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N-Acetyl-L-tyrosine

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Chemical compound Pharmaceutical compound
N-Acetyl-L-tyrosine
Identifiers
IUPAC name
  • (2S)-2-acetamido-3-(4-hydroxyphenyl)propanoic acid
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.007.885 Edit this at Wikidata
Chemical and physical data
FormulaC11H13NO4
Molar mass223.228 g·mol
3D model (JSmol)
SMILES
  • CC(=O)N(CC1=CC=C(C=C1)O)C(=O)O
InChI
  • InChI=1S/C11H13NO4/c1-7(13)12-10(11(15)16)6-8-2-4-9(14)5-3-8/h2-5,10,14H,6H2,1H3,(H,12,13)(H,15,16)/t10-/m0/s1
  • Key:CAHKINHBCWCHCF-JTQLQIEISA-N

N-Acetyl-L-tyrosine is an amino acid, an N-acetyl derivative of tyrosine. It is used for parenteral nutrition and as a dietary supplement.

See also

References

  1. Hoffer LJ, Sher K, Saboohi F, Bernier P, MacNamara EM, Rinzler D (November 2003). "N-Acetyl-L-tyrosine as a tyrosine source in adult parenteral nutrition". Journal of Parenteral and Enteral Nutrition. 27 (6): 419–22. doi:10.1177/0148607103027006419. PMID 14621123.
  2. Jung YP, Earnest CP, Koozehchian M, Galvan E, Dalton R, Walker D, et al. (January 2017). "Effects of acute ingestion of a pre-workout dietary supplement with and without p-synephrine on resting energy expenditure, cognitive function and exercise performance". Journal of the International Society of Sports Nutrition. 14: 3. doi:10.1186/s12970-016-0159-2. PMC 5234109. PMID 28096758.
  3. Fischer F, Ristow M (May 2020). "Endogenous metabolites promote stress resistance through induction of mitohormesis". EMBO Reports. 21 (5): e50340. doi:10.15252/embr.202050340. PMC 7202198. PMID 32329201.


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