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Literature summary for 3.1.1.8 extracted from
- Studies of the inhibition of serum pseudocholinesterase activity in vitro by commonly used drugs (2005), Am. J. Clin. Pathol., 124, 226-228.
Inhibitors
| Inhibitors | Comment | Organism | Structure |
|---|---|---|---|
| additional information | not inhibitory: acetaminophen, chlordiazepoxide, chlorpromazine, desipramine, doxepin, imipramine, methamphetamine, nortryptiline, phenobarbital, phenytoin, procainamide, salicylic acid, theophyline, valproic acid | Homo sapiens | |
| morphine | 0.0013 mM, 6% inhibition | Homo sapiens |  |
| quinidine | 0.007 mM, 5.7% inhibition | Homo sapiens | |
| thioridazine | 0.0054 mM, 10% inhibition | Homo sapiens | |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Homo sapiens | - |
isoform serum pseudocholinesterase | - |
Source Tissue
| Source Tissue | Comment | Organism | Textmining |
|---|---|---|---|
| serum | - |
Homo sapiens | - |
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Release 2023.1 (January 2023)
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