Summary
IMPPAT Phytochemical identifier: IMPHY011846
Phytochemical name: Podofilox
Synonymous chemical names:podophyllotoxin
External chemical identifiers:CID:10607, ChEMBL:CHEMBL61, ChEBI:50305, ZINC:ZINC000003861806, FDASRS:L36H50F353, SureChEMBL:SCHEMBL42243, MolPort-002-493-753
Chemical structure information
SMILES:
COc1cc(cc(c1OC)OC)[C@H]1[C@H]2C(=O)OC[C@@H]2[C@H](c2c1cc1OCOc1c2)OInChI:
InChI=1S/C22H22O8/c1-25-16-4-10(5-17(26-2)21(16)27-3)18-11-6-14-15(30-9-29-14)7-12(11)20(23)13-8-28-22(24)19(13)18/h4-7,13,18-20,23H,8-9H2,1-3H3/t13-,18+,19-,20-/m0/s1InChIKey:
YJGVMLPVUAXIQN-XVVDYKMHSA-NDeepSMILES:
COcccccc6OC)))OC))))[C@H][C@H]C=O)OC[C@@H]5[C@H]cc9ccOCOc5c9)))))))))OFunctional groups:
CO, COC(C)=O, c1cOCO1, cOC
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=C1OCC2Cc3cc4c(cc3C(c3ccccc3)C12)OCO4Scaffold Graph/Node level:
OC1OCC2CC3CC4OCOC4CC3C(C3CCCCC3)C21Scaffold Graph level:
CC1CCC2CC3CC4CCCC4CC3C(C3CCCCC3)C12
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Lignans, neolignans and related compoundsClassyFire Class: Lignan lactones
ClassyFire Subclass: Podophyllotoxins
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Lignans
NP Classifier Class: Arylnaphthalene and aryltetralin lignans
NP-Likeness score: 1.515
Chemical structure download