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Compound Detail

CHEMBL271739

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Cc1oc(-c2ccccc2)nc1CCOc1cccc(CC2C(=O)N(c3ccc(F)cc3)C2C(=O)O)c1

Basic Information

ChEMBL ID CHEMBL271739
Phase Preclinical
Structure Type MOL
InChI Key XUCFNKPVYCHTKK-UHFFFAOYSA-N
2
Targets
4
Activities
2
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

500.5
MW (Da)
5.07
ALogP
5
HBA
1
HBD
92.9
PSA (Ų)
0.32
QED
2
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H25FN2O5
MW 500.53
Aromatic Rings 4
Heavy Atoms 37
NP-Likeness -0.79

Activity Summary

EC50 2 meas. best 7.96
IC50 2 meas. best 6.75

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Peroxisome proliferator-activated receptor alpha
CHEMBL239
EC50 7.96 7.96 11.0 1
Peroxisome proliferator-activated receptor gamma
CHEMBL235
EC50 7.52 7.52 30.0 1
Peroxisome proliferator-activated receptor gamma
CHEMBL235
IC50 6.75 6.75 180.0 1
Peroxisome proliferator-activated receptor alpha
CHEMBL239
IC50 5.62 5.62 2400.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18291645 10.1016/j.bmcl.2008.01.126 Peroxisome proliferator-activated receptor alpha 3
18291645 10.1016/j.bmcl.2008.01.126 Peroxisome proliferator-activated receptor gamma 3
18291645 10.1016/j.bmcl.2008.01.126 Cytochrome P450 3A4 2
18291645 10.1016/j.bmcl.2008.01.126 Voltage-gated inwardly rectifying potassium channel KCNH2 1
18291645 10.1016/j.bmcl.2008.01.126 Cytochrome P450 2C19 1
18291645 10.1016/j.bmcl.2008.01.126 Cytochrome P450 2C9 1

Data from ChEMBL 36 via Core Engine