Compound Detail
CHEMBL153207
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Basic Information
| ChEMBL ID | CHEMBL153207 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | ARRCCCIOHBCTKB-UHFFFAOYSA-N |
2
Targets
5
Activities
2
Assay Types
0
PK Parameters
3
Publications
0
Known Names
Molecular Properties
179.3
MW (Da)
1.34
ALogP
2
HBA
2
HBD
40.7
PSA (Ų)
0.73
QED
0
Ro5 Violations
3
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
Ki 3 meas. best 6.74
EC50 2 meas. best 6.29
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Histamine H3 receptor CHEMBL264 | Ki | 6.74 | 6.74 | 182.0 | 2 |
| Histamine H3 receptor CHEMBL264 | EC50 | 6.29 | 6.29 | 512.9 | 1 |
| Histamine H4 receptor CHEMBL3759 | EC50 | 5.69 | 5.69 | 2041.7 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Histamine H3 receptor | Ki | = | 181.97 | nM | 6.74 | Inhibitory activity measured by [3H]- N alpha- methyl-histamine binding to membr... | 14640553 |
| Histamine H3 receptor | Ki | = | 181.97 | nM | 6.74 | Displacement of [3H]-NR-methylhistamine from human histamine H3 receptor express... | 26390077 |
| Histamine H3 receptor | EC50 | = | 512.86 | nM | 6.29 | Inhibitory activity determined by the inhibition of cAMP- stimulated beta-galact... | 14640553 |
| Histamine H4 receptor | EC50 | = | 2041.74 | nM | 5.69 | Inhibitory activity determined by the inhibition of cAMP- stimulated beta-galact... | 14640553 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 14640553 | 10.1021/jm030905y | Histamine H3 receptor | 4 |
| 14640553 | 10.1021/jm030905y | Histamine H4 receptor | 3 |
| 26390077 | 10.1021/acs.jmedchem.5b00982 | Histamine H3 receptor | 2 |
Data from ChEMBL 36 via Core Engine