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We have synthesized peptidyl fluoromethyl ketones that are specific inhibitors of the serine proteases alpha-chymotrypsin and porcine pancreatic elastase. By analogy with the corresponding aldehydes it is assumed that the fluoromethyl ketones react with the gamma-OH group of the active site serine to form a stable hemiacetal Lowe, G., Chen, R., Gorenstein, D.G., Kennedy, W.P., Lowe, G., Nurse, D., Shah, D.O., Lai, K., Ac-Ala-Ala-Pro-ambo-Ala-CF3, Ki = 0.34 X 10(-6) M) correlates well with the variation in V/K for hydrolysis of the corresponding amide substrates. This trend is indicative of the inhibitors acting as transition-state analogues [Bartlett, P.A., Thompson, R.C. (1973) Biochemistry 12, 47.(ABSTRACT TRUNCATED AT 250 WORDS)
Imperiali et al. (1986) studied this question.