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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.
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4-maleylacetoacetate an isomer of fumarylacetoacetate, formed by oxidation of homogentisate in the degradation of tyrosine and phenylalanine.
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4-methyl-1H-pyrazole fomepizole.
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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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