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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2008-09-16 08:30:09 UTC
Update Date2021-09-14 15:18:00 UTC
HMDB IDHMDB0010357
Secondary Accession Numbers
  • HMDB10357
Metabolite Identification
Common NameTetrahydroaldosterone-3-glucuronide
DescriptionTetrahydroaldosterone-3-glucuronide is a natural human metabolite of Tetrahydroaldosterone 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?1582752818
Synonyms
ValueSource
(3alpha,5beta,11beta)-11,18-Epoxy-18,21-dihydro-20-oxopregnan-3-yl-beta-D-glucopyranosiduronic acidHMDB
(3alpha,5beta,11beta)-11,18-Epoxy-18,21-dihydro-20-oxopregnan-3-yl-beta-delta-glucopyranosiduronic acidHMDB
11beta,18-Epoxy-18,21-dihydroxy-20-oxo-5beta-pregnan-3alpha-yl beta-D-glucopyranosiduronic acidHMDB
11beta,18-Epoxy-18,21-dihydroxy-20-oxo-5beta-pregnan-3alpha-yl beta-delta-glucopyranosiduronic acidHMDB
Tetrahydroaldosterone 3 beta-glucosiduronic acidHMDB
Tetrahydroaldosterone-3-glucuronosideHMDB
11 beta,18-Epoxy-18,21-dihydroxy-20-oxo-5 beta-pregnan-3 alpha-yl beta-D-glucopyranosiduronic acidHMDB
TA-gaHMDB
Chemical FormulaC27H40O11
Average Molecular Weight540.5999
Monoisotopic Molecular Weight540.257062122
IUPAC Name(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-{[(2S,14S,16S)-18-hydroxy-2-(2-hydroxyacetyl)-14-methyl-17-oxapentacyclo[14.2.1.0¹,⁵.0⁶,¹⁵.0⁹,¹⁴]nonadecan-11-yl]oxy}oxane-2-carboxylic acid
Traditional Name(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-{[(2S,14S,16S)-18-hydroxy-2-(2-hydroxyacetyl)-14-methyl-17-oxapentacyclo[14.2.1.0¹,⁵.0⁶,¹⁵.0⁹,¹⁴]nonadecan-11-yl]oxy}oxane-2-carboxylic acid
CAS Registry Number20605-81-6
SMILES
[H][C@@]12CC3(C(O)O1)C(CC[C@@H]3C(=O)CO)C1CCC3CC(CC[C@]3(C)C21)O[C@@H]1O[C@@H]([C@@H](O)[C@@H](O)[C@H]1O)C(O)=O
InChI Identifier
InChI=1S/C27H40O11/c1-26-7-6-12(36-24-21(32)19(30)20(31)22(38-24)23(33)34)8-11(26)2-3-13-14-4-5-15(16(29)10-28)27(14)9-17(18(13)26)37-25(27)35/h11-15,17-22,24-25,28,30-32,35H,2-10H2,1H3,(H,33,34)/t11?,12?,13?,14?,15-,17+,18?,19-,20+,21-,22+,24-,25?,26+,27?/m1/s1
InChI KeyCGIURIOFMWUPSV-RUQPETGGSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as steroid glucuronide conjugates. These are sterol lipids containing a glucuronide moiety linked to the steroid skeleton.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassSteroids and steroid derivatives
Sub ClassSteroidal glycosides
Direct ParentSteroid glucuronide conjugates
Alternative ParentsNot Available
SubstituentsNot Available
Molecular FrameworkAliphatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationRoute of exposureSource
Process
Role
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 Solubility1.49 g/LALOGPS
logP-0.06ALOGPS
logP-0.073ChemAxon
logS-2.6ALOGPS
pKa (Strongest Acidic)3.47ChemAxon
pKa (Strongest Basic)-3.3ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count6ChemAxon
Polar Surface Area183.21 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity127.78 m³·mol⁻¹ChemAxon
Polarizability56.19 ųChemAxon
Number of Rings6ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+224.0631661259
DarkChem[M-H]-215.93231661259
DeepCCS[M-2H]-253.55930932474
DeepCCS[M+Na]+228.53430932474
AllCCS[M+H]+224.832859911
AllCCS[M+H-H2O]+223.632859911
AllCCS[M+NH4]+225.832859911
AllCCS[M+Na]+226.132859911
AllCCS[M-H]-217.132859911
AllCCS[M+Na-2H]-218.832859911
AllCCS[M+HCOO]-220.932859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Tetrahydroaldosterone-3-glucuronide[H][C@@]12CC3(C(O)O1)C(CC[C@@H]3C(=O)CO)C1CCC3CC(CC[C@]3(C)C21)O[C@@H]1O[C@@H]([C@@H](O)[C@@H](O)[C@H]1O)C(O)=O3628.3Standard polar33892256
Tetrahydroaldosterone-3-glucuronide[H][C@@]12CC3(C(O)O1)C(CC[C@@H]3C(=O)CO)C1CCC3CC(CC[C@]3(C)C21)O[C@@H]1O[C@@H]([C@@H](O)[C@@H](O)[C@H]1O)C(O)=O4249.0Standard non polar33892256
Tetrahydroaldosterone-3-glucuronide[H][C@@]12CC3(C(O)O1)C(CC[C@@H]3C(=O)CO)C1CCC3CC(CC[C@]3(C)C21)O[C@@H]1O[C@@H]([C@@H](O)[C@@H](O)[C@H]1O)C(O)=O4468.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Tetrahydroaldosterone-3-glucuronide,1TMS,isomer #1C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124354.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TMS,isomer #2C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124294.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TMS,isomer #3C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124280.7Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TMS,isomer #4C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124285.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TMS,isomer #5C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124290.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TMS,isomer #6C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124283.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TMS,isomer #7C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124276.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TMS,isomer #8C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124273.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #1C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124246.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #10C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124238.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #11C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124235.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #12C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124213.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #13C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124244.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #14C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124226.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #15C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124227.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #16C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124224.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #17C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124212.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #18C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124186.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #19C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124220.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #2C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124251.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #20C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124231.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #21C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124218.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #22C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124179.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #23C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124220.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #24C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124218.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #25C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124185.7Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #26C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124204.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #27C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124160.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #3C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124249.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #4C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124254.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #5C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124257.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #6C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124245.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #7C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124226.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #8C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124223.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TMS,isomer #9C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124232.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #1C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124182.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #10C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124179.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #11C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124147.