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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2008-09-15 17:26:24 UTC
Update Date2021-09-14 15:19:30 UTC
HMDB IDHMDB0010338
Secondary Accession Numbers
  • HMDB10338
Metabolite Identification
Common Name11-Oxo-androsterone glucuronide
Description11-oxo-androsterone glucuronide is a natural human metabolite of 11-oxo-androsterone generated in the liver by UDP glucuonyltransferase. Glucuronidation is used to assist in the excretion of toxic substances, drugs or other substances that cannot be used as an energy source. Glucuronic acid is attached via a glycosidic bond to the substance, and the resulting glucuronide, which has a much higher water solubility than the original substance, is eventually excreted by the kidneys.
Structure
Data?1582752815
Synonyms
ValueSource
1-Palmitoyl-2-lignoceroyl-sn-glycerolHMDB
DAG(16:0/24:0)HMDB
DAG(40:0)HMDB
DG(16:0/24:0)HMDB
DG(40:0)HMDB
DiacylglycerolHMDB
Diacylglycerol(16:0/24:0)HMDB
Diacylglycerol(40:0)HMDB
DiglycerideHMDB
1-Hexadecanoyl-2-tetracosanoyl-sn-glycerolHMDB
11-oxo-Etiocholanolone glucuronideHMDB
11-Oxoandrosterone glucuronideHMDB
11-Oxoetiocholanolone glucuronideHMDB
6-({2,15-dimethyl-14,17-dioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylateGenerator
Chemical FormulaC25H36O9
Average Molecular Weight480.5479
Monoisotopic Molecular Weight480.23593275
IUPAC Name6-({2,15-dimethyl-14,17-dioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid
Traditional Name6-({2,15-dimethyl-14,17-dioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid
CAS Registry NumberNot Available
SMILES
CC12CC(=O)C3C(CCC4CC(CCC34C)OC3OC(C(O)C(O)C3O)C(O)=O)C1CCC2=O
InChI Identifier
InChI=1S/C25H36O9/c1-24-8-7-12(33-23-20(30)18(28)19(29)21(34-23)22(31)32)9-11(24)3-4-13-14-5-6-16(27)25(14,2)10-15(26)17(13)24/h11-14,17-21,23,28-30H,3-10H2,1-2H3,(H,31,32)
InChI KeyQTXWOOLAHRQMGZ-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as 1,2-diacylglycerols. These are diacylglycerols containing a glycerol acylated at positions 1 and 2.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerolipids
Sub ClassDiradylglycerols
Direct Parent1,2-diacylglycerols
Alternative Parents
Substituents
  • 1,2-acyl-sn-glycerol
  • Fatty acid ester
  • Fatty acyl
  • Dicarboxylic acid or derivatives
  • Carboxylic acid ester
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Primary alcohol
  • Organooxygen compound
  • Carbonyl group
  • Alcohol
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Disposition

Biological location

Source

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 Solubility0.55 g/LALOGPS
logP1.55ALOGPS
logP1.39ChemAxon
logS-2.9ALOGPS
pKa (Strongest Acidic)3.47ChemAxon
pKa (Strongest Basic)-3.7ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count9ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area150.59 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity116.76 m³·mol⁻¹ChemAxon
Polarizability50.69 ųChemAxon
Number of Rings5ChemAxon
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]+208.51531661259
DarkChem[M-H]-199.1131661259
DeepCCS[M-2H]-240.83830932474
DeepCCS[M+Na]+216.13630932474

