Compound Detail
CHEMBL3350109
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O=S1(=O)N(Cc2ccc(CO)cc2)[C@@H](COc2ccccc2)[C@@H](O)[C@H](O)[C@H](COc2ccccc2)N1Cc1ccc(CO)cc1
Basic Information
| ChEMBL ID | CHEMBL3350109 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | AWUYZKRFZVNVEM-PSWJWLENSA-N |
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names
Molecular Properties
634.8
MW (Da)
2.85
ALogP
8
HBA
4
HBD
140.0
PSA (Ų)
0.19
QED
1
Ro5 Violations
12
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
Ki 2 meas. best 8.51
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Human immunodeficiency virus type 1 protease CHEMBL243 | Ki | 8.51 | 8.51 | 3.1 | 2 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Human immunodeficiency virus type 1 protease | Ki | = | 3.1 | nM | 8.51 | Inhibition of recombinant HIV-1 protease measured by fluorometric assay | 11170625 |
| Human immunodeficiency virus type 1 protease | Ki | = | 3.09 | nM | 8.51 | Inhibition of HIV-1 protease by fluorometric assay | 11170625 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 11170625 | 10.1021/jm001024j | Human immunodeficiency virus type 1 protease | 2 |
Data from ChEMBL 36 via Core Engine