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #12C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124193.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #13C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124196.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #14C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124169.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #15C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124130.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #16C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124195.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #17C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124175.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #18C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124139.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #19C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124175.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #2C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124164.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #20C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124177.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #21C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124177.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #22C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124171.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #23C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124175.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #24C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124150.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #25C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124156.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #26C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124197.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #27C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124196.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #28C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124171.7Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #29C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124183.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #3C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124175.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #30C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124202.7Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #31C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124168.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #32C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124178.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #33C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124175.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #34C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124182.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #35C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124170.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #36C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124174.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #37C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124156.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #38C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124116.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #39C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124200.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #4C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124177.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #40C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124164.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #41C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124123.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #42C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124166.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #43C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124123.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #44C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124174.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #45C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124142.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #46C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124091.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #47C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124164.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #48C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124119.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #49C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124152.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #5C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124161.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #50C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124104.7Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #6C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124118.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #7C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124191.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #8C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124184.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TMS,isomer #9C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124190.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #1C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124109.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #10C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124103.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #11C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124095.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #12C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124053.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #13C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124102.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #14C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124100.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #15C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124146.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #16C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124139.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #17C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124112.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #18C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124082.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #19C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124124.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #2C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124102.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #20C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124111.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #21C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124077.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #22C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124130.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #23C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124134.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #24C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124136.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #25C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124112.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #26C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124077.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #27C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124117.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #28C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124118.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #29C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124117.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #3C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124117.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #30C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124116.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #31C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124113.