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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2013-06-05 01:09:43 UTC
Update Date2022-03-07 03:03:51 UTC
HMDB IDHMDB0060527
Secondary Accession Numbers
  • HMDB60527
Metabolite Identification
Common NameKukoamine D
DescriptionKukoamine D is an alkaloid from the root bark of Lycium chinense (Chinese boxthorn). UK scientists at the Institute for Food Research have identified blood pressure-lowering compounds called kukoamines in potatoes. Previously only found in Lycium chinense, an exotic herbal plant whose bark is used to make an infusion in Chinese herbal medicine. (http://www.whfoods.com/genpage.php?tname=foodspice&dbid=48)
Structure
Data?1563866072
SynonymsNot Available
Chemical FormulaC28H42N4O6
Average Molecular Weight530.6563
Monoisotopic Molecular Weight530.310435096
IUPAC NameN-[3-(N-{4-[(3-aminopropyl)amino]butyl}-3-(3,4-dihydroxyphenyl)propanamido)propyl]-3-(3,4-dihydroxyphenyl)propanamide
Traditional NameN-[3-(N-{4-[(3-aminopropyl)amino]butyl}-3-(3,4-dihydroxyphenyl)propanamido)propyl]-3-(3,4-dihydroxyphenyl)propanamide
CAS Registry NumberNot Available
SMILES
NCCCNCCCCN(CCCNC(=O)CCC1=CC(O)=C(O)C=C1)C(=O)CCC1=CC(O)=C(O)C=C1
InChI Identifier
InChI=1S/C28H42N4O6/c29-13-3-15-30-14-1-2-17-32(28(38)12-8-22-6-10-24(34)26(36)20-22)18-4-16-31-27(37)11-7-21-5-9-23(33)25(35)19-21/h5-6,9-10,19-20,30,33-36H,1-4,7-8,11-18,29H2,(H,31,37)
InChI KeyVZOUDULKCUBJHR-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as catechols. Catechols are compounds containing a 1,2-benzenediol moiety.
KingdomOrganic compounds
Super ClassBenzenoids
ClassPhenols
Sub ClassBenzenediols
Direct ParentCatechols
Alternative Parents
Substituents
  • Catechol
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Monocyclic benzene moiety
  • Fatty acyl
  • Fatty amide
  • Tertiary carboxylic acid amide
  • Amino acid or derivatives
  • Carboxamide group
  • Secondary carboxylic acid amide
  • Carboxylic acid derivative
  • Secondary amine
  • Secondary aliphatic amine
  • Amine
  • Organonitrogen compound
  • Primary aliphatic amine
  • Organooxygen compound
  • Primary amine
  • Hydrocarbon derivative
  • Organic oxide
  • Organopnictogen compound
  • Carbonyl group
  • Organic oxygen compound
  • Organic nitrogen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External Descriptors
Ontology
Not AvailableNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.041 g/LALOGPS
logP1.3ALOGPS
logP-0.054ChemAxon
logS-4.1ALOGPS
pKa (Strongest Acidic)8.26ChemAxon
pKa (Strongest Basic)9.58ChemAxon
Physiological Charge2ChemAxon
Hydrogen Acceptor Count8ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area168.38 ŲChemAxon
Rotatable Bond Count18ChemAxon
Refractivity148.14 m³·mol⁻¹ChemAxon
Polarizability60.66 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+226.5331661259
DarkChem[M-H]-220.21931661259
DeepCCS[M+H]+224.36930932474
DeepCCS[M-H]-221.97430932474
DeepCCS[M-2H]-254.85630932474
DeepCCS[M+Na]+230.99130932474
AllCCS[M+H]+223.832859911
AllCCS[M+H-H2O]+222.532859911
AllCCS[M+NH4]+224.932859911
AllCCS[M+Na]+225.332859911
AllCCS[M-H]-210.632859911
AllCCS[M+Na-2H]-213.132859911
AllCCS[M+HCOO]-216.032859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Kukoamine DNCCCNCCCCN(CCCNC(=O)CCC1=CC(O)=C(O)C=C1)C(=O)CCC1=CC(O)=C(O)C=C15541.2Standard polar33892256
Kukoamine DNCCCNCCCCN(CCCNC(=O)CCC1=CC(O)=C(O)C=C1)C(=O)CCC1=CC(O)=C(O)C=C14544.4Standard non polar33892256
Kukoamine DNCCCNCCCCN(CCCNC(=O)CCC1=CC(O)=C(O)C=C1)C(=O)CCC1=CC(O)=C(O)C=C15149.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Kukoamine D,1TMS,isomer #1C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O4983.1Semi standard non polar33892256
Kukoamine D,1TMS,isomer #2C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O4988.0Semi standard non polar33892256
Kukoamine D,1TMS,isomer #3C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O4983.0Semi standard non polar33892256
Kukoamine D,1TMS,isomer #4C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O4987.5Semi standard non polar33892256
Kukoamine D,1TMS,isomer #5C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C15214.7Semi standard non polar33892256
Kukoamine D,1TMS,isomer #6C[Si](C)(C)N(CCCN)CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C15080.7Semi standard non polar33892256
Kukoamine D,1TMS,isomer #7C[Si](C)(C)N(CCCN(CCCCNCCCN)C(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C15011.8Semi standard non polar33892256
Kukoamine D,2TMS,isomer #1C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCNC(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C1O4979.1Semi standard non polar33892256
Kukoamine D,2TMS,isomer #10C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O4876.6Semi standard non polar33892256
Kukoamine D,2TMS,isomer #11C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O4920.7Semi standard non polar33892256
Kukoamine D,2TMS,isomer #12C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C4928.1Semi standard non polar33892256
Kukoamine D,2TMS,isomer #13C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C15078.9Semi standard non polar33892256
Kukoamine D,2TMS,isomer #14C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O4928.0Semi standard non polar33892256
Kukoamine D,2TMS,isomer #15C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)=CC=C1O4884.5Semi standard non polar33892256
