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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 20:15:50 UTC
Update Date2022-03-07 02:54:27 UTC
HMDB IDHMDB0035304
Secondary Accession Numbers
  • HMDB35304
Metabolite Identification
Common NameGanoderic acid C2
DescriptionCryptocapsin belongs to the class of organic compounds known as xanthophylls. These are carotenoids containing an oxygenated carotene backbone. Carotenes are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Xanthophylls arise by oxygenation of the carotene backbone. Cryptocapsin is an extremely weak basic (essentially neutral) compound (based on its pKa).
Structure
Data?1563862697
Synonyms
ValueSource
(3's,5'r)-3'-Hydroxy-beta,kappa-caroten-6'-oneHMDB
3'-Hydroxy-b,K-caroten-6'-oneHMDB
KryptocapsinHMDB
Lanost-8-en-26-Oic acid, 3,7,15-trihydroxy-11,23-dioxo-, (3beta,15alpha)- (9ci)HMDB
2-Methyl-4-oxo-6-{5,9,12-trihydroxy-2,6,6,11,15-pentamethyl-17-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}heptanoateGenerator
Ganoderic acid C2MeSH
Ganoderate C2Generator
Chemical FormulaC30H46O7
Average Molecular Weight518.682
Monoisotopic Molecular Weight518.324353826
IUPAC Name2-methyl-4-oxo-6-{5,9,12-trihydroxy-2,6,6,11,15-pentamethyl-17-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}heptanoic acid
Traditional Name2-methyl-4-oxo-6-{5,9,12-trihydroxy-2,6,6,11,15-pentamethyl-17-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}heptanoic acid
CAS Registry Number98296-48-1
SMILES
CC(CC(=O)CC(C)C(O)=O)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O
InChI Identifier
InChI=1S/C30H46O7/c1-15(10-17(31)11-16(2)26(36)37)18-12-23(35)30(7)25-19(32)13-21-27(3,4)22(34)8-9-28(21,5)24(25)20(33)14-29(18,30)6/h15-16,18-19,21-23,32,34-35H,8-14H2,1-7H3,(H,36,37)
InChI KeyRERVSJVGWKIGTJ-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as xanthophylls. These are carotenoids containing an oxygenated carotene backbone. Carotenes are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Xanthophylls arise by oxygenation of the carotene backbone.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassTetraterpenoids
Direct ParentXanthophylls
Alternative Parents
Substituents
  • Xanthophyll
  • Cyclopentanol
  • Alpha,beta-unsaturated ketone
  • Enone
  • Cyclic alcohol
  • Acryloyl-group
  • Secondary alcohol
  • Ketone
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Alcohol
  • Aliphatic homomonocyclic compound
Molecular FrameworkAliphatic homomonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point231 - 232 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.029 g/LALOGPS
logP3.3ALOGPS
logP2.74ChemAxon
logS-4.2ALOGPS
pKa (Strongest Acidic)4.35ChemAxon
pKa (Strongest Basic)-0.81ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count7ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area132.13 ŲChemAxon
Rotatable Bond Count6ChemAxon
Refractivity139.75 m³·mol⁻¹ChemAxon
Polarizability57.97 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+221.59331661259
DarkChem[M-H]-213.97431661259
DeepCCS[M-2H]-254.76830932474
DeepCCS[M+Na]+230.19230932474
AllCCS[M+H]+221.832859911
AllCCS[M+H-H2O]+220.432859911
AllCCS[M+NH4]+223.132859911
AllCCS[M+Na]+223.432859911
AllCCS[M-H]-221.432859911
AllCCS[M+Na-2H]-224.432859911
AllCCS[M+HCOO]-227.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Ganoderic acid C2CC(CC(=O)CC(C)C(O)=O)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O4682.9Standard polar33892256
Ganoderic acid C2CC(CC(=O)CC(C)C(O)=O)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O3270.9Standard non polar33892256
Ganoderic acid C2CC(CC(=O)CC(C)C(O)=O)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O4158.3Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Ganoderic acid C2,1TMS,isomer #1CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C4222.7Semi standard non polar33892256
Ganoderic acid C2,1TMS,isomer #2CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4195.9Semi standard non polar33892256
Ganoderic acid C2,1TMS,isomer #3CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O4246.4Semi standard non polar33892256
Ganoderic acid C2,1TMS,isomer #4CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O4222.9Semi standard non polar33892256
Ganoderic acid C2,1TMS,isomer #5CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4243.1Semi standard non polar33892256
Ganoderic acid C2,1TMS,isomer #6CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4256.7Semi standard non polar33892256
Ganoderic acid C2,1TMS,isomer #7CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4106.3Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #1CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C4122.0Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #10CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4115.2Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #11CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O3942.9Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #12CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O4146.3Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #13CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4202.9Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #14CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4194.4Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #15CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O3980.0Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #16CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O4168.3Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #17CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O4149.7Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #18CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3942.4Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #19CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4019.1Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #2CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C4200.3Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #20CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4037.4Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #3CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C4160.8Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #4CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C4195.7Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #5CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C4185.5Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #6CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C4007.0Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #7CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O4099.2Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #8CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O4076.9Semi standard non polar33892256
Ganoderic acid C2,2TMS,isomer #9CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O4132.9Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #1CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3982.1Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #10CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C4021.5Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #11CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C4008.2Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #12CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3835.7Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #13CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3898.2Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #14CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3894.4Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #15CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3908.5Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #16CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3942.3Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #17CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3933.8Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #18CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O3787.3Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #19CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3922.3Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #2CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3950.5Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #20CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3909.2Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #21CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3770.1Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #22CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3830.9Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #23CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3824.3Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #24CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3994.5Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #25CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3981.2Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #26CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3799.7Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #27CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3869.1Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #28CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3862.4Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #29CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3827.9Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #3CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3989.2Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #30CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3821.1Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #4CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3978.2Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #5CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3830.4Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #6CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C4033.1Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #7CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C4070.1Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #8CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C4067.3Semi standard non polar33892256
Ganoderic acid C2,3TMS,isomer #9CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3882.0Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #1CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3818.9Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #10CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)C3875.2Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #11CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)C3863.8Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #12CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3737.7Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #13CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3763.2Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #14CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3763.9Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #15CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3732.1Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #16CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3736.0Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #17CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3777.1Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #18CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3770.9Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #19CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O3692.9Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #2CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3820.3Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #20CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3704.8Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #21CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O3707.7Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #22CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3702.0Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #23CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3700.3Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #24CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3734.2Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #25CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3734.2Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #3CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3804.0Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #4CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C3716.7Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #5CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3807.0Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #6CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3788.7Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #7CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3701.5Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #8CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3726.7Semi standard non polar33892256
Ganoderic acid C2,4TMS,isomer #9CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3732.1Semi standard non polar33892256
Ganoderic acid C2,5TMS,isomer #1CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)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)C3709.2Semi standard non polar33892256
Ganoderic acid C2,5TMS,isomer #1CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)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)C3902.5Standard non polar33892256
Ganoderic acid C2,5TMS,isomer #10CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3636.7Semi standard non polar33892256
Ganoderic acid C2,5TMS,isomer #10CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3750.5Standard non polar33892256
Ganoderic acid C2,5TMS,isomer #11CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3633.4Semi standard non polar33892256
Ganoderic acid C2,5TMS,isomer #11CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3785.1Standard non polar33892256
Ganoderic acid C2,5TMS,isomer #2CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)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)C3682.4Semi standard non polar33892256
Ganoderic acid C2,5TMS,isomer #2CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)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)C3907.5Standard non polar33892256
Ganoderic acid C2,5TMS,isomer #3CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3647.7Semi standard non polar33892256
Ganoderic acid C2,5TMS,isomer #3CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C)C(=O)O[Si](C)(C)C3778.3Standard non polar33892256
Ganoderic acid C2,5TMS,isomer #4CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3631.6Semi standard non polar33892256
Ganoderic acid C2,5TMS,isomer #4CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3834.7Standard non polar33892256
Ganoderic acid C2,5TMS,isomer #5CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)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 C2,5TMS,isomer #5CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3842.0Standard non polar33892256
Ganoderic acid C2,5TMS,isomer #6CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3637.0Semi standard non polar33892256
Ganoderic acid C2,5TMS,isomer #6CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3837.0Standard non polar33892256
Ganoderic acid C2,5TMS,isomer #7CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3627.5Semi standard non polar33892256
Ganoderic acid C2,5TMS,isomer #7CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3842.8Standard non polar33892256
Ganoderic acid C2,5TMS,isomer #8CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)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)C3656.9Semi standard non polar33892256
Ganoderic acid C2,5TMS,isomer #8CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)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)C3850.0Standard non polar33892256
Ganoderic acid C2,5TMS,isomer #9CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)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)C3654.7Semi standard non polar33892256
Ganoderic acid C2,5TMS,isomer #9CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)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)C3857.7Standard non polar33892256
Ganoderic acid C2,1TBDMS,isomer #1CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4473.1Semi standard non polar33892256
Ganoderic acid C2,1TBDMS,isomer #2CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4428.1Semi standard non polar33892256
Ganoderic acid C2,1TBDMS,isomer #3CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O4473.0Semi standard non polar33892256
Ganoderic acid C2,1TBDMS,isomer #4CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4457.5Semi standard non polar33892256
Ganoderic acid C2,1TBDMS,isomer #5CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4479.4Semi standard non polar33892256
Ganoderic acid C2,1TBDMS,isomer #6CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4493.9Semi standard non polar33892256
