Compound Detail
CHEMBL5180552
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Basic Information
| ChEMBL ID | CHEMBL5180552 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | OTZWZUHDCONCKN-UHFFFAOYSA-N |
5
Targets
5
Activities
1
Assay Types
0
PK Parameters
14
Publications
0
Known Names
Molecular Properties
464.5
MW (Da)
1.64
ALogP
10
HBA
2
HBD
153.4
PSA (Ų)
0.51
QED
0
Ro5 Violations
6
Rot. Bonds
Drug Information
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 5 meas. best 7.05
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Pteridine reductase, putative CHEMBL5228 | IC50 | 7.05 | 7.05 | 90.0 | 1 |
| Bifunctional dihydrofolate reductase-thymidylate synthase CHEMBL4614 | IC50 | 6.34 | 6.34 | 460.0 | 1 |
| Dihydrofolate reductase-thymidylate synthase CHEMBL5229 | IC50 | 6.21 | 6.21 | 620.0 | 1 |
| Dihydrofolate reductase CHEMBL202 | IC50 | 5.37 | 5.37 | 4300.0 | 1 |
| Pteridine reductase 1 CHEMBL6194 | IC50 | 4.88 | 4.88 | 13300.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Pteridine reductase, putative | IC50 | = | 90.0 | nM | 7.05 | Inhibition of recombinant Trypanosoma brucei PTR1 expressed in Escherichia coli ... | 35675511 |
| Bifunctional dihydrofolate reductase-thymidylate synthase | IC50 | = | 460.0 | nM | 6.34 | Inhibition of recombinant Leishmania major DHFR-TS expressed in Escherichia coli... | 35675511 |
| Dihydrofolate reductase-thymidylate synthase | IC50 | = | 620.0 | nM | 6.21 | Inhibition of recombinant Trypanosoma brucei DHFR-TS expressed in Escherichia co... | 35675511 |
| Dihydrofolate reductase | IC50 | = | 4300.0 | nM | 5.37 | Inhibition of recombinant human DHFR expressed in Escherichia coli BL21 (DE3) ce... | 35675511 |
| Pteridine reductase 1 | IC50 | = | 13300.0 | nM | 4.88 | Inhibition of recombinant Leishmania major PTR1 expressed in Escherichia coli BL... | 35675511 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 35675511 | 10.1021/acs.jmedchem.2c00232 | ADMET | 4 |
| 35675511 | 10.1021/acs.jmedchem.2c00232 | Pteridine reductase, putative | 1 |
| 35675511 | 10.1021/acs.jmedchem.2c00232 | Pteridine reductase 1 | 1 |
| 35675511 | 10.1021/acs.jmedchem.2c00232 | Dihydrofolate reductase-thymidylate synthase | 1 |
| 35675511 | 10.1021/acs.jmedchem.2c00232 | Bifunctional dihydrofolate reductase-thymidylate synthase | 1 |
| 35675511 | 10.1021/acs.jmedchem.2c00232 | Dihydrofolate reductase | 1 |
| 35675511 | 10.1021/acs.jmedchem.2c00232 | Voltage-gated inwardly rectifying potassium channel KCNH2 | 1 |
| 35675511 | 10.1021/acs.jmedchem.2c00232 | Cytochrome P450 1A2 | 1 |
| 35675511 | 10.1021/acs.jmedchem.2c00232 | Cytochrome P450 2C9 | 1 |
| 35675511 | 10.1021/acs.jmedchem.2c00232 | Cytochrome P450 2C19 | 1 |
| 35675511 | 10.1021/acs.jmedchem.2c00232 | Cytochrome P450 2D6 | 1 |
| 35675511 | 10.1021/acs.jmedchem.2c00232 | Cytochrome P450 3A4 | 1 |
| 35675511 | 10.1021/acs.jmedchem.2c00232 | 786-0 | 1 |
| 35675511 | 10.1021/acs.jmedchem.2c00232 | A549 | 1 |
Data from ChEMBL 36 via Core Engine