Compound Detail
CHEMBL1916716
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Basic Information
| ChEMBL ID | CHEMBL1916716 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | VNIICVCBGDTYHE-JXMROGBWSA-N |
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names
Molecular Properties
484.6
MW (Da)
4.80
ALogP
7
HBA
1
HBD
75.0
PSA (Ų)
0.34
QED
0
Ro5 Violations
9
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 7.37
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| NON-PROTEIN TARGET CHEMBL3879801 | IC50 | 7.37 | 7.37 | 43.1 | 1 |
| Tyrosine-protein kinase BTK CHEMBL5251 | IC50 | 7.34 | 7.34 | 45.3 | 1 |
| Tyrosine-protein kinase Lyn CHEMBL3905 | IC50 | 5.7 | 5.7 | 1980.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| NON-PROTEIN TARGET | IC50 | = | 43.15 | nM | 7.37 | Inhibition of anti-IgM-stimulated human B cell proliferation assessed as [3H]thy... | 21958547 |
| Tyrosine-protein kinase BTK | IC50 | = | 45.3 | nM | 7.34 | Inhibition of human full-length BTK expressed in Sf9 cells using FAM-Srctide pep... | 21958547 |
| Tyrosine-protein kinase Lyn | IC50 | = | 1980.0 | nM | 5.7 | Inhibition of LYN-A expressed in Sf9 cells after 60 mins by TR-FRET Assay | 21958547 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 21958547 | 10.1016/j.bmcl.2011.09.008 | Tyrosine-protein kinase BTK | 1 |
| 21958547 | 10.1016/j.bmcl.2011.09.008 | Tyrosine-protein kinase Lyn | 1 |
| 21958547 | 10.1016/j.bmcl.2011.09.008 | NON-PROTEIN TARGET | 1 |
Data from ChEMBL 36 via Core Engine