Ganoderic acid C2,1TBDMS,isomer #7CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4351.4Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #1CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4601.7Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #10CC(C=C(CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4590.0Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #11CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O4395.9Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #12CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4603.1Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #13CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)O4683.5Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #14CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)O4672.8Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #15CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O4439.1Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #16CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)O4621.3Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #17CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)O4604.6Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #18CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4390.3Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #19CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4472.9Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #2CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4693.4Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #20CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4497.2Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #3CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4628.4Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #4CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)C4678.9Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #5CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)C4669.9Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #6CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4472.5Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #7CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O4562.8Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #8CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4531.1Semi standard non polar33892256
Ganoderic acid C2,2TBDMS,isomer #9CC(CC(=CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4604.9Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #1CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4707.0Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #10CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)C4685.1Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #11CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)C4667.5Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #12CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4493.4Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #13CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)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)C4531.2Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #14CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)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)C4516.6Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #15CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4611.2Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #16CC(CC(=CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)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)O4656.5Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #17CC(C=C(CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)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)O4646.0Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #18CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O4460.7Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #19CC(CC(=CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)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)O4620.5Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #2CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4647.5Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #20CC(C=C(CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)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)O4600.1Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #21CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4439.5Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #22CC(CC(=CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4490.3Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #23CC(C=C(CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)O[Si](C)(C)C(C)(C)C)C(=O)O4476.5Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #24CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)O4692.1Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #25CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)O4673.5Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #26CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O[Si](C)(C)C(C)(C)C)C(=O)O4470.4Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #27CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)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)O4531.3Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #28CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)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)O4520.9Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #29CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)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)O4485.7Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #3CC(CC(=CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)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)C4677.5Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #30CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)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)O4474.4Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #4CC(C=C(CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)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)C4658.9Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #5CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4490.9Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #6CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)C4720.4Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #7CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)C4769.7Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #8CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)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)C4762.3Semi standard non polar33892256
Ganoderic acid C2,3TBDMS,isomer #9CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3O)C(=O)O[Si](C)(C)C(C)(C)C4548.6Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid C2 GC-MS (Non-derivatized) - 70eV, Positivesplash10-0fe0-1115930000-a60eb9896660bfb736442017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ganoderic acid C2 GC-MS (2 TMS) - 70eV, Positivesplash10-0002-4210149000-b7020da91a0e99db76a72017-10-06Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid C2 10V, Positive-QTOFsplash10-0f89-1001970000-41ed07f24bfa88e519af2016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid C2 20V, Positive-QTOFsplash10-0560-1001910000-2164bec2f55b527238c62016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid C2 40V, Positive-QTOFsplash10-0pbl-5103900000-6853f406cf76b77754892016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid C2 10V, Negative-QTOFsplash10-014j-0000980000-4eaad17d545592fe3eed2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid C2 20V, Negative-QTOFsplash10-05fs-5100920000-1b3588e4387ca4a263e62016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid C2 40V, Negative-QTOFsplash10-0adr-9111710000-f8a579490d4cf6afa2932016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid C2 10V, Negative-QTOFsplash10-014i-0000190000-4cceff31bced10c3ec5b2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid C2 20V, Negative-QTOFsplash10-0079-2006910000-e2230e350e1f27cc806e2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid C2 40V, Negative-QTOFsplash10-00ri-6009700000-e37e86325c5a5a78c84f2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid C2 10V, Positive-QTOFsplash10-00sc-0209220000-1e14c720ff2737ab08022021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid C2 20V, Positive-QTOFsplash10-01x9-5609210000-61552fd53ad5adfde2092021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ganoderic acid C2 40V, Positive-QTOFsplash10-01vx-8409100000-5c30579545f14a906d3b2021-09-22Wishart 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 IDFDB015892
KNApSAcK IDC00022984
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound131752094
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.