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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 22:34:50 UTC
Update Date2022-03-07 02:55:17 UTC
HMDB IDHMDB0037343
Secondary Accession Numbers
  • HMDB37343
Metabolite Identification
Common Name2'',3''-Diacetylcosmosiin
Description2'',3''-Diacetylcosmosiin belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. 2'',3''-Diacetylcosmosiin has been detected, but not quantified in, german camomiles (Matricaria recutita) and herbs and spices. This could make 2'',3''-diacetylcosmosiin a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 2'',3''-Diacetylcosmosiin.
Structure
Data?1563863014
Synonyms
ValueSource
Apigenin 7-(2'',3''-diacetylglucoside)HMDB
4-(Acetyloxy)-5-hydroxy-2-{[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl]oxy}-6-(hydroxymethyl)oxan-3-yl acetic acidGenerator
Chemical FormulaC25H24O12
Average Molecular Weight516.4509
Monoisotopic Molecular Weight516.126776232
IUPAC Name4-(acetyloxy)-5-hydroxy-2-{[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl]oxy}-6-(hydroxymethyl)oxan-3-yl acetate
Traditional Name4-(acetyloxy)-5-hydroxy-2-{[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy}-6-(hydroxymethyl)oxan-3-yl acetate
CAS Registry Number84323-20-6
SMILES
CC(=O)OC1C(O)C(CO)OC(OC2=CC(O)=C3C(=O)C=C(OC3=C2)C2=CC=C(O)C=C2)C1OC(C)=O
InChI Identifier
InChI=1S/C25H24O12/c1-11(27)33-23-22(32)20(10-26)37-25(24(23)34-12(2)28)35-15-7-16(30)21-17(31)9-18(36-19(21)8-15)13-3-5-14(29)6-4-13/h3-9,20,22-26,29-30,32H,10H2,1-2H3
InChI KeyRLRNEHZJFFGOEN-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavonoid glycosides
Direct ParentFlavonoid-7-O-glycosides
Alternative Parents
Substituents
  • Flavonoid-7-o-glycoside
  • 4'-hydroxyflavonoid
  • 5-hydroxyflavonoid
  • Hydroxyflavonoid
  • Flavone
  • Phenolic glycoside
  • Hexose monosaccharide
  • O-glycosyl compound
  • Chromone
  • Glycosyl compound
  • Benzopyran
  • 1-benzopyran
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Phenol
  • Pyranone
  • Pyran
  • Benzenoid
  • Oxane
  • Dicarboxylic acid or derivatives
  • Monocyclic benzene moiety
  • Monosaccharide
  • Heteroaromatic compound
  • Vinylogous acid
  • Secondary alcohol
  • Carboxylic acid ester
  • Organoheterocyclic compound
  • Oxacycle
  • Carboxylic acid derivative
  • Acetal
  • Organic oxide
  • Carbonyl group
  • Organic oxygen compound
  • Hydrocarbon derivative
  • Alcohol
  • Primary alcohol
  • Organooxygen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic 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 Solubility25.51 mg/L @ 25 °C (est)The Good Scents Company Information System
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.34 g/LALOGPS
logP2.03ALOGPS
logP1.32ChemAxon
logS-3.2ALOGPS
pKa (Strongest Acidic)8.31ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count10ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area178.28 ŲChemAxon
Rotatable Bond Count8ChemAxon
Refractivity123.36 m³·mol⁻¹ChemAxon
Polarizability50.56 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+214.82830932474
DeepCCS[M-H]-212.43230932474
DeepCCS[M-2H]-245.36130932474
DeepCCS[M+Na]+220.7430932474
AllCCS[M+H]+217.532859911
AllCCS[M+H-H2O]+215.632859911
AllCCS[M+NH4]+219.332859911
AllCCS[M+Na]+219.832859911
AllCCS[M-H]-215.532859911
AllCCS[M+Na-2H]-216.632859911
AllCCS[M+HCOO]-218.032859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
2'',3''-DiacetylcosmosiinCC(=O)OC1C(O)C(CO)OC(OC2=CC(O)=C3C(=O)C=C(OC3=C2)C2=CC=C(O)C=C2)C1OC(C)=O5669.6Standard polar33892256
2'',3''-DiacetylcosmosiinCC(=O)OC1C(O)C(CO)OC(OC2=CC(O)=C3C(=O)C=C(OC3=C2)C2=CC=C(O)C=C2)C1OC(C)=O4081.8Standard non polar33892256
2'',3''-DiacetylcosmosiinCC(=O)OC1C(O)C(CO)OC(OC2=CC(O)=C3C(=O)C=C(OC3=C2)C2=CC=C(O)C=C2)C1OC(C)=O4660.7Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
2'',3''-Diacetylcosmosiin,1TMS,isomer #1CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO)C(O[Si](C)(C)C)C1OC(C)=O4322.8Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,1TMS,isomer #2CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO[Si](C)(C)C)C(O)C1OC(C)=O4361.3Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,1TMS,isomer #3CC(=O)OC1C(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO)C(O)C1OC(C)=O4311.3Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,1TMS,isomer #4CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)OC(CO)C(O)C1OC(C)=O4347.3Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,2TMS,isomer #1CC(=O)OC1C(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO)C(O[Si](C)(C)C)C1OC(C)=O4194.3Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,2TMS,isomer #2CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)OC(CO)C(O[Si](C)(C)C)C1OC(C)=O4240.6Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,2TMS,isomer #3CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1OC(C)=O4305.9Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,2TMS,isomer #4CC(=O)OC1C(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO[Si](C)(C)C)C(O)C1OC(C)=O4234.0Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,2TMS,isomer #5CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)OC(CO[Si](C)(C)C)C(O)C1OC(C)=O4275.6Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,2TMS,isomer #6CC(=O)OC1C(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)OC(CO)C(O)C1OC(C)=O4263.1Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,3TMS,isomer #1CC(=O)OC1C(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)OC(CO)C(O[Si](C)(C)C)C1OC(C)=O4186.5Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,3TMS,isomer #2CC(=O)OC1C(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1OC(C)=O4212.6Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,3TMS,isomer #3CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1OC(C)=O4258.7Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,3TMS,isomer #4CC(=O)OC1C(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)OC(CO[Si](C)(C)C)C(O)C1OC(C)=O4224.0Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,4TMS,isomer #1CC(=O)OC1C(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1OC(C)=O4192.4Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,1TBDMS,isomer #1CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1OC(C)=O4570.3Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,1TBDMS,isomer #2CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO[Si](C)(C)C(C)(C)C)C(O)C1OC(C)=O4586.4Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,1TBDMS,isomer #3CC(=O)OC1C(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO)C(O)C1OC(C)=O4539.2Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,1TBDMS,isomer #4CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)OC(CO)C(O)C1OC(C)=O4577.5Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,2TBDMS,isomer #1CC(=O)OC1C(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1OC(C)=O4672.2Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,2TBDMS,isomer #2CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1OC(C)=O4705.1Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,2TBDMS,isomer #3CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1OC(C)=O4742.3Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,2TBDMS,isomer #4CC(=O)OC1C(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO[Si](C)(C)C(C)(C)C)C(O)C1OC(C)=O4688.2Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,2TBDMS,isomer #5CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)OC(CO[Si](C)(C)C(C)(C)C)C(O)C1OC(C)=O4727.7Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,2TBDMS,isomer #6CC(=O)OC1C(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)OC(CO)C(O)C1OC(C)=O4730.6Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,3TBDMS,isomer #1CC(=O)OC1C(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1OC(C)=O4873.8Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,3TBDMS,isomer #2CC(=O)OC1C(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C=C4)OC3=C2)OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1OC(C)=O4864.1Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,3TBDMS,isomer #3CC(=O)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1OC(C)=O4901.4Semi standard non polar33892256
2'',3''-Diacetylcosmosiin,3TBDMS,isomer #4CC(=O)OC1C(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)OC(CO[Si](C)(C)C(C)(C)C)C(O)C1OC(C)=O4887.7Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 2'',3''-Diacetylcosmosiin GC-MS (Non-derivatized) - 70eV, Positivesplash10-0a4i-8342900000-0b342c793bd34ee248a92017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2'',3''-Diacetylcosmosiin GC-MS (2 TMS) - 70eV, Positivesplash10-0ufr-6115009000-514fb5a80076bc3ba5872017-10-06Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2'',3''-Diacetylcosmosiin 10V, Positive-QTOFsplash10-00di-0080920000-aee332486bb24caf3a752016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2'',3''-Diacetylcosmosiin 20V, Positive-QTOFsplash10-00di-0090200000-45845cfc93422ea7ec082016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2'',3''-Diacetylcosmosiin 40V, Positive-QTOFsplash10-00dl-1290100000-633bf3727e1e1a3d87652016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2'',3''-Diacetylcosmosiin 10V, Negative-QTOFsplash10-066r-2050940000-084246e4ab7de874ae6a2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2'',3''-Diacetylcosmosiin 20V, Negative-QTOFsplash10-066r-4091400000-2899d6d51f9a47941afe2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2'',3''-Diacetylcosmosiin 40V, Negative-QTOFsplash10-0aor-9280000000-8c8da13c46752d1fa9672016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2'',3''-Diacetylcosmosiin 10V, Negative-QTOFsplash10-014i-0000090000-6d72e46d8ac367983cc22021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2'',3''-Diacetylcosmosiin 20V, Negative-QTOFsplash10-014i-0000090000-414379605b357dcc91fb2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2'',3''-Diacetylcosmosiin 40V, Negative-QTOFsplash10-0a4j-0905120000-a3c0aefc25c5bd4300532021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2'',3''-Diacetylcosmosiin 10V, Positive-QTOFsplash10-014i-0000090000-d915fe26ac26372406d22021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2'',3''-Diacetylcosmosiin 20V, Positive-QTOFsplash10-014i-0000090000-d915fe26ac26372406d22021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2'',3''-Diacetylcosmosiin 40V, Positive-QTOFsplash10-014j-0709170000-b1f29e36cd8630fea2422021-09-23Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
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 IDFDB016365
KNApSAcK IDC00004188
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound73829950
PDB IDNot Available
ChEBI ID176206
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1860011
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.. .

Enzymes

General function:
Lipid transport and metabolism
Specific function:
Involved in the detoxification of xenobiotics and in the activation of ester and amide prodrugs. Hydrolyzes aromatic and aliphatic esters, but has no catalytic activity toward amides or a fatty acyl-CoA ester. Hydrolyzes the methyl ester group of cocaine to form benzoylecgonine. Catalyzes the transesterification of cocaine to form cocaethylene. Displays fatty acid ethyl ester synthase activity, catalyzing the ethyl esterification of oleic acid to ethyloleate.
Gene Name:
CES1
Uniprot ID:
P23141
Molecular weight:
62520.62
Reactions
2'',3''-Diacetylcosmosiin → Apigenin 7-O-(2''-O-acetylglucoside)details