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A Library Approach to the Discovery of Small Molecules That Recognize RNA:  Use of a 1,3-Hydroxyamine Motif as Core

A library of compounds based upon an aminoglucopyranoside core has been developed and screened for binding to RNA and specifically to 16S ribosomal RNA. The title molecules simplify the complexity of naturally occurring aminoglycoside antibiotics by embodying a putative recognition motif found withi...

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Published in:Journal of the American Chemical Society 1998-08, Vol.120 (33), p.8319-8327
Main Authors: Wong, Chi-Huey, Hendrix, Martin, Manning, David D, Rosenbohm, Christoph, Greenberg, William A
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cited_by cdi_FETCH-LOGICAL-a326t-761e6c66f31dc5ac018adb0a532211373f78cf15ec29e4144ce46f72e091a7373
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container_issue 33
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creator Wong, Chi-Huey
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description A library of compounds based upon an aminoglucopyranoside core has been developed and screened for binding to RNA and specifically to 16S ribosomal RNA. The title molecules simplify the complexity of naturally occurring aminoglycoside antibiotics by embodying a putative recognition motif found within these structures, namely, a 1,3-hydroxyamine. The core pyranoside bearing the hydroxyamine motif was structurally varied at two points through a combinatorial approach utilizing acylation and reductive amination protocols. The aminoglycoside mimetics were screened in an automated assay based upon surface plasmon resonance (SPR), and some were found effective at binding a 27-nucleotide model (AS-wt) of A-site 16S RNA as well as a drug-resistant mutant RNA in the micromolar range.
doi_str_mv 10.1021/ja980826p
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source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects 1,3-Hydroxyamine
aminoglycosides
rRNA 16S
title A Library Approach to the Discovery of Small Molecules That Recognize RNA:  Use of a 1,3-Hydroxyamine Motif as Core
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