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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 21:26:20 UTC
Update Date2022-03-07 02:54:52 UTC
HMDB IDHMDB0036309
Secondary Accession Numbers
  • HMDB36309
Metabolite Identification
Common NameGanoderic acid eta
DescriptionCentellasapogenol A belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Centellasapogenol A is an extremely weak basic (essentially neutral) compound (based on its pKa).
Structure
Data?1563862854
Synonyms
ValueSource
(+)-Ganoderic acid etaHMDB
(2E)-4-Hydroxy-2-methyl-6-{5,9,16-trihydroxy-2,6,6,11,15-pentamethyl-12,17-dioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}hept-2-enoateGenerator
Ganoderate etaGenerator
Ganoderate ηGenerator
Ganoderic acid ηGenerator
Chemical FormulaC30H44O8
Average Molecular Weight532.6656
Monoisotopic Molecular Weight532.303618384
IUPAC Name(2E)-4-hydroxy-2-methyl-6-{5,9,16-trihydroxy-2,6,6,11,15-pentamethyl-12,17-dioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}hept-2-enoic acid
Traditional Name(2E)-4-hydroxy-2-methyl-6-{5,9,16-trihydroxy-2,6,6,11,15-pentamethyl-12,17-dioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}hept-2-enoic acid
CAS Registry Number294674-12-7
SMILES
CC(CC(O)\C=C(/C)C(O)=O)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O
InChI Identifier
InChI=1S/C30H44O8/c1-14(10-16(31)11-15(2)26(37)38)17-12-21(34)30(7)22-18(32)13-19-27(3,4)20(33)8-9-28(19,5)23(22)24(35)25(36)29(17,30)6/h11,14,16-20,25,31-33,36H,8-10,12-13H2,1-7H3,(H,37,38)/b15-11+
InChI KeySFQSUCWHIWDMMD-RVDMUPIBSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassTriterpenoids
Direct ParentTriterpenoids
Alternative Parents
Substituents
  • Triterpenoid
  • 12-hydroxysteroid
  • Hydroxysteroid
  • Steroid
  • Cyclic alcohol
  • Secondary alcohol
  • Carboxylic acid derivative
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Hydrocarbon derivative
  • Organic oxide
  • Organic oxygen compound
  • Alcohol
  • Carbonyl group
  • Organooxygen compound
  • Primary alcohol
  • Aliphatic homopolycyclic compound
Molecular FrameworkAliphatic homopolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point212 - 214 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.068 g/LALOGPS
logP2.36ALOGPS
logP2.39ChemAxon
logS-3.9ALOGPS
pKa (Strongest Acidic)4.33ChemAxon
pKa (Strongest Basic)-0.81ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count8ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area152.36 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity142.02 m³·mol⁻¹ChemAxon
Polarizability58.1 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityYesChemAxon
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]+222.29931661259
DarkChem[M-H]-213.43931661259
DeepCCS[M-2H]-254.94830932474
DeepCCS[M+Na]+229.93330932474
AllCCS[M+H]+223.732859911
AllCCS[M+H-H2O]+222.432859911
AllCCS[M+NH4]+225.032859911
AllCCS[M+Na]+225.432859911
AllCCS[M-H]-224.732859911
AllCCS[M+Na-2H]-227.732859911
AllCCS[M+HCOO]-231.032859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Ganoderic acid etaCC(CC(O)\C=C(/C)C(O)=O)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O4770.7Standard polar33892256
Ganoderic acid etaCC(CC(O)\C=C(/C)C(O)=O)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O3632.2Standard non polar33892256
Ganoderic acid etaCC(CC(O)\C=C(/C)C(O)=O)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O4131.1Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Ganoderic acid eta,1TMS,isomer #1C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4303.6Semi standard non polar33892256
Ganoderic acid eta,1TMS,isomer #2C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C4212.4Semi standard non polar33892256
Ganoderic acid eta,1TMS,isomer #3C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4252.8Semi standard non polar33892256
Ganoderic acid eta,1TMS,isomer #4C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O4286.5Semi standard non polar33892256
Ganoderic acid eta,1TMS,isomer #5C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O4234.9Semi standard non polar33892256
Ganoderic acid eta,1TMS,isomer #6C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4067.8Semi standard non polar33892256
Ganoderic acid eta,1TMS,isomer #7C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4163.8Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #1C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4173.6Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #10C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3936.4Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #11C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3995.8Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #12C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O4125.3Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #13C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O4096.3Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #14C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O3912.8Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #15C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4028.2Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #16C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O4122.9Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #17C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O3959.9Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #18C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O4011.9Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #19C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3921.0Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #2C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4193.3Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #20C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O4002.1Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #21C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O3868.7Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #3C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O4141.5Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #4C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C4169.6Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #5C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4006.7Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #6C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4059.0Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #7C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C4098.8Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #8C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C4117.8Semi standard non polar33892256
Ganoderic acid eta,2TMS,isomer #9C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C4073.3Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #1C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4024.1Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #10C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3980.6Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #11C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3856.2Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #12C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3892.2Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #13C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3903.4Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #14C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3901.7Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #15C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3794.7Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #16C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3974.5Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #17C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3942.1Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #18C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3792.9Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #19C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3862.1Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #2C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3984.8Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #20C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3966.6Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #21C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3856.3Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #22C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3854.4Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #23C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3817.0Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #24C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3839.8Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #25C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3747.9Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #26C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3973.4Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #27C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O3815.6Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #28C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O3886.6Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #29C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3779.0Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #3C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C4019.8Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #30C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3888.2Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #31C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O3751.2Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #32C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3841.6Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #33C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3880.3Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #34C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O3769.6Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #35C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3754.8Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #4C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3837.7Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #5C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3920.1Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #6C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O4012.9Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #7C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C4031.9Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #8C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3892.3Semi standard non polar33892256
Ganoderic acid eta,3TMS,isomer #9C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3900.9Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #1C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3890.4Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #10C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3709.1Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #11C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3862.8Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #12C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3786.3Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #13C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3785.4Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #14C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3795.0Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #15C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3764.2Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #16C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3714.5Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #17C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3759.9Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #18C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3751.7Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #19C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3716.3Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #2C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3874.2Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #20C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3701.7Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #21C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3849.1Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #22C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3732.5Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #23C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3761.2Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #24C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3704.6Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #25C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3762.3Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #26C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3668.4Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #27C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3764.7Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #28C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3751.6Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #29C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3678.2Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #3C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3760.3Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #30C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3667.0Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #31C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3738.0Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #32C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3801.3Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #33C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O3694.9Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #34C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3684.0Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #35C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3699.8Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #4C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3796.2Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #5C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3857.9Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #6C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3737.9Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #7C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3808.9Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #8C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3741.8Semi standard non polar33892256
Ganoderic acid eta,4TMS,isomer #9C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3780.0Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #1C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3776.5Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #10C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3624.2Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #11C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3703.6Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #12C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3676.1Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #13C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3667.3Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #14C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3628.5Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #15C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3617.9Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #16C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3665.7Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #17C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3701.9Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #18C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3603.8Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #19C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3590.8Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #2C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3711.0Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #20C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3615.5Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #21C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3645.5Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #3C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3737.0Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #4C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3684.8Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #5C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3688.8Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #6C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3654.1Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #7C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3656.0Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #8C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3694.2Semi standard non polar33892256
Ganoderic acid eta,5TMS,isomer #9C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3651.3Semi standard non polar33892256
Ganoderic acid eta,1TBDMS,isomer #1C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4542.7Semi standard non polar33892256
Ganoderic acid eta,1TBDMS,isomer #2C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4463.1Semi standard non polar33892256
Ganoderic acid eta,1TBDMS,isomer #3C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4480.7Semi standard non polar33892256
Ganoderic acid eta,1TBDMS,isomer #4C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O4514.2Semi standard non polar33892256
Ganoderic acid eta,1TBDMS,isomer #5C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4472.3Semi standard non polar33892256
Ganoderic acid eta,1TBDMS,isomer #6C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4348.7Semi standard non polar33892256
