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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2012-09-13 11:41:42 UTC
Update Date2022-09-22 18:34:27 UTC
HMDB IDHMDB0041832
Secondary Accession Numbers
  • HMDB41832
Metabolite Identification
Common NameBaicalin
DescriptionBaicalin is a flavone, a type of flavonoid. It is found in several species in the genus Scutellaria, including Scutellaria lateriflora (blue skullcap). There are 10 mg/g baicalin in Scutellaria galericulata (common skullcap) leaves. Baicalin is the glucuronide of baicalein. It is a component of Chinese medicinal herb Huang-chin (Scutellaria baicalensis) and one of the chemical ingredients of Sho-Saiko-To, an herbal supplement.
Structure
Data?1563863706
Synonyms
ValueSource
5,6,7-Trihydroxyflavone 7-O-beta-D-glucuronideHMDB
5,6-Dihydroxy-4-oxo-2-phenyl-4H-1-benzopyran-7-yl beta-D-glucopyranosiduronic acidHMDB
5,6-Dihydroxy-4-oxo-2-phenyl-4H-chromen-7-yl beta-D-glucopyranosiduronic acidHMDB
7-D-Glucuronic acid-5,6-dihydroxyflavoneHMDB
Baicalein 7-O-glucuronideHMDB
(2S,3S,4S,5R,6R)-6-[(5,6-Dihydroxy-4-oxo-2-phenyl-4H-chromen-7-yl)oxy]-3,4,5-trihydroxyoxane-2-carboxylateHMDB
Chemical FormulaC21H18O11
Average Molecular Weight446.361
Monoisotopic Molecular Weight446.084911418
IUPAC Name(2S,3S,4S,5R,6R)-6-[(5,6-dihydroxy-4-oxo-2-phenyl-4H-chromen-7-yl)oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid
Traditional Name(2S,3S,4S,5R,6R)-6-[(5,6-dihydroxy-4-oxo-2-phenylchromen-7-yl)oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid
CAS Registry Number21967-41-9
SMILES
O[C@@H]1[C@@H](O)[C@@H](OC2=C(O)C(O)=C3C(=O)C=C(OC3=C2)C2=CC=CC=C2)O[C@@H]([C@H]1O)C(O)=O
InChI Identifier
InChI=1S/C21H18O11/c22-9-6-10(8-4-2-1-3-5-8)30-11-7-12(14(23)15(24)13(9)11)31-21-18(27)16(25)17(26)19(32-21)20(28)29/h1-7,16-19,21,23-27H,(H,28,29)/t16-,17-,18+,19-,21-/m0/s1
InChI KeyIKIIZLYTISPENI-UNJWAJPSSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as flavonoid-7-o-glucuronides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to glucuronic acid at the C7-position.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavonoid glycosides
Direct ParentFlavonoid-7-O-glucuronides
Alternative Parents
Substituents
  • Flavonoid-7-o-glucuronide
  • Flavonoid-7-o-glycoside
  • 5-hydroxyflavonoid
  • 6-hydroxyflavonoid
  • Flavone
  • Hydroxyflavonoid
  • Phenolic glycoside
  • 1-o-glucuronide
  • O-glucuronide
  • Glucuronic acid or derivatives
  • Hexose monosaccharide
  • Chromone
  • Glycosyl compound
  • O-glycosyl compound
  • Benzopyran
  • 1-benzopyran
  • Beta-hydroxy acid
  • Pyranone
  • 1-hydroxy-4-unsubstituted benzenoid
  • Monocyclic benzene moiety
  • Benzenoid
  • Pyran
  • Hydroxy acid
  • Monosaccharide
  • Oxane
  • Heteroaromatic compound
  • Vinylogous acid
  • Secondary alcohol
  • Organoheterocyclic compound
  • Polyol
  • Acetal
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Oxacycle
  • Organooxygen compound
  • Carbonyl group
  • Hydrocarbon derivative
  • Organic oxide
  • Alcohol
  • Organic oxygen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Not AvailableNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point202 - 205 °CNot Available
Boiling Point836.62 °C. @ 760.00 mm Hg (est)The Good Scents Company Information System
Water Solubility907 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP1.431 (est)The Good Scents Company Information System
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility1.72 g/LALOGPS
logP1.27ALOGPS
logP0.76ChemAxon
logS-2.4ALOGPS
pKa (Strongest Acidic)2.62ChemAxon
pKa (Strongest Basic)-3.7ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count6ChemAxon
Polar Surface Area183.21 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity104.93 m³·mol⁻¹ChemAxon
Polarizability42.03 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityNoChemAxon
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]+204.1531661259
DarkChem[M-H]-197.2431661259
DeepCCS[M+H]+195.38630932474
DeepCCS[M-H]-193.08230932474
DeepCCS[M-2H]-226.32230932474
DeepCCS[M+Na]+201.29830932474
AllCCS[M+H]+201.832859911
AllCCS[M+H-H2O]+199.432859911
AllCCS[M+NH4]+204.132859911
AllCCS[M+Na]+204.732859911
AllCCS[M-H]-198.632859911
AllCCS[M+Na-2H]-198.832859911
AllCCS[M+HCOO]-199.232859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
BaicalinO[C@@H]1[C@@H](O)[C@@H](OC2=C(O)C(O)=C3C(=O)C=C(OC3=C2)C2=CC=CC=C2)O[C@@H]([C@H]1O)C(O)=O5226.0Standard polar33892256
BaicalinO[C@@H]1[C@@H](O)[C@@H](OC2=C(O)C(O)=C3C(=O)C=C(OC3=C2)C2=CC=CC=C2)O[C@@H]([C@H]1O)C(O)=O3898.6Standard non polar33892256
BaicalinO[C@@H]1[C@@H](O)[C@@H](OC2=C(O)C(O)=C3C(=O)C=C(OC3=C2)C2=CC=CC=C2)O[C@@H]([C@H]1O)C(O)=O4247.9Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Baicalin,1TMS,isomer #1C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@@H]1O3872.3Semi standard non polar33892256
Baicalin,1TMS,isomer #2C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](C(=O)O)O[C@@H]1OC1=CC2=C(C(O)=C1O)C(=O)C=C(C1=CC=CC=C1)O23897.2Semi standard non polar33892256