Kukoamine D,2TMS,isomer #16C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C15086.2Semi standard non polar33892256
Kukoamine D,2TMS,isomer #17C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O4922.9Semi standard non polar33892256
Kukoamine D,2TMS,isomer #18C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O4876.6Semi standard non polar33892256
Kukoamine D,2TMS,isomer #19C[Si](C)(C)N(CCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C5279.8Semi standard non polar33892256
Kukoamine D,2TMS,isomer #2C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)=CC=C1O4963.5Semi standard non polar33892256
Kukoamine D,2TMS,isomer #20C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C5188.8Semi standard non polar33892256
Kukoamine D,2TMS,isomer #21C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C15084.2Semi standard non polar33892256
Kukoamine D,2TMS,isomer #22C[Si](C)(C)N(CCCN)CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C14906.0Semi standard non polar33892256
Kukoamine D,2TMS,isomer #3C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C4927.8Semi standard non polar33892256
Kukoamine D,2TMS,isomer #4C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O)=C15078.8Semi standard non polar33892256
Kukoamine D,2TMS,isomer #5C[Si](C)(C)OC1=CC(CCC(=O)N(CCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)=CC=C1O4883.7Semi standard non polar33892256
Kukoamine D,2TMS,isomer #6C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O4925.5Semi standard non polar33892256
Kukoamine D,2TMS,isomer #7C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O)=C2)C=C1O4995.5Semi standard non polar33892256
Kukoamine D,2TMS,isomer #8C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C1O4977.8Semi standard non polar33892256
Kukoamine D,2TMS,isomer #9C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C15085.0Semi standard non polar33892256
Kukoamine D,3TMS,isomer #1C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCNC(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O4962.6Semi standard non polar33892256
Kukoamine D,3TMS,isomer #10C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O)=C15022.8Semi standard non polar33892256
Kukoamine D,3TMS,isomer #11C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C4832.8Semi standard non polar33892256
Kukoamine D,3TMS,isomer #12C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C4856.1Semi standard non polar33892256
Kukoamine D,3TMS,isomer #13C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O5146.0Semi standard non polar33892256
Kukoamine D,3TMS,isomer #14C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C5042.2Semi standard non polar33892256
Kukoamine D,3TMS,isomer #15C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C14965.4Semi standard non polar33892256
Kukoamine D,3TMS,isomer #16C[Si](C)(C)OC1=CC(CCC(=O)N(CCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)=CC=C1O4789.3Semi standard non polar33892256
Kukoamine D,3TMS,isomer #17C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O4962.3Semi standard non polar33892256
Kukoamine D,3TMS,isomer #18C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C15053.0Semi standard non polar33892256
Kukoamine D,3TMS,isomer #19C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O)=C2)[Si](C)(C)C)C=C1O4872.2Semi standard non polar33892256
Kukoamine D,3TMS,isomer #2C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)=CC=C1O4950.7Semi standard non polar33892256
Kukoamine D,3TMS,isomer #20C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O)=C2)C=C1O4882.9Semi standard non polar33892256
Kukoamine D,3TMS,isomer #21C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C15037.4Semi standard non polar33892256
Kukoamine D,3TMS,isomer #22C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O4855.9Semi standard non polar33892256
Kukoamine D,3TMS,isomer #23C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C1O4876.2Semi standard non polar33892256
Kukoamine D,3TMS,isomer #24C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O5148.4Semi standard non polar33892256
Kukoamine D,3TMS,isomer #25C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C5040.6Semi standard non polar33892256
Kukoamine D,3TMS,isomer #26C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C14970.2Semi standard non polar33892256
Kukoamine D,3TMS,isomer #27C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O4787.5Semi standard non polar33892256
Kukoamine D,3TMS,isomer #28C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C15023.2Semi standard non polar33892256
Kukoamine D,3TMS,isomer #29C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C4858.6Semi standard non polar33892256
Kukoamine D,3TMS,isomer #3C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C15038.8Semi standard non polar33892256
Kukoamine D,3TMS,isomer #30C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C4832.8Semi standard non polar33892256
Kukoamine D,3TMS,isomer #31C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O5146.4Semi standard non polar33892256
Kukoamine D,3TMS,isomer #32C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C5043.9Semi standard non polar33892256
Kukoamine D,3TMS,isomer #33C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C14966.4Semi standard non polar33892256
Kukoamine D,3TMS,isomer #34C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)=CC=C1O4789.6Semi standard non polar33892256
