Compound Detail
CHEMBL5564492
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C[C@H](NC(=O)c1cn(C)c2ccc(-c3ccn4nc(NC(=O)C5CC5(F)F)nc4c3)cc12)c1cccc(F)c1
Basic Information
| ChEMBL ID | CHEMBL5564492 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | DGQZJIGIOBGFCP-UEDXYCIISA-N |
1
Targets
2
Activities
2
Assay Types
5
PK Parameters
3
Publications
0
Known Names
Molecular Properties
532.5
MW (Da)
5.11
ALogP
6
HBA
2
HBD
93.3
PSA (Ų)
0.32
QED
2
Ro5 Violations
6
Rot. Bonds
Drug Information
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
EC50 1 meas.
IC50 1 meas. best 7.8
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Receptor-interacting serine/threonine-protein kinase 1 CHEMBL5464 | IC50 | 7.8 | 7.8 | 16.0 | 1 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| AUC | 747.0 | ng.hr.mL-1 | Rattus norvegicus |
| Cmax | 0.26 | ug.mL-1 | Rattus norvegicus |
| F | 4.47 | % | Rattus norvegicus |
| T1/2 | 2.47 | hr | Rattus norvegicus |
| Tmax | 0.67 | hr | Rattus norvegicus |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Receptor-interacting serine/threonine-protein kinase 1 | IC50 | = | 16.0 | nM | 7.8 | Inhibition of human RIPK1 (1 to 294 residues) preincubated for 15 mins followed ... | 38159286 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 38159286 | 10.1021/acs.jmedchem.3c02102 | ADMET | 5 |
| 38159286 | 10.1021/acs.jmedchem.3c02102 | Receptor-interacting serine/threonine-protein kinase 1 | 1 |
| 38159286 | 10.1021/acs.jmedchem.3c02102 | HT-29 | 1 |
Data from ChEMBL 36 via Core Engine