Showing metabocard for L-Homocysteine sulfonic acid (BMDB0002238)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2016-09-30 22:53:05 UTC
Update Date2020-04-22 15:10:20 UTC
BMDB IDBMDB0002238
Secondary Accession Numbers
  • BMDB02238
Metabolite Identification
Common NameL-Homocysteine sulfonic acid
DescriptionL-Homocysteine sulfonic acid, also known as L-homocysteine sulphonate, belongs to the class of organic compounds known as organosulfonic acids. Organosulfonic acids are compounds containing the sulfonic acid group, which has the general structure RS(=O)2OH (R is not a hydrogen atom). Based on a literature review very few articles have been published on L-Homocysteine sulfonic acid.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
L-Homocysteine sulfonateGenerator
L-Homocysteine sulphonateGenerator
L-Homocysteine sulphonic acidGenerator
(S)-3-amino-3-Carboxy-1-propanesulfonate L-homocysteine (ester)HMDB
(1R)-1-Amino-3-sulfanylpropane-1-sulfonateGenerator, HMDB
(1R)-1-Amino-3-sulphanylpropane-1-sulphonateGenerator, HMDB
(1R)-1-Amino-3-sulphanylpropane-1-sulphonic acidGenerator, HMDB
Chemical FormulaC3H9NO3S2
Average Molecular Weight171.238
Monoisotopic Molecular Weight171.002384539
IUPAC Name(1R)-1-amino-3-sulfanylpropane-1-sulfonic acid
Traditional NameL-homocysteine sulfonate
CAS Registry Number59729-28-1
SMILES
N[C@@H](CCS)S(O)(=O)=O
InChI Identifier
InChI=1S/C3H9NO3S2/c4-3(1-2-8)9(5,6)7/h3,8H,1-2,4H2,(H,5,6,7)/t3-/m1/s1
InChI KeyMHHDKRFQNZZMOE-GSVOUGTGSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as organosulfonic acids. Organosulfonic acids are compounds containing the sulfonic acid group, which has the general structure RS(=O)2OH (R is not a hydrogen atom).
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassOrganic sulfonic acids and derivatives
Sub ClassOrganosulfonic acids and derivatives
Direct ParentOrganosulfonic acids
Alternative Parents
Substituents
  • Alkanesulfonic acid
  • Sulfonyl
  • Organosulfonic acid
  • Alkylthiol
  • Organic nitrogen compound
  • Organic oxygen compound
  • Organopnictogen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organosulfur compound
  • Organonitrogen compound
  • Primary aliphatic amine
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locationsNot Available
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-1.7ALOGPS
logP-1.4ChemAxon
logS-1.2ALOGPS
pKa (Strongest Acidic)-3.2ChemAxon
pKa (Strongest Basic)7.66ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area80.39 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity36.46 m³·mol⁻¹ChemAxon
Polarizability15.63 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0002238
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB022924
KNApSAcK IDNot Available
Chemspider ID13628321
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN ID6566
PubChem Compound21252279
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available