Kukoamine D,3TMS,isomer #35C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O5148.3Semi standard non polar33892256
Kukoamine D,3TMS,isomer #36C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C5041.3Semi standard non polar33892256
Kukoamine D,3TMS,isomer #37C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C14969.2Semi standard non polar33892256
Kukoamine D,3TMS,isomer #38C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O4787.9Semi standard non polar33892256
Kukoamine D,3TMS,isomer #39C[Si](C)(C)N(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C1)CCCN([Si](C)(C)C)[Si](C)(C)C5265.1Semi standard non polar33892256
Kukoamine D,3TMS,isomer #4C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C1O4874.6Semi standard non polar33892256
Kukoamine D,3TMS,isomer #40C[Si](C)(C)N(CCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C15129.9Semi standard non polar33892256
Kukoamine D,3TMS,isomer #41C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C5023.7Semi standard non polar33892256
Kukoamine D,3TMS,isomer #5C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O4854.1Semi standard non polar33892256
Kukoamine D,3TMS,isomer #6C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN)CCCNC(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)=CC=C1O4950.7Semi standard non polar33892256
Kukoamine D,3TMS,isomer #7C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C15023.9Semi standard non polar33892256
Kukoamine D,3TMS,isomer #8C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)=CC=C1O4845.3Semi standard non polar33892256
Kukoamine D,3TMS,isomer #9C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)=CC=C1O4874.7Semi standard non polar33892256
Kukoamine D,4TMS,isomer #1C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C4953.2Semi standard non polar33892256
Kukoamine D,4TMS,isomer #10C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C14913.7Semi standard non polar33892256
Kukoamine D,4TMS,isomer #11C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O4774.1Semi standard non polar33892256
Kukoamine D,4TMS,isomer #12C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C15012.2Semi standard non polar33892256
Kukoamine D,4TMS,isomer #13C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)=CC=C1O4847.5Semi standard non polar33892256
Kukoamine D,4TMS,isomer #14C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)=CC=C1O4833.1Semi standard non polar33892256
Kukoamine D,4TMS,isomer #15C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)=CC=C1O5117.7Semi standard non polar33892256
Kukoamine D,4TMS,isomer #16C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4961.0Semi standard non polar33892256
Kukoamine D,4TMS,isomer #17C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C14909.7Semi standard non polar33892256
Kukoamine D,4TMS,isomer #18C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)=CC=C1O4764.6Semi standard non polar33892256
Kukoamine D,4TMS,isomer #19C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C5112.3Semi standard non polar33892256
Kukoamine D,4TMS,isomer #2C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C15025.4Semi standard non polar33892256
Kukoamine D,4TMS,isomer #20C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C4997.9Semi standard non polar33892256
Kukoamine D,4TMS,isomer #21C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C14935.7Semi standard non polar33892256
Kukoamine D,4TMS,isomer #22C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C4780.4Semi standard non polar33892256
Kukoamine D,4TMS,isomer #23C[Si](C)(C)OC1=CC(CCC(=O)N(CCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)=CC=C1O5070.3Semi standard non polar33892256
Kukoamine D,4TMS,isomer #24C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O5150.0Semi standard non polar33892256
Kukoamine D,4TMS,isomer #25C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C4939.0Semi standard non polar33892256
Kukoamine D,4TMS,isomer #26C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C15025.1Semi standard non polar33892256
Kukoamine D,4TMS,isomer #27C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O4852.5Semi standard non polar33892256
Kukoamine D,4TMS,isomer #28C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O4852.1Semi standard non polar33892256
Kukoamine D,4TMS,isomer #29C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O)=C2)C=C1O5132.2Semi standard non polar33892256
Kukoamine D,4TMS,isomer #3C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O4851.8Semi standard non polar33892256
Kukoamine D,4TMS,isomer #30C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C4978.5Semi standard non polar33892256
Kukoamine D,4TMS,isomer #31C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C14934.5Semi standard non polar33892256
Kukoamine D,4TMS,isomer #32C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O)=C2)[Si](C)(C)C)C=C1O4787.3Semi standard non polar33892256
Kukoamine D,4TMS,isomer #33C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C1O5120.8Semi standard non polar33892256
Kukoamine D,4TMS,isomer #34C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4964.9Semi standard non polar33892256
Kukoamine D,4TMS,isomer #35C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C14916.6Semi standard non polar33892256
