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Compound Detail

CHEMBL418035

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Nc1c(CC(=O)[O-])cc(Cl)cc1C(=O)c1ccc(Br)cc1Cl.[Na+]

Basic Information

ChEMBL ID CHEMBL418035
Phase Preclinical
Structure Type MOL
InChI Key JOAUIYGOIKPNGA-UHFFFAOYSA-M
Parent Compound CHEMBL1207590
Active Moiety CHEMBL1207590
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

403.1
MW (Da)
4.20
ALogP
3
HBA
2
HBD
80.4
PSA (Ų)
0.59
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C15H9BrCl2NNaO3
MW 425.04
Aromatic Rings 2
Heavy Atoms 22
NP-Likeness -0.86

Activity Summary

IC50 1 meas. best 7.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Cyclooxygenase
CHEMBL2096674
IC50 7.3 7.3 50.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Cyclooxygenase IC50 = 50.0 nM 7.3 Inhibition of prostaglandin G/H synthase obtained from bovine seminal vesicles. 6436487

Literature References

PubMed DOI Target Context # Activities
6436487 10.1021/jm00377a001 Rattus norvegicus 7
6436487 10.1021/jm00377a001 Mus musculus 2
6436487 10.1021/jm00377a001 Cyclooxygenase 1

Data from ChEMBL 36 via Core Engine