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Melarsen oxide

Melarsen was used orally or intravenously but doses were very inaccurate. In fact, it seemed to be less active than tryparsamide and numerous deaths were attributed to this drug [32]. It was abandoned in favor of melarsen oxide (Fig. 5) obtained by reduction of melarsen with sulfur dioxide in the presence of... [Pg.6]

Friedheim EAH (1948) Melarsen oxide in the treatment of human African trypanosomiasis. Ann Trop Med 42 357-363... [Pg.17]

Van Schaftingen, E., Opperdoes, F. R. and Hers, H.-G. (1987) Effects of various metabolic conditions of the trivalent arsenical melarsen oxide on the intracellular levels of fructose 2,6-bisphosphate and of glycolytic intermediates in Trypanosoma brucei. Eur. J. Biochem. 166 653-661. [Pg.31]

ANTIPROTOZOAL EFFECTS Melarsoprol is a prodrug that is metabolized rapidly (t j of 30 minutes) to melarsen oxide, the active form. Arsenoxides react avidly and reversibly with sulfhydryl groups and thereby inactivate many enzymes. Melarsoprol reacts with trypanothione to form melarsen oxide-trypanothione adduct, which potently inhibits trypanothione reductase. Both the sequestering of trypanothione and the inhibition of trypanothione reductase are expected to have lethal consequences to the cell, but this remains unproven. [Pg.686]

Melarsoprol is administered IV in multiple doses and multiple sessions. Its major metabolite in humans is the lipophilic melarsen oxide, which can penetrate into the CNS. This metabolite apparently is responsible for the protein-binding characteristic for melarsoprol. [Pg.1678]


See other pages where Melarsen oxide is mentioned: [Pg.277]    [Pg.1203]    [Pg.5]    [Pg.7]    [Pg.8]    [Pg.361]    [Pg.375]    [Pg.328]    [Pg.389]    [Pg.277]    [Pg.277]    [Pg.1203]    [Pg.5]    [Pg.7]    [Pg.8]    [Pg.361]    [Pg.375]    [Pg.328]    [Pg.389]    [Pg.277]   
See also in sourсe #XX -- [ Pg.7 ]




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