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- W2167304948 abstract "N-Aroyl derivatives of aromatic hydrophobic L-amino-acid esters (1)–(7) are hydrolysed by α-chymotrypsin to the corresponding L-amino-acids (8)–(14). When the amidic nitrogen atom is incorporated into a heterocyclic ring, e.g. in the benzotriazinones (15a and b), substrate properties are lost. The N-nitroso-derivatives of N-acetyl-L-tryptophan methyl and ethyl esters are smoothly hydrolysed by α-chymotrypsin; their nitroso-groups are therefore attached to the indolic rather than the amidic nitrogen atom." @default.
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- W2167304948 date "1975-01-01" @default.
- W2167304948 modified "2023-09-25" @default.
- W2167304948 title "Confirmation of the site of nitrosation in tryptophan derivatives by α-chymotrypsin" @default.
- W2167304948 doi "https://doi.org/10.1039/p19750002357" @default.
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