Record Information
Version1.0
Creation Date2016-09-30 22:48:53 UTC
Update Date2020-05-11 20:51:19 UTC
BMDB IDBMDB0001904
Secondary Accession Numbers
  • BMDB01904
Metabolite Identification
Common Name3-Nitrotyrosine
Description3-Nitrotyrosine belongs to the class of organic compounds known as tyrosine and derivatives. Tyrosine and derivatives are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Based on a literature review a significant number of articles have been published on 3-Nitrotyrosine.
Structure
Thumb
Synonyms
ValueSource
(2S)-2-Amino-3-(4-hydroxy-3-nitrophenyl)propanoic acidChEBI
L-3-NitrotyrosineChEBI
META-nitro-tyrosineChEBI
(2S)-2-Amino-3-(4-hydroxy-3-nitrophenyl)propanoateGenerator
3-MononitrotyrosineMeSH
3-Nitrotyrosine, (DL)-isomerMeSH
3-Nitrotyrosine, (L)-isomerMeSH
NitrotyrosineMeSH
Nitro-TyrosineMYCO, HMDB
5-NitrotyrosineHMDB
m-NitrotyrosineHMDB
3-NitrotyrosineChEBI
Chemical FormulaC9H10N2O5
Average Molecular Weight226.1861
Monoisotopic Molecular Weight226.05897144
IUPAC Name(2S)-2-amino-3-(4-hydroxy-3-nitrophenyl)propanoic acid
Traditional Namenitrotyrosine
CAS Registry Number3604-79-3
SMILES
N[C@@H](CC1=CC=C(O)C(=C1)[N+]([O-])=O)C(O)=O
InChI Identifier
InChI=1S/C9H10N2O5/c10-6(9(13)14)3-5-1-2-8(12)7(4-5)11(15)16/h1-2,4,6,12H,3,10H2,(H,13,14)/t6-/m0/s1
InChI KeyFBTSQILOGYXGMD-LURJTMIESA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as tyrosine and derivatives. Tyrosine and derivatives are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentTyrosine and derivatives
Alternative Parents
Substituents
  • Tyrosine or derivatives
  • Phenylalanine or derivatives
  • 3-phenylpropanoic-acid
  • Alpha-amino acid
  • Amphetamine or derivatives
  • Nitrophenol
  • L-alpha-amino acid
  • Nitrobenzene
  • Nitroaromatic compound
  • 1-hydroxy-2-unsubstituted benzenoid
  • Phenol
  • Aralkylamine
  • Monocyclic benzene moiety
  • Benzenoid
  • C-nitro compound
  • Amino acid
  • Organic nitro compound
  • Propargyl-type 1,3-dipolar organic compound
  • Allyl-type 1,3-dipolar organic compound
  • Organic 1,3-dipolar compound
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Organic oxoazanium
  • Organic zwitterion
  • Organonitrogen compound
  • Amine
  • Organic oxide
  • Organic nitrogen compound
  • Organooxygen compound
  • Primary aliphatic amine
  • Hydrocarbon derivative
  • Carbonyl group
  • Organopnictogen compound
  • Organic oxygen compound
  • Primary amine
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External Descriptors
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Cytoplasm
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP-2.1ALOGPS
logP-1.6ChemAxon
logS-2.2ALOGPS
pKa (Strongest Acidic)1.1ChemAxon
pKa (Strongest Basic)9.46ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count6ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area126.69 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity53.42 m³·mol⁻¹ChemAxon
Polarizability20.55 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash Key
GC-MSGC-MS Spectrum - GC-MS (3 TMS)splash10-014i-2790000000-d2985346d8315d1d8794View in MoNA
GC-MSGC-MS Spectrum - GC-MS (Non-derivatized)splash10-014i-2790000000-d2985346d8315d1d8794View in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positivesplash10-0zgi-5910000000-077a7552abc426243e20View in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (2 TMS) - 70eV, Positivesplash10-074l-9238000000-525285189da0213ff3c1View in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, PositiveNot AvailableView in JSpectraViewer
LC-MS/MSLC-MS/MS Spectrum - , negativesplash10-03di-0900000000-ee8213cb39c0e1019f31View in MoNA
