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Catalog: | HY-B1813A |
Brand: | MCE |
CAS: | 120447-62-3 |
MDL | - |
---|---|
Molecular Weight | 295.85 |
Molecular Formula | C17H26ClNO |
SMILES | O[C@H]1[C@H](N2CCC(C3=CC=CC=C3)CC2)CCCC1.[H]Cl |
Ki: 2 nM (Vesicular acetylcholine transport), 26 nM (σ1 receptors) and 34 nM (σ2 receptors) [1]
The pharmacological actions of (±)-Vesamicol have been attributed to inhibition of acetylcholine transport into synaptic vesicles and the subsequent quantal release of acetylcholine [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
(±)-Vesamicol (3 mg/kg; intraperitoneal injection; once; male Wistar rats) treatment increases the levels of cytosolic acetylcholine (ACh) in all regions of the brain, while those of vesicular ACh decreased in all regions except for the striatum [2] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model: | Male Wistar rats (120-300 g) [2] |
Dosage: | 3 mg/kg |
Administration: | Intraperitoneal injection; once |
Result: | The levels of cytosolic acetylcholine (ACh) increased in all regions of the brain, while those of vesicular ACh decreased in all regions except for the striatum. |
Solid
Room temperature in continental US; may vary elsewhere.
4°C, sealed storage, away from moisture
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
DMSO : 20.83 mg/mL ( 70.41 mM ; ultrasonic and warming and heat to 60°C)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 3.3801 mL | 16.9005 mL | 33.8009 mL |
5 mM | 0.6760 mL | 3.3801 mL | 6.7602 mL |
10 mM | 0.3380 mL | 1.6900 mL | 3.3801 mL |
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