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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 21:10:33 UTC
Update Date2022-03-07 02:54:47 UTC
HMDB IDHMDB0036109
Secondary Accession Numbers
  • HMDB36109
Metabolite Identification
Common Name1,3,5-Bisabolatrien-10-one
Description1,3,5-Bisabolatrien-10-one belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Based on a literature review a small amount of articles have been published on 1,3,5-Bisabolatrien-10-one.
Structure
Data?1563862822
Synonyms
ValueSource
2-Methyl-6-(4-methylphenyl)-3-heptanoneHMDB
Chemical FormulaC15H22O
Average Molecular Weight218.3346
Monoisotopic Molecular Weight218.167065326
IUPAC Name2-methyl-6-(4-methylphenyl)heptan-3-one
Traditional Name2-methyl-6-(4-methylphenyl)heptan-3-one
CAS Registry Number76760-40-2
SMILES
CC(C)C(=O)CCC(C)C1=CC=C(C)C=C1
InChI Identifier
InChI=1S/C15H22O/c1-11(2)15(16)10-7-13(4)14-8-5-12(3)6-9-14/h5-6,8-9,11,13H,7,10H2,1-4H3
InChI KeyUWAKTEDKARQVDV-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassSesquiterpenoids
Direct ParentSesquiterpenoids
Alternative Parents
Substituents
  • Bisabolane sesquiterpenoid
  • Sesquiterpenoid
  • P-cymene
  • Toluene
  • Benzenoid
  • Monocyclic benzene moiety
  • Ketone
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic 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 Solubility0.0063 g/LALOGPS
logP4.45ALOGPS
logP4.87ChemAxon
logS-4.5ALOGPS
pKa (Strongest Basic)-7.4ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area17.07 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity68.91 m³·mol⁻¹ChemAxon
Polarizability26.88 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+154.74131661259
DarkChem[M-H]-152.75931661259
DeepCCS[M+H]+160.26930932474
DeepCCS[M-H]-157.91130932474
DeepCCS[M-2H]-190.87130932474
DeepCCS[M+Na]+166.36230932474
AllCCS[M+H]+151.632859911
AllCCS[M+H-H2O]+147.732859911
AllCCS[M+NH4]+155.332859911
AllCCS[M+Na]+156.332859911
AllCCS[M-H]-158.532859911
AllCCS[M+Na-2H]-159.132859911
AllCCS[M+HCOO]-159.932859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
1,3,5-Bisabolatrien-10-oneCC(C)C(=O)CCC(C)C1=CC=C(C)C=C12209.6Standard polar33892256
1,3,5-Bisabolatrien-10-oneCC(C)C(=O)CCC(C)C1=CC=C(C)C=C11619.2Standard non polar33892256
1,3,5-Bisabolatrien-10-oneCC(C)C(=O)CCC(C)C1=CC=C(C)C=C11615.7Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
1,3,5-Bisabolatrien-10-one,1TMS,isomer #1CC(C)=C(CCC(C)C1=CC=C(C)C=C1)O[Si](C)(C)C1807.1Semi standard non polar33892256
1,3,5-Bisabolatrien-10-one,1TMS,isomer #1CC(C)=C(CCC(C)C1=CC=C(C)C=C1)O[Si](C)(C)C1751.7Standard non polar33892256
1,3,5-Bisabolatrien-10-one,1TMS,isomer #2CC1=CC=C(C(C)CC=C(O[Si](C)(C)C)C(C)C)C=C11771.5Semi standard non polar33892256
1,3,5-Bisabolatrien-10-one,1TMS,isomer #2CC1=CC=C(C(C)CC=C(O[Si](C)(C)C)C(C)C)C=C11711.8Standard non polar33892256
1,3,5-Bisabolatrien-10-one,1TBDMS,isomer #1CC(C)=C(CCC(C)C1=CC=C(C)C=C1)O[Si](C)(C)C(C)(C)C2044.7Semi standard non polar33892256
1,3,5-Bisabolatrien-10-one,1TBDMS,isomer #1CC(C)=C(CCC(C)C1=CC=C(C)C=C1)O[Si](C)(C)C(C)(C)C1973.6Standard non polar33892256
1,3,5-Bisabolatrien-10-one,1TBDMS,isomer #2CC1=CC=C(C(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)C)C=C12017.8Semi standard non polar33892256
1,3,5-Bisabolatrien-10-one,1TBDMS,isomer #2CC1=CC=C(C(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)C)C=C11941.0Standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 1,3,5-Bisabolatrien-10-one GC-MS (Non-derivatized) - 70eV, Positivesplash10-014i-5910000000-64781d54b4e730072aab2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 1,3,5-Bisabolatrien-10-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 - 1,3,5-Bisabolatrien-10-one 10V, Negative-QTOFsplash10-014i-0090000000-c6c3be47d293ce1775ef2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,3,5-Bisabolatrien-10-one 20V, Negative-QTOFsplash10-014i-4490000000-fafca550bac7c06dc9212016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,3,5-Bisabolatrien-10-one 40V, Negative-QTOFsplash10-0159-9300000000-254031561aea1dfcb9972016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,3,5-Bisabolatrien-10-one 10V, Negative-QTOFsplash10-014i-0090000000-868e2fb00a2cfbf6c5292021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,3,5-Bisabolatrien-10-one 20V, Negative-QTOFsplash10-014i-5970000000-131bc9ebab8fee25ffdd2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,3,5-Bisabolatrien-10-one 40V, Negative-QTOFsplash10-0006-9400000000-37eb02bc350c51e358b52021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,3,5-Bisabolatrien-10-one 10V, Positive-QTOFsplash10-014i-2290000000-87abcaa639ed319ce8a82016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,3,5-Bisabolatrien-10-one 20V, Positive-QTOFsplash10-00di-9420000000-d412a22c9e130240d6462016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,3,5-Bisabolatrien-10-one 40V, Positive-QTOFsplash10-0603-9300000000-de11eca0d28dc5e9af442016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,3,5-Bisabolatrien-10-one 10V, Positive-QTOFsplash10-00kf-9850000000-44d7089607008d85cac42021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,3,5-Bisabolatrien-10-one 20V, Positive-QTOFsplash10-0006-9300000000-48fb5462fb8672513a3c2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,3,5-Bisabolatrien-10-one 40V, Positive-QTOFsplash10-00kf-9600000000-a5675307e3515aa0f7e22021-09-23Wishart 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 IDFDB014955
KNApSAcK IDC00011627
Chemspider ID35014096
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound71360448
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.