![4- Hydroxyphenylpyruvic acid [156-39-8] 4- Hydroxyphenylpyruvic acid [156-39-8]](https://www.targetmol.com/group3/M00/36/1C/CgoaEGayOAyELmhzAAAAANNQhNw869.png)
4- Hydroxyphenylpyruvic acid [156-39-8]
T4858
CAS Number156-39-8
Product group Chemicals
Estimated Purity97.56%
Molecular Weight180.16
Overview
- SupplierTargetMol Chemicals
- Product Name4-Hydroxyphenylpyruvic acid
- Delivery Days Customer4
- CAS Number156-39-8
- Category SupplierChemical
- CertificationResearch Use Only
- Chemical Name4-Hydroxyphenylpyruvic acid
- Estimated Purity97.56%
- Molecular FormulaC9H8O4
- Molecular Weight180.16
- Scientific Description4-Hydroxyphenylpyruvic acid is an enzyme inhibitor.4-Hydroxyphenylpyruvic acid (4-HPPA) is a keto acid that is involved in the tyrosine catabolism pathway. It is a product of the enzyme (R)-4-hydroxyphenyllactate dehydrogenase (EC 1.1.1.222) and is formed during tyrosine metabolism. The conversion from tyrosine to 4-HPPA is catalyzed by tyrosine aminotransferase. Additionally, 4-HPPA can be converted to homogentisic acid which is one of the precursors to ochronotic pigment. The enzyme 4-hydroxyphenylpyruvic acid dioxygenase (HPD) catalyzes the reaction that converts 4-hydroxyphenylpyruvic acid to homogentisic acid. A deficiency in the catalytic activity of HPD is known to lead to tyrosinemia type III, an autosomal recessive disorder characterized by elevated levels of blood tyrosine and massive excretion of tyrosine derivatives into urine. It has been shown that hawkinsinuria, an autosomal dominant disorder characterized by the excretion of hawkinsin, may also be a result of HPD deficiency . Moreover, 4-hydroxyphenylpyruvic acid is also found to be associated in phenylketonuria, which is also an inborn error of metabolism. There are two isomers of HPPA, specifically 4HPPA and 3HPPA, of which 4HPPA is the most common.
- Shelf life instruction3 years
- SMILESOC(=O)C(O)=CC1=CC=C(O)C=C1
- Storage Instruction-20°C
- UNSPSC12352200