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环烯醚萜苷元衍生物对Taq DNA聚合酶的抑制作用。

Inhibition of Taq DNA polymerase by iridoid aglycone derivates.

作者信息

Pungitore C R, García C, Sotero Martín V, Tonn C E

机构信息

Area de Química Orgánica, Facultad de Química, Bioquímica y Farmacia- Universidad Nacional de San Luis, San Luis, Argentine.

出版信息

Cell Mol Biol (Noisy-le-grand). 2012 Nov 8;58 Suppl:OL1786-90.

Abstract

Faithful replication of DNA molecules by DNA polymerases is essential for genome integrity and correct transmission of genetic information in all living organisms. DNA polymerases have recently emerged as important cellular targets for chemical intervention in the development of anti--cancer agents. Herein we report additional synthesis of simplified bicyclic aglycones of iridoids and their biological activity against Taq DNA polymerase with the object to find out some of the likely molecular targets implicated in the biological activity showed for this kind of compounds. The compounds 14, 33 and 34 showed inhibitory activity against Taq DNA polymerase with IC(50) values of 13.47, 17.65 and 18.31 μM, respectively. These results would allow proposing to DNA polymerases as the molecular targets implicated in this bioactivity and enhance the iridoid aglycones as leader molecule to develop new drugs for cancer therapy.

摘要

DNA聚合酶对DNA分子的忠实复制对于所有生物体的基因组完整性和遗传信息的正确传递至关重要。DNA聚合酶最近已成为抗癌药物开发中化学干预的重要细胞靶点。在此,我们报告了环烯醚萜简化双环苷元的额外合成及其对Taq DNA聚合酶的生物活性,目的是找出这类化合物所显示生物活性中可能涉及的一些分子靶点。化合物14、33和34对Taq DNA聚合酶表现出抑制活性,IC(50)值分别为13.47、17.65和18.31 μM。这些结果表明DNA聚合酶是这种生物活性所涉及的分子靶点,并增强了环烯醚萜苷元作为开发癌症治疗新药的先导分子的作用。

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