N-(4-Aminobutyl)-N′-(2-methoxyethyl)guanidine
(8a) is a potent inhibitor targeting the hDDAH-1 active site (K
i = 18 μM)
and derived from a series of guanidine- and amidine-based inhibitors.
Its nonamino acid nature leads to high selectivities toward other
enzymes of the nitric oxide-modulating system. Crystallographic data
of 8a-bound hDDAH-1 illuminated a unique
binding mode. Together with its developed N-hydroxyguanidine
prodrug 11, 8a will serve as a most widely
applicable, pharmacological tool to target DDAH-1-associated diseases.
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