Baicalin,1TMS,isomer #3C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O3932.3Semi standard non polar33892256
Baicalin,1TMS,isomer #4C[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O23930.8Semi standard non polar33892256
Baicalin,1TMS,isomer #5C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@H]1O3908.4Semi standard non polar33892256
Baicalin,1TMS,isomer #6C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O3926.5Semi standard non polar33892256
Baicalin,2TMS,isomer #1C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@H]1O[Si](C)(C)C3810.4Semi standard non polar33892256
Baicalin,2TMS,isomer #10C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O3850.9Semi standard non polar33892256
Baicalin,2TMS,isomer #11C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O3830.6Semi standard non polar33892256
Baicalin,2TMS,isomer #12C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O[Si](C)(C)C3859.7Semi standard non polar33892256
Baicalin,2TMS,isomer #13C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O3867.1Semi standard non polar33892256
Baicalin,2TMS,isomer #14C[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O23836.8Semi standard non polar33892256
Baicalin,2TMS,isomer #15C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3859.0Semi standard non polar33892256
Baicalin,2TMS,isomer #2C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3803.1Semi standard non polar33892256
Baicalin,2TMS,isomer #3C[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O23799.2Semi standard non polar33892256
Baicalin,2TMS,isomer #4C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O3791.0Semi standard non polar33892256
Baicalin,2TMS,isomer #5C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@@H]1O[Si](C)(C)C3796.6Semi standard non polar33892256
Baicalin,2TMS,isomer #6C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@H]1O3810.3Semi standard non polar33892256
Baicalin,2TMS,isomer #7C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3830.2Semi standard non polar33892256
Baicalin,2TMS,isomer #8C[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O23818.0Semi standard non polar33892256
Baicalin,2TMS,isomer #9C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O3813.0Semi standard non polar33892256
Baicalin,3TMS,isomer #1C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3806.7Semi standard non polar33892256
Baicalin,3TMS,isomer #10C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O3757.6Semi standard non polar33892256
Baicalin,3TMS,isomer #11C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3825.9Semi standard non polar33892256
Baicalin,3TMS,isomer #12C[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O23791.8Semi standard non polar33892256
Baicalin,3TMS,isomer #13C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O3780.6Semi standard non polar33892256
Baicalin,3TMS,isomer #14C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3827.9Semi standard non polar33892256
Baicalin,3TMS,isomer #15C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3805.4Semi standard non polar33892256
Baicalin,3TMS,isomer #16C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O[Si](C)(C)C3802.7Semi standard non polar33892256
Baicalin,3TMS,isomer #17C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O3846.0Semi standard non polar33892256
Baicalin,3TMS,isomer #18C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3823.8Semi standard non polar33892256
Baicalin,3TMS,isomer #19C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O[Si](C)(C)C3820.3Semi standard non polar33892256
Baicalin,3TMS,isomer #2C[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O23783.9Semi standard non polar33892256
Baicalin,3TMS,isomer #20C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3850.3Semi standard non polar33892256
Baicalin,3TMS,isomer #3C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O3768.9Semi standard non polar33892256
Baicalin,3TMS,isomer #4C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](C(=O)O)O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@@H]1O[Si](C)(C)C3782.8Semi standard non polar33892256
Baicalin,3TMS,isomer #5C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3807.0Semi standard non polar33892256
Baicalin,3TMS,isomer #6C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3785.4Semi standard non polar33892256
Baicalin,3TMS,isomer #7C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3784.9Semi standard non polar33892256
Baicalin,3TMS,isomer #8C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O[Si](C)(C)C3789.3Semi standard non polar33892256
Baicalin,3TMS,isomer #9C[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O23776.0Semi standard non polar33892256
Baicalin,4TMS,isomer #1C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3827.5Semi standard non polar33892256
Baicalin,4TMS,isomer #10C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O[Si](C)(C)C3791.6Semi standard non polar33892256
Baicalin,4TMS,isomer #11C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3850.4Semi standard non polar33892256
