EEDQ is a carboxylate activator and an irreversible antagonist at the 5HT2c receptors. It effectively reduces [3H]β-CIT binding to the dopamine transporter (DAT) in rat caudate-putamen (CPu) homogenates with an IC50 value of 78.3 μM. Additionally, EEDQ has demonstrated the ability to inhibit contralateral rotation behavior, making it a useful tool for studying dopamine signaling and behavioral responses in neuropharmacological research.
EEDQ is a carboxylate activator and an irreversible antagonist at the 5HT2c receptors. It effectively reduces [3H]β-CIT binding to the dopamine transporter (DAT) in rat caudate-putamen (CPu) homogenates with an IC50 value of 78.3 μM. Additionally, EEDQ has demonstrated the ability to inhibit contralateral rotation behavior, making it a useful tool for studying dopamine signaling and behavioral responses in neuropharmacological research.
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