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Compound Detail

CHEMBL3301672

ERITORAN TETRASODIUM
🧪 Phase III
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🧪 Phase III
CCCCCC/C=C\CCCCCCCCCC(=O)N[C@H]1[C@H](OC[C@H]2O[C@H](OP(=O)([O-])[O-])[C@H](NC(=O)CC(=O)CCCCCCCCCCC)[C@@H](OCCCCCCCCCC)[C@@H]2O)O[C@H](COC)[C@@H](OP(=O)([O-])[O-])[C@@H]1OCC[C@@H](CCCCCCC)OC.[Na+].[Na+].[Na+].[Na+]

Basic Information

ChEMBL ID CHEMBL3301672
Name ERITORAN TETRASODIUM
Phase Phase III
Structure Type MOL
InChI Key FEMINZOAAWPBPP-RHMAUSBNSA-J
Parent Compound CHEMBL501259
Active Moiety CHEMBL501259

Known Names

B-1287 B1287 E-5564 E5564 Eritoran sodium Eritoran tetrasodium Eritoran tetrasodium salt
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
1
Publications
7
Known Names
2
Indications
1
Mechanisms

Molecular Properties

1313.7
MW (Da)

Drug Information

Molecule Type Small molecule
Chirality Single Enantiomer

Flags

Natural Product
USAN Stem -toran
USAN Year 2000

Extended Properties

Molecular Formula C66H122N2Na4O19P2
MW 1401.60

Mechanism of Action

Mechanism Action Type Target Direct Efficacy
Toll-like receptor 4/MD-2 antagonist ANTAGONIST Toll-like receptor 4/MD-2

Indications

Sepsis Leukemia

Activity Summary

IC50 2 meas. best 8.82

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Toll-like receptor 4
CHEMBL5255
IC50 8.82 8.82 1.5 2

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18828583 10.1021/jm800957k Toll-like receptor 4 2

Data from ChEMBL 36 via Core Engine