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一种对分枝杆菌具有活性的新型酰腙恶二唑衍生物。

A new -acylhydrazone oxadiazole derivative with activity against mycobacteria.

作者信息

Souza Izabella Ventura, Fróes da Motta Dacome Maria Luiza, Frederico Rozada Andrew Matheus, Rosa Jonathan Sanches, Sampiron Eloisa Gibin, Ferreira Deisiany Gomes, Gauze Gisele Freitas, Norman Negri Melyssa Fernanda, de Lima Scodro Regiane Bertin, Cardoso Rosilene Fressatti, Caleffi-Ferracioli Katiany Rizzieri

机构信息

Postgraduate Program of Biosciences and Physiopathology, Department of Clinical Analysis and Biomedicine, State University of Maringa, Maringa, Parana, Brazil.

Department of Chemistry, State University Maringa, Maringa, Parana, Brazil.

出版信息

Future Microbiol. 2025 Jan;20(1):33-44. doi: 10.1080/17460913.2024.2412439. Epub 2024 Oct 23.

Abstract

To evaluate the anti () potential of the hybrid oxadiazol-4-methoxynaphthalene () derived from -acylhydrazone (). The study determined the minimal inhibitory concentration of ( against HRv and clinical isolates, potential combination of ( with anti-tuberculosis drugs and carried out time kill curve assay of HRv. Additional contribution for the analysis of was explored by pharmacokinetics, and and cytotoxicity determinations. The newly synthesized molecule ( demonstrated anti- activity, low cytotoxicity and selectivity for The derivative () emerges as a potential anti-TB drug candidate.

摘要

评估源自酰腙的杂化恶二唑-4-甲氧基萘的抗()潜力。该研究确定了(对人呼吸道合胞病毒(HRv)和临床分离株的最低抑菌浓度,(与抗结核药物的潜在组合,并进行了HRv的时间杀菌曲线测定。通过药代动力学、(和(细胞毒性测定探索了(分析的额外贡献。新合成的分子(显示出抗(活性、低细胞毒性和对(的选择性。衍生物(成为一种潜在的抗结核药物候选物。

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