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揭示酰胺类化合物的抗棘球蚴疗效:一项[具体内容缺失]研究。

Unveiling the anti-echinococcal efficacy of amide-based compounds: An and study.

作者信息

Chauhan V, Farooq U, Fahmi M, A Khan, Tripathi P K

机构信息

Multi-Disciplinary Research Unit, Government Institute of Medical Sciences, Greater Noida, UP, 201310, India.

Department of Basic Oral Medicine and Allied Dental Sciences, Faculty of Dentistry, Taif University, Taif, Kingdom of Saudi Arabia.

出版信息

Heliyon. 2024 May 14;10(10):e31205. doi: 10.1016/j.heliyon.2024.e31205. eCollection 2024 May 30.

Abstract

Cystic echinococcosis (CE) is a significant global public health concern, particularly in regions where livestock rearing is prevalent. Despite its impact on morbidity and mortality, CE has received insufficient attention compared to other neglected tropical diseases. The complexities in CE management arise from challenges in early detection, effective treatment, and parasite eradication. The present study addresses this gap by exploring innovative therapeutic approaches using amide-based compounds. In recent years, computational approaches and studies have become prominent in neglected tropical disease drug discovery. Leveraging insights from previous studies on amide-based compounds with anti-parasitic potential, this study systematically designed, synthesized, and characterized a library of 30 amide compounds. The research integrated screening, molecular docking, and experimentation to assess the anti-echinococcal potential of these compounds. The study identified five promising amide compounds, namely 3,5-dinitro-N-p-tolylbenzamide, N-p-tolyl-1-naphthamide, N-p-tolyl-4-(trifluoromethoxy)benzamide, 4-pentyl-N-p-tolylbenzamide, and 2,3,4,5,6-pentafluoro-N-p-tolylbenzamide, based on their docking scores. These compounds were synthesized and characterized through various spectroscopic techniques, confirming their structural integrity. The cytotoxicity assay on HepG2 cell lines revealed varying degrees of cytotoxicity for the synthesized compounds. Notably, 4-pentyl-N-p-tolylbenzamide demonstrated the least cytotoxicity. Subsequent scolicidal activity assessments on protoscoleces demonstrated the potent protoscolicidal activity of N-p-tolyl-1-naphthamide, indicating its potential as an effective anti-echinococcal agent. Overall, this study presents a comprehensive exploration of amide-based compounds as potential therapeutic agents against CE. The findings contribute to the development of innovative strategies for CE treatment, addressing the urgent need for effective and safe drugs in managing this neglected tropical disease.

摘要

囊性棘球蚴病(CE)是一个重大的全球公共卫生问题,在畜牧业盛行的地区尤为突出。尽管它对发病率和死亡率有影响,但与其他被忽视的热带病相比,CE受到的关注不足。CE管理的复杂性源于早期检测、有效治疗和寄生虫根除方面的挑战。本研究通过探索使用基于酰胺的化合物的创新治疗方法来填补这一空白。近年来,计算方法和研究在被忽视的热带病药物发现中变得突出。利用先前对具有抗寄生虫潜力的基于酰胺的化合物的研究见解,本研究系统地设计、合成并表征了一个包含30种酰胺化合物的文库。该研究整合了筛选、分子对接和实验,以评估这些化合物的抗棘球蚴潜力。基于对接分数,该研究确定了五种有前景的酰胺化合物,即3,5-二硝基-N-对甲苯基苯甲酰胺、N-对甲苯基-1-萘甲酰胺、N-对甲苯基-4-(三氟甲氧基)苯甲酰胺、4-戊基-N-对甲苯基苯甲酰胺和2,3,4,5,6-五氟-N-对甲苯基苯甲酰胺。通过各种光谱技术对这些化合物进行了合成和表征,证实了它们的结构完整性。对HepG2细胞系的细胞毒性测定显示,合成化合物具有不同程度的细胞毒性。值得注意的是,4-戊基-N-对甲苯基苯甲酰胺表现出最小的细胞毒性。随后对原头节的杀原头节活性评估表明,N-对甲苯基-1-萘甲酰胺具有强大的杀原头节活性,表明其作为一种有效的抗棘球蚴病药物的潜力。总体而言,本研究全面探索了基于酰胺的化合物作为抗CE潜在治疗剂的可能性。这些发现有助于开发CE治疗的创新策略,满足管理这种被忽视的热带病对有效和安全药物的迫切需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82b0/11130662/8c38a0bb76a7/gr1.jpg

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