Compound Detail
CHEMBL3651257
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Basic Information
| ChEMBL ID | CHEMBL3651257 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | SIUNALDMRGZQBR-UHFFFAOYSA-N |
3
Targets
6
Activities
1
Assay Types
0
PK Parameters
0
Publications
0
Known Names
Molecular Properties
476.0
MW (Da)
5.58
ALogP
7
HBA
2
HBD
83.4
PSA (Ų)
0.36
QED
1
Ro5 Violations
7
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 6 meas. best 9.15
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Tyrosine-protein kinase Yes CHEMBL2073 | IC50 | 9.15 | 9.15 | 0.7 | 2 |
| Proto-oncogene tyrosine-protein kinase Src CHEMBL267 | IC50 | 8.38 | 8.38 | 4.2 | 2 |
| Platelet-derived growth factor receptor beta CHEMBL1913 | IC50 | 8.24 | 8.24 | 5.7 | 2 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Tyrosine-protein kinase Yes | IC50 | = | 0.7 | nM | 9.15 | Luciferase-Based Assay: Recombinant human c-Src or Yes (28 ng/well, Panvera/Invi... | - |
| Tyrosine-protein kinase Yes | IC50 | = | 0.7 | nM | 9.15 | Inhibition of human recombinant Yes using PTK2 substrate incubated for 90 mins b... | - |
| Proto-oncogene tyrosine-protein kinase Src | IC50 | = | 4.2 | nM | 8.38 | Luciferase-Based Assay: Recombinant human c-Src or Yes (28 ng/well, Panvera/Invi... | - |
| Proto-oncogene tyrosine-protein kinase Src | IC50 | = | 4.2 | nM | 8.38 | Inhibition of human recombinant c-Src using PTK2 substrate incubated for 90 mins... | - |
| Platelet-derived growth factor receptor beta | IC50 | = | 5.7 | nM | 8.24 | Luciferase-Based Assay: Recombinant human c-Src or Yes (28 ng/well, Panvera/Invi... | - |
| Platelet-derived growth factor receptor beta | IC50 | = | 5.7 | nM | 8.24 | Inhibition of human recombinant Yes using PTK2 peptide substrate incubated for 6... | - |
Data from ChEMBL 36 via Core Engine