Showing metabocard for Dopamine 4-sulfate (BMDB0004148)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2016-09-30 23:08:13 UTC
Update Date2020-05-11 20:23:45 UTC
BMDB IDBMDB0004148
Secondary Accession Numbers
  • BMDB04148
Metabolite Identification
Common NameDopamine 4-sulfate
DescriptionDopamine 4-sulfate belongs to the class of organic compounds known as phenylsulfates. Phenylsulfates are compounds containing a sulfuric acid group conjugated to a phenyl group. Based on a literature review a significant number of articles have been published on Dopamine 4-sulfate.
Structure
Thumb
MOLSDF3D-SDFPDBSMILESInChI View 3D Structure
Synonyms
ValueSource
3-Hydroxytyramine-4-O-sulfateChEBI
3-Hydroxytyramine-4-O-sulphateChEBI
4-(2-Aminoethyl)-1,2-benzenediol 1-(hydrogen sulfate)ChEBI
[4-(2-Aminoethyl)-2-hydroxyphenyl]oxidanesulfonic acidChEBI
Dopamine 4-monosulfateChEBI
Dopamine 4-O-sulphateChEBI
3-Hydroxytyramine-4-O-sulfuric acidGenerator
3-Hydroxytyramine-4-O-sulphuric acidGenerator
4-(2-Aminoethyl)-1,2-benzenediol 1-(hydrogen sulfuric acid)Generator
4-(2-Aminoethyl)-1,2-benzenediol 1-(hydrogen sulphate)Generator
4-(2-Aminoethyl)-1,2-benzenediol 1-(hydrogen sulphuric acid)Generator
[4-(2-Aminoethyl)-2-hydroxyphenyl]oxidanesulfonateGenerator
[4-(2-Aminoethyl)-2-hydroxyphenyl]oxidanesulphonateGenerator
[4-(2-Aminoethyl)-2-hydroxyphenyl]oxidanesulphonic acidGenerator
Dopamine 4-monosulfuric acidGenerator
Dopamine 4-monosulphateGenerator
Dopamine 4-monosulphuric acidGenerator
Dopamine 4-O-sulfateGenerator
Dopamine 4-O-sulfuric acidGenerator
Dopamine 4-O-sulphuric acidGenerator
Dopamine 4-sulfuric acidGenerator
Dopamine 4-sulphateGenerator
Dopamine 4-sulphuric acidGenerator
Dopamine 4-sulfateChEBI
Chemical FormulaC8H11NO5S
Average Molecular Weight233.242
Monoisotopic Molecular Weight233.035793157
IUPAC Name[4-(2-aminoethyl)-2-hydroxyphenyl]oxidanesulfonic acid
Traditional Namedopamine 4-O-sulfate
CAS Registry Number38339-02-5
SMILES
NCCC1=CC=C(OS(O)(=O)=O)C(O)=C1
InChI Identifier
InChI=1S/C8H11NO5S/c9-4-3-6-1-2-8(7(10)5-6)14-15(11,12)13/h1-2,5,10H,3-4,9H2,(H,11,12,13)
InChI KeyDEKNNWJXAQTLFA-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as phenylsulfates. Phenylsulfates are compounds containing a sulfuric acid group conjugated to a phenyl group.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassOrganic sulfuric acids and derivatives
Sub ClassArylsulfates
Direct ParentPhenylsulfates
Alternative Parents
Substituents
  • Phenylsulfate
  • Phenethylamine
  • Phenoxy compound
  • 2-arylethylamine
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Phenol
  • Aralkylamine
  • Monocyclic benzene moiety
  • Sulfuric acid monoester
  • Sulfate-ester
  • Sulfuric acid ester
  • Benzenoid
  • Primary amine
  • Organopnictogen compound
  • Organic oxygen compound
  • Organic nitrogen compound
  • Organooxygen compound
  • Amine
  • Primary aliphatic amine
  • Organonitrogen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External Descriptors
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
  • Exogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Cytoplasm
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting Point265 - 270.5 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP-1.2ALOGPS
logP-0.054ChemAxon
logS-1.8ALOGPS
pKa (Strongest Acidic)-2.1ChemAxon
pKa (Strongest Basic)9.64ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area109.85 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity53.24 m³·mol⁻¹ChemAxon
Polarizability21.59 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Biological Properties
Cellular Locations
  • Cytoplasm
Biospecimen Locations
  • Kidney
  • Liver
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
KidneyExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
 details
LiverExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
 details
Abnormal Concentrations
Not Available
HMDB IDHMDB0004148
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB023320
KNApSAcK IDNot Available
Chemspider ID110461
KEGG Compound IDC13691
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound123932
PDB IDNot Available
ChEBI ID34729
References
Synthesis ReferenceLernhardt U; Strobel G; Schell H; Werle E; Weicker H Modified syntheses of dopamine-4-sulfate, epinephrine-3-sulfate, and norepinephrine-3-sulfate: determination of the position of the sulfate group by 1H-NMR spectroscopy. International journal of sports medicine (1988), 9 Suppl 2 S89-92.
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available