Compound Detail
CHEMBL378194
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CC(C)CN([C@H](CO)CCCCNC(=O)[C@@H](NC(=O)c1ccc(O)c([N+](=O)[O-])c1)C(c1ccccc1)c1ccccc1)S(=O)(=O)c1ccc(N)cc1
Basic Information
| ChEMBL ID | CHEMBL378194 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | ILRBKIMZTBAVNG-NWWLCHBLSA-N |
2
Targets
3
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
731.9
MW (Da)
4.81
ALogP
9
HBA
5
HBD
205.2
PSA (Ų)
0.04
QED
1
Ro5 Violations
18
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
EC50 2 meas. best 7.46
IC50 1 meas. best 9.25
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Human immunodeficiency virus type 1 protease CHEMBL243 | IC50 | 9.25 | 9.25 | 0.6 | 1 |
| Human immunodeficiency virus 1 CHEMBL378 | EC50 | 7.46 | 7.36 | 35.0 | 2 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Human immunodeficiency virus type 1 protease | IC50 | = | 0.56 | nM | 9.25 | Inhibition of HIV aspartyl protease | 16644213 |
| Human immunodeficiency virus 1 | EC50 | = | 35.0 | nM | 7.46 | Antiviral activity against HIV1 multi PI resistant strain 4596 | 16644213 |
| Human immunodeficiency virus 1 | EC50 | = | 55.0 | nM | 7.26 | Antiviral activity against HIV1 NL4-3 in MT4 cells | 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