Compound Detail
CHEMBL89150
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Basic Information
| ChEMBL ID | CHEMBL89150 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | KDBDIVVITSSJRH-UHFFFAOYSA-N |
3
Targets
4
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names
Molecular Properties
356.5
MW (Da)
4.22
ALogP
4
HBA
3
HBD
63.0
PSA (Ų)
0.34
QED
0
Ro5 Violations
7
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 4 meas. best 6.16
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Leishmania major CHEMBL612879 | IC50 | 6.16 | 6.16 | 700.0 | 1 |
| Jurkat CHEMBL397 | IC50 | 5.4 | 5.4 | 4000.0 | 1 |
| P388 CHEMBL389 | IC50 | 4.9 | 4.625 | 12500.0 | 2 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Leishmania major | IC50 | = | 700.0 | nM | 6.16 | Concentration required to reduce incorporation of [3H]TdR in drug-treated cultur... | 9258370 |
| Jurkat | IC50 | = | 4000.0 | nM | 5.4 | Concentration required to reduce the growth of human Jurkat cells to 50% of cont... | 9258370 |
| P388 | IC50 | = | 12500.0 | nM | 4.9 | In vitro inhibition of P388 (murine leukemia) cell growth. | 2231598 |
| P388 | IC50 | = | 45000.0 | nM | 4.35 | In vitro inhibition of Pt resistant P388 (murine leukemia) cell growth. | 2231598 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 2231598 | 10.1021/jm00173a015 | P388 | 4 |
| 9258370 | 10.1021/jm970232h | Leishmania major | 2 |
| 9258370 | 10.1021/jm970232h | Jurkat | 1 |
Data from ChEMBL 36 via Core Engine