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #32C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124106.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #33C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124107.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #34C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124113.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #35C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124116.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #36C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124096.7Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #37C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124096.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #38C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124101.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #39C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124101.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #4C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124108.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #40C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O)C124161.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #41C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124125.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #42C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124140.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #43C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124120.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #44C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124133.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #45C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124129.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #46C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)C34C[C@H](OC4O)C124138.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #47C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O)C124121.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #48C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124089.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #49C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124053.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #5C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124069.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #50C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124088.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #51C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124049.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #52C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124137.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #53C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124094.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #54C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124087.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #55C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O)C124047.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #6C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)CC1CCC1C3CC[C@H](C(=O)CO)C34C[C@H](OC4O[Si](C)(C)C)C124104.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #7C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=O)CO[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124110.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #8C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CCC(=C(CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124088.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,4TMS,isomer #9C[C@]12CCC(O[C@@H]3O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)CC1CCC1C3CC[C@H](C(=CO)O[Si](C)(C)C)C34C[C@H](OC4O[Si](C)(C)C)C124041.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1O[C@H]2CC13C(CC[C@@H]3C(=O)CO)C1CCC3CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]4O)CC[C@]3(C)C124570.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34532.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)[C@H](O)[C@@H]1O4493.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)[C@@H]1O4498.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)O[C@H](C(=O)O)[C@@H](O)[C@H]1O4509.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)[C@H](O)[C@H](O)[C@@H]1O4527.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(CO)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC12C(O)O34516.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,1TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34483.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O[Si](C)(C)C(C)(C)C)O34730.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34691.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC21C(O)O34703.7Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC12C(O)O34679.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34694.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)[C@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4675.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4656.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #16CC(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](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)[C@@H]1O4649.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC(CO)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC12C(O)O34656.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34602.7Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4666.7Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O[Si](C)(C)C(C)(C)C)C43)C2)[C@H](O)[C@H](O)[C@@H]1O4709.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)O[C@H](C(=O)O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4660.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC(CO)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC12C(O)O34659.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34600.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O4681.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC(CO)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC12C(O)O34673.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC21C(O)O34619.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CCC(=C(CO)O[Si](C)(C)C(C)(C)C)C56C[C@H](OC6O)C43)C2)[C@H](O)[C@H](O)[C@@H]1O4665.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=CO)O[Si](C)(C)C(C)(C)C)C56C[C@H](OC6O)C43)C2)[C@H](O)[C@H](O)[C@@H]1O4601.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1O[C@H]2CC13C(CC[C@@H]3C(=O)CO)C1CCC3CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]4O)CC[C@]3(C)C124686.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1O[C@H]2CC13C(CC[C@@H]3C(=O)CO)C1CCC3CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)CC[C@]3(C)C124688.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1O[C@H]2CC13C(CC[C@@H]3C(=O)CO)C1CCC3CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)CC[C@]3(C)C124708.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(CO)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC12C(O[Si](C)(C)C(C)(C)C)O34702.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O[Si](C)(C)C(C)(C)C)O34652.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34693.7Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34680.7Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O[Si](C)(C)C(C)(C)C)O34871.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CCC(=C(CO)O[Si](C)(C)C(C)(C)C)C56C[C@H](OC6O[Si](C)(C)C(C)(C)C)C43)C2)[C@H](O)[C@H](O)[C@@H]1O4832.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=CO)O[Si](C)(C)C(C)(C)C)C56C[C@H](OC6O[Si](C)(C)C(C)(C)C)C43)C2)[C@H](O)[C@H](O)[C@@H]1O4762.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1O[C@H]2CC13C(CC[C@@H]3C(=O)CO)C1CCC3CC(O[C@@H]4O[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]4O)CC[C@]3(C)C124813.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1O[C@H]2CC13C(CC[C@@H]3C(=O)CO)C1CCC3CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)CC[C@]3(C)C124823.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(CO)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC12C(O[Si](C)(C)C(C)(C)C)O34826.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O[Si](C)(C)C(C)(C)C)O34765.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1O[C@H]2CC13C(CC[C@@H]3C(=O)CO)C1CCC3CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]4O[Si](C)(C)C(C)(C)C)CC[C@]3(C)C124827.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC(CO)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC12C(O[Si](C)(C)C(C)(C)C)O34815.