Abstract
Bioluminescent and spectroscopic properties of luciferin analogues with cyclic amino substituents (1-pyrrolidinyl, piperidino, 1-azepanyl, and morpholino groups) at the 6′ position were investigated by comparing with those of 6′-dimethylaminoluciferin, to provide information on spatial and molecular environmental properties of the active site in Photinus pyralis luciferase.
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