Summary
IMPPAT Phytochemical identifier: IMPHY001274
Phytochemical name: Pelargonidin 3-glucoside
Synonymous chemical names:pelargonidin 3-glucoside, pelargonidin-3-glucoside, pelargonidin-3-o-glucoside
External chemical identifiers:CID:443648, ChEBI:31967, ZINC:ZINC000004102353, FDASRS:W623YHH61A, SureChEMBL:SCHEMBL347415
Chemical structure information
SMILES:
OC[C@H]1O[C@@H](Oc2cc3c(O)cc(cc3[o+]c2c2ccc(cc2)O)O)[C@@H]([C@H]([C@@H]1O)O)OInChI:
InChI=1S/C21H20O10/c22-8-16-17(26)18(27)19(28)21(31-16)30-15-7-12-13(25)5-11(24)6-14(12)29-20(15)9-1-3-10(23)4-2-9/h1-7,16-19,21-22,26-28H,8H2,(H2-,23,24,25)/p+1/t16-,17-,18+,19-,21-/m1/s1InChIKey:
ABVCUBUIXWJYSE-GQUPQBGVSA-ODeepSMILES:
OC[C@H]O[C@@H]OccccO)cccc6[o+]c%10cccccc6))O)))))))))O))))))))[C@@H][C@H][C@@H]6O))O))OFunctional groups:
CO, cO, cO[C@@H](C)OC, c[o+]c
Molecular scaffolds
Scaffold Graph/Node/Bond level:
c1ccc(-c2[o+]c3ccccc3cc2OC2CCCCO2)cc1Scaffold Graph/Node level:
C1CCC(C2OC3CCCCC3CC2OC2CCCCO2)CC1Scaffold Graph level:
C1CCC(CC2CC3CCCCC3CC2C2CCCCC2)CC1
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: Anthocyanidins
NP-Likeness score: 2.003
Chemical structure download