Cinanserin hydrochloride is a potent and selective antagonist of the 5-HT2 receptor, exhibiting a binding affinity with a Ki of 41 nM. This compound demonstrates a much higher selectivity for the 5-HT2 receptor compared to the 5-HT1 receptor, which has a Ki value of 3500 nM. Additionally, Cinanserin hydrochloride inhibits the 3C-like proteinase of the severe acute respiratory syndrome coronavirus, effectively reducing viral replication in vitro. This dual functionality makes it a valuable tool for research in neuropharmacology and virology.
Cinanserin hydrochloride is a potent and selective antagonist of the 5-HT2 receptor, exhibiting a binding affinity with a Ki of 41 nM. This compound demonstrates a much higher selectivity for the 5-HT2 receptor compared to the 5-HT1 receptor, which has a Ki value of 3500 nM. Additionally, Cinanserin hydrochloride inhibits the 3C-like proteinase of the severe acute respiratory syndrome coronavirus, effectively reducing viral replication in vitro. This dual functionality makes it a valuable tool for research in neuropharmacology and virology.
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