Summary
SMILES: O=C(/C=C/c1ccc(cc1)O)OC[C@H]1OC(O)[C@@H]([C@H]([C@@H]1O)O)OInChI: InChI=1S/C15H18O8/c16-9-4-1-8(2-5-9)3-6-11(17)22-7-10-12(18)13(19)14(20)15(21)23-10/h1-6,10,12-16,18-21H,7H2/b6-3+/t10-,12-,13+,14-,15?/m1/s1InChIKey: GKUSDFCBGXFHIL-CXXZEMTDSA-N
DeepSMILES: O=C/C=C/cccccc6))O)))))))OC[C@H]OCO)[C@@H][C@H][C@@H]6O))O))O
Scaffold Graph/Node/Bond level: O=C(C=Cc1ccccc1)OCC1CCCCO1
Scaffold Graph/Node level: OC(CCC1CCCCC1)OCC1CCCCO1
Scaffold Graph level: CC(CCC1CCCCC1)CCC1CCCCC1
Functional groups: CO; COC(C)O; c/C=C/C(=O)OC; cO
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Phenylpropanoids and polyketidesClassyFire Class: Cinnamic acids and derivatives
ClassyFire Subclass: Hydroxycinnamic acids and derivatives
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Phenylpropanoids (C6-C3)
NP Classifier Class: Cinnamic acids and derivatives
Synonymous chemical names:6-o-(e)-p-coumaroyl glucopyranose
External chemical identifiers:CID:10087731; ChEMBL:CHEMBL3590582
Chemical structure download