Compound Detail
CHEMBL4081661
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CC1(C(=O)N2CCC[C@@H](c3nc(-c4ccc(C(=O)Nc5cc(C(F)(F)F)ccn5)cc4F)c4c(N)nccn34)C2)CCC1
Basic Information
| ChEMBL ID | CHEMBL4081661 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | RUMYVPRQDWQCDK-GOSISDBHSA-N |
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
595.6
MW (Da)
5.68
ALogP
7
HBA
2
HBD
118.5
PSA (Ų)
0.29
QED
2
Ro5 Violations
5
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 9.52
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Tyrosine-protein kinase BTK CHEMBL5251 | IC50 | 9.52 | 8.835 | 0.3 | 2 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Tyrosine-protein kinase BTK | IC50 | = | 0.3 | nM | 9.52 | Inhibition of recombinant full-length His6-tagged BTK (unknown origin) expressed... | 28720503 |
| Tyrosine-protein kinase BTK | IC50 | = | 7.0 | nM | 8.15 | Inhibition of BTK in human PBMC assessed as reduction in anti-IgM-induced MIP1be... | 28720503 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 28720503 | 10.1016/j.bmcl.2017.03.040 | Tyrosine-protein kinase BTK | 2 |
| 28720503 | 10.1016/j.bmcl.2017.03.040 | Voltage-gated inwardly rectifying potassium channel KCNH2 | 1 |
Data from ChEMBL 36 via Core Engine