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Discovery and optimisation studies of antimalarial phenotypic hits

There is an urgent need for the development of new antimalarial compounds. As a result of a phenotypic screen, several compounds with potent activity against the parasite Plasmodium falciparum were identified. Characterization of these compounds is discussed, along with approaches to optimise the ph...

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Detalles Bibliográficos
Autores principales: Mital, Alka, Murugesan, Dinakaran, Kaiser, Marcel, Yeates, Clive, Gilbert, Ian H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editions Scientifiques Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4607724/
https://www.ncbi.nlm.nih.gov/pubmed/26408453
http://dx.doi.org/10.1016/j.ejmech.2015.08.044
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author Mital, Alka
Murugesan, Dinakaran
Kaiser, Marcel
Yeates, Clive
Gilbert, Ian H.
author_facet Mital, Alka
Murugesan, Dinakaran
Kaiser, Marcel
Yeates, Clive
Gilbert, Ian H.
author_sort Mital, Alka
collection PubMed
description There is an urgent need for the development of new antimalarial compounds. As a result of a phenotypic screen, several compounds with potent activity against the parasite Plasmodium falciparum were identified. Characterization of these compounds is discussed, along with approaches to optimise the physicochemical properties. The in vitro antimalarial activity of these compounds against P. falciparum K1 had EC(50) values in the range of 0.09–29 μM, and generally good selectivity (typically >100-fold) compared to a mammalian cell line (L6). One example showed no significant activity against a rodent model of malaria, and more work is needed to optimise these compounds.
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spelling pubmed-46077242015-11-02 Discovery and optimisation studies of antimalarial phenotypic hits Mital, Alka Murugesan, Dinakaran Kaiser, Marcel Yeates, Clive Gilbert, Ian H. Eur J Med Chem Research Paper There is an urgent need for the development of new antimalarial compounds. As a result of a phenotypic screen, several compounds with potent activity against the parasite Plasmodium falciparum were identified. Characterization of these compounds is discussed, along with approaches to optimise the physicochemical properties. The in vitro antimalarial activity of these compounds against P. falciparum K1 had EC(50) values in the range of 0.09–29 μM, and generally good selectivity (typically >100-fold) compared to a mammalian cell line (L6). One example showed no significant activity against a rodent model of malaria, and more work is needed to optimise these compounds. Editions Scientifiques Elsevier 2015-10-20 /pmc/articles/PMC4607724/ /pubmed/26408453 http://dx.doi.org/10.1016/j.ejmech.2015.08.044 Text en © 2015 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Paper
Mital, Alka
Murugesan, Dinakaran
Kaiser, Marcel
Yeates, Clive
Gilbert, Ian H.
Discovery and optimisation studies of antimalarial phenotypic hits
title Discovery and optimisation studies of antimalarial phenotypic hits
title_full Discovery and optimisation studies of antimalarial phenotypic hits
title_fullStr Discovery and optimisation studies of antimalarial phenotypic hits
title_full_unstemmed Discovery and optimisation studies of antimalarial phenotypic hits
title_short Discovery and optimisation studies of antimalarial phenotypic hits
title_sort discovery and optimisation studies of antimalarial phenotypic hits
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4607724/
https://www.ncbi.nlm.nih.gov/pubmed/26408453
http://dx.doi.org/10.1016/j.ejmech.2015.08.044
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