The quinine , of C20H24N2O2 chemical formula, is a natural Alcaloïde having properties Antipyrétique, antipaludic and Analgésique. It was used for the prevention of the Paludisme before being supplanted by its derivatives, Quinacrine, Chloroquine, and Primaquine. Quinine can always be used to treat the resistant malaria, and to treat the night Crampe S of the legs. It was also used in a test to treat people infected by the prion S, but success was limited.
However: it is toxic for the Nervous system, one thus sought to synthesize analogues not having this defect:
the Artémisinine, nonrelated with quinine, is very active. It is about a sesquiterpenic lactone containing a bridge endopéroxyde and which is resulting from a Chinese Armoise ( Artemisia annua ). It is effective against the shapes of plasmodiums resistant to chloroquine (case of the neuropaludisms in particular) and until now, no resistance of the stocks of Plasmodium to the artémisinine or its derivatives semisynthetic (artéméther, artesunate in particular) appeared.
Quinine is component aromatic of tonic water. According to the tradition, the sour taste of the quinine used against the Paludisme encouraged the colonial British in India to mix it with gin, thus creating the tonic Cocktail Gin.
However, the current gin tonic is very different from drink of this time, in particular because the quinine amount employed is from now on only approximately the quarter of what it was. With the the United States, the authorized maximum amount is of 83 ppm.
In March 2006, of the researchers of the Université of Lille I announced to have developed a new molecule, the ferroquine (SR), by associating the chloroquinine with Fer which attracts the parasite, this new molecule would be up to 30 times more effective than the chloroquinine.
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