Baicalin,4TMS,isomer #12C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3836.2Semi standard non polar33892256
Baicalin,4TMS,isomer #13C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O[Si](C)(C)C3808.5Semi standard non polar33892256
Baicalin,4TMS,isomer #14C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3837.4Semi standard non polar33892256
Baicalin,4TMS,isomer #15C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3853.8Semi standard non polar33892256
Baicalin,4TMS,isomer #2C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3799.9Semi standard non polar33892256
Baicalin,4TMS,isomer #3C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3825.2Semi standard non polar33892256
Baicalin,4TMS,isomer #4C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O[Si](C)(C)C3803.6Semi standard non polar33892256
Baicalin,4TMS,isomer #5C[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O23789.4Semi standard non polar33892256
Baicalin,4TMS,isomer #6C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O3773.7Semi standard non polar33892256
Baicalin,4TMS,isomer #7C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3808.2Semi standard non polar33892256
Baicalin,4TMS,isomer #8C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3809.6Semi standard non polar33892256
Baicalin,4TMS,isomer #9C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3786.5Semi standard non polar33892256
Baicalin,5TMS,isomer #1C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3807.7Semi standard non polar33892256
Baicalin,5TMS,isomer #2C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3833.6Semi standard non polar33892256
Baicalin,5TMS,isomer #3C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3828.0Semi standard non polar33892256
Baicalin,5TMS,isomer #4C[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O[Si](C)(C)C3803.1Semi standard non polar33892256
Baicalin,5TMS,isomer #5C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3803.6Semi standard non polar33892256
Baicalin,5TMS,isomer #6C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3839.0Semi standard non polar33892256
Baicalin,6TMS,isomer #1C[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3835.0Semi standard non polar33892256
Baicalin,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@@H]1O4117.6Semi standard non polar33892256
Baicalin,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](C(=O)O)O[C@@H]1OC1=CC2=C(C(O)=C1O)C(=O)C=C(C1=CC=CC=C1)O24146.5Semi standard non polar33892256
Baicalin,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O4167.1Semi standard non polar33892256
Baicalin,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O24190.3Semi standard non polar33892256
Baicalin,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@H]1O4136.4Semi standard non polar33892256
Baicalin,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O4191.8Semi standard non polar33892256
Baicalin,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4247.8Semi standard non polar33892256
Baicalin,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O[Si](C)(C)C(C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O4320.6Semi standard non polar33892256
Baicalin,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O4280.6Semi standard non polar33892256
Baicalin,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O[Si](C)(C)C(C)(C)C4311.0Semi standard non polar33892256
Baicalin,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C(C)(C)C)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O4349.0Semi standard non polar33892256
Baicalin,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O24304.7Semi standard non polar33892256
Baicalin,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4318.7Semi standard non polar33892256
Baicalin,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4283.3Semi standard non polar33892256
Baicalin,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O24286.0Semi standard non polar33892256
Baicalin,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O4268.0Semi standard non polar33892256
Baicalin,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@@H]1O[Si](C)(C)C(C)(C)C4238.1Semi standard non polar33892256
Baicalin,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4247.3Semi standard non polar33892256
Baicalin,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4309.1Semi standard non polar33892256
Baicalin,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O24300.6Semi standard non polar33892256
Baicalin,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O4280.0Semi standard non polar33892256
Baicalin,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C4439.3Semi standard non polar33892256
Baicalin,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O4437.8Semi standard non polar33892256
Baicalin,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4479.6Semi standard non polar33892256
Baicalin,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O24454.5Semi standard non polar33892256
