Selective inhibition of low affinity IgE receptor (CD23) processing: P1' bicyclomethyl substituents
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Updated: Oct 18, 2026

Identification of Mediators of T-cell Receptor Signaling via the Screening of Chemical Inhibitor Libraries
Published on: January 22, 2019
S Bailey1, B Bolognese, A Faller
1SmithKline Beecham Pharmaceuticals, UK.
Abstract:
Using a variety of alpha-hydroxy hydroxamic acid derivatives, the size and shape of the S1' pocket for the CD23 processing metalloprotease has been explored. It has been demonstrated that a P1' 2-naphthylmethyl group occupies most of the available space and gives excellent selectivity against fibroblast collagenase (matrix metalloproteinase-1, MMP-1) and other MMPs.
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