Summary
SMILES: O=C1C=CC2(C(=C1)OCC1(C2Oc2c1cc1c(c2)OC(C=C1)(C)C)O)OInChI: InChI=1S/C20H18O6/c1-18(2)5-3-11-7-13-15(9-14(11)26-18)25-17-19(22)6-4-12(21)8-16(19)24-10-20(13,17)23/h3-9,17,22-23H,10H2,1-2H3InChIKey: PDSPTIAGLVOKKO-UHFFFAOYSA-N
DeepSMILES: O=CC=CCC=C6)OCCC6Occ5cccc6)OCC=C6))C)C))))))))))O)))))O
Scaffold Graph/Node/Bond level: O=C1C=CC2C(=C1)OCC1c3cc4c(cc3OC21)OCC=C4
Scaffold Graph/Node level: OC1CCC2C(C1)OCC1C3CC4CCCOC4CC3OC21
Scaffold Graph level: CC1CCC2C(CCC3C4CC5CCCCC5CC4CC23)C1
Functional groups: CO; COC1=CC(=O)C=CC1; cC=CC; cOC
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Organoheterocyclic compoundsClassyFire Class: Benzopyrans
ClassyFire Subclass: 1-benzopyrans
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Isoflavonoids
NP Classifier Class: Pterocarpan
Synonymous chemical names:hydroxytuberosone
External chemical identifiers:CID:4302704
Chemical structure download