Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Chemical Compound Review:

AC1MHWLP cyclohexatrienesulfonate; hydrogen(+1)...

Synonyms:

This record was replaced with 7371.

Horne, D.W. et al., Bruns, K.A. et al., Kimura, M. et al.

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High impact information on benzenesulfonic acid

The solubilized acetylcarnitine hydrolase activity was inhibited by p-hydroxymercuriphenylsulfonate, but not by the specific acetylcholinesterase inhibitors, eserine or BW63C47 [1].
5. Conjugase activity from both bile and plasma was inhibited in the presence of the sulfhydryl reagent, p-hydroxymercuriphenylsulfonate, and stimulated in the presence of 2-mercaptoethanol [2].

Analytical, diagnostic and therapeutic context of benzenesulfonic acid

First, titration of the zinc-chelating -SH groups with p-hydroxymercuriphenylsulfonate led to dissociation of the BSD tetramer into unstable monomers or dimers [3].

References

The metabolism of acetylcarnitine and acetate by bovine and hamster epididymal spermatozoa. Bruns, K.A., Casillas, E.R. Biol. Reprod. (1989) [Pubmed]
Properties of folic acid gamma-glutamyl hydrolase (conjugase) in rat bile and plasma. Horne, D.W., Krumdieck, C.L., Wagner, C. J. Nutr. (1981) [Pubmed]
Expression, purification, and characterization of blasticidin S deaminase (BSD) from Aspergillus terreus: the role of catalytic zinc in enzyme structure. Kimura, M., Sekido, S., Isogai, Y., Yamaguchi, I. J. Biochem. (2000) [Pubmed]

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