| Literature DB >> 27556138 |
Marilena Tauro1, Antonio Laghezza2, Fulvio Loiodice2, Luca Piemontese2, Alessia Caradonna2, Davide Capelli3, Roberta Montanari3, Giorgio Pochetti3, Antonella Di Pizio4, Mariangela Agamennone5, Cristina Campestre5, Paolo Tortorella2.
Abstract
New catechol-containing chemical entities have been investigated as matrix metalloproteinase inhibitors as well as antioxidant molecules. The combination of the two properties could represent a useful feature due to the potential application in all the pathological processes characterized by increased proteolytic activity and radical oxygen species (ROS) production, such as inflammation and photoaging. A series of catechol-based molecules were synthesized and tested for both proteolytic and oxidative inhibitory activity, and the detailed binding mode was assessed by crystal structure determination of the complex between a catechol derivative and the matrix metalloproteinase-8. Surprisingly, X-ray structure reveals that the catechol oxygens do not coordinates the zinc atom.Entities:
Keywords: Antioxidants; X-ray crystallography; inhibitors; metalloenzymes; structure–activity relationships
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Year: 2016 PMID: 27556138 DOI: 10.1080/14756366.2016.1217853
Source DB: PubMed Journal: J Enzyme Inhib Med Chem ISSN: 1475-6366 Impact factor: 5.051