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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 17:39:11 UTC
Update Date2022-03-07 02:52:42 UTC
HMDB IDHMDB0030812
Secondary Accession Numbers
  • HMDB30812
Metabolite Identification
Common NameAcerosin
DescriptionAcerosin belongs to the class of organic compounds known as 8-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone. Thus, acerosin is considered to be a flavonoid. Acerosin is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Based on a literature review very few articles have been published on Acerosin.
Structure
Data?1563862041
Synonyms
ValueSource
5,7,3'-Trihydroxy-6,8,4'-trimethoxyflavoneChEBI
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-6,8-dimethoxy-4H-1-benzopyran-4-oneHMDB
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-6,8-dimethoxy-4H-1-benzopyran-4-one, 9ciHMDB
Chemical FormulaC18H16O8
Average Molecular Weight360.3148
Monoisotopic Molecular Weight360.084517488
IUPAC Name5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-6,8-dimethoxy-4H-chromen-4-one
Traditional Nameacerosin
CAS Registry Number15835-74-2
SMILES
COC1=C(O)C=C(C=C1)C1=CC(=O)C2=C(O)C(OC)=C(O)C(OC)=C2O1
InChI Identifier
InChI=1S/C18H16O8/c1-23-11-5-4-8(6-9(11)19)12-7-10(20)13-14(21)17(24-2)15(22)18(25-3)16(13)26-12/h4-7,19,21-22H,1-3H3
InChI KeyBTMNGQCCCWTUQH-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as 8-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassO-methylated flavonoids
Direct Parent8-O-methylated flavonoids
Alternative Parents
Substituents
  • 4p-methoxyflavonoid-skeleton
  • 6-methoxyflavonoid-skeleton
  • 8-methoxyflavonoid-skeleton
  • 3'-hydroxyflavonoid
  • 5-hydroxyflavonoid
  • 7-hydroxyflavonoid
  • Flavone
  • Hydroxyflavonoid
  • Chromone
  • Benzopyran
  • Methoxyphenol
  • 1-benzopyran
  • Phenoxy compound
  • Anisole
  • Methoxybenzene
  • Phenol ether
  • Pyranone
  • Phenol
  • Alkyl aryl ether
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Benzenoid
  • Pyran
  • Monocyclic benzene moiety
  • Vinylogous acid
  • Heteroaromatic compound
  • Organoheterocyclic compound
  • Oxacycle
  • Ether
  • Organic oxygen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organooxygen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
RoleNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point239 - 241 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility56.1 mg/L @ 25 °C (est)The Good Scents Company Information System
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.075 g/LALOGPS
logP2.72ALOGPS
logP2.23ChemAxon
logS-3.7ALOGPS
pKa (Strongest Acidic)6.63ChemAxon
pKa (Strongest Basic)-4.2ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count8ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area114.68 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity92.3 m³·mol⁻¹ChemAxon
Polarizability35.49 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+183.30231661259
DarkChem[M-H]-186.86931661259
DeepCCS[M+H]+180.03230932474
DeepCCS[M-H]-177.67430932474
DeepCCS[M-2H]-211.75830932474
DeepCCS[M+Na]+186.98630932474
AllCCS[M+H]+183.332859911
AllCCS[M+H-H2O]+180.132859911
AllCCS[M+NH4]+186.232859911
AllCCS[M+Na]+187.132859911
AllCCS[M-H]-184.432859911
AllCCS[M+Na-2H]-184.232859911
AllCCS[M+HCOO]-184.132859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
AcerosinCOC1=C(O)C=C(C=C1)C1=CC(=O)C2=C(O)C(OC)=C(O)C(OC)=C2O15409.9Standard polar33892256
AcerosinCOC1=C(O)C=C(C=C1)C1=CC(=O)C2=C(O)C(OC)=C(O)C(OC)=C2O13370.5Standard non polar33892256
AcerosinCOC1=C(O)C=C(C=C1)C1=CC(=O)C2=C(O)C(OC)=C(O)C(OC)=C2O13392.3Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Acerosin,1TMS,isomer #1COC1=CC=C(C2=CC(=O)C3=C(O)C(OC)=C(O)C(OC)=C3O2)C=C1O[Si](C)(C)C3423.0Semi standard non polar33892256
Acerosin,1TMS,isomer #2COC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC)=C(O)C(OC)=C3O2)C=C1O3407.7Semi standard non polar33892256
