Compound Detail
CHEMBL2170609
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Basic Information
| ChEMBL ID | CHEMBL2170609 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | VQGJOZLBMBECDD-UHFFFAOYSA-N |
4
Targets
5
Activities
1
Assay Types
6
PK Parameters
12
Publications
0
Known Names
Molecular Properties
370.4
MW (Da)
2.44
ALogP
3
HBA
3
HBD
99.3
PSA (Ų)
0.56
QED
0
Ro5 Violations
3
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 5 meas. best 7.96
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Sodium/hydrogen exchanger 1 CHEMBL2781 | IC50 | 7.96 | 7.735 | 11.0 | 2 |
| Cytochrome P450 2C19 CHEMBL3622 | IC50 | 4.75 | 4.75 | 18000.0 | 1 |
| Cytochrome P450 2C9 CHEMBL3397 | IC50 | 4.68 | 4.68 | 21000.0 | 1 |
| Cytochrome P450 3A4 CHEMBL340 | IC50 | 4.58 | 4.58 | 26000.0 | 1 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| CL | 8.1 | % | Canis lupus familiaris |
| CL | 4.4 | % | Rattus norvegicus |
| F | 49.0 | % | Canis lupus familiaris |
| F | 49.0 | % | Rattus norvegicus |
| MRT | 14.0 | hr | Canis lupus familiaris |
| MRT | 5.3 | hr | Rattus norvegicus |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Sodium/hydrogen exchanger 1 | IC50 | = | 11.0 | nM | 7.96 | Inhibition of NHE1 in human HT-29 cells assessed as intracellular pH change afte... | 22803959 |
| Sodium/hydrogen exchanger 1 | IC50 | = | 31.0 | nM | 7.51 | Inhibition of NHE1 in human platelet rich plasma assessed as reduction of propio... | 22803959 |
| Cytochrome P450 2C19 | IC50 | = | 18000.0 | nM | 4.75 | Inhibition of CYP2C19 in human liver microsomes using 7-ethoxy-3-cyanocoumarin a... | 22803959 |
| Cytochrome P450 2C9 | IC50 | = | 21000.0 | nM | 4.68 | Inhibition of CYP2C9 in human liver microsomes using 7-methoxy-4-(trifluoromethy... | 22803959 |
| Cytochrome P450 3A4 | IC50 | = | 26000.0 | nM | 4.58 | Inhibition of CYP3A4 in human liver microsomes using 7-benzyloxy-4-(trifluoromet... | 22803959 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 22803959 | 10.1021/jm300601d | Canis familiaris | 4 |
| 22803959 | 10.1021/jm300601d | Rattus norvegicus | 4 |
| 22803959 | 10.1021/jm300601d | Liver microsomes | 2 |
| 22803959 | 10.1021/jm300601d | Sodium/hydrogen exchanger 1 | 2 |
| 22803959 | 10.1021/jm300601d | Voltage-gated inwardly rectifying potassium channel KCNH2 | 1 |
| 22803959 | 10.1021/jm300601d | Sodium/hydrogen exchanger 3 | 1 |
| 22803959 | 10.1021/jm300601d | Unchecked | 1 |
| 22803959 | 10.1021/jm300601d | ADMET | 1 |
| 22803959 | 10.1021/jm300601d | Cytochrome P450 3A4 | 1 |
| 22803959 | 10.1021/jm300601d | Cytochrome P450 2D6 | 1 |
| 22803959 | 10.1021/jm300601d | Cytochrome P450 2C9 | 1 |
| 22803959 | 10.1021/jm300601d | Cytochrome P450 2C19 | 1 |
Data from ChEMBL 36 via Core Engine