Hmdb loader
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 20:46:04 UTC
Update Date2022-03-07 02:54:37 UTC
HMDB IDHMDB0035748
Secondary Accession Numbers
  • HMDB35748
Metabolite Identification
Common NameSebiferenic acid
DescriptionSebiferenic acid, also known as sebiferenate, belongs to the class of organic compounds known as scalarane sesterterpenoids. These are sesterterpenoids with a structure based on the scalarane backbone. Scalarane is a tetracyclic compound, which is similar the homoandrostane with five methyl groups at the 4-, 4-, 8-, 17-, 17a-positions. Based on a literature review a significant number of articles have been published on Sebiferenic acid.
Structure
Data?1563862765
Synonyms
ValueSource
SebiferenateGenerator
2a-Hydroxyaleuritolic acidHMDB
2a-Hydroxymaprounic acidHMDB
10,11-Dihydroxy-2,2,6b,9,9,12a,14a-heptamethyl-1,2,3,4,4a,5,6b,7,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydropicene-4a-carboxylateGenerator
Chemical FormulaC30H48O4
Average Molecular Weight472.6997
Monoisotopic Molecular Weight472.355260024
IUPAC Name10,11-dihydroxy-2,2,6b,9,9,12a,14a-heptamethyl-1,2,3,4,4a,5,6b,7,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydropicene-4a-carboxylic acid
Traditional Name10,11-dihydroxy-2,2,6b,9,9,12a,14a-heptamethyl-1,3,4,5,7,8,8a,10,11,12,12b,13,14,14b-tetradecahydropicene-4a-carboxylic acid
CAS Registry Number94390-09-7
SMILES
CC1(C)CCC2(CC=C3C4(C)CCC5C(C)(C)C(O)C(O)CC5(C)C4CCC3(C)C2C1)C(O)=O
InChI Identifier
InChI=1S/C30H48O4/c1-25(2)14-15-30(24(33)34)13-10-20-27(5)11-8-19-26(3,4)23(32)18(31)16-29(19,7)21(27)9-12-28(20,6)22(30)17-25/h10,18-19,21-23,31-32H,8-9,11-17H2,1-7H3,(H,33,34)
InChI KeyJMJVYEINATYJHM-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as scalarane sesterterpenoids. These are sesterterpenoids with a structure based on the scalarane backbone. Scalarane is a tetracyclic compound, which is similar the homoandrostane with five methyl groups at the 4-, 4-, 8-, 17-, 17a-positions.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassSesterterpenoids
Direct ParentScalarane sesterterpenoids
Alternative Parents
Substituents
  • Scalarane sesterterpenoid
  • Cyclic alcohol
  • Secondary alcohol
  • 1,2-diol
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Alcohol
  • Aliphatic homopolycyclic compound
Molecular FrameworkAliphatic homopolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point325 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility0.004 mg/L @ 25 °C (est)The Good Scents Company Information System
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.004 g/LALOGPS
logP5.88ALOGPS
logP5.52ChemAxon
logS-5.1ALOGPS
pKa (Strongest Acidic)4.74ChemAxon
pKa (Strongest Basic)-3.2ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area77.76 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity134.99 m³·mol⁻¹ChemAxon
Polarizability55.95 ųChemAxon
Number of Rings5ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+206.07731661259
DarkChem[M-H]-201.33531661259
DeepCCS[M+H]+215.80330932474
DeepCCS[M-H]-213.44230932474
DeepCCS[M-2H]-246.32730932474
DeepCCS[M+Na]+221.89430932474
AllCCS[M+H]+218.432859911
AllCCS[M+H-H2O]+216.832859911
AllCCS[M+NH4]+219.832859911
AllCCS[M+Na]+220.332859911
AllCCS[M-H]-215.632859911
AllCCS[M+Na-2H]-217.732859911
AllCCS[M+HCOO]-220.132859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Sebiferenic acidCC1(C)CCC2(CC=C3C4(C)CCC5C(C)(C)C(O)C(O)CC5(C)C4CCC3(C)C2C1)C(O)=O2987.2Standard polar33892256
Sebiferenic acidCC1(C)CCC2(CC=C3C4(C)CCC5C(C)(C)C(O)C(O)CC5(C)C4CCC3(C)C2C1)C(O)=O3593.2Standard non polar33892256
Sebiferenic acidCC1(C)CCC2(CC=C3C4(C)CCC5C(C)(C)C(O)C(O)CC5(C)C4CCC3(C)C2C1)C(O)=O3882.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Sebiferenic acid,1TMS,isomer #1CC1(C)CCC2(C(=O)O)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O[Si](C)(C)C)C(O)CC43C)C2C13935.2Semi standard non polar33892256
Sebiferenic acid,1TMS,isomer #2CC1(C)CCC2(C(=O)O)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O)C(O[Si](C)(C)C)CC43C)C2C13941.7Semi standard non polar33892256
Sebiferenic acid,1TMS,isomer #3CC1(C)CCC2(C(=O)O[Si](C)(C)C)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O)C(O)CC43C)C2C13840.4Semi standard non polar33892256
