Record Information
Version1.0
Creation Date2016-09-30 22:48:48 UTC
Update Date2020-05-05 18:40:16 UTC
BMDB IDBMDB0001900
Secondary Accession Numbers
  • BMDB01900
Metabolite Identification
Common NameRibonolactone
DescriptionRibonolactone belongs to the class of organic compounds known as pentoses. These are monosaccharides in which the carbohydrate moiety contains five carbon atoms. Based on a literature review a significant number of articles have been published on Ribonolactone.
Structure
Thumb
Synonyms
ValueSource
D-(+)-Ribonic acid gamma-lactoneChEBI
D-Ribonic acid-1,4-lactoneChEBI
D-Ribono-gamma-lactoneChEBI
D-RibonolactoneChEBI
D-Ribopentono-1,4-lactoneChEBI
Ribono-gamma-lactoneChEBI
D-(+)-Ribonate g-lactoneGenerator
D-(+)-Ribonate gamma-lactoneGenerator
D-(+)-Ribonate γ-lactoneGenerator
D-(+)-Ribonic acid g-lactoneGenerator
D-(+)-Ribonic acid γ-lactoneGenerator
D-Ribonate-1,4-lactoneGenerator
D-Ribono-g-lactoneGenerator
D-Ribono-γ-lactoneGenerator
Ribono-g-lactoneGenerator
Ribono-γ-lactoneGenerator
D(+)-Ribonic acid gamma-lactoneHMDB
D-(+)-Ribonone-1.4-lactoneHMDB
D-ribono-1,4-LactoneHMDB
delta-(+)-Ribonic acid g-lactoneHMDB
delta-(+)-Ribonic acid gamma-lactoneHMDB
delta-(+)-Ribonone-1.4-lactoneHMDB
delta-ribono-1,4-LactoneHMDB
delta-ribono-gamma-LactoneHMDB
delta-RibonolactoneHMDB
delta-ribopentono-1,4-LactoneHMDB
DeoxyribonolactoneHMDB
gamma-Lactone OF ribonateHMDB
gamma-Lactone OF ribonic acidHMDB
gamma-Lactone-ribonateHMDB
gamma-Lactone-ribonic acidHMDB
RibonolactoneChEBI
Chemical FormulaC5H8O5
Average Molecular Weight148.114
Monoisotopic Molecular Weight148.037173366
IUPAC Name(3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-one
Traditional NameD-ribosone
CAS Registry Number5336-08-3
SMILES
OC[C@H]1OC(=O)[C@H](O)[C@@H]1O
InChI Identifier
InChI=1S/C5H8O5/c6-1-2-3(7)4(8)5(9)10-2/h2-4,6-8H,1H2/t2-,3-,4-/m1/s1
InChI KeyCUOKHACJLGPRHD-BXXZVTAOSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as pentoses. These are monosaccharides in which the carbohydrate moiety contains five carbon atoms.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentPentoses
Alternative Parents
Substituents
  • Pentose monosaccharide
  • Gamma butyrolactone
  • Tetrahydrofuran
  • Carboxylic acid ester
  • Lactone
  • Secondary alcohol
  • Monocarboxylic acid or derivatives
  • Carboxylic acid derivative
  • Oxacycle
  • Organoheterocyclic compound
  • Primary alcohol
  • Hydrocarbon derivative
  • Organic oxide
  • Alcohol
  • Carbonyl group
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
External Descriptors
Ontology
StatusDetected but not Quantified
Origin
  • Endogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Cytoplasm
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting Point83 - 85 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP-2ALOGPS
logP-2.1ChemAxon
logS0.76ALOGPS
pKa (Strongest Acidic)11.63ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area86.99 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity28.82 m³·mol⁻¹ChemAxon
Polarizability12.8 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
  • Mammary Gland
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
Mammary GlandDetected but not QuantifiedNot QuantifiedNot SpecifiedNot Specified
Normal
details
Mammary GlandDetected but not QuantifiedNot QuantifiedNot SpecifiedNot Specified
Normal
details
Abnormal Concentrations
Not Available
HMDB IDHMDB0001900
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB022728
KNApSAcK IDNot Available
Chemspider ID99702
KEGG Compound IDC02674
BioCyc IDCPD-13413
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN ID6380
PubChem Compound111064
PDB IDNot Available
ChEBI ID74168
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available