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Compound Detail

CHEMBL601873

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CC(C)OC(=O)C1=CN(C(=O)c2ccc(OCCCN3CCOCC3)cc2)CC(C)(C)c2c1[nH]c1ccccc21

Basic Information

ChEMBL ID CHEMBL601873
Phase Preclinical
Structure Type MOL
InChI Key CCNIWPQOOWKWHQ-UHFFFAOYSA-N
3
Targets
3
Activities
2
Assay Types
2
PK Parameters
5
Publications
0
Known Names

Molecular Properties

545.7
MW (Da)
5.00
ALogP
6
HBA
1
HBD
84.1
PSA (Ų)
0.32
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 C32H39N3O5
MW 545.68
Aromatic Rings 3
Heavy Atoms 40
NP-Likeness -0.62

Activity Summary

EC50 2 meas. best 7.0
IC50 1 meas. best 5.24

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Bile acid receptor
CHEMBL2047
EC50 7.0 7.0 101.0 1
Bile acid receptor
CHEMBL5343
EC50 6.97 6.97 108.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.24 5.24 5740.0 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 0.25 hr Homo sapiens
T1/2 0.1333 hr Mus musculus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
20095622 10.1021/jm901650u Bile acid receptor 4
20095622 10.1021/jm901650u Liver microsomes 1
20095622 10.1021/jm901650u ADMET 1
20095622 10.1021/jm901650u No relevant target 1
20095622 10.1021/jm901650u Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine