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Grant: Project Grant

McGill University

$810,900.00

Development of new lead antimalarials targeting parasite coenzyme A biosynthesis and utilisation.

FY 2022-23

Summary
Malaria is a life-threatening disease caused by Plasmodium parasites transmitted to people through the bites of infected female mosquitoes. There were 241 million cases of malaria worldwide in 2020 (~500/year in Canada), leading to 627,000 deaths (a 12% increase compared to 2019). Most of the deaths were children under the age of 5 years. Unfortunately, the effectiveness of current antimalarial drugs is decreasing progressively, a phenomenon known as drug resistance, and the disease is expected to disperse to higher latitudes as earth's climate warms up, making the discovery of new drugs to treat malaria ever more crucial. New classes of molecules with a novel mechanism of action are particularly desirable to bypass drug resistance. Interestingly, we have identified a new class of compounds that can reduce proliferation of the malaria-causing parasites. These molecules have a unique mechanism of action, are easy to prepare, potent, and typically non-toxic. We propose here to test them in several biological assays to guide the synthesis of derivatives with improved pharmaceutical profiles, and evaluate the efficacy of the most promising compounds in a mouse model of malaria. This project will generate excellent candidates for the development of new antimalarial drugs.
Program
Project Grant
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
468862
Name
Auclair Karine
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Pharmaceutical Sciences
Projecttitle
Development of new lead antimalarials targeting parasite coenzyme A biosynthesis and utilisation.
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$810,900
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Antimalarial; Antiplasmodial; Coenzyme A Biosynthesis; In Vitro Assays; In Vivo Studies; Medicinal Chemistry
Abstract
Malaria is a life-threatening disease caused by Plasmodium parasites transmitted to people through the bites of infected female mosquitoes. There were 241 million cases of malaria worldwide in 2020 (~500/year in Canada), leading to 627,000 deaths (a 12% increase compared to 2019). Most of the deaths were children under the age of 5 years. Unfortunately, the effectiveness of current antimalarial drugs is decreasing progressively, a phenomenon known as drug resistance, and the disease is expected to disperse to higher latitudes as earth's climate warms up, making the discovery of new drugs to treat malaria ever more crucial. New classes of molecules with a novel mechanism of action are particularly desirable to bypass drug resistance. Interestingly, we have identified a new class of compounds that can reduce proliferation of the malaria-causing parasites. These molecules have a unique mechanism of action, are easy to prepare, potent, and typically non-toxic. We propose here to test them in several biological assays to guide the synthesis of derivatives with improved pharmaceutical profiles, and evaluate the efficacy of the most promising compounds in a mouse model of malaria. This project will generate excellent candidates for the development of new antimalarial drugs.
Competitiondate
202209
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Auclair, Karine
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $810,900~ $0~