Record Information
Version1.0
Creation Date2016-05-22 06:17:40 UTC
Update Date2016-11-09 01:16:01 UTC
Accession NumberCHEM019574
Identification
Common NameAcamprosate calcium
ClassSmall Molecule
Description
Contaminant Sources
  • ToxCast & Tox21 Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
1-Propanesulfonic acid, 3-(acetylamino)-, calcium salt (2:1)ChEBI
Calcium 3-(acetylamino)propane-1-sulfonateChEBI
CampralKegg
RegtectKegg
1-Propanesulfonate, 3-(acetylamino)-, calcium salt (2:1)Generator
1-Propanesulphonate, 3-(acetylamino)-, calcium salt (2:1)Generator
1-Propanesulphonic acid, 3-(acetylamino)-, calcium salt (2:1)Generator
Calcium 3-(acetylamino)propane-1-sulfonic acidGenerator
Calcium 3-(acetylamino)propane-1-sulphonateGenerator
Calcium 3-(acetylamino)propane-1-sulphonic acidGenerator
Acamprosic acid calciumGenerator
N-AcetylhomotaurineMeSH
Calcium acetylhomotaurineMeSH
Sodium acetylhomotaurineMeSH
Campral ecMeSH
N-Acetylhomotaurine, monopotassium saltMeSH
N-Acetylhomotaurine, zinc (2:1) saltMeSH
AotalMeSH
N-Acetylhomotaurine, calcium (2:1) saltMeSH
N-Acetylhomotaurine, magnesium (2:1) saltMeSH
N-Acetylhomotaurine, monolithium saltMeSH
N-Acetylhomotaurine, monosodium saltMeSH
ZulexMeSH
Calcium acetyl homotaurinateMeSH
AOTAMeSH
AcamprosateMeSH
AcamprostateMeSH
Calcium acetylhomotaurinateMeSH
Acetyl homotaurinate, calciumMeSH
Acetylhomotaurine, calciumMeSH
Acetylhomotaurinate, calciumMeSH
N Acetylhomotaurine, monolithium saltMeSH
Acetylhomotaurine, sodiumMeSH
N AcetylhomotaurineMeSH
N Acetylhomotaurine, monopotassium saltMeSH
N Acetylhomotaurine, monosodium saltMeSH
Chemical FormulaC10H20CaN2O8S2
Average Molecular Mass400.482 g/mol
Monoisotopic Mass400.029 g/mol
CAS Registry Number77337-73-6
IUPAC Namecalcium N-(3-sulfopropyl)ethanimidic acid N-(3-sulfonatopropyl)ethanecarboximidate
Traditional Namecalcium N-(3-sulfopropyl)ethanimidic acid N-(3-sulfonatopropyl)ethanecarboximidate
SMILES[Ca++].CC(O)=NCCCS(O)(=O)=O.CC([O-])=NCCCS([O-])(=O)=O
InChI IdentifierInChI=1S/2C5H11NO4S.Ca/c2*1-5(7)6-3-2-4-11(8,9)10;/h2*2-4H2,1H3,(H,6,7)(H,8,9,10);/q;;+2/p-2
InChI KeyBUVGWDNTAWHSKI-UHFFFAOYSA-L
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
  • Organosulfonic acid
  • Sulfonyl
  • Acetamide
  • Alkanesulfonic acid
  • Carboxamide group
  • Secondary carboxylic acid amide
  • Carboxylic acid derivative
  • Organic calcium salt
  • Carbonyl group
  • Organic salt
  • Hydrocarbon derivative
  • Organic oxide
  • Organopnictogen compound
  • Organosulfur compound
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxygen compound
  • Organic nitrogen compound
  • Aliphatic acyclic compound
Molecular FrameworkNot Available
External Descriptors
Biological Properties
StatusDetected and Not Quantified
OriginNot Available
Cellular LocationsNot Available
Biofluid LocationsNot Available
Tissue LocationsNot Available
PathwaysNot Available
ApplicationsNot Available
Biological RolesNot Available
Chemical RolesNot Available
Physical Properties
StateNot Available
AppearanceNot Available
Experimental Properties
PropertyValue
Melting PointNot Available
Boiling PointNot Available
SolubilityNot Available
Predicted Properties
PropertyValueSource
Water Solubility1.97 g/LALOGPS
logP0.8ALOGPS
logP-2.3ChemAxon
logS-2.1ALOGPS
pKa (Strongest Acidic)-1.2ChemAxon
pKa (Strongest Basic)4.4ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area92.62 ŲChemAxon
Rotatable Bond Count8ChemAxon
Refractivity48.86 m³·mol⁻¹ChemAxon
Polarizability16.5 ųChemAxon
Number of Rings0ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
SpectraNot Available
Toxicity Profile
Route of ExposureNot Available
Mechanism of ToxicityNot Available
MetabolismNot Available
Toxicity ValuesNot Available
Lethal DoseNot Available
Carcinogenicity (IARC Classification)Not Available
Uses/SourcesNot Available
Minimum Risk LevelNot Available
Health EffectsNot Available
SymptomsNot Available
TreatmentNot Available
Concentrations
Not Available
DrugBank IDDBSALT000002
HMDB IDNot Available
FooDB IDNot Available
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkAcamprosate
Chemspider IDNot Available
ChEBI ID51042
PubChem Compound ID155434
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available