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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 20:15:21 UTC
Update Date2022-03-07 02:54:27 UTC
HMDB IDHMDB0035297
Secondary Accession Numbers
  • HMDB35297
Metabolite Identification
Common NameHeliocide H1
DescriptionHeliocide H1 belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group. Heliocide H1 has been detected, but not quantified in, cottonseeds (Gossypium) and fats and oils. This could make heliocide H1 a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Heliocide H1.
Structure
Data?1563862696
SynonymsNot Available
Chemical FormulaC25H30O5
Average Molecular Weight410.5027
Monoisotopic Molecular Weight410.20932407
IUPAC Name2,3-dihydroxy-7,10a-dimethyl-8-(3-methylbut-2-en-1-yl)-9,10-dioxo-4-(propan-2-yl)-5,8,8a,9,10,10a-hexahydroanthracene-1-carbaldehyde
Traditional Name2,3-dihydroxy-4-isopropyl-7,10a-dimethyl-8-(3-methylbut-2-en-1-yl)-9,10-dioxo-8,8a-dihydro-5H-anthracene-1-carbaldehyde
CAS Registry Number65024-84-2
SMILES
CC(C)C1=C2C(=O)C3(C)CC=C(C)C(CC=C(C)C)C3C(=O)C2=C(C=O)C(O)=C1O
InChI Identifier
InChI=1S/C25H30O5/c1-12(2)7-8-15-14(5)9-10-25(6)20(15)22(28)18-16(11-26)21(27)23(29)17(13(3)4)19(18)24(25)30/h7,9,11,13,15,20,27,29H,8,10H2,1-6H3
InChI KeyFMJIKKXSIVRJGO-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group.
KingdomOrganic compounds
Super ClassBenzenoids
ClassAnthracenes
Sub ClassAnthraquinones
Direct ParentHydroxyanthraquinones
Alternative Parents
Substituents
  • Hydroxyanthraquinone
  • Cadinane sesquiterpenoid
  • Sesquiterpenoid
  • Tetralin
  • Quinone
  • Aryl alkyl ketone
  • Aryl ketone
  • Aryl-aldehyde
  • Vinylogous acid
  • Ketone
  • Hydrocarbon derivative
  • Organic oxide
  • Organooxygen compound
  • Organic oxygen compound
  • Aldehyde
  • Aromatic homopolycyclic compound
Molecular FrameworkAromatic homopolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateNot Available
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 Solubility0.015 g/LALOGPS
logP4.22ALOGPS
logP5.59ChemAxon
logS-4.4ALOGPS
pKa (Strongest Acidic)6.6ChemAxon
pKa (Strongest Basic)-7.1ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area91.67 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity120.05 m³·mol⁻¹ChemAxon
Polarizability45.54 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+194.13531661259
DarkChem[M-H]-187.91331661259
DeepCCS[M+H]+204.95330932474
DeepCCS[M-H]-202.59530932474
DeepCCS[M-2H]-236.21630932474
DeepCCS[M+Na]+211.61530932474
AllCCS[M+H]+198.932859911
AllCCS[M+H-H2O]+196.432859911
AllCCS[M+NH4]+201.132859911
AllCCS[M+Na]+201.832859911
AllCCS[M-H]-207.932859911
AllCCS[M+Na-2H]-208.532859911
AllCCS[M+HCOO]-209.332859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Heliocide H1CC(C)C1=C2C(=O)C3(C)CC=C(C)C(CC=C(C)C)C3C(=O)C2=C(C=O)C(O)=C1O4090.8Standard polar33892256
Heliocide H1CC(C)C1=C2C(=O)C3(C)CC=C(C)C(CC=C(C)C)C3C(=O)C2=C(C=O)C(O)=C1O3083.1Standard non polar33892256
Heliocide H1CC(C)C1=C2C(=O)C3(C)CC=C(C)C(CC=C(C)C)C3C(=O)C2=C(C=O)C(O)=C1O3084.8Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Heliocide H1,1TMS,isomer #1CC(C)=CCC1C(C)=CCC2(C)C(=O)C3=C(C(=O)C12)C(C=O)=C(O[Si](C)(C)C)C(O)=C3C(C)C3214.6Semi standard non polar33892256
Heliocide H1,1TMS,isomer #2CC(C)=CCC1C(C)=CCC2(C)C(=O)C3=C(C(=O)C12)C(C=O)=C(O)C(O[Si](C)(C)C)=C3C(C)C3169.4Semi standard non polar33892256
Heliocide H1,2TMS,isomer #1CC(C)=CCC1C(C)=CCC2(C)C(=O)C3=C(C(=O)C12)C(C=O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C(C)C3166.0Semi standard non polar33892256
Heliocide H1,1TBDMS,isomer #1CC(C)=CCC1C(C)=CCC2(C)C(=O)C3=C(C(=O)C12)C(C=O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3C(C)C3430.6Semi standard non polar33892256
Heliocide H1,1TBDMS,isomer #2CC(C)=CCC1C(C)=CCC2(C)C(=O)C3=C(C(=O)C12)C(C=O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C3C(C)C3374.9Semi standard non polar33892256
Heliocide H1,2TBDMS,isomer #1CC(C)=CCC1C(C)=CCC2(C)C(=O)C3=C(C(=O)C12)C(C=O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3C(C)C3577.1Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Heliocide H1 GC-MS (Non-derivatized) - 70eV, Positivesplash10-0002-3129000000-59406d8c730ce869282a2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Heliocide H1 GC-MS (2 TMS) - 70eV, Positivesplash10-000l-4010290000-cc444f43e68ce441181d2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Heliocide H1 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 - Heliocide H1 10V, Positive-QTOFsplash10-03di-0109700000-f71c274f83aeb917f2672016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Heliocide H1 20V, Positive-QTOFsplash10-0a4i-1397100000-9ca47bd72905a523f5692016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Heliocide H1 40V, Positive-QTOFsplash10-0ue9-9405000000-d50eff1015ce118f9b702016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Heliocide H1 10V, Negative-QTOFsplash10-0a4i-0001900000-5e6b98ad30a9308646ed2016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Heliocide H1 20V, Negative-QTOFsplash10-0a4i-0115900000-c0eecaf14420d8152d9b2016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Heliocide H1 40V, Negative-QTOFsplash10-052f-7259000000-6ae49763cbf1eeee55b42016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Heliocide H1 10V, Positive-QTOFsplash10-08fr-0009800000-e83a4cb3a00e691404752021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Heliocide H1 20V, Positive-QTOFsplash10-02tc-0129200000-2f84e86246616c62895d2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Heliocide H1 40V, Positive-QTOFsplash10-0knc-7659000000-0b98c33674337f2336072021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Heliocide H1 10V, Negative-QTOFsplash10-0a4i-0000900000-db39b11405f8785914dc2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Heliocide H1 20V, Negative-QTOFsplash10-0a4i-0005900000-c33194a6832bfbd0f81e2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Heliocide H1 40V, Negative-QTOFsplash10-0a6r-2029200000-e505756f52ff51c0a57c2021-09-24Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • 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 IDFDB013964
KNApSAcK IDC00000499
Chemspider ID35013896
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound25201307
PDB IDNot Available
ChEBI ID176025
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. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .