| MDL | MFCD01684929 |
|---|---|
| Molecular Weight | 401.93 |
| Molecular Formula | C22H28ClN3O2 |
| SMILES | O=C1N(CCN(CC)CC)C2=C(C=CC=C2)N=C1CC3=CC=C(OC)C=C3.[H]Cl |
Caroverine (Tinnex) hydrochloride is a potent, competitive and reversible antagonist of NMDA and AMPA glutamate receptor . Caroverine hydrochloride is also an antioxidant and calcium-blocking agent that exhibits vasorelaxant action. Caroverine hydrochloride can be used for the research of inner ear tinnitus [1] [2] [3] .
Caroverine (1 μM; pretreated for 10 min) inhibits the pressor response to KCl (80 mM) and noradrenaline (1 μM) in the rat hindquarter preparation. Caroverine markedly suppresses the contraction caused by KCl (40 mM) in the rat isolated aorta [3] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Caroverine (1.44 mg/rat; s.c; 1.0 mL/h for 72 h) attenuates impulse noise-induced hearing loss in the rat [4] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
| Animal Model: | Sprague-Dawley rats of either sex (250-300 g) received impulse noise exposure [4] |
| Dosage: | 1.44 mg/rat |
| Administration: | 20 mg/mL; s.c. 1.0 mL/h for 72 h |
| Result: | Significantly protected the cochlea against impulse noise trauma. |
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 : 100 mg/mL ( 248.80 mM ; Need ultrasonic)
H 2 O : 20 mg/mL ( 49.76 mM ; Need ultrasonic)
| Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
|---|
| 1 mM | 2.4880 mL | 12.4400 mL | 24.8800 mL |
| 5 mM | 0.4976 mL | 2.4880 mL | 4.9760 mL |
| 10 mM | 0.2488 mL | 1.2440 mL | 2.4880 mL |