Compound Detail
CHEMBL274257
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Basic Information
| ChEMBL ID | CHEMBL274257 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | DYVTYPINLOPJMV-UHFFFAOYSA-N |
2
Targets
3
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
366.4
MW (Da)
3.05
ALogP
7
HBA
3
HBD
112.0
PSA (Ų)
0.67
QED
0
Ro5 Violations
6
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
Ki 2 meas. best 9.39
IC50 1 meas. best 5.39
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| MAP kinase p38 CHEMBL2094115 | Ki | 9.39 | 9.385 | 0.4 | 2 |
| PBMC CHEMBL613107 | IC50 | 5.39 | 5.39 | 4100.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| MAP kinase p38 | Ki | = | 0.41 | nM | 9.39 | Binding affinity for human p38 MAP kinase expressed in Escherichia coli using [g... | 16190753 |
| MAP kinase p38 | Ki | = | 0.42 | nM | 9.38 | Binding affinity for human p38 MAP kinase expressed in Escherichia coli using [g... | 16190753 |
| PBMC | IC50 | = | 4100.0 | nM | 5.39 | Concentration required to inhibit LPS-induced TNFalpha production in human perip... | 16190753 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 16190753 | 10.1021/jm0503594 | MAP kinase p38 | 2 |
| 16190753 | 10.1021/jm0503594 | PBMC | 1 |
Data from ChEMBL 36 via Core Engine