LC-MS/MSLC-MS/MS Spectrum - 35V, Negativesplash10-03di-0900000000-57a8fbe1716064623e24View in MoNA
LC-MS/MSLC-MS/MS Spectrum - 35V, Negativesplash10-03ei-0900000000-a0d125a0ba852e048e8aView in MoNA
LC-MS/MSLC-MS/MS Spectrum - 10V, Negativesplash10-03di-0910000000-68c65cb3388619098ac0View in MoNA
LC-MS/MSLC-MS/MS Spectrum - 20V, Negativesplash10-03dr-0900000000-c925ae686673a229c498View in MoNA
LC-MS/MSLC-MS/MS Spectrum - 20V, Negativesplash10-03e9-0900000000-7c1468722dff591a265aView in MoNA
LC-MS/MSLC-MS/MS Spectrum - 40V, Negativesplash10-029b-1900000000-24959b0bc915f14fffbcView in MoNA
LC-MS/MSLC-MS/MS Spectrum - 35V, Negativesplash10-03di-0900000000-99d357953c342185aa6eView in MoNA
LC-MS/MSLC-MS/MS Spectrum - 40V, Negativesplash10-00kb-2900000000-1156a10414012c052611View in MoNA
LC-MS/MSLC-MS/MS Spectrum - 10V, Negativesplash10-03di-0910000000-64ac373769d7b98563f5View in MoNA
LC-MS/MSLC-MS/MS Spectrum - Quattro_QQQ 10V, Positive (Annotated)splash10-001i-0940000000-67e8e69b7a6cdee33f61View in MoNA
LC-MS/MSLC-MS/MS Spectrum - Quattro_QQQ 25V, Positive (Annotated)splash10-05o9-3900000000-fb63e13d7517f3696858View in MoNA
LC-MS/MSLC-MS/MS Spectrum - Quattro_QQQ 40V, Positive (Annotated)splash10-0kdu-9600000000-31b19bfbe0c1fd17697fView in MoNA
LC-MS/MSLC-MS/MS Spectrum - 20V, Positivesplash10-00lr-3900000000-c2d41a5f34510f427609View in MoNA
LC-MS/MSLC-MS/MS Spectrum - 40V, Positivesplash10-0rml-9500000000-caa9509a77fd0aa8355bView in MoNA
LC-MS/MSLC-MS/MS Spectrum - 10V, Positivesplash10-001i-0920000000-a2b1b1fa9734a6b40189View in MoNA
LC-MS/MSLC-MS/MS Spectrum - 35V, Positivesplash10-001i-0900000000-a9d1a6fdb2c29984221eView in MoNA
LC-MS/MSLC-MS/MS Spectrum - 10V, Positivesplash10-001i-0900000000-c18ef0ce904b7b49b8ecView in MoNA
LC-MS/MSLC-MS/MS Spectrum - 20V, Positivesplash10-00lr-1900000000-86a20e9368aceb49ba2eView in MoNA
LC-MS/MSLC-MS/MS Spectrum - 10V, Positivesplash10-001i-0910000000-d885bb0a89378a0c95eeView in MoNA
LC-MS/MSLC-MS/MS Spectrum - 40V, Positivesplash10-0mi6-9600000000-431eacf87ef25d0d6763View in MoNA
LC-MS/MSLC-MS/MS Spectrum - 20V, Positivesplash10-00lr-1900000000-44b00fd33af2a259db2cView in MoNA
LC-MS/MSLC-MS/MS Spectrum - 40V, Positivesplash10-00kf-9600000000-69dafe639edd5ba33f40View in MoNA
LC-MS/MSLC-MS/MS Spectrum - 20V, Positivesplash10-00lr-1900000000-fa3222f7814c77023fa1View in MoNA
LC-MS/MSLC-MS/MS Spectrum - 10V, Positivesplash10-001i-0910000000-eb55137da6de91c54d49View in MoNA
1D NMR1H NMR Spectrum (1D, 500 MHz, H2O, experimental)Not AvailableView in JSpectraViewer
1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)Not AvailableView in JSpectraViewer
2D NMR[1H, 13C]-HSQC NMR Spectrum (2D, 600 MHz, H2O, experimental)Not AvailableView in JSpectraViewer
Biological Properties
Cellular Locations
  • Cytoplasm
Biospecimen Locations
  • Brain
  • Epidermis
  • Fibroblasts
  • Neuron
  • Platelet
  • Skeletal Muscle
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BrainExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
EpidermisExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
FibroblastsExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
NeuronExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
PlateletExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
Skeletal MuscleExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
Abnormal Concentrations
Not Available
HMDB IDHMDB0001904
DrugBank IDDB03867
Phenol Explorer Compound IDNot Available
FooDB IDFDB022731
KNApSAcK IDNot Available
Chemspider ID58633
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNitrotyrosine
METLIN ID6383
PubChem Compound65124
PDB IDNot Available
ChEBI ID44454
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available