Record Information
Version1.0
Creation date2015-10-09 22:31:14 UTC
Update date2017-01-19 02:36:27 UTC
FoodComEx IDPC000535
FoodDB RecordFDB022728
Chemical Information
NameRibonolactone
DescriptionRibonolactone is a metabolite normally not detectable in human biofluids; however, it has been found in the urine of patients with neuroblastoma. (PMID 699273) [HMDB]
CAS Number5336-08-3
Structure
Thumb
Synonyms
SynonymSource
D-(+)-Ribonate g-lactoneGenerator
D-(+)-Ribonate gamma-lactoneGenerator
D-(+)-Ribonate γ-lactoneGenerator
D-(+)-Ribonic acid g-Lactonehmdb
D-(+)-Ribonic acid gamma-lactonehmdb
D-(+)-Ribonic acid γ-lactoneGenerator
D-(+)-Ribonone-1.4-lactonehmdb
D-Ribonate-1,4-lactoneGenerator
D-Ribonic acid-1,4-lactoneChEBI
D-Ribono-1,4-lactonehmdb
D-Ribono-g-lactoneGenerator
D-Ribono-gamma-lactonehmdb
D-Ribono-γ-lactoneGenerator
D-Ribonolactonehmdb
D-Ribopentono-1,4-lactonehmdb
D(+)-Ribonic acid gamma-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
Ribono-g-lactoneGenerator
Ribono-gamma-lactonehmdb
Ribono-γ-lactoneGenerator
Chemical FormulaC5H8O5
IUPAC name(3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-one
InChI IdentifierInChI=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
Isomeric SMILESOC[C@H]1OC(=O)[C@H](O)[C@@H]1O
Average Molecular Weight148.114
Monoisotopic Molecular Weight148.037173366
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
Physico-Chemical Properties - Experimental
PropertyValueReference
Experimental logPNot Available
Experimental Water SolubilityNot Available
Melting PointNot Available
Foods of Origin
FoodContent Range AverageReference
FoodReference
Production Data
Production Methodcommercial
Production Method ReferenceNot Available
Production Method Reference FileNot Available
Quantity AvailableProduction upon request, up to 100 mg
Delivery TimeNot Available
Storage Formsolid
Storage Conditions-80°C
StabilityNot Available
PurityNot Available
Spectra
Spectral Data Upon RequestNot Available
Provider Information
Contact NameContact InstitutionContact Email
Rosa Vazquez Fresnovazquezf@ualberta.ca
Commercial Vendors
AKSci V6455
Toronto Research Chemicals R416000