Compound Detail
CHEMBL1672132
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Basic Information
| ChEMBL ID | CHEMBL1672132 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | OKBCQVXLHZLMAA-UXHICEINSA-N |
2
Targets
3
Activities
1
Assay Types
1
PK Parameters
3
Publications
0
Known Names
Molecular Properties
335.4
MW (Da)
3.51
ALogP
2
HBA
2
HBD
44.4
PSA (Ų)
0.90
QED
0
Ro5 Violations
4
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 8.77
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Bifunctional epoxide hydrolase 2 CHEMBL5669 | IC50 | 8.77 | 8.77 | 1.7 | 1 |
| Bifunctional epoxide hydrolase 2 CHEMBL2409 | IC50 | 8.64 | 8.37 | 2.3 | 2 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| CL | 100.0 | mL.min-1.g-1 | Rattus norvegicus |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Bifunctional epoxide hydrolase 2 | IC50 | = | 1.698 | nM | 8.77 | Inhibition of rat soluble epoxide hydrolase in cell free system | 21192659 |
| Bifunctional epoxide hydrolase 2 | IC50 | = | 2.291 | nM | 8.64 | Inhibition of human soluble epoxide hydrolase in cell free system | 21192659 |
| Bifunctional epoxide hydrolase 2 | IC50 | = | 7.943 | nM | 8.1 | Inhibition of soluble epoxide hydrolase in human HepG2 cells after 30 mins | 21192659 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 21192659 | 10.1021/jm101273e | Bifunctional epoxide hydrolase 2 | 3 |
| 21192659 | 10.1021/jm101273e | No relevant target | 1 |
| 21192659 | 10.1021/jm101273e | Liver microsomes | 1 |
Data from ChEMBL 36 via Core Engine