Substituent effects on the mechanism-based inactivation of prostatic acid phosphatase

DOI: 10.1021/ja00150a002

Source and publish data:

Journal of the American Chemical Society p. 11049 - 11054 (1995)

Update date:2022-08-03

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Authors:

Myers, Jason K.

Cohen, Jonathan D.

Widlanski, Theodore S.

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Article abstract of DOI:10.1021/ja00150a002

The mechanism of the inactivation of prostatic acid phosphatase (PAP) by 4-halomethylaryl phosphates, such as 4-(fluoromethyl)phenyl phosphate (FMPP), was probed by varying the benzylic leaving group and adding a nitro group to the 2 position. These studi

Full text of DOI:10.1021/ja00150a002

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