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
11-Oxo-androsterone glucuronideCC12CC(=O)C3C(CCC4CC(CCC34C)OC3OC(C(O)C(O)C3O)C(O)=O)C1CCC2=O3163.0Standard polar33892256
11-Oxo-androsterone glucuronideCC12CC(=O)C3C(CCC4CC(CCC34C)OC3OC(C(O)C(O)C3O)C(O)=O)C1CCC2=O3734.3Standard non polar33892256
11-Oxo-androsterone glucuronideCC12CC(=O)C3C(CCC4CC(CCC34C)OC3OC(C(O)C(O)C3O)C(O)=O)C1CCC2=O4157.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
11-Oxo-androsterone glucuronide,1TMS,isomer #1CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O)C5O)CCC43C)C1CCC2=O4212.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,1TMS,isomer #2CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C)C5O)CCC43C)C1CCC2=O4237.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,1TMS,isomer #3CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O[Si](C)(C)C)CCC43C)C1CCC2=O4221.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,1TMS,isomer #4CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O)C5O)CCC43C)C1CCC2=O4135.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,1TMS,isomer #5CC12CCC(OC3OC(C(=O)O)C(O)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC124027.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,1TMS,isomer #6CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O)CCC43C)C1CCC2=O4001.7Semi standard non polar33892256
11-Oxo-androsterone glucuronide,1TMS,isomer #7CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C4100.6Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #1CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O)CCC43C)C1CCC2=O4097.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #10CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C)C5O)CCC43C)C1CCC2=O3924.0Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #11CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3992.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #12CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O)C5O[Si](C)(C)C)CCC43C)C1CCC2=O4099.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #13CC12CCC(OC3OC(C(=O)O)C(O)C(O)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123968.6Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #14CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O[Si](C)(C)C)CCC43C)C1CCC2=O3936.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #15CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3996.0Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #16CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123925.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #17CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O)C5O)CCC43C)C1CCC2=O3883.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #18CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3947.0Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #19CC12CCC(OC3OC(C(=O)O)C(O)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123809.6Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #2CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)CCC43C)C1CCC2=O4172.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #20CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3813.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #3CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)CCC43C)C1CCC2=O4167.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #4CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123973.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #5CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O)C5O)CCC43C)C1CCC2=O3932.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #6CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3994.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #7CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O)CCC43C)C1CCC2=O4095.6Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #8CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CCC2=O4186.6Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TMS,isomer #9CC12CCC(OC3OC(C(=O)O)C(O)C(O[Si](C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123995.7Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #1CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)CCC43C)C1CCC2=O4018.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #10CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123888.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #11CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)CCC43C)C1CCC2=O3862.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #12CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3880.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #13CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123703.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #14CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3685.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #15CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CCC2=O4013.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #16CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123836.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #17CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O)CCC43C)C1CCC2=O3772.0Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #18CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3783.0Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #19CC12CCC(OC3OC(C(=O)O)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123891.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #2CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)CCC43C)C1CCC2=O4015.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #20CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CCC2=O3855.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #21CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3873.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #22CC12CCC(OC3OC(C(=O)O)C(O)C(O[Si](C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123693.7Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #23CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3652.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #24CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123825.6Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #25CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O)C5O[Si](C)(C)C)CCC43C)C1CCC2=O3793.0Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #26CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3804.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #27CC12CCC(OC3OC(C(=O)O)C(O)C(O)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123688.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #28CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3680.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #29CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123650.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #3CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123837.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #30CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3627.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #4CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O)CCC43C)C1CCC2=O3795.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #5CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3809.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #6CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CCC2=O4106.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #7CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123890.7Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #8CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)CCC43C)C1CCC2=O3850.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TMS,isomer #9CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3874.0Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #1CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CCC2=O3942.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #10CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123828.6Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #11CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CCC2=O3789.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #12CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3771.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #13CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123613.0Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #14CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3579.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #15CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123616.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #16CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3595.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #17CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123724.6Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #18CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CCC2=O3682.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #19CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3636.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #2CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123752.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #20CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123567.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #21CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3495.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #22CC12CCC(OC3OC(C(=O)O)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123596.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #23CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3561.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #24CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123562.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #25CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3524.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #3CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)CCC43C)C1CCC2=O3705.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #4CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3665.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #5CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123741.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #6CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)CCC43C)C1CCC2=O3704.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #7CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3673.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #8CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123582.7Semi standard non polar33892256
11-Oxo-androsterone glucuronide,4TMS,isomer #9CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3543.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #1CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123684.6Semi standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #1CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC123840.4Standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #1CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(=O)CCC124307.2Standard polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #10CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123481.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #10CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123591.6Standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #10CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC124462.8Standard polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #11CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3417.7Semi standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #11CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3561.9Standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #11CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C4567.9Standard polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #2CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CCC2=O3642.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #2CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CCC2=O3721.2Standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #2CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CCC2=O4369.4Standard polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #3CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3587.6Semi standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #3CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3620.0Standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #3CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C4267.6Standard polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #4CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123509.