Cinnarizine is an orally active, effective and selective inhibitor of L-type calcium channel Cav1.3 with an IC50 of 1.5 µM (in vestibular hair cells). Cinnarizine can cross the blood-brain barrier and regulate calcium homeostasis and dopamine neurotransmission. Cinnarizine inhibits the influx of calcium ions into smooth muscle cells by blocking L-type calcium channels, thereby relaxing vascular smooth muscle, improving cerebral circulation and reducing blood viscosity, while antagonizing dopamine receptors. Cinnarizine can be used in the study of vestibular vertigo, Menieres disease and cerebrovascular diseases[1][2][3][4][5].
Molekulargewicht:
368.51
Reinheit:
99.63
CAS Nummer:
[298-57-7]
Formel:
C26H28N2
Target-Kategorie:
Calcium Channel,Histamine Receptor
Anwendungsbeschreibung:
MCE Product type: Reference compound
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