Baicalin,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O4455.1Semi standard non polar33892256
Baicalin,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C(C)(C)C)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4493.9Semi standard non polar33892256
Baicalin,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O[Si](C)(C)C(C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4485.9Semi standard non polar33892256
Baicalin,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O[Si](C)(C)C(C)(C)C4435.8Semi standard non polar33892256
Baicalin,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C(C)(C)C)=C2O[Si](C)(C)C(C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O4479.5Semi standard non polar33892256
Baicalin,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O[Si](C)(C)C(C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4488.2Semi standard non polar33892256
Baicalin,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O[Si](C)(C)C(C)(C)C4437.2Semi standard non polar33892256
Baicalin,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O24439.7Semi standard non polar33892256
Baicalin,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C(C)(C)C)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4492.4Semi standard non polar33892256
Baicalin,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O4445.6Semi standard non polar33892256
Baicalin,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)O)O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@@H]1O[Si](C)(C)C(C)(C)C4403.3Semi standard non polar33892256
Baicalin,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O[Si](C)(C)C(C)(C)C)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4470.3Semi standard non polar33892256
Baicalin,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O[Si](C)(C)C(C)(C)C)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4462.9Semi standard non polar33892256
Baicalin,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@H](OC2=CC3=C(C(O)=C2O)C(=O)C=C(C2=CC=CC=C2)O3)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4431.3Semi standard non polar33892256
Baicalin,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=C2OC(C3=CC=CC=C3)=CC(=O)C2=C1O[Si](C)(C)C(C)(C)C4423.5Semi standard non polar33892256
Baicalin,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=C(O)C(O[C@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)=CC2=C1C(=O)C=C(C1=CC=CC=C1)O24429.9Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Baicalin GC-MS (Non-derivatized) - 70eV, Positivesplash10-05di-9328400000-21f478bcb7bb93e5bf282017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Baicalin GC-MS (3 TMS) - 70eV, Positivesplash10-0002-3392057000-ae58abaf7f516069457c2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Baicalin 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 - Baicalin 10V, Positive-QTOFsplash10-00fr-0090800000-605bcbd2ffd9fc7890f22017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Baicalin 20V, Positive-QTOFsplash10-00di-0090000000-f684485fa58df61301462017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Baicalin 40V, Positive-QTOFsplash10-0w90-1590000000-6a6f69daef985731b73d2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Baicalin 10V, Negative-QTOFsplash10-00kb-1251900000-33775a5cd1996ce659d32017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Baicalin 20V, Negative-QTOFsplash10-014i-2291200000-5a566a74a1bcab99fdb52017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Baicalin 40V, Negative-QTOFsplash10-014i-4590000000-56ad61dab640ec2290f32017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Baicalin 10V, Positive-QTOFsplash10-00dj-0090400000-10e70971051c82d629462021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Baicalin 20V, Positive-QTOFsplash10-00di-0090000000-60b322ff74af8a7655802021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Baicalin 40V, Positive-QTOFsplash10-00di-0090000000-53bc3f6f773ee367b5a92021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Baicalin 10V, Negative-QTOFsplash10-014j-0090600000-aaea534c6c95d07377be2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Baicalin 20V, Negative-QTOFsplash10-014i-0090000000-0f9cf513153f5787dba62021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Baicalin 40V, Negative-QTOFsplash10-014i-0090000000-74726919fa50baee16372021-09-24Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Blood
  • Urine
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedCancer patients undergoing total body irradiation details
UrineDetected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedCancer patients undergoing total body irradiation details
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDC00001024
Chemspider ID16498738
KEGG Compound IDC10025
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkBaicalin
METLIN IDNot Available
PubChem Compound13654833
PDB IDNot Available
ChEBI ID2981
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1667691
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available