Record Information
Version1.0
Creation Date2016-05-27 01:46:37 UTC
Update Date2016-11-09 01:22:35 UTC
Accession NumberCHEM041983
Identification
Common Name3-methylsulfinylpropyl-glucosinolate
ClassSmall Molecule
DescriptionNot Available
Contaminant Sources
  • FooDB Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
2-(Hydroxymethyl)-6-({4-methanesulphinyl-1-[(sulphonatooxy)imino]butyl}sulphanyl)oxane-3,4,5-triolGenerator
3-Methylsulfinylpropyl-glucosinolic acidGenerator
3-Methylsulphinylpropyl-glucosinolateGenerator
3-Methylsulphinylpropyl-glucosinolic acidGenerator
Chemical FormulaC11H20NO10S3
Average Molecular Mass422.460 g/mol
Monoisotopic Mass422.025 g/mol
CAS Registry NumberNot Available
IUPAC Name2-(hydroxymethyl)-6-({4-methanesulfinyl-1-[(sulfonatooxy)imino]butyl}sulfanyl)oxane-3,4,5-triol
Traditional Name2-(hydroxymethyl)-6-({4-methanesulfinyl-1-[(sulfonatooxy)imino]butyl}sulfanyl)oxane-3,4,5-triol
SMILESCS(=O)CCCC(SC1OC(CO)C(O)C(O)C1O)=NOS([O-])(=O)=O
InChI IdentifierInChI=1S/C11H21NO10S3/c1-24(17)4-2-3-7(12-22-25(18,19)20)23-11-10(16)9(15)8(14)6(5-13)21-11/h6,8-11,13-16H,2-5H2,1H3,(H,18,19,20)/p-1
InChI KeyPHYYADMVYQURSX-UHFFFAOYSA-M
Chemical Taxonomy
Description belongs to the class of organic compounds known as alkylglucosinolates. These are organic compounds containing a glucosinolate moiety that carries an alkyl chain.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentAlkylglucosinolates
Alternative Parents
Substituents
  • Alkylglucosinolate
  • Glycosyl compound
  • S-glycosyl compound
  • Oxane
  • Monothioacetal
  • Organic sulfuric acid or derivatives
  • Secondary alcohol
  • Sulfoxide
  • Polyol
  • Oxacycle
  • Organoheterocyclic compound
  • Sulfinyl compound
  • Sulfenyl compound
  • Primary alcohol
  • Alcohol
  • Hydrocarbon derivative
  • Organosulfur compound
  • Organonitrogen compound
  • Organic nitrogen compound
  • Organopnictogen compound
  • Organic oxide
  • Organic anion
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
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 Solubility39.2 g/LALOGPS
logP-1.2ALOGPS
logP-5.1ChemAxon
logS-1ALOGPS
pKa (Strongest Acidic)-3.7ChemAxon
pKa (Strongest Basic)-0.51ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count10ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area186.01 ŲChemAxon
Rotatable Bond Count9ChemAxon
Refractivity87.9 m³·mol⁻¹ChemAxon
Polarizability38.8 ųChemAxon
Number of Rings1ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-08i0-5193000000-9c4a54bc59dffee3bdebSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-03di-9110000000-a8512ea6d3beae686069Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-03di-9600000000-af8b1d02f822513003e8Spectrum
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 IDNot Available
HMDB IDHMDB0304141
FooDB IDFDB030445
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkNot Available
Chemspider ID3677869
ChEBI IDNot Available
PubChem Compound ID4479896
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available