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Quinine dihydrochloride is an orally active alkaloid extracted from cinchona bark and can be used in anti-malarial studies. Quinine dihydrochloride is also a potassium channel inhibitor that inhibits WT mouse Slo3 (KCa5.1) channel currents evoked by voltage pulses to +100 mV with an IC50 of 169 μM.
Quinine dihydrochloride (37.5-150 μM, 24 hours) significantly reduces viral DENV RNA and protein levels in a dose-dependent manner in human hepatocarcinoma HepG2 cell line.
Quinine dihydrochloride (oral gavage, 12 or 15 mg/kg, every week, 16 weeks) has some tumor suppressing effect on skin cancer in Swiss albino mice. Quinine dihydrochloride (oral gavage, 10 mg/kg, everyday, 8 weeks) causes a decrease in the antioxidant defense system of rat testicular tissue such as SOD, CAT and GSH enzyme activity in male adult albino rats.
| Molecular Weight | 397.34 |
| Formula | C20H26Cl2N2O2 |
| CAS Number | 60-93-5 |
| Solubility (25°C) | DMSO 50 mg/mL Water |
| Storage | 4°C, protect from light, sealed |
[1] Grace I Anderson, et al. IUCrdata. Quinine di-hydro-chloride hemihydrate
[2] Saleem Ahmed Kharal, et al. J Pak Med Assoc. Quinine is bactericidal
[3] Timothy M Miller, et al. Muscle Nerve. Muscle cramps
[4] N J White, et al. Br J Clin Pharmacol. Quinine disposition kinetics
[5] D N Bateman, et al. Adverse Drug React Acute Poisoning Rev. Quinine toxicity
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