Compound Detail
CHEMBL2018146
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CCn1cc(-c2cccc(-c3cnc(N)c(C(=O)N[C@H]4C5CC6CC4C[C@](O)(C6)C5)n3)c2)cn1
Basic Information
| ChEMBL ID | CHEMBL2018146 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | QSRWJNLAANDJCZ-IWPBWAMJSA-N |
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
458.6
MW (Da)
3.28
ALogP
7
HBA
3
HBD
119.0
PSA (Ų)
0.54
QED
0
Ro5 Violations
5
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 7.7
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Tyrosine-protein kinase receptor TYRO3 CHEMBL5314 | IC50 | 7.7 | 7.7 | 20.0 | 1 |
| LAD2 CHEMBL4483253 | IC50 | 6.75 | 6.75 | 180.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Tyrosine-protein kinase receptor TYRO3 | IC50 | = | 20.0 | nM | 7.7 | Inhibition of human recombinant Sky using poly-GT as substrate and [33P]ATP afte... | 22425453 |
| LAD2 | IC50 | = | 180.0 | nM | 6.75 | Inhibition of IgE-mediated human LAD2 cell degranulation assessed as beta-hexosa... | 22425453 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 22425453 | 10.1016/j.bmcl.2012.02.087 | Tyrosine-protein kinase receptor TYRO3 | 1 |
| 22425453 | 10.1016/j.bmcl.2012.02.087 | LAD2 | 1 |
Data from ChEMBL 36 via Core Engine