1. GPCR/G Protein Neuronal Signaling
  2. Opioid Receptor
  3. MK-1925

MK-1925 (compound 39) is a ORL1 receptor antagonist with human IC50 values of 8.2 nM and 4.6 nM, as well as oral bioavailability and blood-brain barrier penetration. MK-1925 selectively inhibits the ORL1 receptor and shows no significant activity against other opioid receptors or the hERG potassium channel.

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MK-1925

MK-1925 Chemical Structure

CAS No. : 932705-04-9

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Description

MK-1925 (compound 39) is a ORL1 receptor antagonist with human IC50 values of 8.2 nM and 4.6 nM, as well as oral bioavailability and blood-brain barrier penetration. MK-1925 selectively inhibits the ORL1 receptor and shows no significant activity against other opioid receptors or the hERG potassium channel[1].

In Vitro

MK-1925 (compound 39) is highly selective for ORL1 receptors over human μ, κ, and δ opioid receptors, with ORL1 binding IC50 of 8.2 nM and minimal binding to other opioid receptors (IC50 values ≥9800 nM or >10,000 nM)[1].
MK-1925 has minimal binding affinity for hERG potassium channels, with an IC50 of 9500 nM[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

362.40

Formula

C19H21F3N4

CAS No.
SMILES

C(CC#N)N1C(=C(C)C(CN[C@@H]2C[C@H](F)CC2)=N1)C3=CC(F)=CC(F)=C3

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Room temperature in continental US; may vary elsewhere.

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Please store the product under the recommended conditions in the Certificate of Analysis.

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MK-1925
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HY-122561
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