Kukoamine D,4TMS,isomer #36C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O4774.8Semi standard non polar33892256
Kukoamine D,4TMS,isomer #37C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O5072.2Semi standard non polar33892256
Kukoamine D,4TMS,isomer #38C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O5152.5Semi standard non polar33892256
Kukoamine D,4TMS,isomer #39C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C4941.3Semi standard non polar33892256
Kukoamine D,4TMS,isomer #4C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O4850.7Semi standard non polar33892256
Kukoamine D,4TMS,isomer #40C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C5112.3Semi standard non polar33892256
Kukoamine D,4TMS,isomer #41C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4997.7Semi standard non polar33892256
Kukoamine D,4TMS,isomer #42C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C14937.1Semi standard non polar33892256
Kukoamine D,4TMS,isomer #43C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C4780.6Semi standard non polar33892256
Kukoamine D,4TMS,isomer #44C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O5150.0Semi standard non polar33892256
Kukoamine D,4TMS,isomer #45C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)=CC=C1O5070.3Semi standard non polar33892256
Kukoamine D,4TMS,isomer #46C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4939.0Semi standard non polar33892256
Kukoamine D,4TMS,isomer #47C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O5151.8Semi standard non polar33892256
Kukoamine D,4TMS,isomer #48C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O5072.2Semi standard non polar33892256
Kukoamine D,4TMS,isomer #49C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C4941.8Semi standard non polar33892256
Kukoamine D,4TMS,isomer #5C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C15012.5Semi standard non polar33892256
Kukoamine D,4TMS,isomer #50C[Si](C)(C)N(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C1)CCCN([Si](C)(C)C)[Si](C)(C)C5167.7Semi standard non polar33892256
Kukoamine D,4TMS,isomer #6C[Si](C)(C)OC1=CC(CCC(=O)N(CCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)=CC=C1O4834.4Semi standard non polar33892256
Kukoamine D,4TMS,isomer #7C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)=CC=C1O4847.4Semi standard non polar33892256
Kukoamine D,4TMS,isomer #8C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C1O5121.7Semi standard non polar33892256
Kukoamine D,4TMS,isomer #9C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C4966.0Semi standard non polar33892256
Kukoamine D,5TMS,isomer #1C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C15022.2Semi standard non polar33892256
Kukoamine D,5TMS,isomer #1C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C14454.8Standard non polar33892256
Kukoamine D,5TMS,isomer #1C[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C15053.7Standard polar33892256
Kukoamine D,5TMS,isomer #10C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C14923.9Semi standard non polar33892256
Kukoamine D,5TMS,isomer #10C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C14525.8Standard non polar33892256
Kukoamine D,5TMS,isomer #10C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C15284.0Standard polar33892256
Kukoamine D,5TMS,isomer #11C[Si](C)(C)OC1=CC(CCC(=O)N(CCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)=CC=C1O4787.8Semi standard non polar33892256
Kukoamine D,5TMS,isomer #11C[Si](C)(C)OC1=CC(CCC(=O)N(CCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)=CC=C1O4331.1Standard non polar33892256
Kukoamine D,5TMS,isomer #11C[Si](C)(C)OC1=CC(CCC(=O)N(CCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)=CC=C1O5864.2Standard polar33892256
Kukoamine D,5TMS,isomer #12C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C1O5117.4Semi standard non polar33892256
Kukoamine D,5TMS,isomer #12C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C1O4566.4Standard non polar33892256
Kukoamine D,5TMS,isomer #12C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C1O5544.3Standard polar33892256
Kukoamine D,5TMS,isomer #13C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O5084.2Semi standard non polar33892256
Kukoamine D,5TMS,isomer #13C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O4614.0Standard non polar33892256
Kukoamine D,5TMS,isomer #13C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O5482.2Standard polar33892256
Kukoamine D,5TMS,isomer #14C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C4889.3Semi standard non polar33892256
Kukoamine D,5TMS,isomer #14C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C4515.6Standard non polar33892256
Kukoamine D,5TMS,isomer #14C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C5517.0Standard polar33892256
Kukoamine D,5TMS,isomer #15C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)=CC=C1O5112.8Semi standard non polar33892256
Kukoamine D,5TMS,isomer #15C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)=CC=C1O4562.1Standard non polar33892256
Kukoamine D,5TMS,isomer #15C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)=CC=C1O5310.7Standard polar33892256
Kukoamine D,5TMS,isomer #16C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4940.4Semi standard non polar33892256
Kukoamine D,5TMS,isomer #16C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4444.1Standard non polar33892256
