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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 22:02:37 UTC
Update Date2022-03-07 02:55:05 UTC
HMDB IDHMDB0036863
Secondary Accession Numbers
  • HMDB36863
Metabolite Identification
Common NameAnhydrocinnzeylanol
DescriptionAnhydrocinnzeylanol belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. Anhydrocinnzeylanol is an extremely weak basic (essentially neutral) compound (based on its pKa).
Structure
Data?1563862940
SynonymsNot Available
Chemical FormulaC20H30O6
Average Molecular Weight366.4486
Monoisotopic Molecular Weight366.204238692
IUPAC Name2,6,8,12-tetrahydroxy-3,7,11-trimethyl-4-(propan-2-yl)-13-oxatetracyclo[5.5.3.0¹,⁸.0²,⁶]pentadec-3-en-14-one
Traditional Name2,6,8,12-tetrahydroxy-4-isopropyl-3,7,11-trimethyl-13-oxatetracyclo[5.5.3.0¹,⁸.0²,⁶]pentadec-3-en-14-one
CAS Registry Number65230-04-8
SMILES
CC(C)C1=C(C)C2(O)C(O)(C1)C1(C)CC(=O)OC22C(O)C(C)CCC12O
InChI Identifier
InChI=1S/C20H30O6/c1-10(2)13-8-18(24)16(5)9-14(21)26-20(19(18,25)12(13)4)15(22)11(3)6-7-17(16,20)23/h10-11,15,22-25H,6-9H2,1-5H3
InChI KeyJFDHTDLZWVKRQT-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassTerpene lactones
Direct ParentTerpene lactones
Alternative Parents
Substituents
  • Terpene lactone
  • Sesquiterpenoid
  • Caprolactone
  • Delta valerolactone
  • Delta_valerolactone
  • Oxepane
  • Oxane
  • Cyclic alcohol
  • Tertiary alcohol
  • Lactone
  • Carboxylic acid ester
  • Secondary alcohol
  • Polyol
  • Organoheterocyclic compound
  • Oxacycle
  • Monocarboxylic acid or derivatives
  • Carboxylic acid derivative
  • Organooxygen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Alcohol
  • Carbonyl group
  • Organic oxygen compound
  • Aliphatic heteropolycyclic compound
Molecular FrameworkAliphatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
RoleNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point205 - 207 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility5.37 g/LALOGPS
logP0.86ALOGPS
logP0.44ChemAxon
logS-1.8ALOGPS
pKa (Strongest Acidic)11.89ChemAxon
pKa (Strongest Basic)-3.4ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area107.22 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity93.2 m³·mol⁻¹ChemAxon
Polarizability38.55 ųChemAxon
Number of Rings4ChemAxon
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]+182.32131661259
DarkChem[M-H]-178.17431661259
DeepCCS[M-2H]-222.90130932474
DeepCCS[M+Na]+198.41330932474
AllCCS[M+H]+184.432859911
AllCCS[M+H-H2O]+181.832859911
AllCCS[M+NH4]+186.932859911
AllCCS[M+Na]+187.632859911
AllCCS[M-H]-192.632859911
AllCCS[M+Na-2H]-193.032859911
AllCCS[M+HCOO]-193.632859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
AnhydrocinnzeylanolCC(C)C1=C(C)C2(O)C(O)(C1)C1(C)CC(=O)OC22C(O)C(C)CCC12O4199.7Standard polar33892256
AnhydrocinnzeylanolCC(C)C1=C(C)C2(O)C(O)(C1)C1(C)CC(=O)OC22C(O)C(C)CCC12O2623.3Standard non polar33892256
AnhydrocinnzeylanolCC(C)C1=C(C)C2(O)C(O)(C1)C1(C)CC(=O)OC22C(O)C(C)CCC12O2776.7Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Anhydrocinnzeylanol,1TMS,isomer #1CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O)C(C)CCC34O)C12O[Si](C)(C)C2852.2Semi standard non polar33892256
Anhydrocinnzeylanol,1TMS,isomer #2CC1=C(C(C)C)CC2(O[Si](C)(C)C)C3(C)CC(=O)OC4(C(O)C(C)CCC34O)C12O2863.2Semi standard non polar33892256
Anhydrocinnzeylanol,1TMS,isomer #3CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O[Si](C)(C)C)C(C)CCC34O)C12O2852.7Semi standard non polar33892256
