Compound Detail
CHEMBL496605
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Basic Information
| ChEMBL ID | CHEMBL496605 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | NMKSBEVTNZMDAE-UHFFFAOYSA-N |
5
Targets
7
Activities
1
Assay Types
9
PK Parameters
12
Publications
0
Known Names
Molecular Properties
372.5
MW (Da)
4.33
ALogP
5
HBA
1
HBD
51.3
PSA (Ų)
0.58
QED
0
Ro5 Violations
4
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 7 meas. best 7.9
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Unchecked CHEMBL612545 | IC50 | 7.9 | 7.6 | 12.6 | 2 |
| Cytochrome P450 3A4 CHEMBL340 | IC50 | 4.89 | 4.605 | 13000.0 | 2 |
| Cytochrome P450 2C9 CHEMBL3397 | IC50 | 4.77 | 4.77 | 17000.0 | 1 |
| Cytochrome P450 2D6 CHEMBL289 | IC50 | 4.01 | 4.01 | 97000.0 | 1 |
| Cytochrome P450 1A2 CHEMBL3356 | IC50 | 4.0 | 4.0 | 100000.0 | 1 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| CL | 1.9 | mL.min-1.g-1 | Homo sapiens |
| CL | 1.0 | mL.min-1.g-1 | Canis lupus familiaris |
| CL | 6.0 | mL.min-1.g-1 | Rattus norvegicus |
| CL | 48.0 | mL.min-1.kg-1 | Rattus norvegicus |
| CL | 21.0 | mL.min-1.kg-1 | Canis lupus familiaris |
| F | 33.0 | % | Rattus norvegicus |
| F | 61.0 | % | Canis lupus familiaris |
| T1/2 | 0.5 | hr | Rattus norvegicus |
| T1/2 | 2.5 | hr | Canis lupus familiaris |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Unchecked | IC50 | = | 12.59 | nM | 7.9 | Inhibition of H+/K+ ATPase | 19467868 |
| Unchecked | IC50 | = | 50.12 | nM | 7.3 | Inhibition of H+/K+ ATPase in parietal cells assessed as inhibition of pentagast... | 19467868 |
| Cytochrome P450 3A4 | IC50 | = | 13000.0 | nM | 4.89 | Inhibition of CYP3A4 using diethoxyfluorescein as substrate | 19467868 |
| Cytochrome P450 2C9 | IC50 | = | 17000.0 | nM | 4.77 | Inhibition of CYP2C9 | 19467868 |
| Cytochrome P450 3A4 | IC50 | = | 48000.0 | nM | 4.32 | Inhibition of CYP3A4 using 7-benzyloxyquinoline as substrate | 19467868 |
| Cytochrome P450 2D6 | IC50 | = | 97000.0 | nM | 4.01 | Inhibition of CYP2D6 | 19467868 |
| Cytochrome P450 1A2 | IC50 | = | 100000.0 | nM | 4.0 | Inhibition of CYP1A2 | 19467868 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 19467868 | 10.1016/j.bmcl.2009.04.127 | Rattus norvegicus | 6 |
| 19467868 | 10.1016/j.bmcl.2009.04.127 | Canis familiaris | 4 |
| 19467868 | 10.1016/j.bmcl.2009.04.127 | Unchecked | 3 |
| 19467868 | 10.1016/j.bmcl.2009.04.127 | Cytochrome P450 3A4 | 2 |
| 19467868 | 10.1016/j.bmcl.2009.04.127 | Liver microsomes | 2 |
| 19467868 | 10.1016/j.bmcl.2009.04.127 | No relevant target | 1 |
| 19467868 | 10.1016/j.bmcl.2009.04.127 | Cytochrome P450 2D6 | 1 |
| 19467868 | 10.1016/j.bmcl.2009.04.127 | Cytochrome P450 2C19 | 1 |
| 19467868 | 10.1016/j.bmcl.2009.04.127 | Cytochrome P450 2C9 | 1 |
| 19467868 | 10.1016/j.bmcl.2009.04.127 | Cytochrome P450 1A2 | 1 |
| 19467868 | 10.1016/j.bmcl.2009.04.127 | ADMET | 1 |
| 19467868 | 10.1016/j.bmcl.2009.04.127 | Blood | 1 |
Data from ChEMBL 36 via Core Engine