Compound Detail
CHEMBL429734
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Cc1oc(-c2cccc(Cl)c2)nc1CCOc1cccc(C[C@@H]2C(=O)N(c3ccc(C(C)(C)C)cc3)[C@@H]2C(=O)O)c1
Basic Information
| ChEMBL ID | CHEMBL429734 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | RFKDHOWUSOAINF-YTMVLYRLSA-N |
6
Targets
8
Activities
2
Assay Types
0
PK Parameters
6
Publications
0
Known Names
Molecular Properties
573.1
MW (Da)
6.88
ALogP
5
HBA
1
HBD
92.9
PSA (Ų)
0.22
QED
2
Ro5 Violations
9
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 6 meas. best 6.6
EC50 2 meas. best 7.22
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Peroxisome proliferator-activated receptor alpha CHEMBL239 | EC50 | 7.22 | 7.22 | 60.0 | 1 |
| Peroxisome proliferator-activated receptor gamma CHEMBL235 | EC50 | 7.0 | 7.0 | 100.0 | 1 |
| Peroxisome proliferator-activated receptor gamma CHEMBL235 | IC50 | 6.6 | 6.6 | 250.0 | 1 |
| Cytochrome P450 2C9 CHEMBL3397 | IC50 | 6.17 | 6.17 | 670.0 | 1 |
| Peroxisome proliferator-activated receptor alpha CHEMBL239 | IC50 | 6.07 | 6.07 | 860.0 | 1 |
| Voltage-gated inwardly rectifying potassium channel KCNH2 CHEMBL240 | IC50 | 5.75 | 5.75 | 1800.0 | 1 |
| Cytochrome P450 2C19 CHEMBL3622 | IC50 | 5.28 | 5.28 | 5300.0 | 1 |
| Cytochrome P450 3A4 CHEMBL340 | IC50 | 4.7 | 4.7 | 20000.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Peroxisome proliferator-activated receptor alpha | EC50 | = | 60.0 | nM | 7.22 | Agonist activity at PPARalpha in HEK293 cells by GAL4 transactivation assay | 18291645 |
| Peroxisome proliferator-activated receptor gamma | EC50 | = | 100.0 | nM | 7.0 | Agonist activity at PPARgamma in HEK293 cells by GAL4 transactivation assay | 18291645 |
| Peroxisome proliferator-activated receptor gamma | IC50 | = | 250.0 | nM | 6.6 | Inhibition of PPARgamma | 18291645 |
| Cytochrome P450 2C9 | IC50 | = | 670.0 | nM | 6.17 | Inhibition of CYP2C9 | 18291645 |
| Peroxisome proliferator-activated receptor alpha | IC50 | = | 860.0 | nM | 6.07 | Inhibition of PPARalpha | 18291645 |
| Voltage-gated inwardly rectifying potassium channel KCNH2 | IC50 | = | 1800.0 | nM | 5.75 | Inhibition of human ERG by FLIPR assay | 18291645 |
| Cytochrome P450 2C19 | IC50 | = | 5300.0 | nM | 5.28 | Inhibition of CYP2C19 | 18291645 |
| Cytochrome P450 3A4 | IC50 | = | 20000.0 | nM | 4.7 | Inhibition of CYP3A4 in presence of 7-benzyloxyresorufin substrate | 18291645 |
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