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L-tyrosine

File:L-Tyrosin_-_L-Tyrosine.svg · Wikimedia Commons · See Wikimedia Commons

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L-tyrosine

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Also known as Tyr, Y, (2S)-2-amino-3-(4-hydroxyphenyl)propanoic acid, (−)-α-amino-p-hydroxyhydrocinnamic acid, (S)-α-amino-4-hydroxybenzenepropanoic acid, 4-hydroxy-L-phenylalanine, (2S)-2-amino-3-(4-hydroxyphenyl)propionic acid, (2S)-2-azanyl-3-(4-hydroxyphenyl)propanoic acid

thumb|Tyrosine ball and stick model spinning -Tyrosine or tyrosine (symbol Tyr or Y) or 4-hydroxyphenylalanine is one of the 20 standard amino acids that are used by cells to synthesize proteins. It is a conditionally essential amino acid with a polar side group. The word "tyrosine" is from the Greek tyrós, meaning cheese, as it was first discovered in 1846 by German chemist Justus von Liebig in the protein casein from cheese. It is called tyrosyl when referred to as a functional group or side chain. While tyrosine is generally classified as a hydrophobic amino acid, it is more hydrophilic tha

AI overview

L-tyrosine is one of the 20 standard amino acids that cells use to build proteins, and it was first discovered in cheese in 1846. Your body can produce tyrosine on its own, making it a "conditionally essential" amino acid, meaning you only need to get it from food or supplements under certain conditions.

AI-generated from the Wikipedia summary — may contain errors.

Chemical data

Formula
C9H11NO3
Molecular weight
181.19 g/mol
IUPAC name
(2S)-2-azaniumyl-3-(4-hydroxyphenyl)propanoate
SMILES
C1=CC(=CC=C1C[C@@H](C(=O)[O-])[NH3+])O
InChIKey
OUYCCCASQSFEME-QMMMGPOBSA-N
XLogP
-1.6
Polar surface area
88 Ų
H-bond donors
2
H-bond acceptors
3
Formal charge
0

via PubChem

~10 min read

Encyclopedic overview

14 sections
Contents
  • Functions
  • Dietary requirements and sources
  • Biosynthesis
  • Metabolism
  • Phosphorylation and sulfation
  • Precursor to neurotransmitters and hormones
  • Precursor to other compounds
  • Degradation
  • Ortho- and meta-tyrosine
  • Medical use
  • Industrial synthesis
  • See also
  • References
  • External links

thumb|Tyrosine ball and stick model spinning -Tyrosine or tyrosine (symbol Tyr or Y) or 4-hydroxyphenylalanine is one of the 20 standard amino acids that are used by cells to synthesize proteins. It is a conditionally essential amino acid with a polar side group. The word "tyrosine" is from the Greek tyrós, meaning cheese, as it was first discovered in 1846 by German chemist Justus von Liebig in the protein casein from cheese. It is called tyrosyl when referred to as a functional group or side chain. While tyrosine is generally classified as a hydrophobic amino acid, it is more hydrophilic than phenylalanine. It is encoded by the codons UAC and UAU in messenger RNA.

The one-letter symbol Y was assigned to tyrosine for being alphabetically nearest of those letters available. Note that T was assigned to the structurally simpler threonine, U was avoided for its similarity with V for valine, W was assigned to tryptophan, while X was reserved for undetermined or atypical amino acids. The mnemonic tYrosine was also proposed.

Excerpted from Wikipedia’s “L-tyrosine” article, available under the CC BY-SA 4.0 licence.

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