Compound Detail
CHEMBL419580
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CC(C)[C@H](NC(=O)C1Cc2ccccc2CN1)C(=O)N[C@@H](Cc1ccccc1)C(O)[C@H](Cc1ccccc1)NC(=O)[C@H](NC(=O)C1Cc2ccccc2CN1)C(C)C
Basic Information
| ChEMBL ID | CHEMBL419580 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | IIXQQSAAGXCYDM-UHDQTCBSSA-N |
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
787.0
MW (Da)
3.51
ALogP
7
HBA
7
HBD
160.7
PSA (Ų)
0.09
QED
2
Ro5 Violations
16
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 1 meas. best 8.15
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Human immunodeficiency virus type 1 protease CHEMBL243 | IC50 | 8.15 | 8.15 | 7.1 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Human immunodeficiency virus type 1 protease | IC50 | = | 7.1 | nM | 8.15 | Inhibition of purified recombinant HIV-1 protease in a fluorogenic assay | 8426362 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 8426362 | 10.1021/jm00055a003 | MT4 | 2 |
| 8426362 | 10.1021/jm00055a003 | Human immunodeficiency virus type 1 protease | 1 |
Data from ChEMBL 36 via Core Engine