-Based Design, Synthesis, and A-Site rRNA Cocrystal Complexes of Functionally Novel Aminoglycoside Antibiotics:  C2‘ ‘ Ether Analogues of Paromomycin
Journal of Medicinal Chemistry 2007.0