Summary
SMILES: OCC1OC(OC(CC/C=C(/CC/C=C(/CC/C=C(COC2OC(C)C(C(C2O)OC2OC(COC3OC(C)C(C(C3O)OC(=O)/C(=C/CC/C(=C/CC/C(=C/CCC(OC3OC(CO)C(C(C3OC3OC(CO)C(C(C3O)O)O)O)O)(C=C)C)/C)/C)/C)O)C(C(C2O)O)O)O)/C)C)C)(C=C)C)C(C(C1O)O)OC1OC(CO)C(C(C1O)O)OInChI: InChI=1S/C82H134O37/c1-13-81(11,118-79-71(62(97)56(91)49(35-85)111-79)116-76-64(99)59(94)54(89)47(33-83)109-76)31-19-28-41(5)23-15-21-39(3)25-17-27-43(7)37-105-74-68(103)70(53(88)46(10)107-74)115-78-66(101)61(96)58(93)51(113-78)38-106-75-67(102)69(52(87)45(9)108-75)114-73(104)44(8)30-18-26-40(4)22-16-24-42(6)29-20-32-82(12,14-2)119-80-72(63(98)57(92)50(36-86)112-80)117-77-65(100)60(95)55(90)48(34-84)110-77/h13-14,21-22,27-30,45-72,74-80,83-103H,1-2,15-20,23-26,31-38H2,3-12H3/b39-21+,40-22+,41-28+,42-29+,43-27-,44-30+InChIKey: XIQPUQZGYSYODK-JZKHGTLTSA-N
DeepSMILES: OCCOCOCCC/C=C/CC/C=C/CC/C=CCOCOCC)CCC6O))OCOCCOCOCC)CCC6O))OC=O)/C=C/CC/C=C/CC/C=C/CCCOCOCCO))CCC6OCOCCO))CCC6O))O))O)))))))O))O))))))C=C))C)))))/C)))))/C)))))/C)))))O)))))))CCC6O))O))O)))))))O)))))))/C)))))C)))))C)))))C=C))C)))CCC6O))O))OCOCCO))CCC6O))O))O
Scaffold Graph/Node/Bond level: O=C(C=CCCC=CCCC=CCCCOC1OCCCC1OC1CCCCO1)OC1CCOC(OCC2CCCC(OC3CCOC(OCC=CCCC=CCCC=CCCCOC4OCCCC4OC4CCCCO4)C3)O2)C1
Scaffold Graph/Node level: OC(CCCCCCCCCCCCCOC1OCCCC1OC1CCCCO1)OC1CCOC(OCC2CCCC(OC3CCOC(OCCCCCCCCCCCCCCOC4OCCCC4OC4CCCCO4)C3)O2)C1
Scaffold Graph level: CC(CCCCCCCCCCCCCCC1CCCCC1CC1CCCCC1)CC1CCCC(CCC2CCCC(CC3CCCC(CCCCCCCCCCCCCCCCC4CCCCC4CC4CCCCC4)C3)C2)C1
Functional groups: C/C=C(/C)C; C/C=C(C)C; C/C=C(C)C(=O)OC; C=CC; CO; COC(C)OC
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Lipids and lipid-like moleculesClassyFire Class: Fatty Acyls
ClassyFire Subclass: Fatty acyl glycosides
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Diterpenoids
NP Classifier Class: Labdane diterpenoids|Phytane diterpenoids
Synonymous chemical names:capsianoside f
External chemical identifiers:CID:131751078
Chemical structure download
