dc.contributor.authorAnusha, Sebastian
dc.contributor.authorSinha, Ameya
dc.contributor.authorBabu Rajeev, C. P.
dc.contributor.authorChu, Trang T. T.
dc.contributor.authorMathai, Jessin
dc.contributor.authorHuang, Ximei
dc.contributor.authorFuchs, Julian E.
dc.contributor.authorShivananju, NanjundaSwamy
dc.contributor.authorBender, Andreas
dc.contributor.authorPreiser, Peter Rainer
dc.contributor.authorRangappa, Kanchugarakoppal S.
dc.contributor.authorBasappa
dc.contributor.authorChandramohanadas, Rajesh
dc.date.accessioned2016-01-21T04:22:12Z
dc.date.available2016-01-21T04:22:12Z
dc.date.issued2015
dc.identifier.citationAnusha, S., Sinha, A., Babu Rajeev, C. P., Chu, T. T. T., Mathai, J., Huang, X., et al.. (2015). Synthesis, characterization and in vitro evaluation of novel enantiomerically-pure sulphonamide antimalarials. Org. Biomol. Chem., 13(43), 10681-10690.en_US
dc.identifier.issn1477-0520en_US
dc.identifier.urihttp://hdl.handle.net/10220/39739
dc.description.abstractMalaria parasites are currently gaining drug-resistance rapidly, across countries and continents. Hence, the discovery and development of novel chemical scaffolds, with superior antimalarial activity remain an important priority, for the developing world. Our report describes the development, characterization and evaluation of novel bepotastine-based sulphonamide antimalarials inhibiting asexual stage development of Plasmodium falciparum parasites in vitro. The screening results showed potent inhibitory activity of a number of novel sulphonamides against P. falciparum at low micromolar concentrations, in particular in late-stage parasite development. Based on computational studies we hypothesize N-myristoyltransferase as the target of the compounds developed here. Our results demonstrate the value of novel bepotastine-based sulphonamide compounds for targeting the asexual developmental stages of P. falciparum.en_US
dc.description.sponsorshipNRF (Natl Research Foundation, S’pore)en_US
dc.description.sponsorshipMOE (Min. of Education, S’pore)en_US
dc.format.extent23 p.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesOrganic & Biomolecular Chemistryen_US
dc.rights© 2015 The Royal Society of Chemistry. This is the author created version of a work that has been peer reviewed and accepted for publication by Organic & Biomolecular Chemistry, The Royal Society of Chemistry. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1039/C5OB01479D].en_US
dc.subjectPlasmodium falciparumen_US
dc.subjectAnti-malarials
dc.subjectIn-vitro screening
dc.subjectDrug discovery
dc.subjectGiemsa-staining
dc.subjectMicroscopy
dc.subjectFlow cytometry
dc.titleSynthesis, characterization and in vitro evaluation of novel enantiomerically-pure sulphonamide antimalarialsen_US
dc.typeJournal Article
dc.contributor.schoolSchool of Biological Sciencesen_US
dc.identifier.doihttp://dx.doi.org/10.1039/C5OB01479D
dc.description.versionAccepted versionen_US


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