Kukoamine D,5TMS,isomer #16C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C5351.8Standard polar33892256
Kukoamine D,5TMS,isomer #17C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C14924.3Semi standard non polar33892256
Kukoamine D,5TMS,isomer #17C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C14525.6Standard non polar33892256
Kukoamine D,5TMS,isomer #17C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C15283.5Standard polar33892256
Kukoamine D,5TMS,isomer #18C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)=CC=C1O4786.9Semi standard non polar33892256
Kukoamine D,5TMS,isomer #18C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)=CC=C1O4331.1Standard non polar33892256
Kukoamine D,5TMS,isomer #18C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)=CC=C1O5863.8Standard polar33892256
Kukoamine D,5TMS,isomer #19C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)=CC=C1O5073.9Semi standard non polar33892256
Kukoamine D,5TMS,isomer #19C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)=CC=C1O4621.5Standard non polar33892256
Kukoamine D,5TMS,isomer #19C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)=CC=C1O5552.5Standard polar33892256
Kukoamine D,5TMS,isomer #2C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C4872.5Semi standard non polar33892256
Kukoamine D,5TMS,isomer #2C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C4275.9Standard non polar33892256
Kukoamine D,5TMS,isomer #2C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C5617.6Standard polar33892256
Kukoamine D,5TMS,isomer #20C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)=CC=C1O5114.9Semi standard non polar33892256
Kukoamine D,5TMS,isomer #20C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)=CC=C1O4572.8Standard non polar33892256
Kukoamine D,5TMS,isomer #20C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)=CC=C1O5612.4Standard polar33892256
Kukoamine D,5TMS,isomer #21C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4876.0Semi standard non polar33892256
Kukoamine D,5TMS,isomer #21C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4523.3Standard non polar33892256
Kukoamine D,5TMS,isomer #21C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C5581.5Standard polar33892256
Kukoamine D,5TMS,isomer #22C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C5079.7Semi standard non polar33892256
Kukoamine D,5TMS,isomer #22C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C4579.8Standard non polar33892256
Kukoamine D,5TMS,isomer #22C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C5349.5Standard polar33892256
Kukoamine D,5TMS,isomer #23C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C5148.9Semi standard non polar33892256
Kukoamine D,5TMS,isomer #23C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C4529.5Standard non polar33892256
Kukoamine D,5TMS,isomer #23C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C5411.9Standard polar33892256
Kukoamine D,5TMS,isomer #24C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C4927.3Semi standard non polar33892256
Kukoamine D,5TMS,isomer #24C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C4480.4Standard non polar33892256
Kukoamine D,5TMS,isomer #24C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C5386.3Standard polar33892256
Kukoamine D,5TMS,isomer #25C[Si](C)(C)OC1=CC(CCC(=O)N(CCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)=CC=C1O5097.9Semi standard non polar33892256
Kukoamine D,5TMS,isomer #25C[Si](C)(C)OC1=CC(CCC(=O)N(CCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)=CC=C1O4617.2Standard non polar33892256
Kukoamine D,5TMS,isomer #25C[Si](C)(C)OC1=CC(CCC(=O)N(CCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)=CC=C1O5645.0Standard polar33892256
Kukoamine D,5TMS,isomer #26C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O5125.9Semi standard non polar33892256
Kukoamine D,5TMS,isomer #26C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O4553.1Standard non polar33892256
Kukoamine D,5TMS,isomer #26C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O5235.1Standard polar33892256
Kukoamine D,5TMS,isomer #27C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4949.6Semi standard non polar33892256
Kukoamine D,5TMS,isomer #27C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4430.1Standard non polar33892256
Kukoamine D,5TMS,isomer #27C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C5275.8Standard polar33892256
Kukoamine D,5TMS,isomer #28C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C14945.5Semi standard non polar33892256
Kukoamine D,5TMS,isomer #28C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C14517.7Standard non polar33892256
Kukoamine D,5TMS,isomer #28C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C15208.1Standard polar33892256
Kukoamine D,5TMS,isomer #29C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O4804.7Semi standard non polar33892256
Kukoamine D,5TMS,isomer #29C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O4324.4Standard non polar33892256
Kukoamine D,5TMS,isomer #29C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O5801.3Standard polar33892256
Kukoamine D,5TMS,isomer #3C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C4862.1Semi standard non polar33892256
Kukoamine D,5TMS,isomer #3C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C4227.2Standard non polar33892256
