Summary
IMPPAT Phytochemical identifier: IMPHY014859
Phytochemical name: Chrysin 7-glucuronide
Synonymous chemical names:chrysin 7-glucuronide, chrysin-7-glucuronide
External chemical identifiers:CID:44257628
Chemical structure information
SMILES:
OC(=O)C1O[C@@H](Oc2cc(O)c3c(c2)oc(cc3=O)c2ccccc2)C([C@H]([C@@H]1O)O)OInChI:
InChI=1S/C21H18O10/c22-11-6-10(29-21-18(26)16(24)17(25)19(31-21)20(27)28)7-14-15(11)12(23)8-13(30-14)9-4-2-1-3-5-9/h1-8,16-19,21-22,24-26H,(H,27,28)/t16-,17-,18?,19?,21+/m0/s1InChIKey:
IDRSJGHHZXBATQ-ZAJNMQHRSA-NDeepSMILES:
OC=O)CO[C@@H]OcccO)ccc6)occc6=O)))cccccc6))))))))))))))C[C@H][C@@H]6O))O))OFunctional groups:
CC(=O)O, CO, c=O, cO, cO[C@@H](C)OC, coc
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=c1cc(-c2ccccc2)oc2cc(OC3CCCCO3)ccc12Scaffold Graph/Node level:
OC1CC(C2CCCCC2)OC2CC(OC3CCCCO3)CCC12Scaffold Graph level:
CC1CC(C2CCCCC2)CC2CC(CC3CCCCC3)CCC12
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire 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
NP-Likeness score: 1.621
Chemical structure download