Compound Detail
CHEMBL597383
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Basic Information
| ChEMBL ID | CHEMBL597383 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | KPMDOQJJXIXPQH-UHFFFAOYSA-N |
2
Targets
3
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
336.2
MW (Da)
3.60
ALogP
4
HBA
3
HBD
93.6
PSA (Ų)
0.68
QED
0
Ro5 Violations
4
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 5.91
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Bifunctional dihydrofolate reductase-thymidylate synthase CHEMBL2425 | IC50 | 5.91 | 5.91 | 1240.0 | 1 |
| Dihydrofolate reductase CHEMBL2363 | IC50 | 5.32 | 5.32 | 4786.3 | 2 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Bifunctional dihydrofolate reductase-thymidylate synthase | IC50 | = | 1240.0 | nM | 5.91 | Inhibition of Toxoplasma gondii DHFR by spectrophotometric assay | 20117005 |
| Dihydrofolate reductase | IC50 | = | 4800.0 | nM | 5.32 | Inhibition of rat liver DHFR by spectrophotometric assay | 20117005 |
| Dihydrofolate reductase | IC50 | = | 4786.3 | nM | 5.32 | Inhibition of rat liver DHFR by spectrophotometric assay | 20117005 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 20117005 | 10.1016/j.bmc.2009.12.066 | Dihydrofolate reductase | 2 |
| 20117005 | 10.1016/j.bmc.2009.12.066 | Bifunctional dihydrofolate reductase-thymidylate synthase | 1 |
Data from ChEMBL 36 via Core Engine