Metabolite Carveol

Name
Carveol
Description
Not Available
Structure
Synonyms
Not Available
UNII
1L9KXT85R9
CAS number
Not Available
Weight
Average: 152.237
Monoisotopic: 152.120115135
Chemical Formula
C10H16O
InChI Key
BAVONGHXFVOKBV-UHFFFAOYSA-N
InChI
InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3
IUPAC Name
2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-ol
SMILES
[H]C([H])=C(C([H])([H])[H])C1([H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])(O)C1([H])[H]
Reactions
Spectra
SpectrumSpectrum TypeSplash Key
Predicted GC-MS Spectrum - GC-MSPredicted GC-MSsplash10-0gc9-9200000000-d270baae0672bddf4630
GC-MS Spectrum - EI-BGC-MSsplash10-001i-9300000000-c0df06475a23b1847e64
GC-MS Spectrum - EI-BGC-MSsplash10-0a5c-9400000000-20e9d5aa724b146ecbe0
Mass Spectrum (Electron Ionization)MSsplash10-00kf-9600000000-b8936fad384c0f501d3a
Predicted MS/MS Spectrum - 10V, Positive (Annotated)Predicted LC-MS/MSsplash10-0006-9500000000-ec2eb3b5a4967383ca68
Predicted MS/MS Spectrum - 10V, Negative (Annotated)Predicted LC-MS/MSsplash10-0udi-0900000000-b535426807c4f97438d3
Predicted MS/MS Spectrum - 20V, Negative (Annotated)Predicted LC-MS/MSsplash10-0f89-0900000000-077e4939e1980ef8b014
Predicted MS/MS Spectrum - 20V, Positive (Annotated)Predicted LC-MS/MSsplash10-0006-9100000000-e8cdd3b4e0e477a07595
Predicted MS/MS Spectrum - 40V, Negative (Annotated)Predicted LC-MS/MSsplash10-0159-8900000000-f14a712ef9a048f65154
Predicted MS/MS Spectrum - 40V, Positive (Annotated)Predicted LC-MS/MSsplash10-0006-9000000000-44d5523c60ee0f896de3
Chromatographic Properties
Collision Cross Sections (CCS)
AdductCCS Value (Å2)Source typeSource
[M-H]-136.5099868
predicted
DarkChem Lite v0.1.0
[M-H]-135.77342
predicted
DeepCCS 1.0 (2019)
[M+H]+136.4997868
predicted
DarkChem Lite v0.1.0
[M+H]+138.32417
predicted
DeepCCS 1.0 (2019)
[M+Na]+136.6295868
predicted
DarkChem Lite v0.1.0
[M+Na]+147.34383
predicted
DeepCCS 1.0 (2019)
Human Metabolome Database
HMDB0036083
ChemSpider
7160
ChEBI
23046
ChEMBL
CHEMBL1385229
Wikipedia
Carveol
Predicted Properties
PropertyValueSource
Water Solubility2.82 mg/mLALOGPS
logP2.41ALOGPS
logP1.99Chemaxon
logS-1.7ALOGPS
pKa (Strongest Acidic)18.21Chemaxon
pKa (Strongest Basic)-1.4Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count1Chemaxon
Hydrogen Donor Count1Chemaxon
Polar Surface Area20.23 Å2Chemaxon
Rotatable Bond Count1Chemaxon
Refractivity48 m3·mol-1Chemaxon
Polarizability18.34 Å3Chemaxon
Number of Rings1Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleYesChemaxon
MDDR-like RuleNoChemaxon