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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2005-11-16 15:48:42 UTC
Update Date2023-02-21 17:15:17 UTC
HMDB IDHMDB0000909
Secondary Accession Numbers
  • HMDB00909
Metabolite Identification
Common Nametrans-4-Hydroxycyclohexylacetic acid
Descriptiontrans-4-Hydroxycyclohexylacetic acid, also known as 4-hydroxycyclohexyl acetate, belongs to the class of organic compounds known as cyclohexanols. Cyclohexanols are compounds containing an alcohol group attached to a cyclohexane ring. trans-4-Hydroxycyclohexylacetic acid has been detected, but not quantified in, a few different foods, such as anatidaes (Anatidae), chickens (Gallus gallus), and domestic pigs (Sus scrofa domestica). This could make trans-4-hydroxycyclohexylacetic acid a potential biomarker for the consumption of these foods. trans-4-Hydroxycyclohexylacetic acid, with regard to humans, has been linked to the inborn metabolic disorder hawkinsinuria. Based on a literature review a small amount of articles have been published on trans-4-Hydroxycyclohexylacetic acid.
Structure
Data?1676999717
Synonyms
ValueSource
trans-4-HydroxycyclohexylacetateGenerator
4-Hydroxy-cyclohexyl acetic acid esterHMDB
4-Hydroxycyclohexyl acetateHMDB
2-[(1R,4R)-4-Hydroxycyclohexyl]acetateHMDB
Chemical FormulaC8H14O3
Average Molecular Weight158.195
Monoisotopic Molecular Weight158.094294314
IUPAC Name2-[(1r,4r)-4-hydroxycyclohexyl]acetic acid
Traditional Name[(1r,4r)-4-hydroxycyclohexyl]acetic acid
CAS Registry Number68592-23-4
SMILES
O[C@H]1CC[C@H](CC(O)=O)CC1
InChI Identifier
InChI=1S/C8H14O3/c9-7-3-1-6(2-4-7)5-8(10)11/h6-7,9H,1-5H2,(H,10,11)/t6-,7-
InChI KeyALTAAUJNHYWOGS-LJGSYFOKSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as cyclohexanols. Cyclohexanols are compounds containing an alcohol group attached to a cyclohexane ring.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassAlcohols and polyols
Direct ParentCyclohexanols
Alternative Parents
Substituents
  • Cyclohexanol
  • Cyclic alcohol
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Organic oxide
  • Hydrocarbon derivative
  • Carbonyl group
  • Aliphatic homomonocyclic compound
Molecular FrameworkAliphatic homomonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
RoleNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility27.1 g/LALOGPS
logP0.93ALOGPS
logP0.69ChemAxon
logS-0.77ALOGPS
pKa (Strongest Acidic)4.65ChemAxon
pKa (Strongest Basic)-1.5ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area57.53 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity40.09 m³·mol⁻¹ChemAxon
Polarizability16.85 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+135.37831661259
DarkChem[M-H]-129.52231661259
AllCCS[M+H]+136.35632859911
AllCCS[M-H]-135.72732859911
DeepCCS[M+H]+134.90830932474
DeepCCS[M-H]-132.51230932474
DeepCCS[M-2H]-167.81430932474
DeepCCS[M+Na]+142.27330932474
AllCCS[M+H]+136.432859911
AllCCS[M+H-H2O]+132.132859911
AllCCS[M+NH4]+140.332859911
AllCCS[M+Na]+141.532859911
AllCCS[M-H]-135.732859911
AllCCS[M+Na-2H]-137.232859911
AllCCS[M+HCOO]-138.932859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
trans-4-Hydroxycyclohexylacetic acidO[C@H]1CC[C@H](CC(O)=O)CC12625.2Standard polar33892256
trans-4-Hydroxycyclohexylacetic acidO[C@H]1CC[C@H](CC(O)=O)CC11420.4Standard non polar33892256
trans-4-Hydroxycyclohexylacetic acidO[C@H]1CC[C@H](CC(O)=O)CC11473.0Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
trans-4-Hydroxycyclohexylacetic acid,1TMS,isomer #1C[Si](C)(C)O[C@H]1CC[C@H](CC(=O)O)CC11514.7Semi standard non polar33892256
trans-4-Hydroxycyclohexylacetic acid,1TMS,isomer #2C[Si](C)(C)OC(=O)C[C@H]1CC[C@H](O)CC11521.4Semi standard non polar33892256
trans-4-Hydroxycyclohexylacetic acid,2TMS,isomer #1C[Si](C)(C)OC(=O)C[C@H]1CC[C@H](O[Si](C)(C)C)CC11576.7Semi standard non polar33892256
trans-4-Hydroxycyclohexylacetic acid,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)O[C@H]1CC[C@H](CC(=O)O)CC11785.8Semi standard non polar33892256
trans-4-Hydroxycyclohexylacetic acid,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)C[C@H]1CC[C@H](O)CC11766.1Semi standard non polar33892256
