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首页> 外文期刊>Journal of Medicinal Chemistry >N,N'-Dihydroxyamidines;A New Prodrug Principle To Improve the Oral Bioavailability of Amidines
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N,N'-Dihydroxyamidines;A New Prodrug Principle To Improve the Oral Bioavailability of Amidines

机译:N,N'-二羟基am;提高Pro的口服生物利用度的新前药原理

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摘要

N,N'-Dihydroxybenzamdine represents a model compound for a new prodrug principle to improve the oral bioavailability of drags containing amidine functions.The activation of the prodrug could be demonstrated in vitro by porcine and human subcellular enzyme fractions,the mitochondrial benzamidoxime reducing system,and porcine hepatocytes.In vivo,the bioavailability of benzamidine after oral application of N,N'-dihydroxybenzamidine was about 91% and exceeded that of benzamidine after oral application of benzamidoxime,being about 74% (Liu,L.;Ling,Y.;Havel,C;Bashnick,L.;Young,W.;Rai,R.;Vijaykumar,D.;Riggs,J.R.;Ton,T.;Shaghafi,M.;Graupe,D.;Mordenti,J.;Sukbuntherng,J.Species comparison of in vitro and in vivo conversion of five N-hydroxyamidine prodrugs of fVIIA inhibitors to their corresponding active amidines.Presented at the 13th North America ISSX Meeting,Maui,HI,2005).
机译:N,N'-Dihydroxybenzamdine代表一种新的前药原理的模型化合物,可提高含am功能的药物的口服生物利用度。猪,人亚细胞酶组分,线粒体苯甲酰胺肟还原体系,体内,苯甲idine口服N,N'-二羟基苯甲m后的生物利用度约为91%,超过苯甲mid肟口服后的苯am的生物利用度,约为74%(Liu,L。 ; Havel,C; Bashnick,L。; Young,W。; Rai,R。; Vijaykumar,D。; Riggs,JR; Ton,T。; Shaghafi,M。; Graupe,D。; Mordenti,J。; Sukbuntherng ,J.5种fVIIA抑制剂的N-羟基am前药向其相应的活性am的体内外转化的物种比较(在第13届北美ISSX会议上发表,夏威夷,毛伊岛,2005年)。

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