Summary
SMILES: OCC1O[C@@H](Oc2cc3oc(cc(=O)c3c(c2[C@@H]2OC(CO)[C@H]([C@@H](C2O)O)O)O)c2ccc(c(c2)O)O)C([C@H]([C@@H]1O)O)OInChI: InChI=1S/C27H30O16/c28-6-15-19(33)22(36)24(38)26(41-15)18-14(42-27-25(39)23(37)20(34)16(7-29)43-27)5-13-17(21(18)35)11(32)4-12(40-13)8-1-2-9(30)10(31)3-8/h1-5,15-16,19-20,22-31,33-39H,6-7H2/t15?,16?,19-,20-,22+,23+,24?,25?,26+,27-/m1/s1InChIKey: OQKYVRDRDIXQMK-QSKBEBRPSA-N
DeepSMILES: OCCO[C@@H]Occcoccc=O)c6cc%10[C@@H]OCCO))[C@H][C@@H]C6O))O))O))))))O)))))cccccc6)O))O)))))))))))C[C@H][C@@H]6O))O))O
Scaffold Graph/Node/Bond level: O=c1cc(-c2ccccc2)oc2cc(OC3CCCCO3)c(C3CCCCO3)cc12
Scaffold Graph/Node level: OC1CC(C2CCCCC2)OC2CC(OC3CCCCO3)C(C3CCCCO3)CC12
Scaffold Graph level: CC1CC(C2CCCCC2)CC2CC(CC3CCCCC3)C(C3CCCCC3)CC12
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:lutonarin, lutonarin (7-o-beta-d-glucopyranosyl-6-c-beta-d-glucopyranosylluteolin)
External chemical identifiers:CID:44257976
Chemical structure download