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O[Si](C)(C)C(C)(C)C)O34754.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC(CO)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC12C(O[Si](C)(C)C(C)(C)C)O34837.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O[Si](C)(C)C(C)(C)C)O34865.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC21C(O[Si](C)(C)C(C)(C)C)O34769.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34850.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34837.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC21C(O)O34857.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC12C(O)O34830.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34828.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[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]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34835.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC21C(O)O34843.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC12C(O)O34827.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34829.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O[Si](C)(C)C(C)(C)C)O34864.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC21C(O)O34848.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC12C(O)O34826.6Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34829.5Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC12C(O)O34840.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC21C(O)O34844.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4815.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C4804.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #37CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CCC(=C(CO)O[Si](C)(C)C(C)(C)C)C56C[C@H](OC6O)C43)C2)[C@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4810.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #38CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=CO)O[Si](C)(C)C(C)(C)C)C56C[C@H](OC6O)C43)C2)[C@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4744.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C4817.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC21C(O[Si](C)(C)C(C)(C)C)O34879.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #40CC(C)(C)[Si](C)(C)OC(CO)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC12C(O)O34804.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #41CC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC21C(O)O34737.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #42CC(C)(C)[Si](C)(C)OC(CO)=C1CCC2C3CCC4CC(O[C@@H]5O[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]5O)CC[C@]4(C)C3[C@@H]3CC12C(O)O34794.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #43CC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[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]5O)CC[C@]4(C)C3[C@@H]3CC21C(O)O34731.7Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #44CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O)C43)C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4814.3Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #45CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CCC(=C(CO)O[Si](C)(C)C(C)(C)C)C56C[C@H](OC6O)C43)C2)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4796.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #46CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=CO)O[Si](C)(C)C(C)(C)C)C56C[C@H](OC6O)C43)C2)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4723.7Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #47CC(C)(C)[Si](C)(C)OC(CO)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC12C(O)O34805.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #48CC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]5O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H]3CC21C(O)O34738.0Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #49CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CCC(=C(CO)O[Si](C)(C)C(C)(C)C)C56C[C@H](OC6O)C43)C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O4817.1Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC12C(O[Si](C)(C)C(C)(C)C)O34850.8Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #50CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=CO)O[Si](C)(C)C(C)(C)C)C56C[C@H](OC6O)C43)C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O4746.2Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CCC2C3CCC4CC(O[C@@H]5O[C@H](C(=O)O)[C@@H](O)[C@@H](O)[C@H]5O)CC[C@]4(C)C3[C@@H]3CC21C(O[Si](C)(C)C(C)(C)C)O34844.4Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O[Si](C)(C)C(C)(C)C)C43)C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O4848.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O[Si](C)(C)C(C)(C)C)C43)C2)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4823.9Semi standard non polar33892256
Tetrahydroaldosterone-3-glucuronide,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2CC[C@@]3(C)C(CCC4C5CC[C@H](C(=O)CO)C56C[C@H](OC6O[Si](C)(C)C(C)(C)C)C43)C2)[C@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4841.5Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (Non-derivatized) - 70eV, Positivesplash10-0ab9-6103690000-14047f2bdb0ef3dd341e2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (2 TMS) - 70eV, Positivesplash10-01b9-6100219000-9d173de05066ac0a8d122017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_1_8) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Tetrahydroaldosterone-3-glucuronide GC-MS (TMS_2_16) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Tetrahydroaldosterone-3-glucuronide 10V, Positive-QTOFsplash10-01bd-0009160000-22ec70399a690aea5bda2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Tetrahydroaldosterone-3-glucuronide 20V, Positive-QTOFsplash10-014j-0109000000-e0d766932d3840e4913d2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Tetrahydroaldosterone-3-glucuronide 40V, Positive-QTOFsplash10-0pvi-0229000000-c69b52480d42244e92a02016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Tetrahydroaldosterone-3-glucuronide 10V, Negative-QTOFsplash10-01pa-2208490000-09855d6e39bfbeb9aa782016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Tetrahydroaldosterone-3-glucuronide 20V, Negative-QTOFsplash10-03dj-2109210000-4ded13a1278e25bc26302016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Tetrahydroaldosterone-3-glucuronide 40V, Negative-QTOFsplash10-08fr-4109000000-dfd16e49a098227e09d32016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Tetrahydroaldosterone-3-glucuronide 10V, Positive-QTOFsplash10-0006-0000090000-39e628b55b951b77518f2021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Tetrahydroaldosterone-3-glucuronide 20V, Positive-QTOFsplash10-000b-0249130000-ba4c979ef6f5eec9393d2021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Tetrahydroaldosterone-3-glucuronide 40V, Positive-QTOFsplash10-0005-1916070000-9ed3e990712d132a80092021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Tetrahydroaldosterone-3-glucuronide 10V, Negative-QTOFsplash10-000i-0000390000-33110ebe67045c65c29a2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Tetrahydroaldosterone-3-glucuronide 20V, Negative-QTOFsplash10-0a4i-9101420000-e3cc0020a34c77863fcb2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Tetrahydroaldosterone-3-glucuronide 40V, Negative-QTOFsplash10-0a4r-9003610000-08c23161a8e55aa0a0b72021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-29Wishart 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 IDFDB027509
KNApSAcK IDNot Available
Chemspider ID146888
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound167918
PDB IDNot Available
ChEBI ID88728
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 18 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. 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
References
  1. Girard C, Barbier O, Veilleux G, El-Alfy M, Belanger A: Human uridine diphosphate-glucuronosyltransferase UGT2B7 conjugates mineralocorticoid and glucocorticoid metabolites. Endocrinology. 2003 Jun;144(6):2659-68. [PubMed:12746330 ]
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
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. The major substrates of this isozyme are eugenol > 4-methylumbelliferone > dihydrotestosterone (DHT) > androstane-3-alpha,17-beta-diol (3-alpha-diol) > testosterone > androsterone (ADT).
Gene Name:
UGT2B17
Uniprot ID:
O75795
Molecular weight:
61094.915

Only showing the first 10 proteins. There are 18 proteins in total.