Sebiferenic acid,2TMS,isomer #1CC1(C)CCC2(C(=O)O[Si](C)(C)C)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O[Si](C)(C)C)C(O)CC43C)C2C13755.4Semi standard non polar33892256
Sebiferenic acid,2TMS,isomer #2CC1(C)CCC2(C(=O)O)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)CC43C)C2C13916.2Semi standard non polar33892256
Sebiferenic acid,2TMS,isomer #3CC1(C)CCC2(C(=O)O[Si](C)(C)C)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O)C(O[Si](C)(C)C)CC43C)C2C13759.8Semi standard non polar33892256
Sebiferenic acid,3TMS,isomer #1CC1(C)CCC2(C(=O)O[Si](C)(C)C)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)CC43C)C2C13695.4Semi standard non polar33892256
Sebiferenic acid,1TBDMS,isomer #1CC1(C)CCC2(C(=O)O)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O[Si](C)(C)C(C)(C)C)C(O)CC43C)C2C14147.4Semi standard non polar33892256
Sebiferenic acid,1TBDMS,isomer #2CC1(C)CCC2(C(=O)O)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O)C(O[Si](C)(C)C(C)(C)C)CC43C)C2C14161.9Semi standard non polar33892256
Sebiferenic acid,1TBDMS,isomer #3CC1(C)CCC2(C(=O)O[Si](C)(C)C(C)(C)C)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O)C(O)CC43C)C2C14080.9Semi standard non polar33892256
Sebiferenic acid,2TBDMS,isomer #1CC1(C)CCC2(C(=O)O[Si](C)(C)C(C)(C)C)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O[Si](C)(C)C(C)(C)C)C(O)CC43C)C2C14193.9Semi standard non polar33892256
Sebiferenic acid,2TBDMS,isomer #2CC1(C)CCC2(C(=O)O)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)CC43C)C2C14355.9Semi standard non polar33892256
Sebiferenic acid,2TBDMS,isomer #3CC1(C)CCC2(C(=O)O[Si](C)(C)C(C)(C)C)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O)C(O[Si](C)(C)C(C)(C)C)CC43C)C2C14203.7Semi standard non polar33892256
Sebiferenic acid,3TBDMS,isomer #1CC1(C)CCC2(C(=O)O[Si](C)(C)C(C)(C)C)CC=C3C(C)(CCC4C3(C)CCC3C(C)(C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)CC43C)C2C14355.9Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Sebiferenic acid GC-MS (Non-derivatized) - 70eV, Positivesplash10-0aor-0015900000-e4428aac7085846476452017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Sebiferenic acid GC-MS (3 TMS) - 70eV, Positivesplash10-00di-1000029000-783149581e8ad250f2e32017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Sebiferenic acid 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 - Sebiferenic acid 10V, Positive-QTOFsplash10-0ab9-0000900000-d3966df9b42d9f17e2f12015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sebiferenic acid 20V, Positive-QTOFsplash10-0a4i-0100900000-bcf0d409c210ccfc274d2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sebiferenic acid 40V, Positive-QTOFsplash10-0a4i-3466900000-e227dce04a3054befd892015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sebiferenic acid 10V, Negative-QTOFsplash10-00di-0000900000-6ed93980da7f98eb7a162015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sebiferenic acid 20V, Negative-QTOFsplash10-05di-0000900000-57ecdbc0a40e25cb03582015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sebiferenic acid 40V, Negative-QTOFsplash10-0bt9-0000900000-acfd71c6de5fd68a51162015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sebiferenic acid 10V, Positive-QTOFsplash10-00di-0000900000-d033a7f37b12ad112a712021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sebiferenic acid 20V, Positive-QTOFsplash10-0ab9-0024900000-eb21ee1fbd42fedffcde2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sebiferenic acid 40V, Positive-QTOFsplash10-00di-2392200000-20440f0626655adc43292021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sebiferenic acid 10V, Negative-QTOFsplash10-00di-0000900000-ce83f241675374237da42021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sebiferenic acid 20V, Negative-QTOFsplash10-00di-0000900000-e8ebc97bac06940335ca2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sebiferenic acid 40V, Negative-QTOFsplash10-00di-0000900000-d590b76896839b8292152021-09-24Wishart 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 IDFDB014478
KNApSAcK IDC00057674
Chemspider ID35014012
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound75049017
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1851391
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.