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Compound Detail

CHEMBL544841

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Cl.O=C(O)C1CCCN(CCOC(c2ccc(Cl)c(Cl)c2)c2ccc(Cl)c(Cl)c2)C1

Basic Information

ChEMBL ID CHEMBL544841
Phase Preclinical
Structure Type MOL
InChI Key SMJFNRXKTYILRI-UHFFFAOYSA-N
Parent Compound CHEMBL1193435
Active Moiety CHEMBL1193435
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

477.2
MW (Da)
6.20
ALogP
3
HBA
1
HBD
49.8
PSA (Ų)
0.52
QED
1
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C21H22Cl5NO3
MW 513.68
Aromatic Rings 2
Heavy Atoms 29
NP-Likeness -0.83

Activity Summary

IC50 1 meas. best 5.6

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Rattus norvegicus
CHEMBL376
IC50 5.6 5.6 2500.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Rattus norvegicus IC50 = 2500.0 nM 5.6 In vitro inhibition of [3H]GABA uptake in rat Hippocampal slices. 1433224

Literature References

PubMed DOI Target Context # Activities
1433224 10.1021/jm00100a032 Rattus norvegicus 1

Data from ChEMBL 36 via Core Engine