Compound Detail
CHEMBL486162
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Basic Information
| ChEMBL ID | CHEMBL486162 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | CQMWNSQCEMHNIW-UHFFFAOYSA-N |
4
Targets
5
Activities
2
Assay Types
10
PK Parameters
10
Publications
0
Known Names
Molecular Properties
406.5
MW (Da)
2.05
ALogP
8
HBA
1
HBD
92.1
PSA (Ų)
0.71
QED
0
Ro5 Violations
4
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
Ki 3 meas. best 9.15
IC50 2 meas. best 8.15
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Adenosine receptor A2a CHEMBL251 | Ki | 9.15 | 9.15 | 0.7 | 1 |
| Adenosine receptor A2a CHEMBL251 | IC50 | 8.15 | 8.15 | 7.0 | 1 |
| Adenosine receptor A2a CHEMBL302 | Ki | 8.15 | 8.15 | 7.0 | 1 |
| Adenosine receptor A1 CHEMBL226 | Ki | 6.92 | 6.92 | 120.0 | 1 |
| Voltage-gated inwardly rectifying potassium channel KCNH2 CHEMBL240 | IC50 | 6.27 | 6.27 | 540.0 | 1 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| AUC | 1430.0 | ng.hr.mL-1 | Rattus norvegicus |
| AUC | 18700.0 | ng.hr.mL-1 | Rattus norvegicus |
| AUC | 28900.0 | ng.hr.mL-1 | Rattus norvegicus |
| AUC | 36800.0 | ng.hr.mL-1 | Rattus norvegicus |
| CL | 3.0 | mL.min-1.kg-1 | Homo sapiens |
| CL | 25.0 | mL.min-1.kg-1 | Rattus norvegicus |
| Cmax | 1008.63 | nM | Rattus norvegicus |
| Cmax | 6396.22 | nM | Rattus norvegicus |
| Cmax | 8364.29 | nM | Rattus norvegicus |
| Cmax | 10332.36 | nM | Rattus norvegicus |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Adenosine receptor A2a | Ki | = | 0.71 | nM | 9.15 | Displacement of [3H]ZM241685 from human adenosine A2A receptor expressed in HEK2... | 18947224 |
| Adenosine receptor A2a | IC50 | = | 7.0 | nM | 8.15 | Antagonist activity at human adenosine A2A receptor expressed in CHO cells asses... | 18947224 |
| Adenosine receptor A2a | Ki | = | 7.0 | nM | 8.15 | Displacement of [3H]ZM241685 from rat adenosine A2A receptor expressed in CHO ce... | 18947224 |
| Adenosine receptor A1 | Ki | = | 120.0 | nM | 6.92 | Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in HEK293 c... | 18947224 |
| Voltage-gated inwardly rectifying potassium channel KCNH2 | IC50 | = | 540.0 | nM | 6.27 | Inhibition of human ERG by electrophysiology assay | 18947224 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 18947224 | 10.1021/jm800851u | Rattus norvegicus | 10 |
| 18947224 | 10.1021/jm800851u | Adenosine receptor A2a | 3 |
| 18947224 | 10.1021/jm800851u | No relevant target | 3 |
| 18947224 | 10.1021/jm800851u | Liver microsomes | 2 |
| 18947224 | 10.1021/jm800851u | Adenosine receptor A1 | 1 |
| 18947224 | 10.1021/jm800851u | Unchecked | 1 |
| 18947224 | 10.1021/jm800851u | Cytochrome P450 3A4 | 1 |
| 18947224 | 10.1021/jm800851u | Brain | 1 |
| 18947224 | 10.1021/jm800851u | MDCK | 1 |
| 18947224 | 10.1021/jm800851u | Voltage-gated inwardly rectifying potassium channel KCNH2 | 1 |
Data from ChEMBL 36 via Core Engine