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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 02:03:32 UTC
Update Date2022-03-07 02:56:37 UTC
HMDB IDHMDB0040504
Secondary Accession Numbers
  • HMDB40504
Metabolite Identification
Common NameCamellianin B
DescriptionCamellianin B belongs to the class of organic compounds known as flavonoid o-glycosides. Flavonoid O-glycosides are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. Camellianin B has been detected, but not quantified in, several different foods, such as black tea, green tea, herbal tea, red tea, and teas (Camellia sinensis). This could make camellianin b a potential biomarker for the consumption of these foods. Based on a literature review a small amount of articles have been published on Camellianin B.
Structure
Data?1563863557
Synonyms
ValueSource
CamellinHMDB
Chemical FormulaC27H30O14
Average Molecular Weight578.5187
Monoisotopic Molecular Weight578.163555668
IUPAC Name5-{[3,4-dihydroxy-6-(hydroxymethyl)-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-7-hydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one
Traditional Name5-{[3,4-dihydroxy-6-(hydroxymethyl)-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-7-hydroxy-2-(4-hydroxyphenyl)chromen-4-one
CAS Registry Number109232-76-0
SMILES
CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(O4)C3=CC=C(O)C=C3)C(O)C2O)C(O)C(O)C1O
InChI Identifier
InChI=1S/C27H30O14/c1-10-20(32)21(33)23(35)26(37-10)41-25-18(9-28)40-27(24(36)22(25)34)39-17-7-13(30)6-16-19(17)14(31)8-15(38-16)11-2-4-12(29)5-3-11/h2-8,10,18,20-30,32-36H,9H2,1H3
InChI KeyLRFDUPNLCDXZOE-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as flavonoid o-glycosides. Flavonoid O-glycosides are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavonoid glycosides
Direct ParentFlavonoid O-glycosides
Alternative Parents
Substituents
  • Flavonoid-5-o-glycoside
  • Flavonoid o-glycoside
  • 4'-hydroxyflavonoid
  • 7-hydroxyflavonoid
  • Flavone
  • Hydroxyflavonoid
  • Phenolic glycoside
  • Chromone
  • Disaccharide
  • Glycosyl compound
  • O-glycosyl compound
  • Benzopyran
  • 1-benzopyran
  • 1-hydroxy-2-unsubstituted benzenoid
  • Phenol
  • Pyranone
  • Monocyclic benzene moiety
  • Oxane
  • Pyran
  • Benzenoid
  • Heteroaromatic compound
  • Vinylogous ester
  • Secondary alcohol
  • Acetal
  • Polyol
  • Oxacycle
  • Organoheterocyclic compound
  • Organic oxide
  • Organic oxygen compound
  • Hydrocarbon derivative
  • Organooxygen compound
  • Primary alcohol
  • Alcohol
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point328 - 330 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility2.58 g/LALOGPS
logP-0.04ALOGPS
logP-0.94ChemAxon
logS-2.4ALOGPS
pKa (Strongest Acidic)6.53ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count14ChemAxon
Hydrogen Donor Count8ChemAxon
Polar Surface Area225.06 ŲChemAxon
Rotatable Bond Count6ChemAxon
Refractivity135.93 m³·mol⁻¹ChemAxon
Polarizability57.35 ųChemAxon
Number of Rings5ChemAxon
BioavailabilityNoChemAxon
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]+230.82631661259
DarkChem[M-H]-225.95831661259
DeepCCS[M+H]+226.24930932474
DeepCCS[M-H]-223.85330932474
DeepCCS[M-2H]-257.01730932474
DeepCCS[M+Na]+232.15130932474
AllCCS[M+H]+228.432859911
AllCCS[M+H-H2O]+227.132859911
AllCCS[M+NH4]+229.632859911
AllCCS[M+Na]+230.032859911
AllCCS[M-H]-221.832859911
AllCCS[M+Na-2H]-223.932859911
AllCCS[M+HCOO]-226.332859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Camellianin BCC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(O4)C3=CC=C(O)C=C3)C(O)C2O)C(O)C(O)C1O5792.2Standard polar33892256
Camellianin BCC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(O4)C3=CC=C(O)C=C3)C(O)C2O)C(O)C(O)C1O4990.1Standard non polar33892256
Camellianin BCC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(O4)C3=CC=C(O)C=C3)C(O)C2O)C(O)C(O)C1O5623.6Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Camellianin B,1TMS,isomer #1CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O)C1O5276.4Semi standard non polar33892256
Camellianin B,1TMS,isomer #2CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O)C1O5302.2Semi standard non polar33892256
Camellianin B,1TMS,isomer #3CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O)C1O5314.3Semi standard non polar33892256
Camellianin B,1TMS,isomer #4CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O5293.7Semi standard non polar33892256
Camellianin B,1TMS,isomer #5CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O5286.7Semi standard non polar33892256
Camellianin B,1TMS,isomer #6CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O5294.2Semi standard non polar33892256
Camellianin B,1TMS,isomer #7CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O5290.0Semi standard non polar33892256
Camellianin B,1TMS,isomer #8CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C5305.1Semi standard non polar33892256
Camellianin B,2TMS,isomer #1CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O)C1O5216.8Semi standard non polar33892256
Camellianin B,2TMS,isomer #10CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O5205.1Semi standard non polar33892256
