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pubmed-article:12217374pubmed:abstractTextWater soluble N-benzyltriazolium or N-benzylimidazolium salt type prodrugs of several highly lipophilic triazole or imidazole antifungals have been synthesized. They were designed to undergo an enzymatic activation followed by a self-cleavage to release a parent drug. The prodrugs such as 16 had enough chemical stability and water solubility for parenteral use and were rapidly and quantitatively converted to the active substance in human plasma.lld:pubmed
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pubmed-article:12217374pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:12217374pubmed:articleTitleSynthesis of novel water soluble benzylazolium prodrugs of lipophilic azole antifungals.lld:pubmed
pubmed-article:12217374pubmed:affiliationDepartment of Chemistry, Nippon Roche Research Center, 200 Kajiwara, Kamakura, Kanagawa, Japan.lld:pubmed
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