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Novel prodrugs of N-H bond-containing compounds and methods of making thereof

机译:含有N-H键的化合物的新型前药及其制备方法

摘要

The present invention relates to novel prodrugs of pharmaceutical compounds containing one or more N-H bonds. More specifically, the present embodiment of the invention relates to prodrugs wherein sulfur-containing promoieties are attached to pharmaceutical compounds which contain one or more N-H bonds to produce prodrugs containing at least one N-S bond. These N-S bond-containing prodrugs could have optimized stability, solubility, cell membrane permeability, pharmacokinetic properties and other pharmaceutical properties over the pharmaceutical compounds from which they are formed, depending upon the nature of the promoiety. Reversion of the prodrug to the parent pharmaceutical compound occurs by the reaction of the prodrugs with thiol molecules such as cysteine, glutathione or any other thiol containing molecule. Further, the present invention relates to methods of making N-S bond-containing prodrugs of pharmaceutical compounds containing one or more N-H bonds whereby sulfur-containing promoieties are attached to the parent compounds to create at least one N-S bond.
机译:本发明涉及含有一个或多个N-H键的药物化合物的新前药。更具体地,本发明的本实施方案涉及前药,其中将含硫的部分连接到含有一个或多个N-H键的药物化合物上以产生含有至少一个N-S键的前药。相对于形成它们的药物化合物,这些含N-S键的前药可具有优化的稳定性,溶解度,细胞膜通透性,药代动力学性质和其他药物性质,这取决于药物性质。前药与母体药物化合物的还原通过前药与硫醇分子(例如半胱氨酸,谷胱甘肽或任何其他含硫醇的分子)反应而发生。此外,本发明涉及制备含有一个或多个N-H键的药物化合物的含N-S键的前药的方法,其中含硫的部分与母体化合物连接以产生至少一个N-S键。

著录项

  • 公开/公告号AU2002337861B2

    专利类型

  • 公开/公告日2009-04-02

    原文格式PDF

  • 申请/专利权人 UNIVERSITY OF KANSAS;

    申请/专利号AU20020337861

  • 申请日2002-10-16

  • 分类号C07C313/12;C07C313/20;C07C313/28;C07D209/48;C07D223/20;C07D223/26;C07D261/20;C07D263/20;C07D305/14;

  • 国家 AU

  • 入库时间 2022-08-21 19:22:44

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