Camellianin B,2TMS,isomer #11CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O5198.9Semi standard non polar33892256
Camellianin B,2TMS,isomer #12CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O5173.8Semi standard non polar33892256
Camellianin B,2TMS,isomer #13CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C5212.3Semi standard non polar33892256
Camellianin B,2TMS,isomer #14CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O5231.9Semi standard non polar33892256
Camellianin B,2TMS,isomer #15CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O5215.1Semi standard non polar33892256
Camellianin B,2TMS,isomer #16CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O5210.2Semi standard non polar33892256
Camellianin B,2TMS,isomer #17CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O5179.9Semi standard non polar33892256
Camellianin B,2TMS,isomer #18CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C5219.4Semi standard non polar33892256
Camellianin B,2TMS,isomer #19CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O5258.6Semi standard non polar33892256
Camellianin B,2TMS,isomer #2CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O)C1O5222.7Semi standard non polar33892256
Camellianin B,2TMS,isomer #20CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O5219.7Semi standard non polar33892256
Camellianin B,2TMS,isomer #21CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O5204.4Semi standard non polar33892256
Camellianin B,2TMS,isomer #22CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C5235.5Semi standard non polar33892256
Camellianin B,2TMS,isomer #23CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O5205.6Semi standard non polar33892256
Camellianin B,2TMS,isomer #24CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O5190.6Semi standard non polar33892256
Camellianin B,2TMS,isomer #25CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C5221.8Semi standard non polar33892256
Camellianin B,2TMS,isomer #26CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O5199.6Semi standard non polar33892256
Camellianin B,2TMS,isomer #27CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C5201.8Semi standard non polar33892256
Camellianin B,2TMS,isomer #28CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C5210.2Semi standard non polar33892256
Camellianin B,2TMS,isomer #3CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O5250.6Semi standard non polar33892256
Camellianin B,2TMS,isomer #4CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O5224.5Semi standard non polar33892256
Camellianin B,2TMS,isomer #5CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O5205.2Semi standard non polar33892256
Camellianin B,2TMS,isomer #6CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O5189.9Semi standard non polar33892256
Camellianin B,2TMS,isomer #7CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C5221.4Semi standard non polar33892256
Camellianin B,2TMS,isomer #8CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O)C1O5227.9Semi standard non polar33892256
Camellianin B,2TMS,isomer #9CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O5220.6Semi standard non polar33892256
Camellianin B,3TMS,isomer #1CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O)C1O5141.2Semi standard non polar33892256
Camellianin B,3TMS,isomer #10CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O5084.9Semi standard non polar33892256
Camellianin B,3TMS,isomer #11CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C5132.0Semi standard non polar33892256
Camellianin B,3TMS,isomer #12CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O5167.1Semi standard non polar33892256
Camellianin B,3TMS,isomer #13CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O5146.1Semi standard non polar33892256
Camellianin B,3TMS,isomer #14CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O5116.3Semi standard non polar33892256
Camellianin B,3TMS,isomer #15CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C5163.7Semi standard non polar33892256
Camellianin B,3TMS,isomer #16CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O5076.9Semi standard non polar33892256
Camellianin B,3TMS,isomer #17CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O5048.0Semi standard non polar33892256
Camellianin B,3TMS,isomer #18CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C5093.9Semi standard non polar33892256
Camellianin B,3TMS,isomer #19CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O5082.0Semi standard non polar33892256
Camellianin B,3TMS,isomer #2CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O5145.6Semi standard non polar33892256
Camellianin B,3TMS,isomer #20CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C5096.8Semi standard non polar33892256
Camellianin B,3TMS,isomer #21CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C5083.5Semi standard non polar33892256
Camellianin B,3TMS,isomer #22CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O5131.7Semi standard non polar33892256
Camellianin B,3TMS,isomer #23CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O5097.8Semi standard non polar33892256
Camellianin B,3TMS,isomer #24CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O5108.0Semi standard non polar33892256
