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High affinity ligand for the NOP site (Ki = 1.5 nM). Antagonizes nociceptin-stimulated GTP binding in rat brain and the chronotropic effect of nociceptin on rat cardiomyocytes. However, displays potent agonist properties in vivo, inhibiting locomotor activity in mice.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $201 | Inquiry | Inquiry |
| Description | High affinity ligand for the NOP site (Ki = 1.5 nM). Antagonizes nociceptin-stimulated GTP binding in rat brain and the chronotropic effect of nociceptin on rat cardiomyocytes. However, displays potent agonist properties in vivo, inhibiting locomotor activity in mice. |
| Molecular Weight | 939.12 |
| Formula | C44H70N14O9 |
| Cas No. | 200959-48-4 |
| Smiles | [C@@H](CC1=CC=C(O)C=C1)(NC([C@H](CC2=CC=C(O)C=C2)NC([C@H](CCCNC(=N)N)NC(C)=O)=O)=O)C(N[C@H](C(N[C@H](C(N[C@@H](CCCCN)C(N)=O)=O)[C@H](CC)C)=O)CCCNC(=N)N)=O |
| Relative Density. | 1.39 g/cm3 (Predicted) |
| Sequence | Ac-Arg-Tyr-Tyr-Arg-Ile-Lys-NH2 |
| Sequence Short | RYYRIK |
| Storage | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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