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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(F)=C(O)C=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

Molecular Formula C9H10FNO3
Molecular Weight 199.179
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
In vivo metabolism and partitioning of 6-[18F]fluoro-L-meta-tyrosine in whole blood: a unified compartment model.
2002 Jun 7
Hydrogen bonding in human manganese superoxide dismutase containing 3-fluorotyrosine.
2005 Dec
Structural and spectral response of Aequorea victoria green fluorescent proteins to chromophore fluorination.
2005 Mar 15
Mono-, di-, tri-, and tetra-substituted fluorotyrosines: new probes for enzymes that use tyrosyl radicals in catalysis.
2006 Feb 8
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 Jul
Structural mobility in human manganese superoxide dismutase.
2006 Jul 11
An expanded set of amino acid analogs for the ribosomal translation of unnatural peptides.
2007 Oct 3
Probing the coupling between proton and electron transfer in photosystem II core complexes containing a 3-fluorotyrosine.
2009 Apr 1
A mutagenesis-free approach to assignment of (19)F NMR resonances in biosynthetically labeled proteins.
2009 Feb 18
Precursor-directed biosynthesis of fluorinated iturin A in Bacillus spp.
2009 Feb 21
Comparison of the folding mechanism of highly homologous proteins in the lipid-binding protein family.
2009 Jun
19F NMR studies of alpha-synuclein conformation and fibrillation.
2009 Sep 15
Site-specific incorporation of fluorotyrosines into proteins in Escherichia coli by photochemical disguise.
2010 Mar 2
19F NMR studies of α-synuclein-membrane interactions.
2010 Sep
Substance Class Chemical
Created
by admin
on Sat Dec 16 03:10:40 UTC 2023
Edited
by admin
on Sat Dec 16 03:10:40 UTC 2023
Record UNII
174NRG3M2X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-FLUOROTYROSINE, L-
Common Name English
L-M-FLUOROTYROSINE
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 Sat Dec 16 03:10:40 UTC 2023 , Edited by admin on Sat Dec 16 03:10:40 UTC 2023
PRIMARY
CHEBI
46534
Created by admin on Sat Dec 16 03:10:40 UTC 2023 , Edited by admin on Sat Dec 16 03:10:40 UTC 2023
PRIMARY
PUBCHEM
643330
Created by admin on Sat Dec 16 03:10:40 UTC 2023 , Edited by admin on Sat Dec 16 03:10:40 UTC 2023
PRIMARY
CAS
7423-96-3
Created by admin on Sat Dec 16 03:10:40 UTC 2023 , Edited by admin on Sat Dec 16 03:10:40 UTC 2023
PRIMARY
DRUG BANK
DB04436
Created by admin on Sat Dec 16 03:10:40 UTC 2023 , Edited by admin on Sat Dec 16 03:10:40 UTC 2023
PRIMARY
EPA CompTox
DTXSID10225227
Created by admin on Sat Dec 16 03:10:40 UTC 2023 , Edited by admin on Sat Dec 16 03:10:40 UTC 2023
PRIMARY