Compound Detail
CHEMBL113626
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CC(C)[C@H](NC(=O)/C=C/c1cccnc1)C(=O)N[C@@H](Cc1ccccc1)C(O)[C@H](Cc1ccccc1)NC(=O)[C@H](NC(=O)/C=C/c1cccnc1)C(C)C
Basic Information
| ChEMBL ID | CHEMBL113626 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | CTEIKHWGBFKWFC-SBTGMTKMSA-N |
2
Targets
2
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names
Molecular Properties
730.9
MW (Da)
4.30
ALogP
7
HBA
5
HBD
162.4
PSA (Ų)
0.10
QED
1
Ro5 Violations
18
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
EC50 1 meas. best 5.55
IC50 1 meas. best 8.66
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Human immunodeficiency virus type 1 protease CHEMBL243 | IC50 | 8.66 | 8.66 | 2.2 | 1 |
| Human immunodeficiency virus 1 CHEMBL378 | EC50 | 5.55 | 5.55 | 2800.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Human immunodeficiency virus type 1 protease | IC50 | = | 2.2 | nM | 8.66 | Inhibition of purified recombinant HIV-1 protease in a fluorogenic assay | 8426362 |
| Human immunodeficiency virus 1 | EC50 | = | 2800.0 | nM | 5.55 | In vitro for inhibition of cytopathic effect of HIV-1 3B in MT-4 lymphocytes. | 8426362 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 8426362 | 10.1021/jm00055a003 | Human immunodeficiency virus type 1 protease | 1 |
| 8426362 | 10.1021/jm00055a003 | Human immunodeficiency virus 1 | 1 |
| 8426362 | 10.1021/jm00055a003 | MT4 | 1 |
| 8426362 | 10.1021/jm00055a003 | ADMET | 1 |
Data from ChEMBL 36 via Core Engine