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Compound Detail

CHEMBL592647

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CC(C)OC(=O)C1=CN(C(=O)c2ccc(OCCCN3CCN(C)CC3)cc2)CC(C)(C)c2c1[nH]c1ccccc21

Basic Information

ChEMBL ID CHEMBL592647
Phase Preclinical
Structure Type MOL
InChI Key IDTFOXWTCZBUNZ-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
2
PK Parameters
4
Publications
0
Known Names

Molecular Properties

558.7
MW (Da)
4.91
ALogP
6
HBA
1
HBD
78.1
PSA (Ų)
0.31
QED
1
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C33H42N4O4
MW 558.72
Aromatic Rings 3
Heavy Atoms 41
NP-Likeness -0.56

Activity Summary

EC50 1 meas. best 6.71

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Bile acid receptor
CHEMBL2047
EC50 6.71 6.71 194.0 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 0.3 hr Homo sapiens
T1/2 0.1833 hr Mus musculus

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Bile acid receptor EC50 = 194.0 nM 6.71 Agonist activity at human FXR-LBD expressed in HEL293 cells by Gal4-luciferase a... 20095622

Literature References

PubMed DOI Target Context # Activities
20095622 10.1021/jm901650u Bile acid receptor 2
20095622 10.1021/jm901650u Liver microsomes 1
20095622 10.1021/jm901650u ADMET 1
20095622 10.1021/jm901650u No relevant target 1

Data from ChEMBL 36 via Core Engine