Compound Detail
CHEMBL2448738
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Basic Information
| ChEMBL ID | CHEMBL2448738 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | CIFZHDRCJUNMFW-LQKURTRISA-N |
3
Targets
3
Activities
1
Assay Types
6
PK Parameters
5
Publications
0
Known Names
Molecular Properties
412.4
MW (Da)
3.95
ALogP
7
HBA
1
HBD
94.3
PSA (Ų)
0.38
QED
0
Ro5 Violations
6
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 8.6
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Trypanosoma cruzi CHEMBL368 | IC50 | 8.6 | 8.6 | 2.5 | 1 |
| Cytochrome P450 3A4 CHEMBL340 | IC50 | 5.1 | 5.1 | 8000.0 | 1 |
| L6 CHEMBL614793 | IC50 | 4.23 | 4.23 | 58680.0 | 1 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| CL | 29.0 | mL.min-1.g-1 | Mus musculus |
| CL | 30.0 | mL.min-1.g-1 | Homo sapiens |
| CL | 50.0 | mL.min-1.g-1 | Rattus norvegicus |
| T1/2 | 0.9667 | hr | Homo sapiens |
| T1/2 | 1.017 | hr | Mus musculus |
| T1/2 | 0.5833 | hr | Rattus norvegicus |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Trypanosoma cruzi | IC50 | = | 2.533 | nM | 8.6 | DNDI: Chagas in Vitro | - |
| Cytochrome P450 3A4 | IC50 | = | 8000.0 | nM | 5.1 | DNDI: Human CYP3A4 inhibition determined using 6b-hydroxylation of testosterone | - |
| L6 | IC50 | = | 58680.0 | nM | 4.23 | DNDI: Cytotoxicity in vitro, against rat skeletal myoblast (L-6) cells | - |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| - | 10.6019/CHEMBL2448688 | ADMET | 13 |
| - | 10.6019/CHEMBL2448688 | No relevant target | 4 |
| - | 10.6019/CHEMBL2448688 | Cytochrome P450 3A4 | 3 |
| - | 10.6019/CHEMBL2448688 | Trypanosoma cruzi | 2 |
| - | 10.6019/CHEMBL2448688 | L6 | 1 |
Data from ChEMBL 36 via Core Engine