Compound Detail
CHEMBL1779193
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CC1(C)c2cc(OCCN3CCS(=O)(=O)CC3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Basic Information
| ChEMBL ID | CHEMBL1779193 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | XBLAPMPMKLEWHJ-UHFFFAOYSA-N |
2
Targets
2
Activities
1
Assay Types
2
PK Parameters
4
Publications
0
Known Names
Molecular Properties
463.6
MW (Da)
3.02
ALogP
6
HBA
1
HBD
103.3
PSA (Ų)
0.64
QED
0
Ro5 Violations
4
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 8.43
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| ALK tyrosine kinase receptor CHEMBL4247 | IC50 | 8.43 | 8.43 | 3.7 | 1 |
| KARPAS-299 CHEMBL2366156 | IC50 | 7.06 | 7.06 | 87.5 | 1 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| CL | 24.9 | mL.min-1.g-1 | Mus musculus |
| CL | 67.0 | mL.min-1.g-1 | Homo sapiens |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| ALK tyrosine kinase receptor | IC50 | = | 3.7 | nM | 8.43 | Inhibition of ALK assessed as biotin-EGPWLEEEEEAYGWMDF peptide phosphorylation b... | 21561771 |
| KARPAS-299 | IC50 | = | 87.5 | nM | 7.06 | Cytotoxicity against human KARPAS299 cells expressing NPM-ALK after 96 hrs by ce... | 21561771 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 21561771 | 10.1016/j.bmcl.2011.04.020 | ALK tyrosine kinase receptor | 1 |
| 21561771 | 10.1016/j.bmcl.2011.04.020 | KARPAS-299 | 1 |
| 21561771 | 10.1016/j.bmcl.2011.04.020 | Liver | 1 |
| 21561771 | 10.1016/j.bmcl.2011.04.020 | Liver microsomes | 1 |
Data from ChEMBL 36 via Core Engine