Publication Type Journal Article
Title Hydroxypyridinones as privileged chelating structures for the design of medicinal drugs
Authors M. Amélia Santos Sergio M. Marques Sílvia Chaves
Groups BIOIN
Journal COORDINATION CHEMISTRY REVIEWS
Year 2012
Month January
Volume 256
Number 1
Pages 240-259
Abstract Hydroxypyridinones (HPs) are a family of N-heterocyclic core chelators which, based on their specific metal-coordination, easy manipulation/derivatization and biocompatibility, have been an attractive target for the development of new pharmaceutical drugs with manifold uses. Herein we describe the most recent advances reported in the literature on HPs, with a special focus on the metal chelating properties of the 3-hydroxy-4-pyridinone (3,4-HP) derivatives, and the different approaches used to functionalize these chelators to improve their biological properties, namely in terms of bioavailability and specific biotargeting abilities. Representative examples of HPs are included, mostly for applications as chelating drugs for sequestration or passivation of metal overload or deregulated biometals, but also as metallodrugs for potential diagnostic/therapeutic purposes. These examples are discussed in terms of the chelating properties and structure-activity relationships. (C) 2011 Published by Elsevier B.V.
DOI http://dx.doi.org/10.1016/j.ccr.2011.08.008
ISBN
Publisher
Book Title
ISSN 0010-8545
EISSN 1873-3840
Conference Name
Bibtex ID ISI:000298975200017
Observations
Back to Publications List