Summary
IMPPAT Phytochemical identifier: IMPHY010433
Phytochemical name: Scutellarein 7-rutinoside
Synonymous chemical names:scutellarein-7-rutinoside
External chemical identifiers:CID:44258427
Chemical structure information
SMILES:
OC1[C@@H](OC([C@H]([C@@H]1O)O)CO[C@@H]1OC(C)[C@@H]([C@@H](C1O)O)O)Oc1cc2oc(cc(=O)c2c(c1O)O)c1ccc(cc1)OInChI:
InChI=1S/C27H30O15/c1-9-18(30)22(34)24(36)26(39-9)38-8-16-20(32)23(35)25(37)27(42-16)41-15-7-14-17(21(33)19(15)31)12(29)6-13(40-14)10-2-4-11(28)5-3-10/h2-7,9,16,18,20,22-28,30-37H,8H2,1H3/t9?,16?,18-,20+,22-,23-,24?,25?,26+,27+/m0/s1InChIKey:
CMAUMDKYDZZLTH-LZIXYWLMSA-NDeepSMILES:
OC[C@@H]OC[C@H][C@@H]6O))O))CO[C@@H]OCC)[C@@H][C@@H]C6O))O))O)))))))))Occcoccc=O)c6cc%10O))O)))))cccccc6))OFunctional groups:
CO, CO[C@H](C)OC, c=O, cO, cO[C@@H](C)OC, coc
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=c1cc(-c2ccccc2)oc2cc(OC3CCCC(COC4CCCCO4)O3)ccc12Scaffold Graph/Node level:
OC1CC(C2CCCCC2)OC2CC(OC3CCCC(COC4CCCCO4)O3)CCC12Scaffold Graph level:
CC1CC(C2CCCCC2)CC2CC(CC3CCCC(CCC4CCCCC4)C3)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: 1.906
Chemical structure download