N-(Phenylacetyl)-L-phenylalanine is an amino acid analog designed to modulate protein interactions. Synthesized through the enantioselective acylation of L-phenylalanine using penicillin G acylase from Alcaligenes faecalis, it exhibits unique biochemical properties. Under aqueous conditions, N-(Phenylacetyl)-L-phenylalanine is prone to hydrolysis, making it a valuable tool in research applications studying enzyme activity and protein structure.
N-(Phenylacetyl)-L-phenylalanine is an amino acid analog designed to modulate protein interactions. Synthesized through the enantioselective acylation of L-phenylalanine using penicillin G acylase from Alcaligenes faecalis, it exhibits unique biochemical properties. Under aqueous conditions, N-(Phenylacetyl)-L-phenylalanine is prone to hydrolysis, making it a valuable tool in research applications studying enzyme activity and protein structure.
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