Summary
SMILES: Oc1ccc(cc1)c1cc(=O)c2c(o1)c(O[C@@H]1OC(C(=O)O)[C@H]([C@@H](C1O)O)O)c(cc2O)OInChI: InChI=1S/C21H18O12/c22-8-3-1-7(2-4-8)12-6-10(24)13-9(23)5-11(25)17(18(13)31-12)32-21-16(28)14(26)15(27)19(33-21)20(29)30/h1-6,14-16,19,21-23,25-28H,(H,29,30)/t14-,15-,16?,19?,21+/m0/s1InChIKey: FBDUYUDFMFZSDJ-ZGZLJJHASA-N
DeepSMILES: Occcccc6))ccc=O)cco6)cO[C@@H]OCC=O)O))[C@H][C@@H]C6O))O))O))))))ccc6O)))O
Scaffold Graph/Node/Bond level: O=c1cc(-c2ccccc2)oc2c(OC3CCCCO3)cccc12
Scaffold Graph/Node level: OC1CC(C2CCCCC2)OC2C(OC3CCCCO3)CCCC12
Scaffold Graph level: CC1CC(C2CCCCC2)CC2C(CC3CCCCC3)CCCC12
Functional groups: CC(=O)O; CO; 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:isoscutellarein-8-glucuronide
External chemical identifiers:CID:44258568
Chemical structure download