ADL5859


CAS No. : 850305-06-5

850305-06-5
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Cat. No. : HY-14356
M.Wt: 392.49
Formula: C24H28N2O3
Purity: >98 %
Solubility:
Introduction of 850305-06-5 :

ADL-5859 is a selective and orally active δ opioid receptor (DOR) agonist with an Ki and an EC50 value of 0.84 and 20 nM, respectively. ADL-5859 also shows inhibitory activity to hERG channel with an IC50 value of 78 μM. ADL-5859 can be used for the research of pain[1][2]. IC50 & Target:IC50: 78 μM (hERG channel), 43 μM (CYP2D6)[1][2] In Vitro:ADL-5859 (0-10 μM) shows activities to δ opioid receptor with an Ki and an EC50 value of 0.84 and 20 nM, and inhibits 32% and 37% activities to µ and κ opioid receptor, respectively[1].
ADL-5859 (0-100 μM) exhibits inhibitory activity to hERG channel with an IC50 value of 78 μM[1].
ADL-5859 (0-100 μM) inhibits activity of the drug metabolizing enzyme cytochrome P450 2D6 (CYP2D6) in vitro with an IC50 value of 43 μM[2].

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