CTAP is a potent and highly selective μ opioid receptor antagonist, exhibiting an IC50 of 3.5 nM. It demonstrates over 1200-fold selectivity against δ opioid receptors (IC50 = 4500 nM) and somatostatin receptors. CTAP is valuable for research applications focusing on L-DOPA-induced dyskinesia, as well as studies related to opiate overdose and addiction mechanisms.
CTAP is a potent and highly selective μ opioid receptor antagonist, exhibiting an IC50 of 3.5 nM. It demonstrates over 1200-fold selectivity against δ opioid receptors (IC50 = 4500 nM) and somatostatin receptors. CTAP is valuable for research applications focusing on L-DOPA-induced dyskinesia, as well as studies related to opiate overdose and addiction mechanisms.
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