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

CHEMBL5422211

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(O)C1(c2ccc(N3CCC(OCc4c(-c5c(Cl)cccc5Cl)noc4C4CC4)CC3)cc2)CC1

Basic Information

ChEMBL ID CHEMBL5422211
Phase Preclinical
Structure Type MOL
InChI Key ZLEXRRHXLWBTIU-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

527.5
MW (Da)
6.83
ALogP
5
HBA
1
HBD
75.8
PSA (Ų)
0.35
QED
2
Ro5 Violations
8
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H28Cl2N2O4
MW 527.45
Aromatic Rings 3
Heavy Atoms 36
NP-Likeness -0.65

Activity Summary

EC50 1 meas. best 6.03

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Bile acid receptor
CHEMBL2047
EC50 6.03 6.03 926.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Bile acid receptor EC50 = 926.0 nM 6.03 Agonist activity at FXR-LBD (unknown origin) using fluorescein-coactivator pepti... 37079895

Literature References

PubMed DOI Target Context # Activities
37079895 10.1021/acs.jmedchem.2c01918 Bile acid receptor 3
37079895 10.1021/acs.jmedchem.2c01918 Fatty acid-binding protein, liver 2

Data from ChEMBL 36 via Core Engine