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Synthesis of vinca alkaloid–triphenylphosphine derivatives having potential antitumor effect

机译:具有潜在抗肿瘤效应的Vinca生物碱 - 三苯基膦衍生物的合成

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The successful therapy of cancer is still unresolved. For that reason enormous efforts are being made to increase the effectiveness of anticancer drugs and reduce their side effects at least. An important approach to the development of selective molecules is the synthesis of drug conjugates, also called as “hybrids”. Taking this into consideration two Vinca alkaloid derivatives conjugated with triphenylphosphine have been synthetized. The incorporation of the mentioned two pharmacophores in the same molecule could amplify the evolving cumulative antineoplastic impact and/or counterbalance the side effects. Thus a development of hybrid anticancer molecules has been started by synthesis of Vinca alkaloid–triphenylphosphine conjugates, which could have higher efficacies and safety profiles than the present drugs available in market.
机译:癌症的成功治疗仍未得到解决。 因此,正在进行巨大的努力来增加抗癌药物的有效性,并至少减少副作用。 选择性分子的发展的重要方法是药物缀合物的合成,也称为“杂种”。 考虑到这两种与三苯基膦缀合的Vinca生物碱衍生物已经合成。 在相同分子中提到的两种药物的掺入可以扩增进化的累积抗肿瘤撞击和/或逆损副作用。 因此,通过合成vinca生物碱 - 三苯基膦酰胺膦酰胺,开始了杂化抗癌分子的发展,这可能具有比市场上可用的目前药物更高的效率和安全性。

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