Compound Detail
CHEMBL205968
Enter ChEMBL ID:
Free Research Context
This compound will appear in recent viewed items on the research home for this browser.
Research home
View demo workspace
CC(C)CN([C@H](CO)CCCCNC(=O)[C@@H](NC(=O)c1ccccn1)C(c1ccccc1)c1ccccc1)S(=O)(=O)c1ccc(N)cc1
Basic Information
| ChEMBL ID | CHEMBL205968 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | PLKVIGSGPBBXJR-ZJJOJAIXSA-N |
2
Targets
3
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
671.9
MW (Da)
4.59
ALogP
7
HBA
4
HBD
154.7
PSA (Ų)
0.09
QED
1
Ro5 Violations
17
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
EC50 2 meas. best 7.17
IC50 1 meas. best 9.34
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Human immunodeficiency virus type 1 protease CHEMBL243 | IC50 | 9.34 | 9.34 | 0.5 | 1 |
| Human immunodeficiency virus 1 CHEMBL378 | EC50 | 7.17 | 6.98 | 68.0 | 2 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Human immunodeficiency virus type 1 protease | IC50 | = | 0.46 | nM | 9.34 | Inhibition of HIV aspartyl protease | 16644213 |
| Human immunodeficiency virus 1 | EC50 | = | 68.0 | nM | 7.17 | Antiviral activity against HIV1 NL4-3 in MT4 cells | 16644213 |
| Human immunodeficiency virus 1 | EC50 | = | 161.0 | nM | 6.79 | Antiviral activity against HIV1 multi PI resistant strain 4596 | 16644213 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 16644213 | 10.1016/j.bmcl.2006.04.011 | Human immunodeficiency virus 1 | 2 |
| 16644213 | 10.1016/j.bmcl.2006.04.011 | Human immunodeficiency virus type 1 protease | 1 |
Data from ChEMBL 36 via Core Engine