Weight | 264.281 g/mol |
---|---|
Formula | C13H16N2O4 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 1 |
Rotatable Bonds | 7 |
Phenylacetylglutamine (28047-15-6)
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- Sigma-Aldrich - Phenylacetylglutamine51.50 USD
- Fisher Scientific - Search for Phenylacetylglutamine
- TCI - Search for Phenylacetylglutamine
- Phenylacetylglutamine May Replace Urea as a Vehicle for Waste Nitrogen Excretion (Pediatric Research, 1991)
- PHENYLACETYLGLUTAMINE AS A CONSTITUENT OF NORMAL HUMAN URINE (Journal of the American Chemical Society, 1954)
- Synthesis of phenylacetylglutamine by human tissue. (Journal of Biological Chemistry, 1957)
- Disposition of phenylbutyrate and its metabolites, phenylacetate and phenylacetylglutamine (The Journal of Clinical Pharmacology, 1995)
- The determination of urinary phenylacetylglutamine as phenylacetic acid.: Studies on its origin in normal subjects and children with cystic fibrosis (Clinica Chimica Acta, 1971)
- Phenylacetylglutamine and Hippuric Acid in Uremic and Healthy Subjects (Nephron, 1990)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)CC(=O)NC(CCC(=O)N)C(=O)O
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InChIKeyJFLIEFSWGNOPJJ-UHFFFAOYSA-N
- Pubchem - Phenylacetylglutamine
- Wikipedia - N(2)-phenylacetyl-L-glutamine
Phenylacetylglutamine is a product formed by the conjugation of phenylacetate and glutamine. It is a common metabolite that can be found in human urine.
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
benzene
+
Reactant
(Friedel-Crafts alkylation)
2-PHENYLACETAMIDE
+
Reactant
(Alkylation of primary amines)
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