Compound Detail
CHEMBL5181292
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CN1C(=S)[C@@H](NC(=O)c2nc(Cc3ccccc3)n(CC(F)(F)F)n2)COc2ccccc21
Basic Information
| ChEMBL ID | CHEMBL5181292 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | LZVKWDKNNWOLTP-HNNXBMFYSA-N |
2
Targets
2
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
475.5
MW (Da)
3.39
ALogP
6
HBA
1
HBD
72.3
PSA (Ų)
0.57
QED
0
Ro5 Violations
5
Rot. Bonds
Drug Information
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
EC50 1 meas. best 7.44
Kd 1 meas. best 6.57
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| HT-29 CHEMBL384 | EC50 | 7.44 | 7.44 | 36.0 | 1 |
| Receptor-interacting serine/threonine-protein kinase 1 CHEMBL5464 | Kd | 6.57 | 6.57 | 267.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| HT-29 | EC50 | = | 36.0 | nM | 7.44 | Anti-necroptic activity in human HT-29 cells assessed as inhibition of TSZ induc... | 35398729 |
| Receptor-interacting serine/threonine-protein kinase 1 | Kd | = | 267.0 | nM | 6.57 | Binding affinity to wild-type human partial length RIPK1 (M1 to K305 residues) e... | 35398729 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 35398729 | 10.1016/j.ejmech.2022.114345 | HT-29 | 2 |
| 35398729 | 10.1016/j.ejmech.2022.114345 | Receptor-interacting serine/threonine-protein kinase 1 | 1 |
Data from ChEMBL 36 via Core Engine