Compound Detail
CHEMBL5407292
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CC(C)(O)C(=O)N1CCc2nc(Nc3ncc(C(F)(F)F)c(N[C@H]4CC[C@@H](N)CC4)n3)ccc2C1
Basic Information
| ChEMBL ID | CHEMBL5407292 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | UTOOTASPOOSERC-GASCZTMLSA-N |
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names
Molecular Properties
493.5
MW (Da)
2.97
ALogP
8
HBA
4
HBD
129.3
PSA (Ų)
0.50
QED
0
Ro5 Violations
5
Rot. Bonds
Drug Information
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 8.02
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| MV4-11 CHEMBL613835 | IC50 | 8.02 | 8.02 | 9.5 | 1 |
| Receptor-type tyrosine-protein kinase FLT3 CHEMBL1974 | IC50 | 7.26 | 7.26 | 55.4 | 1 |
| Serine/threonine-protein kinase Chk1 CHEMBL4630 | IC50 | 6.6 | 6.6 | 250.4 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| MV4-11 | IC50 | = | 9.51 | nM | 8.02 | Antiproliferative activity against human MV4-11 cells assessed as reduction in c... | 37584545 |
| Receptor-type tyrosine-protein kinase FLT3 | IC50 | = | 55.43 | nM | 7.26 | Inhibition of FLT3 D835Y mutant (unknown origin) using peptide substrate TK-S an... | 37584545 |
| Serine/threonine-protein kinase Chk1 | IC50 | = | 250.45 | nM | 6.6 | Inhibition of CHK1 (unknown origin) using peptide substrate S1 and ATP as substr... | 37584545 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 37584545 | 10.1021/acs.jmedchem.3c00245 | Receptor-type tyrosine-protein kinase FLT3 | 1 |
| 37584545 | 10.1021/acs.jmedchem.3c00245 | Serine/threonine-protein kinase Chk1 | 1 |
| 37584545 | 10.1021/acs.jmedchem.3c00245 | MV4-11 | 1 |
| 37584545 | 10.1021/acs.jmedchem.3c00245 | Voltage-gated inwardly rectifying potassium channel KCNH2 | 1 |
Data from ChEMBL 36 via Core Engine