Compound Detail
CHEMBL4126579
Enter ChEMBL ID:
Free Research Context
This compound will appear in recent viewed items on the research home for this browser.
Research home
View demo workspace
Basic Information
| ChEMBL ID | CHEMBL4126579 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | JQXWHSPGFYOVPN-LJQANCHMSA-N |
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names
Molecular Properties
449.0
MW (Da)
3.49
ALogP
4
HBA
4
HBD
125.1
PSA (Ų)
0.38
QED
0
Ro5 Violations
7
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 7.0
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Serine protease hepsin CHEMBL2079849 | IC50 | 7.0 | 7.0 | 100.0 | 1 |
| Urokinase-type plasminogen activator CHEMBL3286 | IC50 | 4.75 | 4.75 | 18000.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Serine protease hepsin | IC50 | = | 100.0 | nM | 7.0 | Inhibition of recombinant C-terminal His10-tagged human Hepsin (R45 to L17 resid... | 29701962 |
| Urokinase-type plasminogen activator | IC50 | = | 18000.0 | nM | 4.75 | Inhibition of recombinant C-terminal His10-tagged human uPA (M1 to L431 residues... | 29701962 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 29701962 | 10.1021/acs.jmedchem.7b01698 | Serine protease hepsin | 1 |
| 29701962 | 10.1021/acs.jmedchem.7b01698 | Urokinase-type plasminogen activator | 1 |
| 29701962 | 10.1021/acs.jmedchem.7b01698 | Unchecked | 1 |
| 29701962 | 10.1021/acs.jmedchem.7b01698 | No relevant target | 1 |
Data from ChEMBL 36 via Core Engine