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Cover Picture: Targeted Fluoro Positioning for the Discovery of a Potent and Highly Selective Matrix Metalloproteinase Inhibitor (ChemistryOpen 2/2017)

The Front Cover picture shows the design of the highly potent and selective inhibitor ZHAWOC5684 bound to its target protein matrix metalloproteinase‐13 (MMP‐13). The key design principle involves the structure‐based positioning of a single fluorine atom to probe water‐mediated interactions within t...

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Detalles Bibliográficos
Autores principales: Fischer, Thomas, Riedl, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390810/
http://dx.doi.org/10.1002/open.201700043
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author Fischer, Thomas
Riedl, Rainer
author_facet Fischer, Thomas
Riedl, Rainer
author_sort Fischer, Thomas
collection PubMed
description The Front Cover picture shows the design of the highly potent and selective inhibitor ZHAWOC5684 bound to its target protein matrix metalloproteinase‐13 (MMP‐13). The key design principle involves the structure‐based positioning of a single fluorine atom to probe water‐mediated interactions within the allosteric binding site. In combination with a zinc‐binding carboxylic acid fragment blocking the active site this approach delivers a drug‐like small molecule inhibitor of MMP‐13 with excellent microsomal and plasma stability. More information can be found in the Communication by R. Riedl and T. Fischer on page 192 in Issue 2, 2017 (DOI: 10.1002/open.201600158).[Image: see text]
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spelling pubmed-53908102017-04-14 Cover Picture: Targeted Fluoro Positioning for the Discovery of a Potent and Highly Selective Matrix Metalloproteinase Inhibitor (ChemistryOpen 2/2017) Fischer, Thomas Riedl, Rainer ChemistryOpen Cover Pictures The Front Cover picture shows the design of the highly potent and selective inhibitor ZHAWOC5684 bound to its target protein matrix metalloproteinase‐13 (MMP‐13). The key design principle involves the structure‐based positioning of a single fluorine atom to probe water‐mediated interactions within the allosteric binding site. In combination with a zinc‐binding carboxylic acid fragment blocking the active site this approach delivers a drug‐like small molecule inhibitor of MMP‐13 with excellent microsomal and plasma stability. More information can be found in the Communication by R. Riedl and T. Fischer on page 192 in Issue 2, 2017 (DOI: 10.1002/open.201600158).[Image: see text] John Wiley and Sons Inc. 2017-03-10 /pmc/articles/PMC5390810/ http://dx.doi.org/10.1002/open.201700043 Text en © 2017 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim
spellingShingle Cover Pictures
Fischer, Thomas
Riedl, Rainer
Cover Picture: Targeted Fluoro Positioning for the Discovery of a Potent and Highly Selective Matrix Metalloproteinase Inhibitor (ChemistryOpen 2/2017)
title Cover Picture: Targeted Fluoro Positioning for the Discovery of a Potent and Highly Selective Matrix Metalloproteinase Inhibitor (ChemistryOpen 2/2017)
title_full Cover Picture: Targeted Fluoro Positioning for the Discovery of a Potent and Highly Selective Matrix Metalloproteinase Inhibitor (ChemistryOpen 2/2017)
title_fullStr Cover Picture: Targeted Fluoro Positioning for the Discovery of a Potent and Highly Selective Matrix Metalloproteinase Inhibitor (ChemistryOpen 2/2017)
title_full_unstemmed Cover Picture: Targeted Fluoro Positioning for the Discovery of a Potent and Highly Selective Matrix Metalloproteinase Inhibitor (ChemistryOpen 2/2017)
title_short Cover Picture: Targeted Fluoro Positioning for the Discovery of a Potent and Highly Selective Matrix Metalloproteinase Inhibitor (ChemistryOpen 2/2017)
title_sort cover picture: targeted fluoro positioning for the discovery of a potent and highly selective matrix metalloproteinase inhibitor (chemistryopen 2/2017)
topic Cover Pictures
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390810/
http://dx.doi.org/10.1002/open.201700043
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