(+)-Eseroline
(+)-Eseroline is an opioid agonist and adenylate cyclase inhibitor (Ki=6-8 μM). (+)-Eseroline binds specifically to μ-opioid receptors and δ-opioid receptors on rat brain cell membranes (Ka=0.7 μM). (+)-Eseroline exhibits only weak activity in various mouse analgesic models and can be used for studies on pain-related mechanisms.
For research use only. We do not sell to patients.
- CAS No.: 29347-15-7
- Formula: C13H18N2O
- Molecular Weight:218.30
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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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μ Opioid Receptor/MOR |
δ Opioid Receptor/DOR |
(+)-Eseroline (0-100 μM; 10 min) inhibits adenylate cyclase activity in NG108-15 cell membranes with a Ki of 6-8 μM, acts as a lower-efficacy opiate agonist relative to (-)-Eseroline, and functions as an antagonist of both (-)-Eseroline and the opioid peptide dalamid[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 29347-15-7
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Molecular Weight 218.30
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Formula C13H18N2O
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SMILES
C[C@@]12C=3C(N(C)[C@@]1(N(C)CC2)[H])=CC=C(O)C3
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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)