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Compound Detail

CHEMBL2349422

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CO[C@@H](CC(=O)O[C@@H]1C[C@](OC(=O)/C=C/c2ccc(O)c(O)c2)(C(=O)O)C[C@@H](O)[C@H]1O)c1ccc(O)c(O)c1

Basic Information

ChEMBL ID CHEMBL2349422
Phase Preclinical
Structure Type MOL
InChI Key LJQOTSZZGZIZEG-OQJUOGDSSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

548.5
MW (Da)
1.09
ALogP
12
HBA
7
HBD
220.5
PSA (Ų)
0.13
QED
3
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C26H28O13
MW 548.50
Aromatic Rings 2
Heavy Atoms 39
NP-Likeness 1.78

Activity Summary

IC50 2 meas. best 5.33

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
BV-2
CHEMBL614781
IC50 5.33 5.33 4660.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
BV-2 IC50 = 4660.0 nM 5.33 Anti-neuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS... 23462643

Literature References

PubMed DOI Target Context # Activities
23462643 10.1016/j.bmcl.2013.01.115 BV-2 3
23462643 10.1016/j.bmcl.2013.01.115 RAW264.7 2
23462643 10.1016/j.bmcl.2013.01.115 Unchecked 1
23462643 10.1016/j.bmcl.2013.01.115 Nitric oxide synthase, inducible 1

Data from ChEMBL 36 via Core Engine