Cirazoline hydrochloride is a potent full agonist of the α1A-adrenergic receptor, exhibiting a competitive inhibition constant (Ki) of 120 nM. It also acts as a partial agonist at the α1B-adrenergic receptor with a Ki of 960 nM and the α1D-adrenergic receptor with a Ki of 660 nM. This compound is valuable for research applications involving α1-adrenergic signaling pathways and the study of cardiovascular and neurological conditions.
Cirazoline hydrochloride is a potent full agonist of the α1A-adrenergic receptor, exhibiting a competitive inhibition constant (Ki) of 120 nM. It also acts as a partial agonist at the α1B-adrenergic receptor with a Ki of 960 nM and the α1D-adrenergic receptor with a Ki of 660 nM. This compound is valuable for research applications involving α1-adrenergic signaling pathways and the study of cardiovascular and neurological conditions.
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