Summary
SMILES: OCC1O[C@@H](Oc2ccc(cc2)c2cc(=O)c3c(o2)c(c(cc3O)O)[C@@H]2O[C@@H](CO)[C@H](C(C2O)O)O)C(C([C@H]1O)O)OInChI: InChI=1S/C27H30O15/c28-7-15-19(33)21(35)23(37)26(41-15)18-12(31)5-11(30)17-13(32)6-14(40-25(17)18)9-1-3-10(4-2-9)39-27-24(38)22(36)20(34)16(8-29)42-27/h1-6,15-16,19-24,26-31,33-38H,7-8H2/t15-,16?,19+,20-,21?,22?,23?,24?,26-,27+/m0/s1InChIKey: CQJPSSJEHVNDFL-QIPUSLQTSA-N
DeepSMILES: OCCO[C@@H]Occcccc6))ccc=O)cco6)cccc6O)))O))[C@@H]O[C@@H]CO))[C@H]CC6O))O))O))))))))))))))))CC[C@H]6O))O))O
Scaffold Graph/Node/Bond level: O=c1cc(-c2ccc(OC3CCCCO3)cc2)oc2c(C3CCCCO3)cccc12
Scaffold Graph/Node level: OC1CC(C2CCC(OC3CCCCO3)CC2)OC2C1CCCC2C1CCCCO1
Scaffold Graph level: CC1CC(C2CCC(CC3CCCCC3)CC2)CC2C1CCCC2C1CCCCC1
Functional groups: CO; COC; c=O; cO; cO[C@@H](C)OC; coc
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Phenylpropanoids and polyketidesClassyFire Class: Flavonoids
ClassyFire Subclass: Flavonoid glycosides
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Flavonoids
NP Classifier Class: Flavones
Synonymous chemical names:vitexin-4'-o-galactoside
External chemical identifiers:CID:44257743
Chemical structure download