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稠合四氢喹啉正在干扰你的检测。

Fused Tetrahydroquinolines Are Interfering with Your Assay.

机构信息

Structural Genomics Consortium, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.

Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia 30322, United States.

出版信息

J Med Chem. 2023 Nov 9;66(21):14434-14446. doi: 10.1021/acs.jmedchem.3c01277. Epub 2023 Oct 24.

Abstract

Tricyclic tetrahydroquinolines (THQs) have been repeatedly reported as hits across a diverse range of high-throughput screening (HTS) campaigns. The activities of these compounds, however, are likely due to reactive byproducts that interfere with the assay. As a lesser studied class of pan-assay interference compounds, the mechanism by which fused THQs react with protein targets remains largely unknown. During HTS follow-up, we characterized the behavior and stability of several fused tricyclic THQs. We synthesized key analogues to pinpoint the cyclopentene ring double bond as a source of reactivity of fused THQs. We found that these compounds degrade in solution under standard laboratory conditions in days. Importantly, these observations make it likely that fused THQs, which are ubiquitously found within small molecule screening libraries, are unlikely the intact parent compounds. We urge deprioritization of tricylic THQ hits in HTS follow-up and caution against the investment of resources to follow-up on these problematic compounds.

摘要

三环四氢喹啉 (THQs) 在各种高通量筛选 (HTS) 活动中被反复报道为命中。然而,这些化合物的活性可能是由于反应副产物干扰了测定。作为研究较少的一类泛分析干扰化合物,融合的 THQs 与蛋白靶标反应的机制在很大程度上仍然未知。在 HTS 后续研究中,我们对几种融合的三环四氢喹啉的行为和稳定性进行了表征。我们合成了关键的类似物,以确定环戊烯环双键是融合 THQs 反应性的来源。我们发现这些化合物在标准实验室条件下会在数天内在溶液中降解。重要的是,这些观察结果表明,在小分子筛选文库中普遍存在的融合 THQs 不太可能是完整的母体化合物。我们敦促在 HTS 后续研究中优先考虑三环四氢喹啉的命中,并警告不要投入资源来跟进这些有问题的化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/725c/10641811/6f952674bf1a/jm3c01277_0001.jpg

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