Target-Activated prodrugs (TAPs) for the autoregulated inhibition of MMP12

We describe a prodrug concept in which the target enzyme MMP12 produces its own inhibitor in a two-step activation procedure. By using an MMP12-specific peptide sequence and a known sulfonamide drug integrated in the backbone, the active inhibitor is released upon enzyme cleavage. In in vitro experi...

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Bibliographic Details
Main Authors: Cobos-Correa, Amanda (Author) , Stein, Frank (Author) , Schultz, Carsten (Author)
Format: Article (Journal)
Language:English
Published: 20 July 2012
In: ACS medicinal chemistry letters
Year: 2012, Volume: 3, Issue: 8, Pages: 653-657
ISSN:1948-5875
DOI:10.1021/ml3001193
Online Access:Verlag, Volltext: http://dx.doi.org/10.1021/ml3001193
Verlag, Volltext: https://doi.org/10.1021/ml3001193
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Author Notes:Amanda Cobos-Correa, Frank Stein, Carsten Schultz
Description
Summary:We describe a prodrug concept in which the target enzyme MMP12 produces its own inhibitor in a two-step activation procedure. By using an MMP12-specific peptide sequence and a known sulfonamide drug integrated in the backbone, the active inhibitor is released upon enzyme cleavage. In in vitro experiments, we present proof of concept that the activation proceeds with useful kinetics. The approach is highly selective over the closely related MMP8. If applied in vivo in the future, these prodrugs might release the active entity in a highly specific manner only at such sites where enzyme activity resides.
Item Description:Published online 20 July 2012
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Physical Description:Online Resource
ISSN:1948-5875
DOI:10.1021/ml3001193