Summary

IMPPAT Phytochemical identifier: IMPHY001789

Phytochemical name: Murisolin

Synonymous chemical names:
murisolin

External chemical identifiers:
CID:11399084, ChEMBL:CHEMBL81089, ChEBI:176139, ZINC:ZINC000043278594, SureChEMBL:SCHEMBL13144123

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Chemical structure information

SMILES:
CCCCCCCCCCCC[C@H]([C@H]1CC[C@@H](O1)[C@@H](CCCCCCCCCC[C@H](CC1=C[C@@H](OC1=O)C)O)O)O

InChI:
InChI=1S/C35H64O6/c1-3-4-5-6-7-8-9-13-16-19-22-31(37)33-24-25-34(41-33)32(38)23-20-17-14-11-10-12-15-18-21-30(36)27-29-26-28(2)40-35(29)39/h26,28,30-34,36-38H,3-25,27H2,1-2H3/t28-,30+,31+,32+,33+,34+/m0/s1

InChIKey:
PYNFAPLXMQHUNR-YZDQYAEISA-N

DeepSMILES:
CCCCCCCCCCCC[C@H][C@H]CC[C@@H]O5)[C@@H]CCCCCCCCCC[C@H]CC=C[C@@H]OC5=O)))C)))))O))))))))))))O))))))O

Functional groups:
CC1=CCOC1=O, CO, COC

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=C1OCC=C1CCCCCCCCCCCCCC1CCCO1

Scaffold Graph/Node level:
OC1OCCC1CCCCCCCCCCCCCC1CCCO1

Scaffold Graph level:
CC1CCCC1CCCCCCCCCCCCCC1CCCC1

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Lipids and lipid-like molecules

ClassyFire Class: Fatty acyls

ClassyFire Subclass: Fatty alcohols

NP Classifier Biosynthetic pathway: Polyketides

NP Classifier Superclass: Linear polyketides

NP Classifier Class: Acetogenins

NP-Likeness score: 1.791

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Chemical structure download