Camellianin B,3TMS,isomer #25CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O5077.5Semi standard non polar33892256
Camellianin B,3TMS,isomer #26CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C5128.1Semi standard non polar33892256
Camellianin B,3TMS,isomer #27CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O5123.8Semi standard non polar33892256
Camellianin B,3TMS,isomer #28CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O5092.4Semi standard non polar33892256
Camellianin B,3TMS,isomer #29CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O5067.8Semi standard non polar33892256
Camellianin B,3TMS,isomer #3CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O5087.2Semi standard non polar33892256
Camellianin B,3TMS,isomer #30CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C5114.8Semi standard non polar33892256
Camellianin B,3TMS,isomer #31CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O5053.3Semi standard non polar33892256
Camellianin B,3TMS,isomer #32CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O5030.1Semi standard non polar33892256
Camellianin B,3TMS,isomer #33CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C5074.7Semi standard non polar33892256
Camellianin B,3TMS,isomer #34CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O5075.2Semi standard non polar33892256
Camellianin B,3TMS,isomer #35CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C5086.1Semi standard non polar33892256
Camellianin B,3TMS,isomer #36CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C5077.0Semi standard non polar33892256
Camellianin B,3TMS,isomer #37CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O5148.3Semi standard non polar33892256
Camellianin B,3TMS,isomer #38CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O5126.6Semi standard non polar33892256
Camellianin B,3TMS,isomer #39CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O5088.5Semi standard non polar33892256
Camellianin B,3TMS,isomer #4CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O5088.9Semi standard non polar33892256
Camellianin B,3TMS,isomer #40CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C5134.6Semi standard non polar33892256
Camellianin B,3TMS,isomer #41CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O5083.8Semi standard non polar33892256
Camellianin B,3TMS,isomer #42CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O5046.0Semi standard non polar33892256
Camellianin B,3TMS,isomer #43CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C5093.5Semi standard non polar33892256
Camellianin B,3TMS,isomer #44CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O5098.2Semi standard non polar33892256
Camellianin B,3TMS,isomer #45CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C5113.6Semi standard non polar33892256
Camellianin B,3TMS,isomer #46CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C5099.2Semi standard non polar33892256
Camellianin B,3TMS,isomer #47CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O5119.5Semi standard non polar33892256
Camellianin B,3TMS,isomer #48CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O5093.4Semi standard non polar33892256
Camellianin B,3TMS,isomer #49CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C5134.2Semi standard non polar33892256
Camellianin B,3TMS,isomer #5CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O5063.4Semi standard non polar33892256
Camellianin B,3TMS,isomer #50CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O5084.1Semi standard non polar33892256
Camellianin B,3TMS,isomer #51CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C5096.0Semi standard non polar33892256
Camellianin B,3TMS,isomer #52CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C5079.9Semi standard non polar33892256
Camellianin B,3TMS,isomer #53CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O5043.7Semi standard non polar33892256
Camellianin B,3TMS,isomer #54CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C5059.9Semi standard non polar33892256
Camellianin B,3TMS,isomer #55CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C5048.7Semi standard non polar33892256
Camellianin B,3TMS,isomer #56CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C5081.2Semi standard non polar33892256
Camellianin B,3TMS,isomer #6CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C5117.8Semi standard non polar33892256
Camellianin B,3TMS,isomer #7CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O5157.3Semi standard non polar33892256
Camellianin B,3TMS,isomer #8CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O5099.9Semi standard non polar33892256
Camellianin B,3TMS,isomer #9CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O5114.9Semi standard non polar33892256
Camellianin B,4TMS,isomer #1CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O5033.3Semi standard non polar33892256
Camellianin B,4TMS,isomer #10CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4951.2Semi standard non polar33892256
Camellianin B,4TMS,isomer #11CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4924.3Semi standard non polar33892256
