Description
A 5-HT3 receptor antagonist (Ki = 995 nM and IC50 = 308 nM in rat cortical membranes); D2 receptor antagonist (IC50 = 483 nM in rat brain synaptic membranes); oral administration inhibits cisplatin-induced emesis in ferrets and apomorphine-induced emesis in dogs (ED50s = 6.170 and 0.45 mg/kg, respectively); reversibly inhibits human AChE isolated from caudate nucleus (Kis = 9.3 and 82 μM for competitive and non-competitive inhibition, respectively)
Formal name: 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-methoxy-benzamide, monohydrochloride
Synonyms: NSC 354467
Molecular weight: 336.3
CAS: 7232-21-5
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Ion Channel Modulation|Blockers||Product Type|Biochemicals|Small Molecule Inhibitors|Acetylcholine Turnover||Product Type|Biochemicals|Small Molecule Inhibitors|MMPs||Research Area|Neuroscience|Behavioral Neuroscience|Schizophrenia & Psychosis