Selective anti-malarial minor groove binders
Scott, Fraser J. and Khalaf, Abedawn I. and Duffy, Sandra and Avery, Vicky M. and Suckling, Colin J. (2016) Selective anti-malarial minor groove binders. Bioorganic and Medicinal Chemistry Letters, 26. pp. 3326-3329. ISSN 0960-894X (https://doi.org/10.1016/j.bmcl.2016.05.039)
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Abstract
A set of 31 DNA minor groove binders (MGBs) with diverse structural features relating to both physical chemical properties and DNA binding sequence preference has been evaluated as potential drugs to treat Plasmodium falciparum infections using a chloroquine sensitive strain (3D7) and a chloroquine resistant strain (Dd2) in comparison with human embryonic kidney (HEK) cells as an indicator of mammalian cell toxicity. MGBs with an alkene link between the two N-terminal building blocks were demonstrated to be most active with IC50 values in the range 30 – 500 nM and therapeutic ratios in the range 10 - > 500. Many active compounds contained a C-alkylthiazole building block. Active compounds with logD7.4 values of approximately 3 or 7 were identified. Importantly the MGBs tested were essentially equally effective against both chloroquine sensitive and resistant strains. The results show that suitably designed MGBs have the potential for development into clinical candidates for antimalarial drugs effective against resistant strains of Plasmodia.
ORCID iDs
Scott, Fraser J. ORCID: https://orcid.org/0000-0003-0229-3698, Khalaf, Abedawn I. ORCID: https://orcid.org/0000-0001-9162-7527, Duffy, Sandra, Avery, Vicky M. and Suckling, Colin J.;-
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Item type: Article ID code: 56367 Dates: DateEvent15 July 2016Published13 May 2016Published Online12 May 2016AcceptedSubjects: Science > Chemistry
Medicine
Science > MicrobiologyDepartment: Faculty of Science > Pure and Applied Chemistry Depositing user: Pure Administrator Date deposited: 13 May 2016 09:09 Last modified: 21 Nov 2024 01:12 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/56367