Camellianin B,4TMS,isomer #12CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4989.8Semi standard non polar33892256
Camellianin B,4TMS,isomer #13CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4941.6Semi standard non polar33892256
Camellianin B,4TMS,isomer #14CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4964.4Semi standard non polar33892256
Camellianin B,4TMS,isomer #15CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4961.2Semi standard non polar33892256
Camellianin B,4TMS,isomer #16CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O5016.8Semi standard non polar33892256
Camellianin B,4TMS,isomer #17CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O4998.6Semi standard non polar33892256
Camellianin B,4TMS,isomer #18CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O4959.6Semi standard non polar33892256
Camellianin B,4TMS,isomer #19CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C5029.6Semi standard non polar33892256
Camellianin B,4TMS,isomer #2CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O4993.0Semi standard non polar33892256
Camellianin B,4TMS,isomer #20CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4954.0Semi standard non polar33892256
Camellianin B,4TMS,isomer #21CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4923.5Semi standard non polar33892256
Camellianin B,4TMS,isomer #22CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4988.2Semi standard non polar33892256
Camellianin B,4TMS,isomer #23CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4949.4Semi standard non polar33892256
Camellianin B,4TMS,isomer #24CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4977.8Semi standard non polar33892256
Camellianin B,4TMS,isomer #25CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4969.4Semi standard non polar33892256
Camellianin B,4TMS,isomer #26CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4989.1Semi standard non polar33892256
Camellianin B,4TMS,isomer #27CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4964.1Semi standard non polar33892256
Camellianin B,4TMS,isomer #28CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C5015.4Semi standard non polar33892256
Camellianin B,4TMS,isomer #29CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4962.1Semi standard non polar33892256
Camellianin B,4TMS,isomer #3CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O4992.3Semi standard non polar33892256
Camellianin B,4TMS,isomer #30CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4986.0Semi standard non polar33892256
Camellianin B,4TMS,isomer #31CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4983.0Semi standard non polar33892256
Camellianin B,4TMS,isomer #32CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4928.9Semi standard non polar33892256
Camellianin B,4TMS,isomer #33CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4948.2Semi standard non polar33892256
Camellianin B,4TMS,isomer #34CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4949.2Semi standard non polar33892256
Camellianin B,4TMS,isomer #35CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4957.0Semi standard non polar33892256
Camellianin B,4TMS,isomer #36CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O5004.9Semi standard non polar33892256
Camellianin B,4TMS,isomer #37CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O4984.4Semi standard non polar33892256
Camellianin B,4TMS,isomer #38CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O4954.2Semi standard non polar33892256
Camellianin B,4TMS,isomer #39CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C5009.7Semi standard non polar33892256
Camellianin B,4TMS,isomer #4CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O4956.3Semi standard non polar33892256
Camellianin B,4TMS,isomer #40CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4956.7Semi standard non polar33892256
Camellianin B,4TMS,isomer #41CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4926.7Semi standard non polar33892256
Camellianin B,4TMS,isomer #42CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4980.9Semi standard non polar33892256
Camellianin B,4TMS,isomer #43CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4964.0Semi standard non polar33892256
Camellianin B,4TMS,isomer #44CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4980.4Semi standard non polar33892256
Camellianin B,4TMS,isomer #45CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4978.9Semi standard non polar33892256
Camellianin B,4TMS,isomer #46CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4963.3Semi standard non polar33892256
Camellianin B,4TMS,isomer #47CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4935.4Semi standard non polar33892256
Camellianin B,4TMS,isomer #48CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4992.3Semi standard non polar33892256
Camellianin B,4TMS,isomer #49CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4934.2Semi standard non polar33892256
Camellianin B,4TMS,isomer #5CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C5023.3Semi standard non polar33892256
Camellianin B,4TMS,isomer #50CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4952.6Semi standard non polar33892256
