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通过3D药效团建模在美国食品药品监督管理局批准的药物中探索新型抗血吸虫病药物。

The 3D pharmacophore modeling to explore new antischistosomal agents among US FDA approved drugs.

作者信息

Dobrachinski Leandro, Ferreira Leonardo Lg, Cirino Maria E, Andrade-de-Siqueira Allan I, Mafud Ana C, Mascarenhas Yvonne P, Andricopulo Adriano D, de Moraes Josué

机构信息

Núcleo de Pesquisa em Doenças Negligenciadas, Universidade Guarulhos, Guarulhos, SP, Brazil.

Instituto de Física de São Carlos, Universidade de São Paulo, São Carlos, SP, Brazil.

出版信息

Future Med Chem. 2024;16(17):1791-1799. doi: 10.1080/17568919.2024.2379231. Epub 2024 Jul 29.

Abstract

To identify potential antischistosomal agents through 3D pharmacophore-based virtual screening of US FDA approved drugs. A comprehensive virtual screening was conducted on a dataset of 10,000 FDA approved drugs, employing praziquantel as a template. Promising candidates were selected and assessed for their impact on viability and using infected mice. Among the selected drugs, betamethasone and doxazosin demonstrated efficacy, with effective concentration 50% (EC) values ranging from 35 to 60 μM. studies revealed significant (>50%) reductions in worm burden for both drugs. These findings suggest that betamethasone and doxazosin hold promise for repurposing in treating schistosomiasis. Additionally, the study showcases a useful approach for identifying new antischistosomal drugs.

摘要

通过基于3D药效团的美国食品药品监督管理局(FDA)批准药物虚拟筛选来鉴定潜在的抗血吸虫药物。以吡喹酮为模板,对10000种FDA批准药物的数据集进行了全面的虚拟筛选。选择了有前景的候选药物,并评估它们对感染小鼠的生存能力的影响。在所选药物中,倍他米松和多沙唑嗪显示出疗效,其半数有效浓度(EC)值在35至60μM之间。研究表明,这两种药物的虫负荷均显著降低(>50%)。这些发现表明,倍他米松和多沙唑嗪有望用于血吸虫病的重新利用治疗。此外,该研究展示了一种识别新型抗血吸虫药物的有用方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a9/11457623/004d2e941d50/IFMC_A_2379231_UF0001_C.jpg

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