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Compound Detail

CHEMBL253873

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CCC(CC)Oc1cc(/C=C/C(=O)NCCc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)cc(OC(CC)CC)c1O

Basic Information

ChEMBL ID CHEMBL253873
Phase Preclinical
Structure Type MOL
InChI Key AUBAVCRJIBWSPZ-FOCLMDBBSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

567.8
MW (Da)
8.20
ALogP
5
HBA
3
HBD
88.0
PSA (Ų)
0.21
QED
2
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C35H53NO5
MW 567.81
Aromatic Rings 2
Heavy Atoms 41
NP-Likeness 0.19

Activity Summary

IC50 1 meas. best 6.36

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Brain
CHEMBL613617
IC50 6.36 6.36 440.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Brain IC50 = 440.0 nM 6.36 Inhibition of lipid peroxidation in Sprague-Dawley rat brain after 30 mins by TB... 18249541

Literature References

PubMed DOI Target Context # Activities
18249541 10.1016/j.bmcl.2008.01.061 Brain 1
18249541 10.1016/j.bmcl.2008.01.061 Radical scavenging activity 1

Data from ChEMBL 36 via Core Engine