Camellianin B,4TMS,isomer #51CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4950.6Semi standard non polar33892256
Camellianin B,4TMS,isomer #52CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4915.3Semi standard non polar33892256
Camellianin B,4TMS,isomer #53CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4934.8Semi standard non polar33892256
Camellianin B,4TMS,isomer #54CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4929.2Semi standard non polar33892256
Camellianin B,4TMS,isomer #55CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4950.5Semi standard non polar33892256
Camellianin B,4TMS,isomer #56CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4979.6Semi standard non polar33892256
Camellianin B,4TMS,isomer #57CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4940.8Semi standard non polar33892256
Camellianin B,4TMS,isomer #58CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C5002.1Semi standard non polar33892256
Camellianin B,4TMS,isomer #59CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4945.1Semi standard non polar33892256
Camellianin B,4TMS,isomer #6CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O5007.2Semi standard non polar33892256
Camellianin B,4TMS,isomer #60CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4968.9Semi standard non polar33892256
Camellianin B,4TMS,isomer #61CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4960.1Semi standard non polar33892256
Camellianin B,4TMS,isomer #62CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4918.5Semi standard non polar33892256
Camellianin B,4TMS,isomer #63CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4941.9Semi standard non polar33892256
Camellianin B,4TMS,isomer #64CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4933.5Semi standard non polar33892256
Camellianin B,4TMS,isomer #65CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4967.3Semi standard non polar33892256
Camellianin B,4TMS,isomer #66CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4935.6Semi standard non polar33892256
Camellianin B,4TMS,isomer #67CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4959.7Semi standard non polar33892256
Camellianin B,4TMS,isomer #68CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4956.3Semi standard non polar33892256
Camellianin B,4TMS,isomer #69CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4949.2Semi standard non polar33892256
Camellianin B,4TMS,isomer #7CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O4985.0Semi standard non polar33892256
Camellianin B,4TMS,isomer #70CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4927.9Semi standard non polar33892256
Camellianin B,4TMS,isomer #8CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O4959.5Semi standard non polar33892256
Camellianin B,4TMS,isomer #9CC1OC(OC2C(CO[Si](C)(C)C)OC(OC3=CC(O[Si](C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C5026.5Semi standard non polar33892256
Camellianin B,1TBDMS,isomer #1CC1OC(OC2C(CO[Si](C)(C)C(C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O)C1O5486.1Semi standard non polar33892256
Camellianin B,1TBDMS,isomer #2CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C(C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O)C1O5508.0Semi standard non polar33892256
Camellianin B,1TBDMS,isomer #3CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O)C1O5508.2Semi standard non polar33892256
Camellianin B,1TBDMS,isomer #4CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O5534.7Semi standard non polar33892256
Camellianin B,1TBDMS,isomer #5CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O5525.6Semi standard non polar33892256
Camellianin B,1TBDMS,isomer #6CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O5530.9Semi standard non polar33892256
Camellianin B,1TBDMS,isomer #7CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O5533.3Semi standard non polar33892256
Camellianin B,1TBDMS,isomer #8CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C5546.5Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #1CC1OC(OC2C(CO[Si](C)(C)C(C)(C)C)OC(OC3=CC(O[Si](C)(C)C(C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O)C1O5597.8Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #10CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C(C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O5600.7Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #11CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C(C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O5570.6Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #12CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C(C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O5581.1Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #13CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C(C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C5608.9Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #14CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)O4)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O5624.7Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #15CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)O4)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O5