SHR0687
SHR0687 is a selective tetrapeptide kappa opioid receptor (KOR) agonist with an EC50 of 0.53 pM. SHR0687 displays high potency and selectivity over MOR and DOR, with negligible blood-brain barrier penetration. SHR0687 activates KOR specifically, leading to potential modulation of neurological pathways without significant central nervous system effects. SHR0687 can be used for the research of pain.
For research use only. We do not sell to patients.
- CAS No.: 2168573-03-1
- Formula: C39H60N8O5
- Molecular Weight:720.94
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All Opioid Receptor Isoforms
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Biological Activity
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κ Opioid Receptor/KOR 0.53 pM (EC50) |
μ Opioid Receptor/MOR >50000 nM (EC50) |
δ Opioid Receptor/DOR >50000 nM (EC50) |
SHR0687 (Human embryonic kidney cells (HEK293)) does not inhibit hERG channels[1].
SHR0687 (Human liver microsomes) does not significantly inhibit major CYP isoforms, including CYP1A2, CYP2C9, CYP2C19, CYP2D6, and CYP3A4[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
SHR0687 (1 mg/kg; Intravenous (IV); administration) shows minimal BBB penetration in Sprague Dawley rats (SD)[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Sprague Dawley rats (SD) (150-180 g) were subcutaneously injected with 1% carrageenan (100 μL)[1]
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Dosage:0.03 mg/kg, 0.1 mg/kg, 0.3 mg/kg
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Administration:i.v.;30 minutes before detection
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Result:A dose-dependent reduction in pain was observed.
Chemical Information
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CAS No. 2168573-03-1
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Molecular Weight 720.94
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Formula C39H60N8O5
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SMILES
C[C@H](C1=CC=CC=C1)CNCC(N[C@H](CC2=CC=CC=C2)C(N[C@H](CC(C)C)C(N[C@H](CCCCN)C(N3CCC(CC3)NC(NC)=O)=O)=O)=O)=O
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)