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Details

Stereochemistry RACEMIC
Molecular Formula C9H11NO3
Molecular Weight 181.1885
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TYROSINE, DL-

SMILES

NC(CC1=CC=C(O)C=C1)C(O)=O

InChI

InChIKey=OUYCCCASQSFEME-UHFFFAOYSA-N
InChI=1S/C9H11NO3/c10-8(9(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,10H2,(H,12,13)

HIDE SMILES / InChI

Molecular Formula C9H11NO3
Molecular Weight 181.1885
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
The mitochondrial ATPase. Selective modification of a nitrogen residue in the beta subunit.
1975 May
Semisynthetic analogs of cytochrome c reconstructed from natural and synthetic peptides.
1979 Jun 19
Interaction of opioid peptides with model membranes. A carbon-13 nuclear magnetic study of enkephalin binding to phosphatidylserine.
1980 Jan 22
Presence of endogenous calcium ion in horseradish peroxidase. Elucidation of metal-binding site by substitutions of divalent and lanthanide ions for calcium and use of metal-induced NMR (1H and 113Cd) resonances.
1986 Jul 15
[Monoclonal antibodies to an artificial immunogen, specifically demonstrating phosphotyrosine-containing proteins].
1989 Aug
Dopamine beta-hydroxylase inactivation generates a protein-bound quinone derivative.
2001 Feb 23
Aromatic ring-flipping in supercooled water: implications for NMR-based structural biology of proteins.
2001 Jan 24
Unexpected differences between D- and L- tyrosine lead to chiral enhancement in racemic mixtures.
2002 Aug
Conformationally constrained macrocycles that mimic tripeptide beta-strands in water and aprotic solvents.
2002 May 22
Synthesis of novel tyrosinyl FRET cassettes, terminators, and their potential use in DNA sequencing.
2003 May-Aug
Stereospecificity of horseradish peroxidase.
2004 Dec
Thiamine and vasculopathies.
2005 Feb
Vibrational spectroscopy to study the properties of redox-active tyrosines in photosystem II and other proteins.
2005 Feb 25
The long-lived triplet excited state of an elongated ketoprofen derivative and its interactions with amino acids and nucleosides.
2007 Jul 19
[Study on enantioselectivity of celluloses derived by phenylcarbamate at 2,3- or 2,3,6-positions].
2007 Mar
Stereospecificity of mushroom tyrosinase immobilized on a chiral and a nonchiral support.
2007 May 30
UV-light exposed prion protein fails to form amyloid fibrils.
2008 Jul 16
[(2S)-2-(3,5-Dichloro-2-oxidobenzyl-ideneamino)-3-(4-hydroxy-phen-yl)propionato-κO,N,O'](dimethyl-formamide-κO)copper(II).
2008 Mar 29
Aqua-{2-[(3,5-dichloro-2-oxidobenzyl-idene)amino]-3-(4-hydroxy-phen-yl)propionato-κO,N,O}copper(II) sesquihydrate.
2008 May 3
Enantioseparation of dopa and related compounds by cyclodextrin-modified microemulsion electrokinetic chromatography.
2008 Sep 19
(S)-Benzyl 2-amino-3-(4-hydroxy-phen-yl)propanoate.
2009 Jan 10
Amino acid ionic liquids as chiral ligands in ligand-exchange chiral separations.
2009 Sep 28
Selective inhibitors of the JMJD2 histone demethylases: combined nondenaturing mass spectrometric screening and crystallographic approaches.
2010 Feb 25
Ribosylation rapidly induces alpha-synuclein to form highly cytotoxic molten globules of advanced glycation end products.
2010 Feb 4
Non-ionic surfactant modified ligand exchange chromatography using copper (II) complex of N,N-dimethyl-L-phenylalanine as the chiral additive for enantioselective amino acids separation.
2010 Mar 17
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:11:27 GMT 2023
Edited
by admin
on Fri Dec 15 15:11:27 GMT 2023
Record UNII
A9BAT9B32M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TYROSINE, DL-
Systematic Name English
DL-P-TYROSINE
Common Name English
NSC-205006
Code English
2-AMINO-3-(4-HYDROXYPHENYL)PROPANOIC ACID
Systematic Name English
DL-TYROSINE
Systematic Name English
(±)-TYROSINE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29596
Created by admin on Fri Dec 15 15:11:27 GMT 2023 , Edited by admin on Fri Dec 15 15:11:27 GMT 2023
CFR 21 CFR 862.1730
Created by admin on Fri Dec 15 15:11:27 GMT 2023 , Edited by admin on Fri Dec 15 15:11:27 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
209-113-1
Created by admin on Fri Dec 15 15:11:27 GMT 2023 , Edited by admin on Fri Dec 15 15:11:27 GMT 2023
PRIMARY
NCI_THESAURUS
C61997
Created by admin on Fri Dec 15 15:11:27 GMT 2023 , Edited by admin on Fri Dec 15 15:11:27 GMT 2023
PRIMARY
NSC
205006
Created by admin on Fri Dec 15 15:11:27 GMT 2023 , Edited by admin on Fri Dec 15 15:11:27 GMT 2023
PRIMARY
CAS
556-03-6
Created by admin on Fri Dec 15 15:11:27 GMT 2023 , Edited by admin on Fri Dec 15 15:11:27 GMT 2023
PRIMARY
PUBCHEM
1153
Created by admin on Fri Dec 15 15:11:27 GMT 2023 , Edited by admin on Fri Dec 15 15:11:27 GMT 2023
PRIMARY
CHEBI
18186
Created by admin on Fri Dec 15 15:11:27 GMT 2023 , Edited by admin on Fri Dec 15 15:11:27 GMT 2023
PRIMARY
EPA CompTox
DTXSID50859040
Created by admin on Fri Dec 15 15:11:27 GMT 2023 , Edited by admin on Fri Dec 15 15:11:27 GMT 2023
PRIMARY
FDA UNII
A9BAT9B32M
Created by admin on Fri Dec 15 15:11:27 GMT 2023 , Edited by admin on Fri Dec 15 15:11:27 GMT 2023
PRIMARY
Related Record Type Details
METABOLITE -> PARENT