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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 02:19:24 UTC
Update Date2022-03-07 02:56:43 UTC
HMDB IDHMDB0040746
Secondary Accession Numbers
  • HMDB40746
Metabolite Identification
Common Name12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al
Description12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Based on a literature review a small amount of articles have been published on 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al.
Structure
Data?1563863583
SynonymsNot Available
Chemical FormulaC20H26O3
Average Molecular Weight314.4186
Monoisotopic Molecular Weight314.188194698
IUPAC Name6-hydroxy-1,4a-dimethyl-9-oxo-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carbaldehyde
Traditional Name6-hydroxy-7-isopropyl-1,4a-dimethyl-9-oxo-3,4,10,10a-tetrahydro-2H-phenanthrene-1-carbaldehyde
CAS Registry NumberNot Available
SMILES
CC(C)C1=CC2=C(C=C1O)C1(C)CCCC(C)(C=O)C1CC2=O
InChI Identifier
InChI=1S/C20H26O3/c1-12(2)13-8-14-15(9-16(13)22)20(4)7-5-6-19(3,11-21)18(20)10-17(14)23/h8-9,11-12,18,22H,5-7,10H2,1-4H3
InChI KeyWWTJTTLCNJCBCJ-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassDiterpenoids
Direct ParentDiterpenoids
Alternative Parents
Substituents
  • Abietane diterpenoid
  • Diterpenoid
  • Hydrophenanthrene
  • Phenanthrene
  • Tetralin
  • Aryl alkyl ketone
  • Aryl ketone
  • 1-hydroxy-2-unsubstituted benzenoid
  • Benzenoid
  • Ketone
  • Organooxygen compound
  • Aldehyde
  • Organic oxygen compound
  • Carbonyl group
  • Hydrocarbon derivative
  • Organic oxide
  • Aromatic homopolycyclic compound
Molecular FrameworkAromatic homopolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
Role
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.011 g/LALOGPS
logP4.45ALOGPS
logP4.14ChemAxon
logS-4.5ALOGPS
pKa (Strongest Acidic)8.19ChemAxon
pKa (Strongest Basic)-6.7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area54.37 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity91.29 m³·mol⁻¹ChemAxon
Polarizability35.91 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+174.93531661259
DarkChem[M-H]-170.70531661259
DeepCCS[M+H]+180.50330932474
DeepCCS[M-H]-178.14530932474
DeepCCS[M-2H]-211.63630932474
DeepCCS[M+Na]+186.86330932474
AllCCS[M+H]+176.032859911
AllCCS[M+H-H2O]+172.932859911
AllCCS[M+NH4]+178.932859911
AllCCS[M+Na]+179.732859911
AllCCS[M-H]-184.332859911
AllCCS[M+Na-2H]-184.632859911
AllCCS[M+HCOO]-185.032859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
12-Hydroxy-7-oxo-8,11,13-abietatrien-18-alCC(C)C1=CC2=C(C=C1O)C1(C)CCCC(C)(C=O)C1CC2=O3354.9Standard polar33892256
12-Hydroxy-7-oxo-8,11,13-abietatrien-18-alCC(C)C1=CC2=C(C=C1O)C1(C)CCCC(C)(C=O)C1CC2=O2655.6Standard non polar33892256
12-Hydroxy-7-oxo-8,11,13-abietatrien-18-alCC(C)C1=CC2=C(C=C1O)C1(C)CCCC(C)(C=O)C1CC2=O2774.8Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al,1TMS,isomer #1CC(C)C1=CC2=C(C=C1O[Si](C)(C)C)C1(C)CCCC(C)(C=O)C1CC2=O2687.6Semi standard non polar33892256
12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al,1TBDMS,isomer #1CC(C)C1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C1(C)CCCC(C)(C=O)C1CC2=O2930.4Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al GC-MS (Non-derivatized) - 70eV, Positivesplash10-000b-0090000000-2b1504d53a4d02a2dd2c2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al GC-MS (1 TMS) - 70eV, Positivesplash10-00di-1009000000-50c915c660d6c7e76e592017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al 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 - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al 10V, Positive-QTOFsplash10-014i-0049000000-538f778b1daa6d1883602017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al 20V, Positive-QTOFsplash10-000i-0591000000-5d3d7ba37b13302dc5492017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al 40V, Positive-QTOFsplash10-01bj-3290000000-f4d6752191f4c747218b2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al 10V, Negative-QTOFsplash10-03di-0019000000-0c58fffc5af31279db9b2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al 20V, Negative-QTOFsplash10-03di-0049000000-bca958b728ad95f6563e2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al 40V, Negative-QTOFsplash10-00lb-1090000000-bb7ce1e76b6aa5da037c2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al 10V, Positive-QTOFsplash10-000i-0092000000-e9bb512d5c2f5ea0d94e2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al 20V, Positive-QTOFsplash10-000i-0291000000-9cb77bef9db4cdca16f52021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al 40V, Positive-QTOFsplash10-015c-1791000000-899d422854663c6bfa3e2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al 10V, Negative-QTOFsplash10-03di-0009000000-d8638daf32922c2274642021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al 20V, Negative-QTOFsplash10-03di-0009000000-7426e03bdee7b169f6312021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 12-Hydroxy-7-oxo-8,11,13-abietatrien-18-al 40V, Negative-QTOFsplash10-0002-0090000000-7659c340903e46f899e42021-09-24Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • 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 IDFDB020556
KNApSAcK IDNot Available
Chemspider ID8194106
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound10018533
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.