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4-hydroxyphenylpyruvic acid

Known as: (p-hydroxyphenyl)pyruvic acid, 4-hydroxy alpha-oxobenzenepropanoic acid, para-hydroxyphenylpyruvic acid 
National Institutes of Health

Papers overview

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1998
1998
Aromatic amino acid catabolism by Trypanosoma brucei evansi was investigated in vivo using C3HeB/FeJ mice. The major catabolites… 
1997
1997
Tyrosinemia type 3, caused by a genetic deficiency of 4-hydroxyphenylpyruvic acid dioxygenase (HPD) in tyrosine catabolism, is… 
1990
1990
Three types of hereditary tyrosinaemia have been described. Type I disease (McKusick 27670) is clinically characterized by liver… 
1979
1979
The biosynthesis of 4-hydroxybenzaldehyde and 3-bromo-4-hydroxybenzaldehyde from l-[U-(14)C]tyrosine has been demonstrated in… 
Highly Cited
1976
Highly Cited
1976
A metabolic pathway for L-tyrosine catabolism involves 3,4-dihydroxyphenylacetic acid (homoprotocatechuic acid) as substrate for… 
1975
1975
The occurrence from a marine sponge of 4-hydroxyphenylpyruvic acid oxime is good evidence that an oxime (4) is the biogenetic…