Ganoderic acid eta,1TBDMS,isomer #7C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4412.3Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #1C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4615.5Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #10C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4425.7Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #11C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4451.5Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #12C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O4591.8Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #13C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4558.7Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #14C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4406.7Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #15C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4483.5Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #16C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4592.3Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #17C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O4449.8Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #18C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O4488.0Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #19C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4421.3Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #2C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4658.7Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #20C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4471.5Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #21C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4338.8Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #3C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O4585.0Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #4C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4627.4Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #5C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4485.9Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #6C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4515.5Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #7C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4549.5Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #8C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4584.3Semi standard non polar33892256
Ganoderic acid eta,2TBDMS,isomer #9C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4532.5Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #1C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4710.9Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #10C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4684.3Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #11C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O4562.6Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #12C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O4577.1Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #13C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4586.8Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #14C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4577.0Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #15C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4454.8Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #16C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4669.4Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #17C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4640.2Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #18C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4453.5Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #19C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4511.0Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #2C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O4679.0Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #20C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4670.6Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #21C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4541.0Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #22C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4534.2Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #23C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4507.7Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #24C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4517.2Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #25C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4377.1Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #26C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4681.6Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #27C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O4501.2Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #28C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O4556.3Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #29C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4469.2Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #3C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4704.0Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #30C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4564.4Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #31C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4388.8Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #32C/C(=C\C(O)CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4556.7Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #33C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4569.1Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #34C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O4422.0Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #35C/C(=C\C(O)CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4429.0Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #4C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4519.3Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #5C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O[Si](C)(C)C(C)(C)C)C12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4581.0Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #6C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O4714.0Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #7C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4744.6Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #8C/C(=C\C(CC(C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4586.0Semi standard non polar33892256
Ganoderic acid eta,3TBDMS,isomer #9C/C(=C\C(CC(C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4581.4Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (Non-derivatized) - 70eV, Positivesplash10-0gb9-0232590000-2bddece9a8866369bdec2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (2 TMS) - 70eV, Positivesplash10-03di-1111019000-a4741be20dbc7144ce8e2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_16) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid eta GC-MS (TMS_2_17) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid eta 10V, Positive-QTOFsplash10-014j-0000970000-4de0998976349a5cf7fc2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid eta 20V, Positive-QTOFsplash10-00ke-2000910000-6ec2756ca781a100a7212016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid eta 40V, Positive-QTOFsplash10-014i-2103900000-8de86a03697f0db5dd5b2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid eta 10V, Negative-QTOFsplash10-01q9-0000290000-fc27e6830af03e6a6e142016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid eta 20V, Negative-QTOFsplash10-02u9-2000960000-8e23e1bca46bd7cd856a2016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid eta 40V, Negative-QTOFsplash10-0g4i-9021740000-77035cb40d77a16a2f852016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid eta 10V, Negative-QTOFsplash10-001i-0000190000-70771b0b6125490dc3cf2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid eta 20V, Negative-QTOFsplash10-014r-1000910000-21e316b4155f86218dca2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid eta 40V, Negative-QTOFsplash10-014i-2000900000-13f2151b77ec35e736562021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid eta 10V, Positive-QTOFsplash10-05mt-0105930000-f638f9c52ab1806b8cf52021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid eta 20V, Positive-QTOFsplash10-01b9-0104900000-eb30b4f69bf930b3f7ab2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid eta 40V, Positive-QTOFsplash10-01vo-9402200000-b413f095226d56336eb52021-09-23Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB015180
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound73196815
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 References
  1. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
  2. Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
  3. Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
  4. Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
  5. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
  6. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.