loxapine
SMILES | CN1CCN(CC1)C1=Nc2ccccc2Oc2c1cc(Cl)cc2 |
InChIKey | XJGVXQDUIWGIRW-UHFFFAOYSA-N |
Chemical properties
Hydrogen bond acceptors | 4 |
Hydrogen bond donors | 0 |
Rotatable bonds | 0 |
Molecular weight (Da) | 327.1 |
Drug properties
Molecular type | Small molecule |
Endogenous/Surrogate | Surrogate |
Approved drug | Yes |
Database connections
Ligand site mutations | D4 |
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
CCK2 | GASR | Rat | Cholecystokinin | A | pKi | 6.6 | 6.6 | 6.6 | ChEMBL |
CCK1 | CCKAR | Rat | Cholecystokinin | A | pKi | 9.52 | 9.52 | 9.52 | ChEMBL |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
CCK1 | CCKAR | Rat | Cholecystokinin | A | pIC50 | 8.4 | 8.4 | 8.4 | Guide to Pharmacology |
CCK1 | CCKAR | Human | Cholecystokinin | A | pIC50 | 5.72 | 5.72 | 5.72 | ChEMBL |
CCK1 | CCKAR | Rat | Cholecystokinin | A | pIC50 | 10.3 | 10.3 | 10.3 | ChEMBL |