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Quinine
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Product Name Quinine
Price: $30 / 20mg
CAS No.: 130-95-0
Catalog No.: CFN90195
Molecular Formula: C20H24N2O2
Molecular Weight: 324.42 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Cryst.
Source: The barks of Cinchona ledgeriana (Howard) Moens ex Trim.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
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Biological Activity
Description: Quinine is an anti-malaria agent and also a potassium channel inhibitor with an IC50 of 169 μM.Quinine is used for the treatment of acute malaria in pregnant women.
Targets: Antifection | Potassium channel
In vivo:
Homeopathy. 2014 Jul;103(3):165-71.
China rubra for side-effects of quinine: a prospective, randomised study in pregnant women with malaria in Cotonou, Benin.[Pubmed: 24931747]
In endemic areas, gestational malaria is responsible for low birth weight and maternal anaemia. Quinine is the reference treatment for acute malaria in pregnant women, irrespective of term. However, Quinine administration is associated with various side-effects. We evaluated the impact of the homeopathic medicine China rubra 7CH on the side-effects of Quinine used as treatment for acute malaria in pregnant women in Cotonou, Benin.
METHODS AND RESULTS:
This prospective, comparative, randomised study was carried out between June and December 2007 in the Saint Jean-Baptiste Medical Centre, Cotonou. Women were included if they were >3 months pregnant and had a clinical diagnosis of malaria confirmed by a positive thick blood smear. The study population was divided into two groups: (i) patients who presented between the 1st and 15th of each month and who received China rubra 7CH plus Quinine (China group); and (ii) patients who presented from the 16th to the end of each month and who received treatment with Quinine only (Standard group). The aim was to compare the frequency of side-effects of Quinine in the two groups until day 6 after the start of treatment. Neither the patients nor the care givers were blinded to study treatment. Statistical comparison of the two groups was carried out with an alpha risk fixed at 5%. 211 women were recruited: 105 received Quinine plus China rubra 7CH (China group) and 106 received Quinine only (Standard group). A decrease in proportion of patients presenting with side-effects was observed in the China group from day 0 to day 6 of follow-up (53.9%-23.3%) whereas the proportion of patients with side-effects in the Standard group did not change significantly (85.9% on day 0 vs. 82.5% on day 6). Ninety-six (72.4%) patients in the China group and 103 (97.2%) in the Standard group reported at least one side-effect during follow-up (p < 0.0001). The most frequently reported side-effects were tinnitus, dizziness and asthenia.
CONCLUSIONS:
This preliminary study shows the interest of China rubra 7CH in limiting the side-effects of Quinine used for the treatment of acute malaria in pregnant women.
Malar J. 2011 May 24;10:144.
Quinine, an old anti-malarial drug in a modern world: role in the treatment of malaria.[Pubmed: 21609473 ]
Quinine remains an important anti-malarial drug almost 400 years after its effectiveness was first documented. However, its continued use is challenged by its poor tolerability, poor compliance with complex dosing regimens, and the availability of more efficacious anti-malarial drugs. This article reviews the historical role of Quinine, considers its current usage and provides insight into its appropriate future use in the treatment of malaria.
METHODS AND RESULTS:
In light of recent research findings intravenous artesunate should be the first-line drug for severe malaria, with Quinine as an alternative. The role of rectal Quinine as pre-referral treatment for severe malaria has not been fully explored, but it remains a promising intervention. In pregnancy, Quinine continues to play a critical role in the management of malaria, especially in the first trimester, and it will remain a mainstay of treatment until safer alternatives become available. For uncomplicated malaria, artemisinin-based combination therapy (ACT) offers a better option than Quinine though the difficulty of maintaining a steady supply of ACT in resource-limited settings renders the rapid withdrawal of Quinine for uncomplicated malaria cases risky.
CONCLUSIONS:
The best approach would be to identify solutions to ACT stock-outs, maintain Quinine in case of ACT stock-outs, and evaluate strategies for improving Quinine treatment outcomes by combining it with antibiotics. In HIV and TB infected populations, concerns about potential interactions between Quinine and antiretroviral and anti-tuberculosis drugs exist, and these will need further research and pharmacovigilance.
Quinine Description
Source: The barks of Cinchona ledgeriana (Howard) Moens ex Trim.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

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After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.0824 mL 15.4121 mL 30.8242 mL 61.6485 mL 77.0606 mL
5 mM 0.6165 mL 3.0824 mL 6.1648 mL 12.3297 mL 15.4121 mL
10 mM 0.3082 mL 1.5412 mL 3.0824 mL 6.1648 mL 7.7061 mL
50 mM 0.0616 mL 0.3082 mL 0.6165 mL 1.233 mL 1.5412 mL
100 mM 0.0308 mL 0.1541 mL 0.3082 mL 0.6165 mL 0.7706 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Kinase Assay:
Br J Pharmacol. 2015 Sep;172(17):4355-63.
Mechanism of inhibition of mouse Slo3 (KCa 5.1) potassium channels by quinine, quinidine and barium.[Pubmed: 26045093 ]
The Slo3 (KCa 5.1) channel is a major component of mammalian KSper (sperm potassium conductance) channels and inhibition of these channels by Quinine and barium alters sperm motility. The aim of this investigation was to determine the mechanism by which these drugs inhibit Slo3 channels.
METHODS AND RESULTS:
Mouse (m) Slo3 (KCa 5.1) channels or mutant forms were expressed in Xenopus oocytes and currents recorded with 2-electrode voltage-clamp. Gain-of-function mSlo3 mutations were used to explore the state-dependence of the inhibition. The interaction between quinidine and mSlo3 channels was modelled by in silico docking. Several drugs known to block KSper also affected mSlo3 channels with similar levels of inhibition. The inhibition induced by extracellular barium was prevented by increasing the extracellular potassium concentration. R196Q and F304Y mutations in the mSlo3 voltage sensor and pore, respectively, both increased channel activity. The F304Y mutation did not alter the effects of barium, but increased the potency of inhibition by both Quinine and quinidine approximately 10-fold; this effect was not observed with the R196Q mutation.
CONCLUSIONS:
Block of mSlo3 channels by Quinine, quinidine and barium is not state-dependent. Barium inhibits mSlo3 outside the cell by interacting with the selectivity filter, whereas Quinine and quinidine act from the inside, by binding in a hydrophobic pocket formed by the S6 segment of each subunit. Furthermore, we propose that the Slo3 channel activation gate lies deep within the pore between F304 in the S6 segment and the selectivity filter.
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