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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 22:46:31 UTC
Update Date2022-03-07 02:55:22 UTC
HMDB IDHMDB0037524
Secondary Accession Numbers
  • HMDB37524
Metabolite Identification
Common Name(3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol
Description(3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol belongs to the class of organic compounds known as stigmastanes and derivatives. These are sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24. Thus, (3beta,5alpha,24R)-stigmast-8(14)-en-3-ol is considered to be a sterol lipid molecule (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.
Structure
Data?1563863045
Synonyms
ValueSource
(3b,5a,24R)-Stigmast-8(14)-en-3-olGenerator
(3Β,5α,24R)-stigmast-8(14)-en-3-olGenerator
Chemical FormulaC29H50O
Average Molecular Weight414.7067
Monoisotopic Molecular Weight414.386166222
IUPAC Name14-(5-ethyl-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-10-en-5-ol
Traditional Name14-(5-ethyl-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-10-en-5-ol
CAS Registry Number14291-38-4
SMILES
CCC(CCC(C)C1CCC2=C3CCC4CC(O)CCC4(C)C3CCC12C)C(C)C
InChI Identifier
InChI=1S/C29H50O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h19-23,25,27,30H,7-18H2,1-6H3
InChI KeyYQQOGXLLGWWKQH-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as stigmastanes and derivatives. These are sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassSteroids and steroid derivatives
Sub ClassStigmastanes and derivatives
Direct ParentStigmastanes and derivatives
Alternative ParentsNot Available
SubstituentsNot Available
Molecular FrameworkAliphatic homopolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point113.5 - 114 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.00012 g/LALOGPS
logP7.12ALOGPS
logP7.8ChemAxon
logS-6.5ALOGPS
pKa (Strongest Acidic)18.3ChemAxon
pKa (Strongest Basic)-1.4ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area20.23 ŲChemAxon
Rotatable Bond Count6ChemAxon
Refractivity129.5 m³·mol⁻¹ChemAxon
Polarizability53.92 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+198.81131661259
DarkChem[M-H]-195.21331661259
DeepCCS[M-2H]-244.06830932474
DeepCCS[M+Na]+219.60530932474
AllCCS[M+H]+210.032859911
AllCCS[M+H-H2O]+208.132859911
AllCCS[M+NH4]+211.732859911
AllCCS[M+Na]+212.232859911
AllCCS[M-H]-204.732859911
AllCCS[M+Na-2H]-207.032859911
AllCCS[M+HCOO]-209.632859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(3beta,5alpha,24R)-Stigmast-8(14)-en-3-olCCC(CCC(C)C1CCC2=C3CCC4CC(O)CCC4(C)C3CCC12C)C(C)C2537.2Standard polar33892256
(3beta,5alpha,24R)-Stigmast-8(14)-en-3-olCCC(CCC(C)C1CCC2=C3CCC4CC(O)CCC4(C)C3CCC12C)C(C)C3294.1Standard non polar33892256
(3beta,5alpha,24R)-Stigmast-8(14)-en-3-olCCC(CCC(C)C1CCC2=C3CCC4CC(O)CCC4(C)C3CCC12C)C(C)C3336.1Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
(3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol,1TMS,isomer #1CCC(CCC(C)C1CCC2=C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CCC21C)C(C)C3390.3Semi standard non polar33892256
(3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol,1TBDMS,isomer #1CCC(CCC(C)C1CCC2=C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC21C)C(C)C3620.3Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol GC-MS (Non-derivatized) - 70eV, Positivesplash10-000j-2119000000-eacdf6695aa0b98107a72017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol GC-MS (1 TMS) - 70eV, Positivesplash10-05fr-4104900000-8643778b68d8d8ef91292017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 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,5alpha,24R)-Stigmast-8(14)-en-3-ol 10V, Positive-QTOFsplash10-00kb-1019500000-ee4e699f34b201efdc3c2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 20V, Positive-QTOFsplash10-00kb-5149100000-55ef9cb6ea0eae0b0ac82015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 40V, Positive-QTOFsplash10-0002-9156000000-7258b865269008d1488d2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 10V, Positive-QTOFsplash10-00kb-1019500000-ee4e699f34b201efdc3c2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 20V, Positive-QTOFsplash10-00kb-5149100000-55ef9cb6ea0eae0b0ac82015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 40V, Positive-QTOFsplash10-0002-9156000000-7258b865269008d1488d2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 10V, Negative-QTOFsplash10-03di-0002900000-0a4f033c2879dfae51ce2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 20V, Negative-QTOFsplash10-03di-0005900000-ac0e2254635fa785a6482015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 40V, Negative-QTOFsplash10-0002-2009000000-948bc3fcf8e484c728b42015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 10V, Negative-QTOFsplash10-03di-0002900000-0a4f033c2879dfae51ce2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 20V, Negative-QTOFsplash10-03di-0005900000-ac0e2254635fa785a6482015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 40V, Negative-QTOFsplash10-0002-2009000000-948bc3fcf8e484c728b42015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 10V, Negative-QTOFsplash10-03di-0000900000-eda302082c5114b2ab3a2021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 20V, Negative-QTOFsplash10-03di-0001900000-bf25a83a900fbc405c512021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 40V, Negative-QTOFsplash10-01ot-0009500000-4aa80369f60ad476c92c2021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 10V, Positive-QTOFsplash10-014i-4105900000-99bbfbc61a39a84dee962021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 20V, Positive-QTOFsplash10-0900-9123300000-84456b31a1c66d71fbbc2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (3beta,5alpha,24R)-Stigmast-8(14)-en-3-ol 40V, Positive-QTOFsplash10-0a4i-9410000000-9c1b6eed5af4b2aa00742021-09-25Wishart 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 IDFDB016605
KNApSAcK IDNot Available
Chemspider ID550699
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound634400
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.