Flibanserin hydrochloride is a selective agonist of the 5-HT1A receptor and antagonist of the 5-HT2A receptor, exhibiting binding affinities of Ki 1 nM and 49 nM, respectively. Additionally, it interacts with dopamine D4 receptors with a Ki range of 4-24 nM. This compound demonstrates notable antidepressant and anxiolytic effects, making it a valuable tool for researching hypoactive sexual desire disorder (HSDD) and related conditions.
Flibanserin hydrochloride is a selective agonist of the 5-HT1A receptor and antagonist of the 5-HT2A receptor, exhibiting binding affinities of Ki 1 nM and 49 nM, respectively. Additionally, it interacts with dopamine D4 receptors with a Ki range of 4-24 nM. This compound demonstrates notable antidepressant and anxiolytic effects, making it a valuable tool for researching hypoactive sexual desire disorder (HSDD) and related conditions.
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