Publication:
Hundreds of dual-stage antimalarial molecules discovered by a functional gametocyte screen

dc.contributor.authorCelia Miguel-Blancoen_US
dc.contributor.authorIrene Molinaen_US
dc.contributor.authorAna I. Barderaen_US
dc.contributor.authorBeatriz Díazen_US
dc.contributor.authorLaura De Las Herasen_US
dc.contributor.authorSonia Lozanoen_US
dc.contributor.authorCarolina Gonzálezen_US
dc.contributor.authorJanneth Rodriguesen_US
dc.contributor.authorMichael J. Delvesen_US
dc.contributor.authorAndrea Rueckeren_US
dc.contributor.authorGonzalo Colmenarejoen_US
dc.contributor.authorSara Vieraen_US
dc.contributor.authorMaría S. Martínez-Martínezen_US
dc.contributor.authorEsther Fernándezen_US
dc.contributor.authorJake Baumen_US
dc.contributor.authorRobert E. Sindenen_US
dc.contributor.authorEsperanza Herrerosen_US
dc.contributor.otherGlaxoSmithKline plc, Spainen_US
dc.contributor.otherImperial College Londonen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherNuffield Department of Clinical Medicineen_US
dc.date.accessioned2018-12-21T06:48:41Z
dc.date.accessioned2019-03-14T08:02:54Z
dc.date.available2018-12-21T06:48:41Z
dc.date.available2019-03-14T08:02:54Z
dc.date.issued2017-05-17en_US
dc.description.abstract© The Author(s) 2017. Plasmodium falciparum stage V gametocytes are responsible for parasite transmission, and drugs targeting this stage are needed to support malaria elimination. We here screen the Tres Cantos Antimalarial Set (TCAMS) using the previously developed P. falciparum female gametocyte activation assay (Pf FGAA), which assesses stage V female gametocyte viability and functionality using Pfs25 expression. We identify over 400 compounds with activities <2 μM, chemically classified into 57 clusters and 33 singletons. Up to 68% of the hits are chemotypes described for the first time as late-stage gametocyte-targeting molecules. In addition, the biological profile of 90 compounds representing the chemical diversity is assessed. We confirm in vitro transmission-blocking activity of four of the six selected molecules belonging to three distinct scaffold clusters. Overall, this TCAMS gametocyte screen provides 276 promising antimalarial molecules with dual asexual/sexual activity, representing starting points for target identification and candidate selection.en_US
dc.identifier.citationNature Communications. Vol.8, (2017)en_US
dc.identifier.doi10.1038/ncomms15160en_US
dc.identifier.issn20411723en_US
dc.identifier.other2-s2.0-85019859594en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/41890
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85019859594&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.titleHundreds of dual-stage antimalarial molecules discovered by a functional gametocyte screenen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85019859594&origin=inwarden_US

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