| 4-hydroxyphenylpyruvate dioxygenase |
[EC 1.13.11.27] an enzyme of the oxidoreductase class that catalyzes the oxidation of p-hydroxyphenylpyruvate to homogentisate as a step in the use of tyrosine and phenylalanine as fuels. Deficiency of the enzyme, an autosomal dominant trait, causes hawkinsinuria.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| 4-maleylacetoacetate |
an isomer of fumarylacetoacetate, formed by oxidation of homogentisate in the degradation of tyrosine and phenylalanine.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| 4-methyl-1H-pyrazole |
fomepizole.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| 4-dimethylaminopyridine |
A catalyst used in the synthesis of organic chemicals to add acetyl groups to molecules.
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| 4-methylpyrazole |
An intravenous antidote for ethylene glycol poisoning.
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