Kukoamine D,5TMS,isomer #3C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C5655.3Standard polar33892256
Kukoamine D,5TMS,isomer #30C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O)=C2)[Si](C)(C)C)C=C1O5102.9Semi standard non polar33892256
Kukoamine D,5TMS,isomer #30C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O)=C2)[Si](C)(C)C)C=C1O4607.3Standard non polar33892256
Kukoamine D,5TMS,isomer #30C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O)=C2)[Si](C)(C)C)C=C1O5409.6Standard polar33892256
Kukoamine D,5TMS,isomer #31C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O)=C2)C=C1O5127.3Semi standard non polar33892256
Kukoamine D,5TMS,isomer #31C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O)=C2)C=C1O4560.0Standard non polar33892256
Kukoamine D,5TMS,isomer #31C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O)=C2)C=C1O5471.4Standard polar33892256
Kukoamine D,5TMS,isomer #32C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C4913.4Semi standard non polar33892256
Kukoamine D,5TMS,isomer #32C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C4508.7Standard non polar33892256
Kukoamine D,5TMS,isomer #32C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C5446.8Standard polar33892256
Kukoamine D,5TMS,isomer #33C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O5086.0Semi standard non polar33892256
Kukoamine D,5TMS,isomer #33C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O4614.9Standard non polar33892256
Kukoamine D,5TMS,isomer #33C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O5482.1Standard polar33892256
Kukoamine D,5TMS,isomer #34C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C1O5114.9Semi standard non polar33892256
Kukoamine D,5TMS,isomer #34C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C1O4566.5Standard non polar33892256
Kukoamine D,5TMS,isomer #34C[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C1O5544.3Standard polar33892256
Kukoamine D,5TMS,isomer #35C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4889.5Semi standard non polar33892256
Kukoamine D,5TMS,isomer #35C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4516.6Standard non polar33892256
Kukoamine D,5TMS,isomer #35C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)[Si](C)(C)C5516.9Standard polar33892256
Kukoamine D,5TMS,isomer #36C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O5105.3Semi standard non polar33892256
Kukoamine D,5TMS,isomer #36C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O4616.7Standard non polar33892256
Kukoamine D,5TMS,isomer #36C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O5583.1Standard polar33892256
Kukoamine D,5TMS,isomer #37C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C5148.0Semi standard non polar33892256
Kukoamine D,5TMS,isomer #37C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C4529.5Standard non polar33892256
Kukoamine D,5TMS,isomer #37C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C5412.3Standard polar33892256
Kukoamine D,5TMS,isomer #38C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C5079.0Semi standard non polar33892256
Kukoamine D,5TMS,isomer #38C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C4581.6Standard non polar33892256
Kukoamine D,5TMS,isomer #38C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C5350.0Standard polar33892256
Kukoamine D,5TMS,isomer #39C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4927.1Semi standard non polar33892256
Kukoamine D,5TMS,isomer #39C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4481.7Standard non polar33892256
Kukoamine D,5TMS,isomer #39C[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C5386.8Standard polar33892256
Kukoamine D,5TMS,isomer #4C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O5127.0Semi standard non polar33892256
Kukoamine D,5TMS,isomer #4C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O4552.9Standard non polar33892256
Kukoamine D,5TMS,isomer #4C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)CCCNC(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C1O5234.8Standard polar33892256
Kukoamine D,5TMS,isomer #40C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)=CC=C1O5097.6Semi standard non polar33892256
Kukoamine D,5TMS,isomer #40C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)=CC=C1O4618.3Standard non polar33892256
Kukoamine D,5TMS,isomer #40C[Si](C)(C)OC1=CC(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)=CC=C1O5645.0Standard polar33892256
Kukoamine D,5TMS,isomer #41C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O5105.9Semi standard non polar33892256
Kukoamine D,5TMS,isomer #41C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O4617.0Standard non polar33892256
Kukoamine D,5TMS,isomer #41C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C1O5583.1Standard polar33892256
Kukoamine D,5TMS,isomer #5C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C4951.1Semi standard non polar33892256
Kukoamine D,5TMS,isomer #5C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C4430.2Standard non polar33892256
Kukoamine D,5TMS,isomer #5C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C1)[Si](C)(C)C5275.6Standard polar33892256
Kukoamine D,5TMS,isomer #6C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C14942.5Semi standard non polar33892256
Kukoamine D,5TMS,isomer #6C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C14515.6Standard non polar33892256
