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An N‐Acetyl Cysteine Ruthenium Tricarbonyl Conjugate Enables Simultaneous Release of CO and Ablation of Reactive Oxygen Species
Authors:Dr João D Seixas  Dr Miguel Chaves‐Ferreira  Diana Montes‐Grajales  Ana M Gonçalves  Dr Ana R Marques  Dr Lígia M Saraiva  Prof Jesus Olivero‐Verbel  Prof Carlos C Romão  Dr Gonçalo J L Bernardes
Affiliation:1. Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Av. Prof. Egas Moniz, 1649‐028 Lisboa (Portugal) www.gbernardes‐lab.com;2. Instituto de Tecnologia Química e Biológica‐António Xavier, Universidade Nova de Lisboa, Av da República, 2780‐157 Oeiras (Portugal);3. Alfama Ltd., Instituto de Biologia Experimental e Tecnológica, IBET, Av. da República, EAN, 2780‐157 Oeiras (Portugal);4. Department of Chemistry, University of Cambridge, Lensfield Road, CB2 1EW Cambridge (UK);5. School of Pharmaceutical Sciences, University of Cartagena, Campus of Zaragocilla, Cartagena, Bolivar 130015 (Colombia)
Abstract:We have designed and synthesised a Ru(CO)3Cl2(NAC)] pro‐drug that features an N‐acetyl cysteine (NAC) ligand. This NAC carbon monoxide releasing molecule (CORM) conjugate is able to simultaneously release biologically active CO and to ablate the concurrent formation of reactive oxygen species (ROS). Complexes of the general formulae Ru(CO)3(L)3]2+, including Ru(CO)3Cl(glycinate)] (CORM‐3), have been shown to produce ROS through a water–gas shift reaction, which contributes significantly, for example, to their antibacterial activity. In contrast, NAC‐CORM conjugates do not produce ROS or possess antibacterial activity. In addition, we demonstrate the synergistic effect of CO and NAC both for the inhibition of nitric oxide (formation) and in the expression of tumour‐necrosis factor (TNF)‐α. This work highlights the advantages of combining a CO‐releasing scaffold with the anti‐oxidant and anti‐inflammatory drug NAC in a unique pro‐drug.
Keywords:anti‐oxidants  carbon monoxide  N‐acetyl cysteine  prodrugs  reactive oxygen species  ruthenium
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