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

CHEMBL5186962

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
Cc1cccc(-c2nc3cc(NC(=O)c4cc([N+](=O)[O-])ccc4Cl)ccc3o2)c1

Basic Information

ChEMBL ID CHEMBL5186962
Phase Preclinical
Structure Type MOL
InChI Key FTQBNTYNRDNARK-UHFFFAOYSA-N
1
Targets
2
Activities
2
Assay Types
2
PK Parameters
4
Publications
0
Known Names

Molecular Properties

407.8
MW (Da)
5.62
ALogP
5
HBA
1
HBD
98.3
PSA (Ų)
0.35
QED
1
Ro5 Violations
4
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C21H14ClN3O4
MW 407.81
Aromatic Rings 4
Heavy Atoms 29
NP-Likeness -2.30

Activity Summary

EC50 1 meas. best 8.74
IC50 1 meas. best 5.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Peroxisome proliferator-activated receptor gamma
CHEMBL235
EC50 8.74 8.74 1.8 1
Peroxisome proliferator-activated receptor gamma
CHEMBL235
IC50 5.89 5.89 1300.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 7.5 mL.min-1.kg-1 Homo sapiens
CL 70.0 mL.min-1.kg-1 Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
36270630 10.1021/acs.jmedchem.2c01379 ADMET 12
36270630 10.1021/acs.jmedchem.2c01379 Peroxisome proliferator-activated receptor gamma 5
36270630 10.1021/acs.jmedchem.2c01379 Unchecked 2
36270630 10.1021/acs.jmedchem.2c01379 No relevant target 1

Data from ChEMBL 36 via Core Engine