Kukoamine D,5TMS,isomer #6C[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O)=C15207.7Standard polar33892256
Kukoamine D,5TMS,isomer #7C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O4803.6Semi standard non polar33892256
Kukoamine D,5TMS,isomer #7C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O4323.8Standard non polar33892256
Kukoamine D,5TMS,isomer #7C[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C1O5801.3Standard polar33892256
Kukoamine D,5TMS,isomer #8C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)=CC=C1O5112.9Semi standard non polar33892256
Kukoamine D,5TMS,isomer #8C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)=CC=C1O4561.8Standard non polar33892256
Kukoamine D,5TMS,isomer #8C[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)=CC=C1O5311.1Standard polar33892256
Kukoamine D,5TMS,isomer #9C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4940.4Semi standard non polar33892256
Kukoamine D,5TMS,isomer #9C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C4443.8Standard non polar33892256
Kukoamine D,5TMS,isomer #9C[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)C5352.1Standard polar33892256
Kukoamine D,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O5280.1Semi standard non polar33892256
Kukoamine D,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O5285.3Semi standard non polar33892256
Kukoamine D,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O5280.6Semi standard non polar33892256
Kukoamine D,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O5285.2Semi standard non polar33892256
Kukoamine D,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C15461.1Semi standard non polar33892256
Kukoamine D,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)N(CCCN)CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C15317.9Semi standard non polar33892256
Kukoamine D,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)N(CCCN(CCCCNCCCN)C(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C15276.6Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCNC(=O)CCC2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C=C1O5580.0Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C(C)(C)C)C=C1O5420.5Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O5438.8Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C(C)(C)C5481.9Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C15622.8Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O5432.5Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C(C)(C)C)=CC=C1O5409.1Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C15640.7Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O5439.1Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C(C)(C)C)C=C1O5418.9Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)N(CCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C(C)(C)C5717.9Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)=CC=C1O5558.1Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C(C)(C)C5663.4Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C(C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C15592.0Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)N(CCCN)CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C(C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C15388.5Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C(C)(C)C5481.4Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O)=C15621.8Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)N(CCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C(C)(C)C)=CC=C1O5408.1Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O5430.4Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)C=C1O5603.1Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C=C1O5578.9Semi standard non polar33892256
Kukoamine D,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C15641.2Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCNC(=O)CCC2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)C=C1O5766.6Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O)=C15775.7Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C5583.6Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C(C)(C)C5592.0Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O5845.4Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C(C)(C)C5755.4Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)[Si](C)(C)C(C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C15702.5Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)N(CCCN(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C(C)(C)C)=CC=C1O5537.5Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)C=C1O5766.5Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C15862.5Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)[Si](C)(C)C(C)(C)C)C=C1O5669.4Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)=CC=C1O5740.7Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)C(=O)CCC2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)C=C1O5647.8Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C15830.6Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCNCCCN)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)[Si](C)(C)C(C)(C)C)C=C1O5646.7Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C=C1O5634.0Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)NCCCN(CCCCNCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