Summary
SMILES: O=CC(C(C1OC(=O)c2cc(O)c(c(c2-c2c(C(=O)OCC1O)cc(c(c2O)O)O)O)O)OC(=O)c1cc(O)c(c(c1)O)O)OInChI: InChI=1S/C27H22O18/c28-5-14(33)23(44-25(40)7-1-10(29)18(35)11(30)2-7)24-15(34)6-43-26(41)8-3-12(31)19(36)21(38)16(8)17-9(27(42)45-24)4-13(32)20(37)22(17)39/h1-5,14-15,23-24,29-39H,6H2InChIKey: XKVYZLLWKHGKMT-UHFFFAOYSA-N
DeepSMILES: O=CCCCOC=O)cccO)ccc6-ccC=O)OCC%15O)))))cccc6O))O))O))))))O))O))))))))OC=O)cccO)ccc6)O))O))))))))O
Scaffold Graph/Node/Bond level: O=C(OCC1CCOC(=O)c2ccccc2-c2ccccc2C(=O)O1)c1ccccc1
Scaffold Graph/Node level: OC(OCC1CCOC(O)C2CCCCC2C2CCCCC2C(O)O1)C1CCCCC1
Scaffold Graph level: CC(CCC1CCCC(C)C2CCCCC2C2CCCCC2C(C)C1)C1CCCCC1
Functional groups: CC=O; CO; cC(=O)OC; cO
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Phenylpropanoids and polyketidesClassyFire Class: Tannins
ClassyFire Subclass: Hydrolyzable tannins
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Phenolic acids (C6-C1)
NP Classifier Class: Gallotannins
Synonymous chemical names:gemin d
External chemical identifiers:CID:471119
Chemical structure download