Summary
SMILES: OC[C@H]1O[C@@H](Oc2ccc(c(c2)O)/C=C/c2cc(O)cc(c2)O[C@@H]2O[C@H](CO)[C@H]([C@@H]([C@H]2O)O)O)[C@@H]([C@H]([C@@H]1O)O)OInChI: InChI=1S/C26H32O14/c27-9-17-19(31)21(33)23(35)25(39-17)37-14-4-3-12(16(30)8-14)2-1-11-5-13(29)7-15(6-11)38-26-24(36)22(34)20(32)18(10-28)40-26/h1-8,17-36H,9-10H2/b2-1+/t17-,18-,19-,20-,21+,22+,23-,24-,25-,26-/m1/s1InChIKey: HPSWAEGGWLOOKT-VUNDNAJOSA-N
DeepSMILES: OC[C@H]O[C@@H]Occcccc6)O))/C=C/cccO)ccc6)O[C@@H]O[C@H]CO))[C@H][C@@H][C@H]6O))O))O))))))))))))))))))[C@@H][C@H][C@@H]6O))O))O
Scaffold Graph/Node/Bond level: C(=Cc1cccc(OC2CCCCO2)c1)c1ccc(OC2CCCCO2)cc1
Scaffold Graph/Node level: C1CCC(OC2CCC(CCC3CCCC(OC4CCCCO4)C3)CC2)OC1
Scaffold Graph level: C1CCC(CC2CCC(CCC3CCCC(CC4CCCCC4)C3)CC2)CC1
Functional groups: CO; c/C=C/c; cO; cO[C@@H](C)OC
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Phenylpropanoids and polyketidesClassyFire Class: Stilbenes
ClassyFire Subclass: Stilbene glycosides
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Stilbenoids
NP Classifier Class: Monomeric stilbenes
Synonymous chemical names:mulberroside a
External chemical identifiers:CID:6443484; ChEMBL:CHEMBL455619; ZINC:ZINC000044359935; FDASRS:OJU5SVA08B; SureChEMBL:SCHEMBL22498775; MolPort-039-052-276
Chemical structure download