Anhydrocinnzeylanol,1TMS,isomer #4CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O)C(C)CCC34O[Si](C)(C)C)C12O2849.8Semi standard non polar33892256
Anhydrocinnzeylanol,2TMS,isomer #1CC1=C(C(C)C)CC2(O[Si](C)(C)C)C3(C)CC(=O)OC4(C(O)C(C)CCC34O)C12O[Si](C)(C)C2855.9Semi standard non polar33892256
Anhydrocinnzeylanol,2TMS,isomer #2CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O[Si](C)(C)C)C(C)CCC34O)C12O[Si](C)(C)C2850.3Semi standard non polar33892256
Anhydrocinnzeylanol,2TMS,isomer #3CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O)C(C)CCC34O[Si](C)(C)C)C12O[Si](C)(C)C2853.9Semi standard non polar33892256
Anhydrocinnzeylanol,2TMS,isomer #4CC1=C(C(C)C)CC2(O[Si](C)(C)C)C3(C)CC(=O)OC4(C(O[Si](C)(C)C)C(C)CCC34O)C12O2848.2Semi standard non polar33892256
Anhydrocinnzeylanol,2TMS,isomer #5CC1=C(C(C)C)CC2(O[Si](C)(C)C)C3(C)CC(=O)OC4(C(O)C(C)CCC34O[Si](C)(C)C)C12O2852.6Semi standard non polar33892256
Anhydrocinnzeylanol,2TMS,isomer #6CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O[Si](C)(C)C)C(C)CCC34O[Si](C)(C)C)C12O2840.1Semi standard non polar33892256
Anhydrocinnzeylanol,3TMS,isomer #1CC1=C(C(C)C)CC2(O[Si](C)(C)C)C3(C)CC(=O)OC4(C(O[Si](C)(C)C)C(C)CCC34O)C12O[Si](C)(C)C2860.5Semi standard non polar33892256
Anhydrocinnzeylanol,3TMS,isomer #2CC1=C(C(C)C)CC2(O[Si](C)(C)C)C3(C)CC(=O)OC4(C(O)C(C)CCC34O[Si](C)(C)C)C12O[Si](C)(C)C2861.8Semi standard non polar33892256
Anhydrocinnzeylanol,3TMS,isomer #3CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O[Si](C)(C)C)C(C)CCC34O[Si](C)(C)C)C12O[Si](C)(C)C2845.1Semi standard non polar33892256
Anhydrocinnzeylanol,3TMS,isomer #4CC1=C(C(C)C)CC2(O[Si](C)(C)C)C3(C)CC(=O)OC4(C(O[Si](C)(C)C)C(C)CCC34O[Si](C)(C)C)C12O2844.2Semi standard non polar33892256
Anhydrocinnzeylanol,4TMS,isomer #1CC1=C(C(C)C)CC2(O[Si](C)(C)C)C3(C)CC(=O)OC4(C(O[Si](C)(C)C)C(C)CCC34O[Si](C)(C)C)C12O[Si](C)(C)C2872.8Semi standard non polar33892256
Anhydrocinnzeylanol,1TBDMS,isomer #1CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O)C(C)CCC34O)C12O[Si](C)(C)C(C)(C)C3113.7Semi standard non polar33892256
Anhydrocinnzeylanol,1TBDMS,isomer #2CC1=C(C(C)C)CC2(O[Si](C)(C)C(C)(C)C)C3(C)CC(=O)OC4(C(O)C(C)CCC34O)C12O3116.8Semi standard non polar33892256
Anhydrocinnzeylanol,1TBDMS,isomer #3CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O[Si](C)(C)C(C)(C)C)C(C)CCC34O)C12O3099.2Semi standard non polar33892256
Anhydrocinnzeylanol,1TBDMS,isomer #4CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O)C(C)CCC34O[Si](C)(C)C(C)(C)C)C12O3105.4Semi standard non polar33892256
Anhydrocinnzeylanol,2TBDMS,isomer #1CC1=C(C(C)C)CC2(O[Si](C)(C)C(C)(C)C)C3(C)CC(=O)OC4(C(O)C(C)CCC34O)C12O[Si](C)(C)C(C)(C)C3319.8Semi standard non polar33892256
Anhydrocinnzeylanol,2TBDMS,isomer #2CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O[Si](C)(C)C(C)(C)C)C(C)CCC34O)C12O[Si](C)(C)C(C)(C)C3325.6Semi standard non polar33892256
Anhydrocinnzeylanol,2TBDMS,isomer #3CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O)C(C)CCC34O[Si](C)(C)C(C)(C)C)C12O[Si](C)(C)C(C)(C)C3321.3Semi standard non polar33892256
Anhydrocinnzeylanol,2TBDMS,isomer #4CC1=C(C(C)C)CC2(O[Si](C)(C)C(C)(C)C)C3(C)CC(=O)OC4(C(O[Si](C)(C)C(C)(C)C)C(C)CCC34O)C12O3332.8Semi standard non polar33892256
Anhydrocinnzeylanol,2TBDMS,isomer #5CC1=C(C(C)C)CC2(O[Si](C)(C)C(C)(C)C)C3(C)CC(=O)OC4(C(O)C(C)CCC34O[Si](C)(C)C(C)(C)C)C12O3321.6Semi standard non polar33892256
