Summary
IMPPAT Phytochemical identifier: IMPHY002593
Phytochemical name: Moracin O
Synonymous chemical names:moracin o
External chemical identifiers:CID:14539883, ChEMBL:CHEMBL205924, ChEBI:175160
Chemical structure information
SMILES:
Oc1cc(O)cc(c1)c1oc2c(c1)cc1c(c2)OC(C1)C(O)(C)CInChI:
InChI=1S/C19H18O5/c1-19(2,22)18-7-11-3-10-6-15(23-16(10)9-17(11)24-18)12-4-13(20)8-14(21)5-12/h3-6,8-9,18,20-22H,7H2,1-2H3InChIKey:
HMTMYIWMPJSCAZ-UHFFFAOYSA-NDeepSMILES:
OcccO)ccc6)coccc5)cccc6)OCC5)CO)C)CFunctional groups:
CO, cO, cOC, coc
Molecular scaffolds
Scaffold Graph/Node/Bond level:
c1ccc(-c2cc3cc4c(cc3o2)OCC4)cc1Scaffold Graph/Node level:
C1CCC(C2CC3CC4CCOC4CC3O2)CC1Scaffold Graph level:
C1CCC(C2CC3CC4CCCC4CC3C2)CC1
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Phenylpropanoids and polyketidesClassyFire Class: 2-arylbenzofuran flavonoids
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Isoflavonoids
NP Classifier Class: 2-arylbenzofurans
NP-Likeness score: 1.868
Chemical structure download