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新型靶向雄配子传播阻断抗疟药的结构-活性关系研究。

Structure-Activity Relationship Studies of a Novel Class of Transmission Blocking Antimalarials Targeting Male Gametes.

机构信息

Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, White City Campus, Wood Lane, London W12 0BZ, United Kingdom.

Department of Life Sciences, Imperial College London, London SW7 2AZ, United Kingdom.

出版信息

J Med Chem. 2020 Mar 12;63(5):2240-2262. doi: 10.1021/acs.jmedchem.9b00898. Epub 2019 Sep 20.

Abstract

Malaria is still a leading cause of mortality among children in the developing world, and despite the immense progress made in reducing the global burden, further efforts are needed if eradication is to be achieved. In this context, targeting transmission is widely recognized as a necessary intervention toward that goal. After carrying out a screen to discover new transmission-blocking agents, herein we report our medicinal chemistry efforts to study the potential of the most robust hit, DDD01035881, as a male-gamete targeted compound. We reveal key structural features for the activity of this series and identify analogues with greater potency and improved metabolic stability. We believe this study lays the groundwork for further development of this series as a transmission blocking agent.

摘要

疟疾仍然是发展中国家儿童死亡的主要原因,尽管在减轻全球负担方面取得了巨大进展,但如果要实现消除疟疾的目标,还需要进一步努力。在这种情况下,以传播为目标被广泛认为是实现这一目标的必要干预措施。在进行筛选以发现新的阻断传播的药物后,我们在此报告了我们的药物化学研究工作,以研究最有效的化合物 DDD01035881 作为一种靶向精子的化合物的潜力。我们揭示了该系列化合物活性的关键结构特征,并确定了具有更高效力和改善代谢稳定性的类似物。我们相信这项研究为进一步开发该系列作为传播阻断剂奠定了基础。

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