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| Cat. No. : | HY-A0118 |
| M.Wt: | 651.78 |
| Formula: | C34H53NO11 |
| Purity: | >98 % |
| Solubility: | 10 mM in DMSO |
Naloxegol (NKTR-118; AZ-13337019) is an orally active peripherally acting μ-opioid receptor antagonist with a target Ki of 7.42 nM. Naloxegol inhibits the binding of opioids to μ-opioid receptors in the gastrointestinal tract, and alleviates opioid-induced gastrointestinal hypomotility, delayed transit, hypertonicity, and increased fluid reabsorption. Naloxegol is applicable to research related to opioid-induced constipation[1][2]. IC50 & Target:Opioid receptor[1] In Vitro:Naloxegol binds with high affinity to μ-opioid receptors and κ-opioid receptors and low affinity to δ-opioid receptors in vitro, with no significant activity at non-opioid targets[2]. In Vivo:Naloxegol inhibits the binding of opioids to μ-opioid receptors in the gastrointestinal tract, and alleviates the opioid-induced phenomena including slowed gastrointestinal motility and transit, hypertonicity, and increased fluid reabsorption[2].
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