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N-Acetyl-L-tyrosine

From Wikipedia, the free encyclopedia
N-Acetyl-L-tyrosine
Identifiers
  • (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−1
3D model (JSmol)
  • CC(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O
  • 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.[1][2][3]

See also

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References

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  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.