手机版 客户端

选择性识别G-四链体的新先导:结构优化、生物活性及作用机制研究

选择性识别G-四链体的新先导:结构优化、生物活性及作用机制研究
  • 导航:首页 > 科学基金
  • 批准号:81760620
  • 批准年度: 2017年
  • 学科分类:合成药物化学(H3001) |
  • 项目负责人:魏涌标
  • 负责人职称:副教授
  • 依托单位:广西医科大学
  • 资助金额:32万元
  • 项目类别:地区科学基金项目
  • 研究期限:2018年01月01日 至 2021年12月31日
  • 中文关键词: 选择性;识别;链体;生物;活性
  • 英文关键词:G-quadruplex ;anticancer;lead compound;structure optimization

项目摘要

中文摘要

靶向特定G-四链体类化合物能够选择性杀伤癌细胞,有望开发成高效低毒的抗肿瘤药物。前期的预研工作发展了一类对正平行G-四链体具有良好选择性的新月形小分子化合物。该类化合物能够诱导肿瘤细胞发生凋亡,具有开发成抗肿瘤药物的潜在价值,但也存在难溶于水的缺点。基于此,本项目拟对该类化合物进行结构修饰以增强其水溶性,在此基础上,开展化合物诱导细胞凋亡的机理及体内抗肿瘤效果研究。具体为:1、保证整个分子呈新月形的前提下,改变芳环上杂原子的种类、数目及侧链,合成结构多样化的新型化合物;2、评价化合物与不同G-四链体的结合强度、选择性及稳定作用;3、研究化合物对细胞摄取、细胞内定位、选择性杀伤能力、对细胞形态的调控以及抑制原癌基因转录和翻译能力;4、对体内抗肿瘤活性及毒性进行评价。本项目的研究将进一步加深对新月形小分子诱导细胞调亡的理解,为抗肿瘤药物的筛选、开发及应用提供理论和技术指导。

英文摘要

G- quadruplex targeting drugs is characterized by good tumor-cell-selective cytotoxicity, which is expected to develop novel high efficiency and low toxicity antitumor agents. A new series of molecule, 7a-7c for G-quadruplexes, which contains a crescent-shaped π-conjugated planar core, has been developed by our group recently. Such molecules have the properties to induce tumor cell apoptosis, as may provide the possibility to develop antitumor drugs. However,the poor water solubility restricts the pharmacokinetic properties. On the basis of our recent related studies, the project plan to modify the structure of the compounds aiming to improve the water solubility. Furthermore, the mechanism of tumor cell apoptosis by the compounds and the in vivo antitumor effects will be studied. Firstly, a series of derivatives will be synthesized by modifying the type and number of heteroatom on the aromatic ring as well as side-chains on the premise of assuring the compounds with crescent-shaped π-conjugated planar core. Secondly, the bonding strength, selectivity and stability of compounds with various G-quadruplex will be evaluated. Thirdly, the effect of compounds on the cell-uptake, cellular location, cellular selectivity and cellular morphology as well as inhibition of transcription and translation of proto oncogenes will be investigated. Forthly, the in vivo antitumor activity acute toxicity test will be evaluated. In a word, the implementation of this project will further the understandings of the tumor cell apoptosis by the compounds with crescent shape. It provide the reliable theoretical basis and technical guidance for the selection, development and application of antitumor drugs.

评估说明

    国家自然科学基金项目“选择性识别G-四链体的新先导:结构优化、生物活性及作用机制研究”发布于爱科学iikx,并永久归类于相关科学基金导航中,仅供广大科研工作者查询、学习、选题参考。国科金是根据国家发展科学技术的方针、政策和规划,以及科学技术发展方向,面向全国资助基础研究和应用研究,发挥着促进我国基础研究源头创新的作用。国科金的真正价值在于它能否为科学进步和社会发展带来积极的影响。

此文由 爱科学 编辑!:首页 > 科学基金 > 科学基金4 » 选择性识别G-四链体的新先导:结构优化、生物活性及作用机制研究

推荐文章