Comparison of deacylation rates of chymotryptic catalysis within an enantiomeric pair of p-nitrophenyl esters

DOI: 10.1248/cpb.39.2748

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2748 - 2749 (1991)

Update date:2022-08-05

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Authors:

Tanizawa

Yamada Yamada

Itoh Itoh

Kanaoka Kanaoka

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Article abstract of DOI:10.1248/cpb.39.2748

p-Nitrophenyl esters carrying a chiral acyl group were synthesized. These compounds were shown to meet the requirements of chymotrypsin for both the specific binding and the acylation. Therefore, the behavior of p-nitrophenyl esters with chymotrypsin is c

Full text of DOI:10.1248/cpb.39.2748

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