Compound Detail
CHEMBL3357182
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Basic Information
| ChEMBL ID | CHEMBL3357182 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | KMBASEXJNDTEKF-UHFFFAOYSA-N |
2
Targets
3
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names
Molecular Properties
456.6
MW (Da)
1.66
ALogP
8
HBA
2
HBD
114.4
PSA (Ų)
0.36
QED
0
Ro5 Violations
12
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 5.37
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Receptor-type tyrosine-protein kinase FLT3 CHEMBL1974 | IC50 | 5.37 | 5.05 | 4230.0 | 2 |
| MV4-11 CHEMBL613835 | IC50 | 5.12 | 5.12 | 7610.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Receptor-type tyrosine-protein kinase FLT3 | IC50 | = | 4230.0 | nM | 5.37 | Inhibition of recombinant FLT3 ITD mutant (unknown origin) by RBC kinase assay | 25456387 |
| MV4-11 | IC50 | = | 7610.0 | nM | 5.12 | Antiproliferative activity against human MV4-11 cells after 72 hrs by luminescen... | 25456387 |
| Receptor-type tyrosine-protein kinase FLT3 | IC50 | = | 18590.0 | nM | 4.73 | Inhibition of recombinant FLT3 D835Y mutant (unknown origin) by TR-FRET assay | 25456387 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 25456387 | 10.1016/j.bmc.2014.10.006 | Receptor-type tyrosine-protein kinase FLT3 | 3 |
| 25456387 | 10.1016/j.bmc.2014.10.006 | NON-PROTEIN TARGET | 3 |
| 25456387 | 10.1016/j.bmc.2014.10.006 | MV4-11 | 2 |
| 25456387 | 10.1016/j.bmc.2014.10.006 | ADMET | 1 |
| 25456387 | 10.1016/j.bmc.2014.10.006 | K562 | 1 |
Data from ChEMBL 36 via Core Engine