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/C(C/C(=C/CC/C(=C/CCC(OC3OC(CO)C(C(C3OC3OC(CO)C(C(C3O)O)O)O)O)(C=C)C)/C)/C)O)/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/C82H134O38/c1-13-81(11,119-79-71(62(98)56(92)49(34-85)112-79)117-76-64(100)59(95)54(90)47(32-83)110-76)28-18-26-39(4)21-15-20-38(3)23-17-25-42(7)36-106-74-68(104)70(53(89)45(10)108-74)116-78-66(102)61(97)58(94)51(114-78)37-107-75-67(103)69(52(88)44(9)109-75)115-73(105)43(8)31-46(87)30-41(6)24-16-22-40(5)27-19-29-82(12,14-2)120-80-72(63(99)57(93)50(35-86)113-80)118-77-65(101)60(96)55(91)48(33-84)111-77/h13-14,20,24-27,31,44-72,74-80,83-104H,1-2,15-19,21-23,28-30,32-37H2,3-12H3/b38-20+,39-26+,40-27+,41-24+,42-25-,43-31+InChIKey: BHQXDVVPOFDEHV-RPQRBYGFSA-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)))O)))/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 d
External chemical identifiers:CID:131751077
Chemical structure download
