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3-位取代联苯烯丙胺类似物喹诺酮类化合物,具有增强的抗疟性能。

3-Position Biaryl Endochin-like Quinolones with Enhanced Antimalarial Performance.

机构信息

VA Portland Healthcare System, 3710 SW US Veterans Hospital Road, Portland, Oregon 97239, United States.

Department of Microbiology and Immunology, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, Pennsylvania 19129, United States.

出版信息

ACS Infect Dis. 2024 Jul 12;10(7):2419-2442. doi: 10.1021/acsinfecdis.4c00140. Epub 2024 Jun 11.

Abstract

ELQ-300 is a potent antimalarial drug with activity against blood, liver, and vector stages of the disease. A prodrug, , exhibits reduced crystallinity and improved in vivo efficacy in preclinical testing, and currently, it is in the developmental pipeline for once-a-week dosing for oral prophylaxis against malaria. Because of the high cost of developing a new drug for human use and the high risk of drug failure, it is prudent to have a back-up plan in place. Here we describe , a member of a new subseries of 3-biaryl-ELQs, with enhanced potency in vitro against multidrug-resistant parasites. , a prodrug of with diminished crystallinity, is more effective vs murine malaria than its progenitor by 4- to 10-fold, suggesting that correspondingly lower doses could be used to protect and cure humans of malaria. With a longer bloodstream half-life in mice compared to its progenitor, highlights a novel series of next-generation ELQs with the potential for once-monthly dosing for protection against malaria infection. Advances in the preparation of 3-biaryl-ELQs are presented along with preliminary results from experiments to explore key structure-activity relationships for drug potency, selectivity, pharmacokinetics, and safety.

摘要

ELQ-300 是一种强效抗疟药物,对疾病的血液、肝脏和媒介阶段均有活性。前药 表现出降低的结晶度和改善的体内功效,目前正在开发用于每周一次口服预防疟疾的方案。由于开发用于人体的新药成本高,药物失败的风险高,因此明智的做法是制定后备计划。在这里,我们描述了 ,这是一个新的 3-联苯 ELQ 亚系列的成员,对多药耐药的寄生虫具有增强的体外效力。 ,其前药的结晶度降低,对鼠疟的效果比其母体化合物 强 4 至 10 倍,这表明可以使用相应较低的剂量来保护和治疗人类疟疾。与母体化合物相比, 在小鼠中的血液半衰期更长,这突出了一类新的下一代 ELQ 系列,具有每月一次给药预防疟疾感染的潜力。本文介绍了 3-联苯 ELQ 的制备进展,并初步探讨了药物效力、选择性、药代动力学和安全性的关键结构-活性关系的实验结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/767a/11507049/d3ba39da6864/id4c00140_0001.jpg

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