Summary

IMPPAT Phytochemical identifier: IMPHY009420

Phytochemical name: Sumaresinol

Synonymous chemical names:
sumaresinoic-acid

External chemical identifiers:
CID:12443148, ChEMBL:CHEMBL486807, ChEBI:80906, ZINC:ZINC000004349900, FDASRS:ZLX0T88D9C, SureChEMBL:SCHEMBL12447712

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Chemical structure information

SMILES:
O[C@@H]1C[C@]2(C)[C@@H]([C@@]3([C@@H]1C(C)(C)[C@H](CC3)O)C)CC=C1[C@@]2(C)CC[C@@]2([C@H]1CC(CC2)(C)C)C(=O)O

InChI:
InChI=1S/C30H48O4/c1-25(2)12-14-30(24(33)34)15-13-28(6)18(19(30)16-25)8-9-21-27(5)11-10-22(32)26(3,4)23(27)20(31)17-29(21,28)7/h8,19-23,31-32H,9-17H2,1-7H3,(H,33,34)/t19-,20+,21+,22-,23-,27+,28+,29+,30-/m0/s1

InChIKey:
KLHSKTMVSOWVLD-WPDRYGPBSA-N

DeepSMILES:
O[C@@H]C[C@]C)[C@@H][C@@][C@@H]6CC)C)[C@H]CC6))O))))C))CC=C[C@@]6C)CC[C@@][C@H]6CCCC6))C)C))))C=O)O

Functional groups:
CC(=O)O, CC=C(C)C, CO

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
C1=C2C3CCCCC3CCC2C2CCC3CCCCC3C2C1

Scaffold Graph/Node level:
C1CCC2C(C1)CCC1C2CCC2C3CCCCC3CCC21

Scaffold Graph level:
C1CCC2C(C1)CCC1C2CCC2C3CCCCC3CCC21

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Lipids and lipid-like molecules

ClassyFire Class: Prenol lipids

ClassyFire Subclass: Triterpenoids

NP Classifier Biosynthetic pathway: Terpenoids

NP Classifier Superclass: Triterpenoids

NP Classifier Class: Oleanane triterpenoids, Ursane and Taraxastane triterpenoids

NP-Likeness score: 3.425

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Chemical structure download