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Antitumor bioconjugates of hyaluronic acid or its derivatives obtained by indirect chemical conjugation

机译:通过间接化学缀合获得的透明质酸或其衍生物的抗肿瘤生物缀合物

摘要

Pharmaceutical chemical conjugates of hyaluronic acid and / or its derivatives obtained through an indirect union between the polysaccharide and a drug with an antitumor action, through a molecular spacer that forms an ester bond with the carboxylic group of HA and / or its derivative, with the proviso that said spacer is not a hydrazide or a polypeptide, the drug is doxorubicin; said hyaluronic acid derivatives are selected from salified HA with organic and / or inorganic bases having a molecular weight of 50-730 KDa or a high molecular weight of 750-1 230 KDa and the spacer is selected from bromopropionic acid or bromobutyric acid.
机译:透明质酸和/或其衍生物的药物化学共轭物,是通过多糖与具有抗肿瘤作用的药物之间的间接结合而获得的,它是通过与HA和/或其衍生物的羧基形成酯键的分子间隔基与条件是所述间隔物不是酰肼或多肽,所述药物是阿霉素。所述透明质酸衍生物选自具有有机和/或无机碱的成盐的HA,所述有机和/或无机碱的分子量为50-730 KDa或高分子量为750-1 230 KDa,并且间隔基选自溴丙酸或溴丁酸。

著录项

  • 公开/公告号ES2692619T3

    专利类型

  • 公开/公告日2018-12-04

    原文格式PDF

  • 申请/专利权人 FIDIA FARMACEUTICI S.P.A.;

    申请/专利号ES20110159664T

  • 发明设计人 RENIER DAVIDE;BETTELLA FABIO;

    申请日2006-08-02

  • 分类号A61K47/61;A61P35;

  • 国家 ES

  • 入库时间 2022-08-21 11:59:35

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