Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL2181227

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
O=C(c1cnccc1Oc1cc(Cl)c(Cl)cc1Cl)N1CCN(C2CC2)c2ccccc21

Basic Information

ChEMBL ID CHEMBL2181227
Phase Preclinical
Structure Type MOL
InChI Key SLFOKMKKDLQLST-UHFFFAOYSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

474.8
MW (Da)
6.46
ALogP
4
HBA
0
HBD
45.7
PSA (Ų)
0.41
QED
1
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H18Cl3N3O2
MW 474.78
Aromatic Rings 3
Heavy Atoms 31
NP-Likeness -1.15

Activity Summary

EC50 2 meas. best 9.34

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
G-protein coupled bile acid receptor 1
CHEMBL5409
EC50 9.34 9.34 0.5 1
G-protein coupled bile acid receptor 1
CHEMBL1255150
EC50 8.7 8.7 2.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
23148522 10.1021/jm301071h G-protein coupled bile acid receptor 1 2
23148522 10.1021/jm301071h Bile acid receptor 1

Data from ChEMBL 36 via Core Engine