Compound Detail
CHEMBL5089911
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Basic Information
| ChEMBL ID | CHEMBL5089911 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | ZJNSFQCRAJSSCV-UHFFFAOYSA-N |
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names
Molecular Properties
461.6
MW (Da)
2.57
ALogP
8
HBA
4
HBD
114.1
PSA (Ų)
0.40
QED
0
Ro5 Violations
8
Rot. Bonds
Drug Information
| Molecule Type | Unknown |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 8.12
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Proto-oncogene tyrosine-protein kinase receptor Ret CHEMBL2041 | IC50 | 8.12 | 8.015 | 7.5 | 2 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Proto-oncogene tyrosine-protein kinase receptor Ret | IC50 | = | 7.53 | nM | 8.12 | Inhibition of GST-3C fused human RET (705 to 1013 residues) expressed in sf9 bac... | 35081714 |
| Proto-oncogene tyrosine-protein kinase receptor Ret | IC50 | = | 12.32 | nM | 7.91 | Inhibition of human RET V804M mutant using 5-FAM- peptide as substrate preincuba... | 35081714 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 35081714 | 10.1021/acs.jmedchem.1c01280 | Proto-oncogene tyrosine-protein kinase receptor Ret | 2 |
Data from ChEMBL 36 via Core Engine