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Diaconu et al

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The IRAP inhibitor 48 was the best inhibitor in a second series of bioisosteric diaminobenzoic acid inhibitors but was both less potent and selective as compared 47 ( Most small molecule binders of the oxytocinase subfamily of M1 aminopeptidases, e.g., the phosphinic pseudotripeptides 4346 address the active site and establish strong interactions with the catalytic zinc ion

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research-stage peptides show even more dramatic individual differences