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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 20:48:21 UTC
Update Date2022-03-07 02:54:37 UTC
HMDB IDHMDB0035783
Secondary Accession Numbers
  • HMDB35783
Metabolite Identification
Common Name(+)-Menthone
Description(+)-Menthone, also known as (1S,4R)-menthone, belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. Based on a literature review a small amount of articles have been published on (+)-Menthone.
Structure
Data?1563862771
Synonyms
ValueSource
(1S,4R)-MenthoneChEBI
(1S,4R)-p-Menthan-3-oneChEBI
(2R,5S)-2-Isopropyl-5-methylcyclohexanoneChEBI
(+)-(1S,4R)-MenthoneHMDB
(2R,5S)-5-Methyl-2-(propan-2-yl)cyclohexanoneHMDB
MenthoneMeSH, HMDB
(+)-MenthoneHMDB
(2R,5S)-5-Methyl-2-(1-methylethyl)cyclohexanoneHMDB
D-MenthoneHMDB
Chemical FormulaC10H18O
Average Molecular Weight154.2493
Monoisotopic Molecular Weight154.135765198
IUPAC Name(2R,5S)-5-methyl-2-(propan-2-yl)cyclohexan-1-one
Traditional Name(+)-menthone
CAS Registry Number3391-87-5
SMILES
CC(C)[C@H]1CC[C@H](C)CC1=O
InChI Identifier
InChI=1S/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-9H,4-6H2,1-3H3/t8-,9+/m0/s1
InChI KeyNFLGAXVYCFJBMK-DTWKUNHWSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassMonoterpenoids
Direct ParentMenthane monoterpenoids
Alternative Parents
Substituents
  • P-menthane monoterpenoid
  • Monocyclic monoterpenoid
  • Cyclic ketone
  • Ketone
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic homomonocyclic compound
Molecular FrameworkAliphatic homomonocyclic compounds
External Descriptors
Ontology
Physiological effect
Disposition
Process
Role
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling Point208.00 to 210.00 °C. @ 760.00 mm HgThe Good Scents Company Information System
Water Solubility180.5 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP2.625 (est)The Good Scents Company Information System
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.26 g/LALOGPS
logP3.05ChemAxon
pKa (Strongest Basic)-7.4ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area17.07 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity46.52 m³·mol⁻¹ChemAxon
Polarizability18.94 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+137.2331661259
DarkChem[M-H]-132.32831661259
DeepCCS[M+H]+136.50330932474
DeepCCS[M-H]-133.2130932474
DeepCCS[M-2H]-170.24430932474
DeepCCS[M+Na]+145.78330932474
AllCCS[M+H]+133.532859911
AllCCS[M+H-H2O]+129.132859911
AllCCS[M+NH4]+137.632859911
AllCCS[M+Na]+138.832859911
AllCCS[M-H]-140.032859911
AllCCS[M+Na-2H]-141.632859911
AllCCS[M+HCOO]-143.532859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(+)-MenthoneCC(C)[C@H]1CC[C@H](C)CC1=O1485.7Standard polar33892256
(+)-MenthoneCC(C)[C@H]1CC[C@H](C)CC1=O1142.9Standard non polar33892256
(+)-MenthoneCC(C)[C@H]1CC[C@H](C)CC1=O1146.9Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
(+)-Menthone,1TMS,isomer #1CC(C)C1=C(O[Si](C)(C)C)C[C@@H](C)CC11342.3Semi standard non polar33892256
(+)-Menthone,1TMS,isomer #1CC(C)C1=C(O[Si](C)(C)C)C[C@@H](C)CC11360.6Standard non polar33892256
(+)-Menthone,1TMS,isomer #2CC(C)[C@H]1CC[C@H](C)C=C1O[Si](C)(C)C1290.0Semi standard non polar33892256
(+)-Menthone,1TMS,isomer #2CC(C)[C@H]1CC[C@H](C)C=C1O[Si](C)(C)C1346.5Standard non polar33892256
(+)-Menthone,1TBDMS,isomer #1CC(C)C1=C(O[Si](C)(C)C(C)(C)C)C[C@@H](C)CC11565.8Semi standard non polar33892256
(+)-Menthone,1TBDMS,isomer #1CC(C)C1=C(O[Si](C)(C)C(C)(C)C)C[C@@H](C)CC11544.0Standard non polar33892256
(+)-Menthone,1TBDMS,isomer #2CC(C)[C@H]1CC[C@H](C)C=C1O[Si](C)(C)C(C)(C)C1493.2Semi standard non polar33892256
(+)-Menthone,1TBDMS,isomer #2CC(C)[C@H]1CC[C@H](C)C=C1O[Si](C)(C)C(C)(C)C1503.7Standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Menthone GC-MS (Non-derivatized) - 70eV, Positivesplash10-06r7-9300000000-1d150f2cf0a23dbfef0b2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Menthone 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 - (+)-Menthone 10V, Positive-QTOFsplash10-0a4i-0900000000-fa99f8c083212e4f2fc32016-08-02Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Menthone 20V, Positive-QTOFsplash10-0bt9-9800000000-7bf975ea31bcef83aa612016-08-02Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Menthone 40V, Positive-QTOFsplash10-0aor-9000000000-3f8923896797c44866932016-08-02Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Menthone 10V, Negative-QTOFsplash10-0udi-0900000000-d55afdef2faae68197a62016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Menthone 20V, Negative-QTOFsplash10-0udi-0900000000-91ec697d11dad181a3422016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Menthone 40V, Negative-QTOFsplash10-01oy-9600000000-7933610ac6051fc8ef812016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Menthone 10V, Negative-QTOFsplash10-0udi-0900000000-d2363ae8d4dbdcccda802021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Menthone 20V, Negative-QTOFsplash10-0udi-0900000000-084e13e285859f435a612021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Menthone 40V, Negative-QTOFsplash10-0gbc-9700000000-57929498deae48afce7a2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Menthone 10V, Positive-QTOFsplash10-0bti-3900000000-5b9ac9ca9aaff729e2d12021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Menthone 20V, Positive-QTOFsplash10-0532-9200000000-ac0243da1ad4aa3d859e2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Menthone 40V, Positive-QTOFsplash10-0006-9000000000-d3a7bbb5abb9a0381a392021-09-22Wishart 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 IDFDB014530
KNApSAcK IDC00010903
Chemspider ID391431
KEGG Compound IDC11390
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound443159
PDB IDNot Available
ChEBI ID31
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1450831
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.