Anhydrocinnzeylanol,2TBDMS,isomer #6CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O[Si](C)(C)C(C)(C)C)C(C)CCC34O[Si](C)(C)C(C)(C)C)C12O3330.4Semi standard non polar33892256
Anhydrocinnzeylanol,3TBDMS,isomer #1CC1=C(C(C)C)CC2(O[Si](C)(C)C(C)(C)C)C3(C)CC(=O)OC4(C(O[Si](C)(C)C(C)(C)C)C(C)CCC34O)C12O[Si](C)(C)C(C)(C)C3540.0Semi standard non polar33892256
Anhydrocinnzeylanol,3TBDMS,isomer #2CC1=C(C(C)C)CC2(O[Si](C)(C)C(C)(C)C)C3(C)CC(=O)OC4(C(O)C(C)CCC34O[Si](C)(C)C(C)(C)C)C12O[Si](C)(C)C(C)(C)C3526.0Semi standard non polar33892256
Anhydrocinnzeylanol,3TBDMS,isomer #3CC1=C(C(C)C)CC2(O)C3(C)CC(=O)OC4(C(O[Si](C)(C)C(C)(C)C)C(C)CCC34O[Si](C)(C)C(C)(C)C)C12O[Si](C)(C)C(C)(C)C3532.9Semi standard non polar33892256
Anhydrocinnzeylanol,3TBDMS,isomer #4CC1=C(C(C)C)CC2(O[Si](C)(C)C(C)(C)C)C3(C)CC(=O)OC4(C(O[Si](C)(C)C(C)(C)C)C(C)CCC34O[Si](C)(C)C(C)(C)C)C12O3536.3Semi standard non polar33892256
Anhydrocinnzeylanol,4TBDMS,isomer #1CC1=C(C(C)C)CC2(O[Si](C)(C)C(C)(C)C)C3(C)CC(=O)OC4(C(O[Si](C)(C)C(C)(C)C)C(C)CCC34O[Si](C)(C)C(C)(C)C)C12O[Si](C)(C)C(C)(C)C3744.1Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Anhydrocinnzeylanol GC-MS (Non-derivatized) - 70eV, Positivesplash10-0udi-3901000000-6d66a5bb2b2288b457852017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Anhydrocinnzeylanol GC-MS (4 TMS) - 70eV, Positivesplash10-0574-9131026000-aab7ef03c6546d5925bb2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Anhydrocinnzeylanol 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 - Anhydrocinnzeylanol 10V, Positive-QTOFsplash10-014i-0009000000-fc63b92b6ca0e17f5f172015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Anhydrocinnzeylanol 20V, Positive-QTOFsplash10-014j-9016000000-a6175ca9b4d88e9542762015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Anhydrocinnzeylanol 40V, Positive-QTOFsplash10-1003-9000000000-9841360efab974ec05692015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Anhydrocinnzeylanol 10V, Negative-QTOFsplash10-014i-0009000000-7ce58161a87c450d8d912015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Anhydrocinnzeylanol 20V, Negative-QTOFsplash10-01ba-2009000000-3b6904ba9bbfcfec6db12015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Anhydrocinnzeylanol 40V, Negative-QTOFsplash10-052f-9302000000-72e75e256ed4f01abc0a2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Anhydrocinnzeylanol 10V, Positive-QTOFsplash10-014i-0009000000-edc663139e42443c63702021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Anhydrocinnzeylanol 20V, Positive-QTOFsplash10-014i-0029000000-7bd36de55235b4d135022021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Anhydrocinnzeylanol 40V, Positive-QTOFsplash10-0006-9112000000-b7edb82dc386144c70b72021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Anhydrocinnzeylanol 10V, Negative-QTOFsplash10-014i-0009000000-b429e707756684188b3f2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Anhydrocinnzeylanol 20V, Negative-QTOFsplash10-014i-0009000000-b429e707756684188b3f2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Anhydrocinnzeylanol 40V, Negative-QTOFsplash10-0zfr-2911000000-9eba85cded9a2be25d512021-09-23Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • 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 IDFDB015817
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound73099741
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.