Compound Detail
CHEMBL1765101
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Basic Information
| ChEMBL ID | CHEMBL1765101 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | OVYVQHHATBRNQF-UHFFFAOYSA-N |
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names
Molecular Properties
322.4
MW (Da)
3.98
ALogP
3
HBA
2
HBD
58.1
PSA (Ų)
0.75
QED
0
Ro5 Violations
5
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 8.0
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Steroid 17-alpha-hydroxylase/17,20 lyase CHEMBL4430 | IC50 | 8.0 | 8.0 | 10.0 | 1 |
| Steroid 17-alpha-hydroxylase/17,20 lyase CHEMBL3522 | IC50 | 6.89 | 6.89 | 130.0 | 1 |
| Cytochrome P450 3A4 CHEMBL340 | IC50 | 5.7 | 5.7 | 2000.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Steroid 17-alpha-hydroxylase/17,20 lyase | IC50 | = | 10.0 | nM | 8.0 | Inhibition of 17,20 lyase activity in Sprague-Dawley rat testicular microsomes | 21429754 |
| Steroid 17-alpha-hydroxylase/17,20 lyase | IC50 | = | 130.0 | nM | 6.89 | Inhibition of human 17,20 lyase activity | 21429754 |
| Cytochrome P450 3A4 | IC50 | = | 2000.0 | nM | 5.7 | Inhibition of human CYP3A4 after 30 mins | 21429754 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 21429754 | 10.1016/j.bmc.2011.02.009 | Steroid 17-alpha-hydroxylase/17,20 lyase | 2 |
| 21429754 | 10.1016/j.bmc.2011.02.009 | Cytochrome P450 3A4 | 1 |
| 21429754 | 10.1016/j.bmc.2011.02.009 | Unchecked | 1 |
Data from ChEMBL 36 via Core Engine