Record Information
Version1.0
Creation date2010-04-08 22:12:04 UTC
Update date2019-11-26 03:12:16 UTC
Primary IDFDB015819
Secondary Accession NumbersNot Available
Chemical Information
FooDB NameLepidiumterpenyl ester
DescriptionLepidiumterpenyl ester 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 Lepidiumterpenyl ester.
CAS Number255833-57-9
Structure
Thumb
Synonyms
Predicted Properties
PropertyValueSource
Water Solubility0.00028 g/LALOGPS
logP6.54ALOGPS
logP7.22ChemAxon
logS-6.1ALOGPS
pKa (Strongest Acidic)5.04ChemAxon
pKa (Strongest Basic)-7.1ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area63.6 ŲChemAxon
Rotatable Bond Count19ChemAxon
Refractivity111.11 m³·mol⁻¹ChemAxon
Polarizability47.51 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Chemical FormulaC23H42O4
IUPAC name13-(hept-6-en-1-yloxy)-4,8,12-trimethyl-13-oxotridecanoic acid
InChI IdentifierInChI=1S/C23H42O4/c1-5-6-7-8-9-18-27-23(26)21(4)15-11-14-19(2)12-10-13-20(3)16-17-22(24)25/h5,19-21H,1,6-18H2,2-4H3,(H,24,25)
InChI KeyPASMASQJCDKBJK-UHFFFAOYSA-N
Isomeric SMILESCC(CCCC(C)CCC(O)=O)CCCC(C)C(=O)OCCCCCC=C
Average Molecular Weight382.5772
Monoisotopic Molecular Weight382.308309832
Classification
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
  • Farsesane sesquiterpenoid
  • Long-chain fatty acid
  • Branched fatty acid
  • Fatty acid ester
  • Methyl-branched fatty acid
  • Dicarboxylic acid or derivatives
  • Fatty acyl
  • Carboxylic acid ester
  • Carboxylic acid
  • Carboxylic acid derivative
  • Organic oxide
  • Organooxygen compound
  • Organic oxygen compound
  • Hydrocarbon derivative
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Disposition

Route of exposure:

Biological location:

Source:

Process

Naturally occurring process:

Role

Industrial application:

Biological role:

Physico-Chemical Properties
Physico-Chemical Properties - Experimental
Spectra
Spectra
EI-MS/GC-MS
TypeDescriptionSplash KeyView
Predicted GC-MSLepidiumterpenyl ester, non-derivatized, Predicted GC-MS Spectrum - 70eV, Positivesplash10-00kg-9561000000-0b9dde46d6105301237dSpectrum
Predicted GC-MSLepidiumterpenyl ester, 1 TMS, Predicted GC-MS Spectrum - 70eV, Positivesplash10-03ki-9147100000-0a987d0d3158fac0d8ceSpectrum
Predicted GC-MSLepidiumterpenyl ester, non-derivatized, Predicted GC-MS Spectrum - 70eV, PositiveNot AvailableSpectrum
MS/MS
TypeDescriptionSplash KeyView
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-00ls-2139000000-9b83c36fff7be9284dcf2016-08-02View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-9342000000-d62a90b24e59cdfb88e72016-08-02View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0002-9810000000-b93305ecdbde69a9b6e62016-08-02View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-001i-1039000000-25c1329ae676d9858c7a2016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-000i-2092000000-2b7edad5e2c50231e6052016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0a4u-9180000000-f9fa5edeabee00fd74ff2016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-001r-0019000000-c59e4bf7fa3241cfe4a42021-09-24View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-052r-7469000000-b421ef5448a50d24f4052021-09-24View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-07br-2390000000-cedd9adc623e03224c772021-09-24View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-00kk-9071000000-41959250badaf42560f12021-09-24View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-07bs-5290000000-bad466fae8bdb4785d9e2021-09-24View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0002-9200000000-29c0380869f95304ad0b2021-09-24View Spectrum
NMRNot Available
ChemSpider ID9968992
ChEMBL IDNot Available
KEGG Compound IDNot Available
Pubchem Compound ID11794320
Pubchem Substance IDNot Available
ChEBI IDNot Available
Phenol-Explorer IDNot Available
DrugBank IDNot Available
HMDB IDHMDB36865
CRC / DFC (Dictionary of Food Compounds) IDKJG57-O:KJO99-Q
EAFUS IDNot Available
Dr. Duke IDNot Available
BIGG IDNot Available
KNApSAcK IDNot Available
HET IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
Flavornet IDNot Available
GoodScent IDNot Available
SuperScent IDNot Available
Wikipedia IDNot Available
Phenol-Explorer Metabolite IDNot Available
Duplicate IDSNot Available
Old DFC IDSNot Available
Associated Foods
FoodContent Range AverageReference
No data available in table
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Biological Effects and Interactions
Health Effects / BioactivitiesNot Available
EnzymesNot Available
PathwaysNot Available
MetabolismNot Available
BiosynthesisNot Available
Organoleptic Properties
FlavoursNot Available
Files
MSDSNot Available
References
Synthesis ReferenceNot Available
General ReferenceNot Available
Content Reference