Summary of project PR001955

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001955. The data can be accessed directly via it's Project DOI: 10.21228/M8172C This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

Project ID: PR001955
Project DOI:doi: 10.21228/M8172C
Project Title:On-target, dual aminopeptidase inhibition provides cross-1 species antimalarial activity
Project Summary:To combat the global burden of malaria, development of new drugs to replace or complement current therapies are urgently required. Here we show that the compound MMV1557817 is a selective, nanomolar inhibitor of both Plasmodium falciparum and Plasmodium vivax aminopeptidases M1 and M17, leading to inhibition of end stage haemoglobin digestion in asexual parasites. MMV1557817 can kill sexual stage P. falciparum, is active against murine malaria and did not show any shift in activity against a panel of parasites resistant to other antimalarials. MMV1557817-resistant P. falciparum exhibited a slow growth rate that was quickly outcompeted by wild type parasites and were sensitised to the current clinical drug, artemisinin. Overall, these results confirm MMV1557817 as a lead compound for further drug development and highlight the potential of dual inhibition of M1 and M17 as an effective multi-species drug targeting strategy.
Institute:Monash University
Last Name:Siddiqui
First Name:Ghizal
Address:381 Royal Parade, Parkville, Melbourne, Victoria, 3052, Australia
Email:ghizal.siddiqui@monash.edu
Phone:99039282

Summary of all studies in project PR001955

Study IDStudy TitleSpeciesInstituteAnalysis
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ST003144 On-target, dual aminopeptidase inhibition provides cross-species antimalarial activity Plasmodium falciparum Monash University MS 2024-04-18 1 4 Uploaded data (455.2M)*
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