Compound Detail
CHEMBL2029992
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COc1cc2ncnc(Sc3cccc(NC(=O)Nc4cc(C5(C(F)(F)F)CC5)on4)c3)c2cc1OC
Basic Information
| ChEMBL ID | CHEMBL2029992 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | WKWHUIXJXMGBLU-UHFFFAOYSA-N |
2
Targets
3
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
531.5
MW (Da)
6.02
ALogP
8
HBA
2
HBD
111.4
PSA (Ų)
0.28
QED
2
Ro5 Violations
7
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 6.65
Kd 1 meas. best 7.51
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Serine/threonine-protein kinase B-raf CHEMBL5145 | Kd | 7.51 | 7.51 | 31.0 | 1 |
| A-375 CHEMBL613859 | IC50 | 6.65 | 6.65 | 222.0 | 1 |
| Serine/threonine-protein kinase B-raf CHEMBL5145 | IC50 | 6.33 | 6.33 | 469.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Serine/threonine-protein kinase B-raf | Kd | = | 31.0 | nM | 7.51 | Inhibition of BRAF V600E mutant in human HEK293 cells after 1 hr by competition ... | 22168626 |
| A-375 | IC50 | = | 222.0 | nM | 6.65 | Cytotoxicity against human A375 cells expressing BRAF V600E mutant after 72 hrs ... | 22168626 |
| Serine/threonine-protein kinase B-raf | IC50 | = | 469.0 | nM | 6.33 | Inhibition of BRAF V600E mutant-mediated MEK phosphorylation in human A375 cells... | 22168626 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 22168626 | 10.1021/jm2009925 | Serine/threonine-protein kinase B-raf | 2 |
| 22168626 | 10.1021/jm2009925 | A-375 | 1 |
Data from ChEMBL 36 via Core Engine