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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2012-09-11 20:01:41 UTC
Update Date2021-10-13 06:45:46 UTC
HMDB IDHMDB0035084
Secondary Accession Numbers
  • HMDB35084
Metabolite Identification
Common Name(+)-1(10),4-Cadinadiene
Description(+)-1(10),4-Cadinadiene, also known as (1S,8ar)-delta-cadinene or delta-amorphene, belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Thus, (+)-1(10),4-cadinadiene is considered to be an isoprenoid. Based on a literature review a small amount of articles have been published on (+)-1(10),4-Cadinadiene.
Structure
Data?1563862663
Synonyms
ValueSource
(1S,8AR)-4,7-dimethyl-1-(propan-2-yl)-1,2,3,5,6,8a-hexahydronaphthaleneChEBI
(1S,8AR)-delta-cadineneChEBI
delta-AmorpheneChEBI
delta-CadineneChEBI
(+)-delta-CadineneKegg
(1S,8AR)-δ-cadineneGenerator
Δ-amorpheneGenerator
Δ-cadineneGenerator
(+)-Δ-cadineneGenerator
(+)-1S,8AR-cadina-1(10),4-dieneHMDB
(+)-D-CadineneHMDB
1,2,3,5,6,8a-hexahydro-4,7-Dimethyl-1-(1-methylethyl)-(1S,8ar)-naphthaleneHMDB
D-CadineneHMDB
Cadina-1(10),4-dienePhytoBank
(±)-delta-CadinenePhytoBank
(±)-δ-CadinenePhytoBank
DysoxylonenePhytoBank
DysoxylonenPhytoBank
delta-CardinenePhytoBank
δ-CardinenePhytoBank
Chemical FormulaC15H24
Average Molecular Weight204.357
Monoisotopic Molecular Weight204.187800773
IUPAC Name(1S,8aR)-4,7-dimethyl-1-(propan-2-yl)-1,2,3,5,6,8a-hexahydronaphthalene
Traditional Namedelta-cadinene
CAS Registry Number483-76-1
SMILES
[H][C@@]12C=C(C)CCC1=C(C)CC[C@H]2C(C)C
InChI Identifier
InChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h9-10,13,15H,5-8H2,1-4H3/t13-,15-/m0/s1
InChI KeyFUCYIEXQVQJBKY-ZFWWWQNUSA-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
  • Sesquiterpenoid
  • Cadinane sesquiterpenoid
  • Branched unsaturated hydrocarbon
  • Polycyclic hydrocarbon
  • Cyclic olefin
  • Unsaturated aliphatic hydrocarbon
  • Unsaturated hydrocarbon
  • Olefin
  • Hydrocarbon
  • Aliphatic homopolycyclic compound
Molecular FrameworkAliphatic homopolycyclic compounds
External Descriptors
Ontology
Disposition

Biological location

Source

Route of exposure

Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling Point120.00 to 121.00 °C. @ 9.00 mm HgThe Good Scents Company Information System
Water Solubility0.049 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP6.271 (est)The Good Scents Company Information System
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.042 g/LALOGPS
logP10(4.92) g/LALOGPS
logP10(4.4) g/LChemAxon
logS10(-3.7) g/LALOGPS
Physiological Charge0ChemAxon
Hydrogen Acceptor Count0ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area0 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity68.33 m³·mol⁻¹ChemAxon
Polarizability26.34 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]+150.16431661259
DarkChem[M-H]-146.91731661259

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(+)-1(10),4-Cadinadiene[H][C@@]12C=C(C)CCC1=C(C)CC[C@H]2C(C)C1711.5Standard polar33892256
(+)-1(10),4-Cadinadiene[H][C@@]12C=C(C)CCC1=C(C)CC[C@H]2C(C)C1499.7Standard non polar33892256
(+)-1(10),4-Cadinadiene[H][C@@]12C=C(C)CCC1=C(C)CC[C@H]2C(C)C1530.8Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental GC-MSGC-MS Spectrum - (+)-1(10),4-Cadinadiene EI-B (Non-derivatized)splash10-03e9-4910000000-d866d006ef5edc06b50d2017-09-12HMDB team, MONA, MassBankView Spectrum
Experimental GC-MSGC-MS Spectrum - (+)-1(10),4-Cadinadiene EI-B (Non-derivatized)splash10-03e9-4910000000-d866d006ef5edc06b50d2018-05-18HMDB team, MONA, MassBankView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-1(10),4-Cadinadiene GC-MS (Non-derivatized) - 70eV, Positivesplash10-01p2-2900000000-7e0e6d0a32506b6eb9332016-09-22Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-1(10),4-Cadinadiene 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(10),4-Cadinadiene 10V, Positive-QTOFsplash10-0a4i-0490000000-85ec97b8032d4370cfe02016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-1(10),4-Cadinadiene 20V, Positive-QTOFsplash10-0bta-2920000000-51a0b00ff6967440ef072016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-1(10),4-Cadinadiene 40V, Positive-QTOFsplash10-02bk-5900000000-d0bfeebca8e74869b58e2016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-1(10),4-Cadinadiene 10V, Negative-QTOFsplash10-0udi-0090000000-fe8dc7c5f863461e974f2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-1(10),4-Cadinadiene 20V, Negative-QTOFsplash10-0udi-0190000000-55a43b599b1e9bc5b16a2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-1(10),4-Cadinadiene 40V, Negative-QTOFsplash10-0h2s-0910000000-6ad78804a6c28a720abf2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-1(10),4-Cadinadiene 10V, Positive-QTOFsplash10-0a4i-0490000000-5d5cdcbbeb2b24c287012021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-1(10),4-Cadinadiene 20V, Positive-QTOFsplash10-0c01-3930000000-6aa320f1e378f197caf22021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-1(10),4-Cadinadiene 40V, Positive-QTOFsplash10-0006-9300000000-011ac33d2677c648ab892021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-1(10),4-Cadinadiene 10V, Negative-QTOFsplash10-0udi-0090000000-7ccf03fa1149a1e9f55f2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-1(10),4-Cadinadiene 20V, Negative-QTOFsplash10-0udi-0090000000-7ccf03fa1149a1e9f55f2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-1(10),4-Cadinadiene 40V, Negative-QTOFsplash10-0udi-0090000000-0b1ac00c3b3c6c0a73b92021-09-22Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen Locations
  • Saliva
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
SalivaDetected but not QuantifiedNot QuantifiedAdult (>18 years old)Not SpecifiedNormal details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB013710
KNApSAcK IDC00007636
Chemspider ID389830
KEGG Compound IDC06394
BioCyc IDCPD-1722
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound441005
PDB IDNot Available
ChEBI ID15385
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1054621
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.