Hmdb loader
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 21:44:51 UTC
Update Date2022-03-07 02:54:58 UTC
HMDB IDHMDB0036589
Secondary Accession Numbers
  • HMDB36589
Metabolite Identification
Common Name1,2-Dehydro-alpha-cyperone
Description1,2-Dehydro-alpha-cyperone belongs to the class of organic compounds known as eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids. These are sesquiterpenoids with a structure based on the eudesmane skeleton. Based on a literature review a small amount of articles have been published on 1,2-Dehydro-alpha-cyperone.
Structure
Data?1563862893
Synonyms
ValueSource
1,2-Dehydro-a-cyperoneGenerator
1,2-Dehydro-α-cyperoneGenerator
(+)-Eudesma-1,4,11-trien-3-oneHMDB
(4AS-cis)-5,6,7,8-tetrahydro-1,4a-dimethyl-7-(1-methylethenyl)-2(4ah)-naphthalenoneHMDB
1,4,11-Eudesmatrien-3-oneHMDB
1,4,11-Selinatrien-3-oneHMDB
Chemical FormulaC15H20O
Average Molecular Weight216.3187
Monoisotopic Molecular Weight216.151415262
IUPAC Name1,4a-dimethyl-7-(prop-1-en-2-yl)-2,4a,5,6,7,8-hexahydronaphthalen-2-one
Traditional Name1,4a-dimethyl-7-(prop-1-en-2-yl)-5,6,7,8-tetrahydronaphthalen-2-one
CAS Registry Number17081-85-5
SMILES
CC(=C)C1CCC2(C)C=CC(=O)C(C)=C2C1
InChI Identifier
InChI=1S/C15H20O/c1-10(2)12-5-7-15(4)8-6-14(16)11(3)13(15)9-12/h6,8,12H,1,5,7,9H2,2-4H3
InChI KeyYFZICPBAKZACEG-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids. These are sesquiterpenoids with a structure based on the eudesmane skeleton.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassSesquiterpenoids
Direct ParentEudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Alternative Parents
Substituents
  • Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoid
  • Cyclic ketone
  • Ketone
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic homopolycyclic compound
Molecular FrameworkAliphatic 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 Solubility2.88 mg/L @ 25 °C (est)The Good Scents Company Information System
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.054 g/LALOGPS
logP4.28ALOGPS
logP3.81ChemAxon
logS-3.6ALOGPS
pKa (Strongest Basic)-5ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area17.07 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity68.97 m³·mol⁻¹ChemAxon
Polarizability25.58 ųChemAxon
Number of Rings2ChemAxon
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]+151.39731661259
DarkChem[M-H]-148.32231661259
DeepCCS[M+H]+152.75130932474
DeepCCS[M-H]-150.39330932474
DeepCCS[M-2H]-183.72830932474
DeepCCS[M+Na]+158.84430932474
AllCCS[M+H]+149.132859911
AllCCS[M+H-H2O]+145.132859911
AllCCS[M+NH4]+152.832859911
AllCCS[M+Na]+153.832859911
AllCCS[M-H]-157.332859911
AllCCS[M+Na-2H]-157.632859911
AllCCS[M+HCOO]-158.032859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
1,2-Dehydro-alpha-cyperoneCC(=C)C1CCC2(C)C=CC(=O)C(C)=C2C12509.0Standard polar33892256
1,2-Dehydro-alpha-cyperoneCC(=C)C1CCC2(C)C=CC(=O)C(C)=C2C11742.1Standard non polar33892256
1,2-Dehydro-alpha-cyperoneCC(=C)C1CCC2(C)C=CC(=O)C(C)=C2C11787.6Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 1,2-Dehydro-alpha-cyperone GC-MS (Non-derivatized) - 70eV, Positivesplash10-0uel-1910000000-329add8ad291a6424dd52017-09-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 1,2-Dehydro-alpha-cyperone GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 1,2-Dehydro-alpha-cyperone 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 - 1,2-Dehydro-alpha-cyperone 10V, Positive-QTOFsplash10-014i-0690000000-ab6abafc77bbed80cc592016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,2-Dehydro-alpha-cyperone 20V, Positive-QTOFsplash10-014i-2930000000-614876051a26654914f02016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,2-Dehydro-alpha-cyperone 40V, Positive-QTOFsplash10-0udl-8900000000-3b3151768bb2a06efe3b2016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,2-Dehydro-alpha-cyperone 10V, Negative-QTOFsplash10-014i-0090000000-71005072ad6282db9d4f2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,2-Dehydro-alpha-cyperone 20V, Negative-QTOFsplash10-014i-0290000000-282e11f38d01fb072ee42016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,2-Dehydro-alpha-cyperone 40V, Negative-QTOFsplash10-0002-0900000000-9a8b066ef8d0f992ad982016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,2-Dehydro-alpha-cyperone 10V, Negative-QTOFsplash10-014i-0090000000-93c59166c81b3b7c46b82021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,2-Dehydro-alpha-cyperone 20V, Negative-QTOFsplash10-014i-0090000000-27395fa42ed8c0e0fb8f2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,2-Dehydro-alpha-cyperone 40V, Negative-QTOFsplash10-02aj-0920000000-838f1780ad56fd3839d42021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,2-Dehydro-alpha-cyperone 10V, Positive-QTOFsplash10-016r-0960000000-a61db63e8791e82da7762021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,2-Dehydro-alpha-cyperone 20V, Positive-QTOFsplash10-00s9-3900000000-f5d659b6059517dae8912021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1,2-Dehydro-alpha-cyperone 40V, Positive-QTOFsplash10-014i-9600000000-f9a769948974a26087192021-09-25Wishart 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 IDFDB015501
KNApSAcK IDC00012761
Chemspider ID35014166
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound13192441
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1855811
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.