Compound Detail
CHEMBL310321
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O=C(NNc1ccc([N+](=O)[O-])cc1[N+](=O)[O-])c1ccc2ccc(C(=O)O)c(O)c2n1
Basic Information
| ChEMBL ID | CHEMBL310321 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | PKZCZJOXJSYLGZ-UHFFFAOYSA-N |
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names
Molecular Properties
413.3
MW (Da)
2.21
ALogP
9
HBA
4
HBD
197.8
PSA (Ų)
0.34
QED
0
Ro5 Violations
6
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 5.52
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Serine/threonine-protein kinase pim-1 CHEMBL2147 | IC50 | 5.52 | 5.52 | 3000.0 | 1 |
| Human immunodeficiency virus type 1 integrase CHEMBL3471 | IC50 | 5.52 | 5.52 | 3000.0 | 1 |
| Molecular identity unknown CHEMBL612546 | IC50 | 5.52 | 5.52 | 3000.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Human immunodeficiency virus type 1 integrase | IC50 | = | 3000.0 | nM | 5.52 | In vitro inhibition of recombinant integrase activity in a standard 3'-processin... | 15109635 |
| Serine/threonine-protein kinase pim-1 | IC50 | = | 3000.0 | nM | 5.52 | Inhibition of PIM1 | 20363627 |
| Molecular identity unknown | IC50 | = | 3000.0 | nM | 5.52 | Inhibition of HIV-1 integrase | 33609889 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 15109635 | 10.1016/j.bmcl.2004.03.005 | Human immunodeficiency virus type 1 integrase | 1 |
| 15109635 | 10.1016/j.bmcl.2004.03.005 | Human immunodeficiency virus 1 | 1 |
| 15109635 | 10.1016/j.bmcl.2004.03.005 | CCRF-CEM | 1 |
| 20363627 | 10.1016/j.bmcl.2010.03.061 | Serine/threonine-protein kinase pim-1 | 1 |
| 33609889 | 10.1016/j.ejmech.2021.113220 | Molecular identity unknown | 1 |
Data from ChEMBL 36 via Core Engine