ASP-2205 is a potent agonist of the 5-HT2C receptor, with an EC50 of 0.85 nM for the human receptor and 2.5 nM for the rat receptor. This compound enhances the pudendal nerve-mediated urethral closure reflex, making it a valuable tool for research into therapies for urinary incontinence. ASP-2205 may be instrumental in studying the physiological roles of the 5-HT2C receptor in urogenital function and related disorders.
ASP-2205 is a potent agonist of the 5-HT2C receptor, with an EC50 of 0.85 nM for the human receptor and 2.5 nM for the rat receptor. This compound enhances the pudendal nerve-mediated urethral closure reflex, making it a valuable tool for research into therapies for urinary incontinence. ASP-2205 may be instrumental in studying the physiological roles of the 5-HT2C receptor in urogenital function and related disorders.
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