Summary

IMPPAT Phytochemical identifier: IMPHY011860

Phytochemical name: Epiisopodophyllotoxin

Synonymous chemical names:
epiisopodophyllotoxin

External chemical identifiers:
CID:1549055, ChEMBL:CHEMBL3244929, ZINC:ZINC000001532026

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Chemical structure information

SMILES:
COc1cc(cc(c1OC)OC)[C@@H]1[C@H]2C(=O)OC[C@@H]2[C@@H](c2c1cc1OCOc1c2)O

InChI:
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/s1

InChIKey:
YJGVMLPVUAXIQN-XCXWGBRNSA-N

DeepSMILES:
COcccccc6OC)))OC))))[C@@H][C@H]C=O)OC[C@@H]5[C@@H]cc9ccOCOc5c9)))))))))O

Functional groups:
CO, COC(C)=O, c1cOCO1, cOC

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=C1OCC2Cc3cc4c(cc3C(c3ccccc3)C12)OCO4

Scaffold Graph/Node level:
OC1OCC2CC3CC4OCOC4CC3C(C3CCCCC3)C21

Scaffold Graph level:
CC1CCC2CC3CC4CCCC4CC3C(C3CCCCC3)C12

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Lignans, neolignans and related compounds

ClassyFire 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

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Chemical structure download