trans-4-Hydroxycyclohexylacetic acid,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)C[C@H]1CC[C@H](O[Si](C)(C)C(C)(C)C)CC12045.8Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - trans-4-Hydroxycyclohexylacetic acid GC-MS (Non-derivatized) - 70eV, Positivesplash10-0005-9400000000-abc03a0f8f17c7d423a22017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - trans-4-Hydroxycyclohexylacetic acid GC-MS (2 TMS) - 70eV, Positivesplash10-00g0-6950000000-e954349d2bba3a1f7bda2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - trans-4-Hydroxycyclohexylacetic acid GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - trans-4-Hydroxycyclohexylacetic acid GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - trans-4-Hydroxycyclohexylacetic acid GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - trans-4-Hydroxycyclohexylacetic acid GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - trans-4-Hydroxycyclohexylacetic acid GC-MS (TBDMS_1_1) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - trans-4-Hydroxycyclohexylacetic acid GC-MS (TBDMS_1_2) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - trans-4-Hydroxycyclohexylacetic acid GC-MS (TBDMS_2_1) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - trans-4-Hydroxycyclohexylacetic acid 10V, Positive-QTOFsplash10-052f-2900000000-cdb682550fd7986a0a1c2016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - trans-4-Hydroxycyclohexylacetic acid 20V, Positive-QTOFsplash10-01ot-9800000000-a24c028ad8e3ba7b50492016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - trans-4-Hydroxycyclohexylacetic acid 40V, Positive-QTOFsplash10-00o4-9000000000-3cefeadb5ca0dbfbb8e72016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - trans-4-Hydroxycyclohexylacetic acid 10V, Negative-QTOFsplash10-0a4i-1900000000-228641a4fa5e65521acf2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - trans-4-Hydroxycyclohexylacetic acid 20V, Negative-QTOFsplash10-0bt9-3900000000-2731aa44b1316101793f2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - trans-4-Hydroxycyclohexylacetic acid 40V, Negative-QTOFsplash10-0a4m-9300000000-382927881c2cd816ee472016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - trans-4-Hydroxycyclohexylacetic acid 10V, Positive-QTOFsplash10-0005-7900000000-8822dbd01cb75d38d0992021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - trans-4-Hydroxycyclohexylacetic acid 20V, Positive-QTOFsplash10-000w-9300000000-94fda51f4a569a75c11e2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - trans-4-Hydroxycyclohexylacetic acid 40V, Positive-QTOFsplash10-05po-9000000000-a9825eb303905399d98c2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - trans-4-Hydroxycyclohexylacetic acid 10V, Negative-QTOFsplash10-0a4i-0900000000-74b6873659b7a591064c2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - trans-4-Hydroxycyclohexylacetic acid 20V, Negative-QTOFsplash10-0a4i-3900000000-aec6e520c4013fbac56c2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - trans-4-Hydroxycyclohexylacetic acid 40V, Negative-QTOFsplash10-0006-9100000000-e2229c7ab1d4ae401bf22021-09-25Wishart LabView Spectrum

IR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-)2023-02-03FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)2023-02-03FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)2023-02-03FELIX labView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Blood
  • Feces
  • Urine
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodExpected but not QuantifiedNot QuantifiedNot AvailableNot Available
Normal
      Not Available
details
FecesDetected but not QuantifiedNot QuantifiedAdult (>18 years old)Both
Normal
details
FecesDetected but not QuantifiedNot QuantifiedNot SpecifiedNot Specified
Normal
details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
UrineDetected but not QuantifiedNot QuantifiedNot AvailableNot AvailableHawkinsinuria details
Associated Disorders and Diseases
Disease References
Hawkinsinuria
  1. Kumps A, Duez P, Mardens Y: Metabolic, nutritional, iatrogenic, and artifactual sources of urinary organic acids: a comprehensive table. Clin Chem. 2002 May;48(5):708-17. [PubMed:11978597 ]
Associated OMIM IDs
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB022313
KNApSAcK IDNot Available
Chemspider ID17216021
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN ID5865
PubChem CompoundNot Available
PDB IDNot Available
ChEBI ID88508
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceUngnade, Herbert E.; Morriss, Francis V. Hydrogenation of phenolic acids. Journal of the American Chemical Society (1948), 70 1898-9.
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Niederwieser A, Wadman SK, Danks DM: Excretion of cis- and trans-4-hydroxycyclohexylacetic acid in addition to hawkinsin in a family with a postulated defect of 4-hydroxyphenylpyruvate dioxygenase. Clin Chim Acta. 1978 Dec 1;90(2):195-200. [PubMed:719903 ]
  2. Hocart CH, Halpern B, Hick LA, Wong CO: Hawkinsinuria--identification of quinolacetic acid and pyroglutamic acid during an acidotic phase. J Chromatogr. 1983 Jul 8;275(2):237-43. [PubMed:6619234 ]
  3. Niederwieser A, Matasovic A, Neuheiser F, Wetzel E: New tyrosine metabolites in humans: hawkinsin and cis- and trans-4-hydroxycyclohexylacetic acids. Unusual adsorption of deuterated and non-deuterated hawkinsin during gas chromatography. J Chromatogr. 1978 Sep 1;146(2):207-12. [PubMed:701419 ]