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Details

Stereochemistry ABSOLUTE
Molecular Formula C9H10FNO3
Molecular Weight 199.179
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-FLUOROTYROSINE, L-

SMILES

N[C@@H](CC1=CC=C(O)C(F)=C1)C(O)=O

InChI

InChIKey=VIIAUOZUUGXERI-ZETCQYMHSA-N
InChI=1S/C9H10FNO3/c10-6-3-5(1-2-8(6)12)4-7(11)9(13)14/h1-3,7,12H,4,11H2,(H,13,14)/t7-/m0/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
19F NMR studies of α-synuclein-membrane interactions.
2010-09
Residue-specific global fluorination of Candida antarctica lipase B in Pichia pastoris.
2010-09
Site-specific incorporation of fluorotyrosines into proteins in Escherichia coli by photochemical disguise.
2010-03-02
Protein (19)F NMR in Escherichia coli.
2010-01-13
Approaches for the measurement of solvent exposure in proteins by 19F NMR.
2009-11
19F NMR studies of alpha-synuclein conformation and fibrillation.
2009-09-15
Comparison of the folding mechanism of highly homologous proteins in the lipid-binding protein family.
2009-06
Probing the coupling between proton and electron transfer in photosystem II core complexes containing a 3-fluorotyrosine.
2009-04-01
Precursor-directed biosynthesis of fluorinated iturin A in Bacillus spp.
2009-02-21
A mutagenesis-free approach to assignment of (19)F NMR resonances in biosynthetically labeled proteins.
2009-02-18
Metabolism of no-carrier-added 2-[18F]fluoro-L-tyrosine in rats.
2008-11-07
Red fluorescent protein variants with incorporated non-natural amino acid analogues.
2008-02
Combined NMR and computational study for azide binding to human manganese superoxide dismutase.
2007-12-27
An expanded set of amino acid analogs for the ribosomal translation of unnatural peptides.
2007-10-03
Identification of a potential general acid/base in the reversible phosphoryl transfer reactions catalyzed by tyrosine recombinases: Flp H305.
2007-02
Site-specific incorporation of fluorotyrosines into the R2 subunit of E. coli ribonucleotide reductase by expressed protein ligation.
2007
Electron transfer reactions of fluorotyrosyl radicals.
2006-10-25
Aminoacrylate intermediates in the reaction of Citrobacter freundii tyrosine phenol-lyase.
2006-08-08
Structural mobility in human manganese superoxide dismutase.
2006-07-11
Aspartic acid 214 in Citrobacter freundii tyrosine phenol-lyase ensures sufficient C--H-acidity of the external aldimine intermediate and proper orientation of the cofactor at the active site.
2006-07
Mono-, di-, tri-, and tetra-substituted fluorotyrosines: new probes for enzymes that use tyrosyl radicals in catalysis.
2006-02-08
Hydrogen bonding in human manganese superoxide dismutase containing 3-fluorotyrosine.
2005-12
Structural and spectral response of Aequorea victoria green fluorescent proteins to chromophore fluorination.
2005-03-15
Crystallographic evidence for isomeric chromophores in 3-fluorotyrosyl-green fluorescent protein.
2004-05-03
Chemically amplified 19F-1H nuclear Overhauser effects.
2004-05
The role of acidic dissociation of substrate's phenol group in the mechanism of tyrosine phenol-lyase.
2003-04-11
Evaluating the potential of fluorinated tyrosines as spectroscopic probes of local protein environments: a UV resonance Raman study.
2003-03-04
In vivo metabolism and partitioning of 6-[18F]fluoro-L-meta-tyrosine in whole blood: a unified compartment model.
2002-06-07
Name Type Language
L-M-FLUOROTYROSINE
Preferred Name English
3-FLUOROTYROSINE, L-
Common Name English
TYROSINE, 3-FLUORO-, L-
Systematic Name English
L-TYROSINE, 3-FLUORO-
Systematic Name English
3-FLUORO-L-TYROSINE
Systematic Name English
Code System Code Type Description
FDA UNII
174NRG3M2X
Created by admin on Mon Mar 31 21:17:17 GMT 2025 , Edited by admin on Mon Mar 31 21:17:17 GMT 2025
PRIMARY
CHEBI
46534
Created by admin on Mon Mar 31 21:17:17 GMT 2025 , Edited by admin on Mon Mar 31 21:17:17 GMT 2025
PRIMARY
PUBCHEM
643330
Created by admin on Mon Mar 31 21:17:17 GMT 2025 , Edited by admin on Mon Mar 31 21:17:17 GMT 2025
PRIMARY
CAS
7423-96-3
Created by admin on Mon Mar 31 21:17:17 GMT 2025 , Edited by admin on Mon Mar 31 21:17:17 GMT 2025
PRIMARY
DRUG BANK
DB04436
Created by admin on Mon Mar 31 21:17:17 GMT 2025 , Edited by admin on Mon Mar 31 21:17:17 GMT 2025
PRIMARY
EPA CompTox
DTXSID10225227
Created by admin on Mon Mar 31 21:17:17 GMT 2025 , Edited by admin on Mon Mar 31 21:17:17 GMT 2025
PRIMARY