Compound Detail
CHEMBL326566
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CCCC1(CCc2ccccc2)CC(=O)C(C(CC)c2cccc(NS(=O)(=O)c3ccc(F)cc3)c2)=C(O)O1
Basic Information
| ChEMBL ID | CHEMBL326566 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | ZBHMRNYMELLCAK-UHFFFAOYSA-N |
1
Targets
4
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
551.7
MW (Da)
7.05
ALogP
5
HBA
2
HBD
92.7
PSA (Ų)
0.27
QED
2
Ro5 Violations
11
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 5.92
Ki 2 meas. best 8.22
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Human immunodeficiency virus type 1 protease CHEMBL243 | Ki | 8.22 | 8.215 | 6.0 | 2 |
| Human immunodeficiency virus type 1 protease CHEMBL243 | IC50 | 5.92 | 5.92 | 1200.0 | 2 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Human immunodeficiency virus type 1 protease | Ki | = | 6.0 | nM | 8.22 | Tested for inhibition of HIV protease | 8893827 |
| Human immunodeficiency virus type 1 protease | Ki | = | 6.1 | nM | 8.21 | Inhibitory activity against HIV-1 protease in tandem assay. | 9719600 |
| Human immunodeficiency virus type 1 protease | IC50 | = | 1200.0 | nM | 5.92 | Tested for inhibition of HIV protease | 8893827 |
| Human immunodeficiency virus type 1 protease | IC50 | = | 1200.0 | nM | 5.92 | Inhibition of HIV-1 protease in a cell culture assay using HIV-1 IIIB infected H... | 9719600 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 8893827 | 10.1021/jm960541s | Human immunodeficiency virus type 1 protease | 3 |
| 9719600 | 10.1021/jm9802158 | Human immunodeficiency virus type 1 protease | 3 |
Data from ChEMBL 36 via Core Engine