Publication | Open Access
Determination of the inhibitory effects of N-methylpyrrole derivatives on glutathione reductase enzyme
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Citations
17
References
2018
Year
Antiparasitic AgentMalariaEnzymatic ModificationRedox BiologyMedicinal ChemistryGlutathione Reductase EnzymeN-methylpyrrole DerivativesStructure-function Enzyme KineticsInhibitory ActivityGlutathione ReductaseBiochemistryMechanism Of ActionDrug DevelopmentPharmacologyInhibitory EffectsNatural SciencesEnzyme CatalysisBetter Inhibitory ActivityCrucial Antioxidant EnzymeMedicineDrug Discovery
Glutathione reductase (GR) is a crucial antioxidant enzyme which is responsible for the maintenance of antioxidant GSH molecule. Antimalarial effects of some chemical molecules are attributed to their inhibition of GR, thus inhibitors of this enzyme are expected to be promising candidates for the treatment of malaria. In this work, GR inhibitory properties of N-Methylpyrrole derivatives are reported. It was found that all compounds have better inhibitory activity than the strong GR inhibitor N,N-bis(2-chloroethyl)-N-nitrosourea, especially three molecules, 8 m, 8 n, and 8 q, were determined to be the most powerful among them. Findings of our study indicates that these Schiff base derivatives are strong GR inhibitors which can be used as leads for designation of novel antimalarial candidates.
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