alpha-Hydroxyhippuric acid
CAS: 16555-77-4
Ref. 3D-FH158929
5g | 70.00 € | ||
10g | 112.00 € | ||
25g | 224.00 € | ||
50g | 367.00 € | ||
100g | 560.00 € |
Product Information
- (2R)-hydroxy[(phenylcarbonyl)amino]ethanoate
- (2S)-hydroxy[(phenylcarbonyl)amino]ethanoate
- (Benzoylamino)(Hydroxy)Acetic Acid
- 2-(Benzoylamino)-2-hydroxyacetic acid
- 2-Benzamido-2-hydroxyacetic acid
- 2-Benzamido-2-hydroxyaceticacid
- 2-Hydroxy-2-(phenylformamido)acetic acid
- Acetic acid, (benzoylamino)hydroxy-
- Acetic acid, 2-(benzoylamino)-2-hydroxy-
- Benzamidohydroxyacetic acid
- See more synonyms
- Hippuric acid, α-hydroxy-
- N-(2-hydroxybenzoyl)glycine
- Salicylglycine
- [(Benzoylamino)Oxy]Acetic Acid
- alpha-Hydroxybenzoylglycine
- {[(2-Hydroxyphenyl)Carbonyl]Amino}Acetate
- Α-Hydroxyhippuric Acid
Alpha-hydroxyhippuric acid (AHA) is a metabolite of benzoic acid. It is the end product of the hydrolysis of the benzyl ester linkage in metoprolol succinate, and it can be detected in urine samples. AHA is a diagnostic marker for renal dysfunction and nephrology dialysis. The reaction mechanism for AHA formation is not known, but it may involve gamma-aminobutyric acid (GABA), which has been shown to inhibit carboxylesterase activity. In addition to being used as an indicator of renal function, AHA has also been used as a probe for gamma-aminobutyric acid receptors.
AHA has been shown to bind to thiophosphorylcholine (TPC) better than other amino acids, such as glycine or glutamic acid. This binding leads to conformational changes that are critical for TPC function and protein stability.
Chemical properties
Technical inquiry about: 3D-FH158929 alpha-Hydroxyhippuric acid
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