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- W2059362419 abstract "The previously reported irreversible inhibition of thermolysin by (dl)-N-chloroacetyl-N-hydroxyleucine methyl ester, an active site directed inactivator, is found to be due to the d-enantiomer. Thus, while the d-enantiomer inactivated the enzyme, no inhibitory activity was found with the l-enantiomer. A possible explanation is presented for the reversed stereochemistry in the inactivation reaction compared with that of substrate." @default.
- W2059362419 created "2016-06-24" @default.
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- W2059362419 date "1996-01-01" @default.
- W2059362419 modified "2023-09-24" @default.
- W2059362419 title "Inhibitory stereochemistry of N-chloroacetyl-N-hydroxyleucine methyl ester for thermolysin" @default.
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- W2059362419 doi "https://doi.org/10.1016/0960-894x(95)00576-f" @default.
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