606.3Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #16CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O5571.5Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #17CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O5582.9Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #18CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C5610.7Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #19CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O5631.7Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #2CC1OC(OC2C(CO[Si](C)(C)C(C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O)C1O5607.8Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #20CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O5585.5Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #21CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O5589.9Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #22CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C5625.2Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #23CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O5564.2Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #24CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O5575.1Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #25CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C5604.3Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #26CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O5563.0Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #27CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C5585.8Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #28CC1OC(OC2C(CO)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C5594.3Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #3CC1OC(OC2C(CO[Si](C)(C)C(C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O5619.4Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #4CC1OC(OC2C(CO[Si](C)(C)C(C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O5594.3Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #5CC1OC(OC2C(CO[Si](C)(C)C(C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O5563.7Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #6CC1OC(OC2C(CO[Si](C)(C)C(C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O5570.2Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #7CC1OC(OC2C(CO[Si](C)(C)C(C)(C)C)OC(OC3=CC(O)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C5600.7Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #8CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C(C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)O4)C(O)C2O)C(O)C(O)C1O5628.3Semi standard non polar33892256
Camellianin B,2TBDMS,isomer #9CC1OC(OC2C(CO)OC(OC3=CC(O[Si](C)(C)C(C)(C)C)=CC4=C3C(=O)C=C(C3=CC=C(O)C=C3)O4)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O5617.9Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (Non-derivatized) - 70eV, Positivesplash10-044j-6382190000-98a6aa3adf3658eab8a32017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (1 TMS) - 70eV, Positivesplash10-0080-9536117000-87c56b7fbeb1f89117592017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS ("Camellianin B,1TMS,#1" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_1_8) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Camellianin B GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Camellianin B 10V, Positive-QTOFsplash10-00di-0090760000-38cf111c08c67092a1c02017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Camellianin B 20V, Positive-QTOFsplash10-00di-0190300000-6d9412c12240d580d9592017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Camellianin B 40V, Positive-QTOFsplash10-00di-1290100000-2b60c7f57756219599162017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Camellianin B 10V, Negative-QTOFsplash10-016r-2390580000-6f95d977a51c5728b4272017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Camellianin B 20V, Negative-QTOFsplash10-014i-1290320000-a26f3140afe273de96b02017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Camellianin B 40V, Negative-QTOFsplash10-014i-2390000000-5b7bad3db6d6817045a32017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Camellianin B 10V, Positive-QTOFsplash10-004i-0000090000-ed76a1e0332f667006022021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Camellianin B 20V, Positive-QTOFsplash10-004i-0000090000-ed76a1e0332f667006022021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Camellianin B 40V, Positive-QTOFsplash10-03fr-0600960000-42cd3f2954e566cebbfa2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Camellianin B 10V, Negative-QTOFsplash10-004i-0000090000-205d908166a11e471cd92021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Camellianin B 20V, Negative-QTOFsplash10-004i-0000090000-6ecc991f16d1ad27701f2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Camellianin B 40V, Negative-QTOFsplash10-0a4i-0900530000-72a2c6f9d30c8b330d1e2021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • 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 IDFDB020268
KNApSAcK IDC00053961
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound73989750
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. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .