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带有脒基尾基的S-单糖基甘油二酯是强效、选择性抗疟原虫剂。

S-MGBs bearing amidine tail groups are potent, selective antiplasmodial agents.

作者信息

Perieteanu Marina, Garzon Tayner Rodriguez, McGee Leah M C, Khalaf Abedawn I, Suckling Colin J, Beveridge Rebecca, Avery Vicky M, Scott Fraser J

机构信息

Department of Pure and Applied Chemistry, University of Strathclyde Glasgow UK

Discovery Biology, Centre for Cellular Phenomics, Griffith University Nathan Queensland 4111 Australia.

出版信息

RSC Med Chem. 2024 Oct 16;16(1):412-9. doi: 10.1039/d4md00619d.

Abstract

There were an estimated 249 million cases of malaria globally in 2022, causing approximately 608 000 deaths. Most of these are attributed to infection by . Strathclyde minor groove binders (S-MGBs) are a promising new class of anti-infective agent that have been shown to be effective against many infectious organisms, including . A panel of 25 S-MGBs was synthesised, including those bearing an amidine tail group, and their antiplasmodial activity against 3D7 and Dd2 strains was determined using an asexual imaging assay. Determination of activity against HEK293 cells allowed for selective cytotoxicity to be measured. DNA binding studies were carried out using native mass spectrometry and DNA thermal shift assays. A comparison of 3D7 (chloroquine sensitive) and Dd2 (chloroquine resistant) potency showed no evidence of cross-resistance across the S-MGB set. , and , amidine tail containing S-MGBs, were identified as the most promising hit compounds based on their selectivity indices (HEK293/3D7) of >612.6, >335.8 and >264.8, respectively. , and were confirmed to bind to DNA as dimers, with gDNA thermal shifts (Δ ) of 12 °C, 3 °C and 16 °C, respectively. Together, these data demonstrate that amidine tail bearing S-MGBs are promising hit compounds against , and can be further optimised into lead compounds.

摘要

2022年,全球估计有2.49亿例疟疾病例,导致约60.8万人死亡。其中大多数归因于感染。斯特拉斯克莱德小沟结合剂(S-MGBs)是一类很有前景的新型抗感染药物,已被证明对许多感染性生物体有效,包括。合成了一组25种S-MGBs,包括带有脒尾基团的那些,并使用无性成像测定法测定了它们对3D7和Dd2菌株的抗疟原虫活性。通过测定对HEK293细胞的活性来测量选择性细胞毒性。使用原生质谱和DNA热迁移测定法进行了DNA结合研究。对3D7(氯喹敏感)和Dd2(氯喹耐药)效力的比较表明,在整个S-MGB组中没有交叉耐药的证据。基于它们分别大于612.6、大于335.8和大于264.8的选择性指数(HEK293/3D7),含有脒尾的S-MGBs 、和被确定为最有前景的命中化合物。、和被证实在结合DNA时形成二聚体,其基因组DNA热迁移(Δ)分别为12℃、3℃和16℃。总之,这些数据表明,带有脒尾的S-MGBs是针对的有前景的命中化合物,并且可以进一步优化成先导化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d63/11756258/5d47f5c5628a/d4md00619d-f1.jpg

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