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Significantly, the antimalarial potency of these compounds correlated well with their ability to disrupt erythrocyte redox balance in vitro (and slightly less strongly in vivo in mice), leading the authors to conclude that erythrocyte enolase is likely the common target that links these two characteristics
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and wherein covalent bonds 1 , 2 and 3 are selected from the group consisting of peptide bonds and reduced peptide bonds
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