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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 20:05:20 UTC
Update Date2022-03-07 02:54:22 UTC
HMDB IDHMDB0035144
Secondary Accession Numbers
  • HMDB35144
Metabolite Identification
Common Name(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one
Description(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one is an extremely weak basic (essentially neutral) compound (based on its pKa).
Structure
Data?1563862673
Synonyms
ValueSource
(3b,17a,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-oneGenerator
(3Β,17α,23S,24S)-17,23-epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-oneGenerator
Chemical FormulaC29H46O5
Average Molecular Weight474.6725
Monoisotopic Molecular Weight474.334524582
IUPAC Name5'-hydroxy-6'-(hydroxymethyl)-5-(1-hydroxypropyl)-2',3,6',11',15'-pentamethylspiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-en-12'-one
Traditional Name5'-hydroxy-6'-(hydroxymethyl)-5-(1-hydroxypropyl)-2',3,6',11',15'-pentamethylspiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-en-12'-one
CAS Registry NumberNot Available
SMILES
CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(O)C(C)(CO)C2CC4)O1
InChI Identifier
InChI=1S/C29H46O5/c1-7-20(31)21-14-17(2)29(34-21)15-24(33)28(6)19-8-9-22-25(3,18(19)10-13-27(28,29)5)12-11-23(32)26(22,4)16-30/h17,20-23,30-32H,7-16H2,1-6H3
InChI KeyFGFZDTLKZFGANR-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassTriterpenoids
Direct ParentTriterpenoids
Alternative ParentsNot Available
SubstituentsNot Available
Molecular FrameworkAliphatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point234 - 236 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.0081 g/LALOGPS
logP3.93ALOGPS
logP3.65ChemAxon
logS-4.8ALOGPS
pKa (Strongest Acidic)14.02ChemAxon
pKa (Strongest Basic)-2.8ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area86.99 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity132.43 m³·mol⁻¹ChemAxon
Polarizability55.12 ųChemAxon
Number of Rings5ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+210.35431661259
DarkChem[M-H]-202.331661259
DeepCCS[M-2H]-245.49130932474
DeepCCS[M+Na]+220.90830932474
AllCCS[M+H]+215.432859911
AllCCS[M+H-H2O]+213.732859911
AllCCS[M+NH4]+217.032859911
AllCCS[M+Na]+217.432859911
AllCCS[M-H]-215.232859911
AllCCS[M+Na-2H]-217.632859911
AllCCS[M+HCOO]-220.332859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-oneCCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(O)C(C)(CO)C2CC4)O13326.2Standard polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-oneCCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(O)C(C)(CO)C2CC4)O13637.5Standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-oneCCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(O)C(C)(CO)C2CC4)O13991.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,1TMS,isomer #1CCC(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO)C2CC4)O13766.7Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,1TMS,isomer #2CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(C)(CO)C2CC4)O13758.8Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,1TMS,isomer #3CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO[Si](C)(C)C)C2CC4)O13720.6Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,1TMS,isomer #4CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO)C2CC4)O13661.8Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,2TMS,isomer #1CCC(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(C)(CO)C2CC4)O13748.9Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,2TMS,isomer #2CCC(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO[Si](C)(C)C)C2CC4)O13715.2Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,2TMS,isomer #3CCC(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO)C2CC4)O13651.2Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,2TMS,isomer #4CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O13704.5Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,2TMS,isomer #5CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(C)(CO)C2CC4)O13604.5Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,2TMS,isomer #6CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO[Si](C)(C)C)C2CC4)O13566.7Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,3TMS,isomer #1CCC(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O13696.5Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,3TMS,isomer #2CCC(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(C)(CO)C2CC4)O13598.0Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,3TMS,isomer #3CCC(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO[Si](C)(C)C)C2CC4)O13563.5Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,3TMS,isomer #4CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O13550.5Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,4TMS,isomer #1CCC(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O13542.2Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,4TMS,isomer #1CCC(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O13533.8Standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,1TBDMS,isomer #1CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO)C2CC4)O14008.6Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,1TBDMS,isomer #2CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O13984.4Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,1TBDMS,isomer #3CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O13959.2Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,1TBDMS,isomer #4CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO)C2CC4)O13898.8Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,2TBDMS,isomer #1CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O14204.8Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,2TBDMS,isomer #2CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O14174.9Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,2TBDMS,isomer #3CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO)C2CC4)O14101.9Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,2TBDMS,isomer #4CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O14152.5Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,2TBDMS,isomer #5CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O14038.2Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,2TBDMS,isomer #6CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O14011.1Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,3TBDMS,isomer #1CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O14352.7Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,3TBDMS,isomer #2CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O14235.5Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,3TBDMS,isomer #3CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O14206.5Semi standard non polar33892256
(3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one,3TBDMS,isomer #4CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O14182.9Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one GC-MS (Non-derivatized) - 70eV, Positivesplash10-05ue-2116900000-8ed9f8642e36b38c72cb2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one GC-MS (3 TMS) - 70eV, Positivesplash10-004i-2120219000-83d5fe18250930ffa8e42017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one 10V, Positive-QTOFsplash10-0a4r-0001900000-3d1fd9d7d566143e66722016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one 20V, Positive-QTOFsplash10-052r-3127900000-fde08932ad461968ba902016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one 40V, Positive-QTOFsplash10-00y0-3097100000-c31b8d7b8e8d6f73412c2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one 10V, Negative-QTOFsplash10-00di-0000900000-44713eba1ca1d5c8279d2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one 20V, Negative-QTOFsplash10-0abc-1001900000-a07a8b357d15018f55562016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one 40V, Negative-QTOFsplash10-0abi-2029400000-4f07bd2443f7aeb50f7a2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one 10V, Positive-QTOFsplash10-056r-0001900000-258b414c4c36771c63ed2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one 20V, Positive-QTOFsplash10-0a4i-0022900000-03a37fb94593cfa45a972021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one 40V, Positive-QTOFsplash10-00kf-9233700000-c1617048853cdd4407cf2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one 10V, Negative-QTOFsplash10-00di-0000900000-c53cb709661bcae07a512021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one 20V, Negative-QTOFsplash10-0829-0002900000-96c8d64926f07c9266412021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,17alpha,23S,24S)-17,23-Epoxy-3,24,29-trihydroxy-27-norlanost-8-en-15-one 40V, Negative-QTOFsplash10-0adi-3000900000-227a62596bc2dbcb46042021-09-22Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB013780
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound131751674
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
  2. Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
  3. Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
  4. Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
  5. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
  6. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.