Villalba, MM, Litchfield, VJ, Smith, RB, Franklin, AM, Livingstone, C and Davis, J (2007) A chromatographic tool for preparing combinatorial quinone-thiol conjugate libraries. JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 70 (5). pp. 797-802. [Journal article]
Full text not available from this repository.
Quinones are well established as key players in the production of reactive oxygen species within cellular environments. Many factors govern their cytotoxicity but most studies have been restricted to a few, core, derivatives. A new strategy for the in situ production of quinone derivatives has been developed such that libraries of diverse functionality can be rapidly created without recourse to extensive synthetic procedures. The approach relies upon nucleophilic addition by reduced thiol derivatives to the quinone core within a pre-culture assay mixture and provides a generic strategy that exploits the large reservoir of commercial thiols currently available. A readily accessible chromatographic method has been developed that allows the derivatisation process to be easily monitored and the purity of the resulting one pot preparation to be assessed. The viability of the combinatorial approach has been fully validated through comparison with a range of quinone-S-conjugates prepared using conventional bench synthesis. The latter have been fully characterised. (c) 2007 Elsevier B.V. All rights reserved.
|Item Type:||Journal article|
|Faculties and Schools:||Faculty of Computing & Engineering|
Faculty of Computing & Engineering > School of Engineering
|Research Institutes and Groups:||Engineering Research Institute|
Engineering Research Institute > Nanotechnology & Integrated BioEngineering Centre (NIBEC)
|Deposited By:||Professor James Davis|
|Deposited On:||24 Jun 2010 15:39|
|Last Modified:||18 Aug 2011 11:19|
Repository Staff Only: item control page