Zimelidine is an orally active selective serotonin reuptake inhibitor. Zimelidine competitively inhibits central 5-HT uptake and desensitizes 5-HT autoreceptors in dorsal raphe nucleus. Zimelidine time-dependently modulates 5-HT neuronal firing and hippocampal CA3 responses. Zimelidine strengthens central serotonergic neurotransmission and produces related behavioral changes. Zimelidine exerts anxiolytic, analgesic, feeding-suppressive and tolerance-attenuating effects. Zimelidine is used for the study of depressive disorders and analgesic tolerance[1][2][3][4].
Molekulargewicht:
317.22
CAS Nummer:
[56775-88-3]
Formel:
C16H17BrN2
Target-Kategorie:
Serotonin Transporter
Anwendungsbeschreibung:
MCE Product type: Reference compound
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