HomeProductsBioactive CompoundsSmall MoleculesN-Acetyl-L-tyrosine
Chemical structure of CAS 537-55-3

N-Acetyl-L-tyrosine

In Stock•Starting at $6 for 25 g•Purity ≥ 98%
CAS No.537-55-3
MDL No.MFCD00037190
MFC11H13NO4
MW223.22
InChI KeyCAHKINHBCWCHCF-JTQLQIEISA-N
CUSTOM SYNTHESISPRECLINICAL SUPPORT

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
25 g98%$6In Stock
100 g98%$8In Stock
500 g98%$23In Stock
1 kg98%$44In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

N-acetyl-L-tyrosine is an N-acetyltyrosine with the L configuration at the chiral center. It functions as an inhibitor of EC 2.1.1.4 (acetylserotonin O-methyltransferase), a biomarker, and a human urinary metabolite. It is also a N-acyl-L-tyrosine and the conjugate acid of N-acetyl-L-tyrosinate.

CAS No.537-55-3
Product NameN-Acetyl-L-tyrosine
CorrosiveCorrosive
Signal Word:Danger
HCode:H318
PCode:P264+P265-P280-P305+P354+P338-P317

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Studies related to this compound and its mechanism of action

Comparative studies on the properties of the extrinsic manganese-stabilizing protein from higher plants and of a synthetic peptide of its C-terminus.

Biochimica et biophysica acta • Vol. 1604, Issue 2 • 2003
PMID: 12765766DOI: 10.1016/s0005-2728(03)00025-2

N-acetyl-L-tyrosine as a tyrosine source in adult parenteral nutrition.

JPEN. Journal of parenteral and enteral nutrition • Vol. 27, Issue 6 • 2003
PMID: 14621123DOI: 10.1177/0148607103027006419

Effects of surfactants on the photosensitized production of tyrosine radicals studied by photo-CIDNP.

Photochemistry and photobiology • Vol. 75, Issue 1 • 2002
PMID: 11841041DOI: 10.1562/0031-8655(2002)075<0006:eosotp>2.0.co;2

Second derivative fluorescence spectra of indole compounds.

Journal of biochemistry • Vol. 131, Issue 3 • 2002
PMID: 11872172DOI: 10.1093/oxfordjournals.jbchem.a003118

Documentation

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