Acerosin,1TMS,isomer #3COC1=CC=C(C2=CC(=O)C3=C(O)C(OC)=C(O[Si](C)(C)C)C(OC)=C3O2)C=C1O3412.0Semi standard non polar33892256
Acerosin,2TMS,isomer #1COC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC)=C(O)C(OC)=C3O2)C=C1O[Si](C)(C)C3303.8Semi standard non polar33892256
Acerosin,2TMS,isomer #2COC1=CC=C(C2=CC(=O)C3=C(O)C(OC)=C(O[Si](C)(C)C)C(OC)=C3O2)C=C1O[Si](C)(C)C3291.5Semi standard non polar33892256
Acerosin,2TMS,isomer #3COC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC)=C(O[Si](C)(C)C)C(OC)=C3O2)C=C1O3335.7Semi standard non polar33892256
Acerosin,3TMS,isomer #1COC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC)=C(O[Si](C)(C)C)C(OC)=C3O2)C=C1O[Si](C)(C)C3226.0Semi standard non polar33892256
Acerosin,1TBDMS,isomer #1COC1=CC=C(C2=CC(=O)C3=C(O)C(OC)=C(O)C(OC)=C3O2)C=C1O[Si](C)(C)C(C)(C)C3632.6Semi standard non polar33892256
Acerosin,1TBDMS,isomer #2COC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC)=C(O)C(OC)=C3O2)C=C1O3633.3Semi standard non polar33892256
Acerosin,1TBDMS,isomer #3COC1=CC=C(C2=CC(=O)C3=C(O)C(OC)=C(O[Si](C)(C)C(C)(C)C)C(OC)=C3O2)C=C1O3629.9Semi standard non polar33892256
Acerosin,2TBDMS,isomer #1COC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC)=C(O)C(OC)=C3O2)C=C1O[Si](C)(C)C(C)(C)C3772.8Semi standard non polar33892256
Acerosin,2TBDMS,isomer #2COC1=CC=C(C2=CC(=O)C3=C(O)C(OC)=C(O[Si](C)(C)C(C)(C)C)C(OC)=C3O2)C=C1O[Si](C)(C)C(C)(C)C3750.1Semi standard non polar33892256
Acerosin,2TBDMS,isomer #3COC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC)=C(O[Si](C)(C)C(C)(C)C)C(OC)=C3O2)C=C1O3783.1Semi standard non polar33892256
Acerosin,3TBDMS,isomer #1COC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC)=C(O[Si](C)(C)C(C)(C)C)C(OC)=C3O2)C=C1O[Si](C)(C)C(C)(C)C3877.3Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Acerosin GC-MS (Non-derivatized) - 70eV, Positivesplash10-000w-0319000000-8ee1f78603a1d7ea06442017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Acerosin GC-MS (3 TMS) - 70eV, Positivesplash10-03di-1021190000-da86b7c39113f92c753d2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Acerosin 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 - Acerosin 10V, Positive-QTOFsplash10-03di-0009000000-5637e7acf708407798812016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Acerosin 20V, Positive-QTOFsplash10-03di-0009000000-4edc9c652e08904376c92016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Acerosin 40V, Positive-QTOFsplash10-00xr-3798000000-86dbbc7c8a028d3662fd2016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Acerosin 10V, Negative-QTOFsplash10-0a4i-0009000000-6b97991c47f6da239b8e2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Acerosin 20V, Negative-QTOFsplash10-0a4l-0009000000-0039e6cb00709a0dbd6f2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Acerosin 40V, Negative-QTOFsplash10-0229-0196000000-26348a4cb07389fa55d72016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Acerosin 10V, Positive-QTOFsplash10-03di-0009000000-1c8c4a2b4efd0f2d032d2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Acerosin 20V, Positive-QTOFsplash10-03di-0009000000-6ab3e7c3a52a09d619e22021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Acerosin 40V, Positive-QTOFsplash10-014i-0029000000-4a97d1d60e54a2ccd3b22021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Acerosin 10V, Negative-QTOFsplash10-0a4i-0009000000-d442391e53f6220e2ea32021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Acerosin 20V, Negative-QTOFsplash10-0006-0009000000-ada8326de9b6bd844b522021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Acerosin 40V, Negative-QTOFsplash10-0a4i-0249000000-cdb3ef43e4889c84e4512021-09-24Wishart 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 IDFDB002768
KNApSAcK IDC00003930
Chemspider ID154695
KEGG Compound IDC09982
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound177696
PDB IDNot Available
ChEBI ID2382
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1822971
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.. .