)C=C1O5860.6Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C(C)(C)C5770.8Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)[Si](C)(C)C(C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C15722.9Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCN(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C(C)(C)C)C=C1O5543.8Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C15776.4Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O[Si](C)(C)C(C)(C)C5591.3Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C15832.2Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C5583.0Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)=CC=C1O5846.2Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)[Si](C)(C)C(C)(C)C5755.5Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C(C)(C)C)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C15702.5Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C(C)(C)C)=CC=C1O5537.7Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O)=C2)C=C1O5860.4Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)NCCCN(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)[Si](C)(C)C(C)(C)C5769.9Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #37CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C(C)(C)C)C(=O)CCC1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C15722.8Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #38CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)CCCN(C(=O)CCC2=CC=C(O)C(O)=C2)[Si](C)(C)C(C)(C)C)C=C1O5543.2Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)N(CCCCN(CCCNC(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C1)CCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C5904.8Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)CCCNC(=O)CCC2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C=C1O5634.2Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #40CC(C)(C)[Si](C)(C)N(CCCN(CCCCNCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C1)C(=O)CCC1=CC=C(O)C(O)=C15804.4Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #41CC(C)(C)[Si](C)(C)NCCCN(CCCCN(CCCN(C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C(C)(C)C)C(=O)CCC1=CC=C(O)C(O)=C1)[Si](C)(C)C(C)(C)C5735.4Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)[Si](C)(C)C(C)(C)C)C=C1O5643.4Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN)CCCNC(=O)CCC2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)=CC=C1O5739.4Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)NCCCNCCCCN(CCCNC(=O)CCC1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)CCC1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C15798.7Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)N(CCCCNCCCN)CCCN(C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)[Si](C)(C)C(C)(C)C)=CC=C1O5622.3Semi standard non polar33892256
Kukoamine D,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)NCCCN(CCCCN(CCCN)[Si](C)(C)C(C)(C)C)C(=O)CCC2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)=CC=C1O5621.5Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (Non-derivatized) - 70eV, Positivesplash10-00kr-5914100000-30e7d1a6e0fdff4322802017-09-20Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (2 TMS) - 70eV, Positivesplash10-0a59-9661228000-891984051c357995cf1a2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D GC-MS (TMS_2_16) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kukoamine D 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 - Kukoamine D 10V, Positive-QTOFsplash10-02u0-1527190000-5da242b636ad0555687e2017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kukoamine D 20V, Positive-QTOFsplash10-0uxu-7897130000-3336e26b2b0f9cb6538c2017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kukoamine D 40V, Positive-QTOFsplash10-0a4r-7950000000-226af79607e818e40e2f2017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kukoamine D 10V, Negative-QTOFsplash10-004i-0102190000-966171b576765d9dbd5a2017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kukoamine D 20V, Negative-QTOFsplash10-0ge9-1519340000-56fd2e4be394d698d7cb2017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kukoamine D 40V, Negative-QTOFsplash10-056c-4942000000-2fbec696d1511cfe5f742017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kukoamine D 10V, Positive-QTOFsplash10-001i-0000190000-c76cd694e4b30b32f9ff2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kukoamine D 20V, Positive-QTOFsplash10-06sr-0405970000-218d6da39c5ea5a266162021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kukoamine D 40V, Positive-QTOFsplash10-0kfx-1659000000-e160da7a826c5980d3b02021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kukoamine D 10V, Negative-QTOFsplash10-004i-0000090000-231ab71351cad87801282021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kukoamine D 20V, Negative-QTOFsplash10-004i-0326490000-b5745fa72e93cae5aae82021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kukoamine D 40V, Negative-QTOFsplash10-0a4l-5409600000-a821b64f5b91eb4b4af02021-10-12Wishart 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 LocationsNot Available
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 IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDC17618
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound10075692
PDB IDNot Available
ChEBI ID81223
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available