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #4CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123605.1Standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #4CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC124469.3Standard polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #5CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3451.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #5CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C3573.0Standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #5CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C4574.6Standard polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #6CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123509.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #6CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123636.3Standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #6CC12CCC(OC3OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC124498.0Standard polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #7CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3459.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #7CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3609.0Standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #7CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C4597.0Standard polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #8CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123537.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #8CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC123570.5Standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #8CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C)CC2(C)C(O[Si](C)(C)C)=CCC124435.4Standard polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #9CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3510.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #9CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C3535.4Standard non polar33892256
11-Oxo-androsterone glucuronide,5TMS,isomer #9CC12C=C(O[Si](C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C4543.1Standard polar33892256
11-Oxo-androsterone glucuronide,1TBDMS,isomer #1CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C5O)CCC43C)C1CCC2=O4446.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,1TBDMS,isomer #2CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)CCC43C)C1CCC2=O4466.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,1TBDMS,isomer #3CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CCC2=O4455.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,1TBDMS,isomer #4CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C5O)CCC43C)C1CCC2=O4380.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,1TBDMS,isomer #5CC12CCC(OC3OC(C(=O)O)C(O)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(=O)CCC124303.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,1TBDMS,isomer #6CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O)CCC43C)C1CCC2=O4238.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,1TBDMS,isomer #7CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4318.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #1CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C5O)CCC43C)C1CCC2=O4557.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #10CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)CCC43C)C1CCC2=O4386.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #11CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4440.7Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #12CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CCC2=O4551.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #13CC12CCC(OC3OC(C(=O)O)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(=O)CCC124440.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #14CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CCC2=O4383.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #15CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4432.6Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #16CC12CCC(OC3OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(=O)CCC124402.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #17CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C5O)CCC43C)C1CCC2=O4328.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #18CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4392.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #19CC12CCC(OC3OC(C(=O)O)C(O)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(O[Si](C)(C)C(C)(C)C)=CCC124284.0Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #2CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C5O)CCC43C)C1CCC2=O4605.7Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #20CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4246.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #3CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CCC2=O4606.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #4CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(=O)CCC124437.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #5CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C5O)CCC43C)C1CCC2=O4381.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #6CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4433.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #7CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)CCC43C)C1CCC2=O4556.7Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #8CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CCC2=O4624.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,2TBDMS,isomer #9CC12CCC(OC3OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(=O)CCC124459.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #1CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C5O)CCC43C)C1CCC2=O4671.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #10CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(=O)CCC124554.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #11CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CCC2=O4515.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #12CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4532.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #13CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(O[Si](C)(C)C(C)(C)C)=CCC124385.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #14CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4358.0Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #15CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CCC2=O4677.6Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #16CC12CCC(OC3OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(=O)CCC124525.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #17CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)CCC43C)C1CCC2=O4439.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #18CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4485.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #19CC12CCC(OC3OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(=O)CCC124573.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #2CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CCC2=O4669.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #20CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CCC2=O4525.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #21CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4542.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #22CC12CCC(OC3OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(O[Si](C)(C)C(C)(C)C)=CCC124402.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #23CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4356.2Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #24CC12CCC(OC3OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(=O)CCC124516.5Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #25CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CCC2=O4452.7Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #26CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4492.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #27CC12CCC(OC3OC(C(=O)O)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(O[Si](C)(C)C(C)(C)C)=CCC124383.0Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #28CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O)C(O)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4351.4Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #29CC12CCC(OC3OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(O[Si](C)(C)C(C)(C)C)=CCC124354.8Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #3CC12CCC(OC3OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(=O)CCC124523.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #30CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4318.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #4CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C5O)CCC43C)C1CCC2=O4456.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #5CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C5O)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4498.9Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #6CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C5O[Si](C)(C)C(C)(C)C)CCC43C)C1CCC2=O4740.0Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #7CC12CCC(OC3OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)CC1CCC1C2=C(O[Si](C)(C)C(C)(C)C)CC2(C)C(=O)CCC124559.1Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #8CC12C=C(O[Si](C)(C)C(C)(C)C)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C5O)CCC43C)C1CCC2=O4512.3Semi standard non polar33892256
11-Oxo-androsterone glucuronide,3TBDMS,isomer #9CC12CC(=O)C3C(CCC4CC(OC5OC(C(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C5O)CCC43C)C1CC=C2O[Si](C)(C)C(C)(C)C4532.3Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 11-Oxo-androsterone glucuronide GC-MS (Non-derivatized) - 70eV, Positivesplash10-0gw0-5155900000-870bd7a832d7d2c361642017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 11-Oxo-androsterone glucuronide GC-MS (3 TMS) - 70eV, Positivesplash10-001i-1041019000-4e5f7a8123a7a7cbc8712017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 11-Oxo-androsterone glucuronide 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 - 11-Oxo-androsterone glucuronide 10V, Positive-QTOFsplash10-0bu9-0165900000-16c7db2f63801f613d212016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 11-Oxo-androsterone glucuronide 20V, Positive-QTOFsplash10-0a4r-0294100000-4eba2ad81023da15bb132016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 11-Oxo-androsterone glucuronide 40V, Positive-QTOFsplash10-0bti-0390000000-61d45ba48b345dd844f92016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 11-Oxo-androsterone glucuronide 10V, Negative-QTOFsplash10-0fbi-1224900000-4c49bc973ae05ffd8ead2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 11-Oxo-androsterone glucuronide 20V, Negative-QTOFsplash10-0udi-2339300000-cec8e4fce848f8069b062016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 11-Oxo-androsterone glucuronide 40V, Negative-QTOFsplash10-0udi-8379000000-d638f0624c6b8f4d39722016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 11-Oxo-androsterone glucuronide 10V, Positive-QTOFsplash10-01q9-0000900000-ad56031b86c584612e022021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 11-Oxo-androsterone glucuronide 20V, Positive-QTOFsplash10-02ti-2293500000-129e71f76254cda1d3992021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 11-Oxo-androsterone glucuronide 40V, Positive-QTOFsplash10-0002-4639200000-54f7927182f9b5d85daa2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 11-Oxo-androsterone glucuronide 10V, Negative-QTOFsplash10-004i-0000900000-90787777dc3cdc6176722021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 11-Oxo-androsterone glucuronide 20V, Negative-QTOFsplash10-004i-6304900000-e8f8d5f009d6bb1e45bc2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 11-Oxo-androsterone glucuronide 40V, Negative-QTOFsplash10-0a4i-9023400000-d1ba590eff5bccb273ba2021-09-23Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
  • Membrane
Biospecimen Locations
  • Blood
  • Urine
Tissue Locations
  • Kidney
  • Liver
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodExpected but not QuantifiedNot QuantifiedNot AvailableNot AvailableNormal
      Not Available
details
UrineDetected but not QuantifiedNot QuantifiedAdult (>18 years old)BothNormal details
UrineDetected but not QuantifiedNot QuantifiedAdult (>18 years old)BothNot Available details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB024316
KNApSAcK IDNot Available
Chemspider ID24765936
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound53478031
PDB IDNot Available
ChEBI IDNot Available
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 ReferencesNot Available

Only showing the first 10 proteins. There are 19 proteins in total.

Enzymes

General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGTs are of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isozyme has glucuronidating capacity with steroid substrates such as 5-beta-androstane 3-alpha,17-beta-diol, estradiol, ADT, eugenol and bile acids. Only isoform 1 seems to be active.
Gene Name:
UGT2B28
Uniprot ID:
Q9BY64
Molecular weight:
38742.9
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGTs are of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isozyme is active on polyhydroxylated estrogens (such as estriol, 4-hydroxyestrone and 2-hydroxyestriol) and xenobiotics (such as 4-methylumbelliferone, 1-naphthol, 4-nitrophenol, 2-aminophenol, 4-hydroxybiphenyl and menthol). It is capable of 6 alpha-hydroxyglucuronidation of hyodeoxycholic acid.
Gene Name:
UGT2B4
Uniprot ID:
P06133
Molecular weight:
60512.035
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform glucuronidates bilirubin IX-alpha to form both the IX-alpha-C8 and IX-alpha-C12 monoconjugates and diconjugate.
Gene Name:
UGT1A4
Uniprot ID:
P22310
Molecular weight:
60024.535
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds.
Gene Name:
UGT2B10
Uniprot ID:
P36537
Molecular weight:
60773.485
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. Its unique specificity for 3,4-catechol estrogens and estriol suggests it may play an important role in regulating the level and activity of these potent and active estrogen metabolites. Is also active with androsterone, hyodeoxycholic acid and tetrachlorocatechol (in vitro).
Gene Name:
UGT2B7
Uniprot ID:
P16662
Molecular weight:
60720.15
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGTs are of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isozyme displays activity toward several classes of xenobiotic substrates, including simple phenolic compounds, 7-hydroxylated coumarins, flavonoids, anthraquinones, and certain drugs and their hydroxylated metabolites. It also catalyzes the glucuronidation of endogenous estrogens and androgens.
Gene Name:
UGT2B15
Uniprot ID:
P54855
Molecular weight:
61035.815
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDP-glucuronosyltransferases catalyze phase II biotransformation reactions in which lipophilic substrates are conjugated with glucuronic acid to increase water solubility and enhance excretion. They are of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. Active on odorants and seems to be involved in olfaction; it could help clear lipophilic odorant molecules from the sensory epithelium.
Gene Name:
UGT2A1
Uniprot ID:
Q9Y4X1
Molecular weight:
60771.605
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform glucuronidates bilirubin IX-alpha to form both the IX-alpha-C8 and IX-alpha-C12 monoconjugates and diconjugate. Is also able to catalyze the glucuronidation of 17beta-estradiol, 17alpha-ethinylestradiol, 1-hydroxypyrene, 4-methylumbelliferone, 1-naphthol, paranitrophenol, scopoletin, and umbelliferone.
Gene Name:
UGT1A1
Uniprot ID:
P22309
Molecular weight:
59590.91
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform has specificity for phenols.
Gene Name:
UGT1A9
Uniprot ID:
O60656
Molecular weight:
59940.495
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds.
Gene Name:
UGT1A3
Uniprot ID:
P35503
Molecular weight:
60337.835

Only showing the first 10 proteins. There are 19 proteins in total.