Compound Detail
CHEMBL416958
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Basic Information
| ChEMBL ID | CHEMBL416958 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | UWOVKSLBXBRCJZ-UHFFFAOYSA-N |
2
Targets
5
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names
Molecular Properties
315.4
MW (Da)
3.88
ALogP
5
HBA
4
HBD
103.0
PSA (Ų)
0.33
QED
0
Ro5 Violations
2
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 5 meas. best 7.6
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Plasmodium falciparum CHEMBL364 | IC50 | 7.6 | 7.5275 | 25.0 | 4 |
| Jurkat CHEMBL397 | IC50 | 4.82 | 4.82 | 15000.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Plasmodium falciparum | IC50 | = | 25.0 | nM | 7.6 | Inhibitory concentration IC50 against Plasmodium falciparum K1 by [3H]hypoxanthi... | 8182707 |
| Plasmodium falciparum | IC50 | = | 25.0 | nM | 7.6 | Inhibitory concentration against Plasmodium falciparum K1 infected erythrocytes | 8182707 |
| Plasmodium falciparum | IC50 | = | 33.0 | nM | 7.48 | Inhibitory concentration against Plasmodium falciparum D6 infected erythrocytes | 8182707 |
| Plasmodium falciparum | IC50 | = | 37.0 | nM | 7.43 | Inhibitory concentration against Plasmodium falciparum W2 infected erythrocytes | 8182707 |
| Jurkat | IC50 | = | 15000.0 | nM | 4.82 | Concentration required to reduce growth of human jurkat leukemia cells to 50% of... | 8182707 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 8182707 | 10.1021/jm00036a014 | Plasmodium falciparum | 4 |
| 8182707 | 10.1021/jm00036a014 | Jurkat | 2 |
| 8182707 | 10.1021/jm00036a014 | DNA topoisomerase II | 1 |
| 8182707 | 10.1021/jm00036a014 | DNA topoisomerase 2 | 1 |
Data from ChEMBL 36 via Core Engine