Compound Detail
CHEMBL2335892
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Basic Information
| ChEMBL ID | CHEMBL2335892 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | IDMVTOZYZLLLTD-UHFFFAOYSA-N |
1
Targets
2
Activities
1
Assay Types
1
PK Parameters
7
Publications
0
Known Names
Molecular Properties
427.5
MW (Da)
4.65
ALogP
6
HBA
2
HBD
89.0
PSA (Ų)
0.43
QED
0
Ro5 Violations
8
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 7.4
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Serine/threonine-protein kinase B-raf CHEMBL5145 | IC50 | 7.4 | 7.275 | 40.0 | 2 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| CL | 76.0 | mL.min-1.g-1 | Homo sapiens |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Serine/threonine-protein kinase B-raf | IC50 | = | 40.0 | nM | 7.4 | Inhibition of human recombinant N-terminus His-tagged BRAF V600E mutant expresse... | 23398453 |
| Serine/threonine-protein kinase B-raf | IC50 | = | 71.0 | nM | 7.15 | Inhibition of BRAF V600E mutant-mediated ERK phosphorylation in human A375 cells... | 23398453 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 23398453 | 10.1021/jm301658d | Serine/threonine-protein kinase B-raf | 2 |
| 23398453 | 10.1021/jm301658d | Liver microsomes | 1 |
| 23398453 | 10.1021/jm301658d | Hepatocyte | 1 |
| 23398453 | 10.1021/jm301658d | Plasma | 1 |
| 23398453 | 10.1021/jm301658d | No relevant target | 1 |
| - | 10.6019/CHEMBL3301361 | No relevant target | 1 |
| - | 10.6019/CHEMBL3301361 | ADMET | 1 |
Data from ChEMBL 36 via Core Engine