开发具有in vivo抗胞体活性的非镇静二胺
Md Yeunus Mian1,2, Dishary Sharmin1,2, Prithu Mondal1,2
1Department of Chemistry and Biochemistry, University of Wisconsin-Milwaukee, Milwaukee, Wisconsin, USA.
Antimicrobial agents and chemotherapy
|August 13, 2024
概括
新的二甲衍生物显示出对治疗被忽视的热带疾病 - - 石病的前景. 这些化合物对寄生虫有效,与原始候选药物相比,降低了镇静副作用.
科学领域:
- 药用化学 医学化学
- 寄生虫学的寄生虫学
- 药物发现 药物发现 药物发现
背景情况:
- 全球有超过2亿人患上istosomiasis,治疗选择有限,主要依赖于praziquantel.
- 实验量子耐药性和治疗失败需要开发替代抗寄生虫药物.
- 孟佐迪亚泽类药物麦克洛纳泽帕姆 (Meclonazepam) 显示出有效性,但由于镇静剂的副作用而被置.
研究的目的:
- 设计和合成具有抗寄生虫活性但降低宿主镇静性的梅克洛纳泽类型.
- 探索结构-活性关系,以优化治疗指数在潜在的杆菌病治疗.
主要方法:
- 合成了18种梅克洛纳泽衍生物,对二胺环系统进行了修改.
- 在体外评估了对schistosoma寄生虫的抗寄生虫活性.
- 使用小鼠模型在体内选有前途的化合物,并通过旋转杆测试评估镇静效应.
主要成果:
- 五种合成的化合物在体外表现出抗寄生虫活性.
- 两种衍生药物在治疗小鼠杆菌病方面表现出有效性,与麦克洛纳泽帕姆相当.
- 这两种优化化合物与麦克洛纳泽相比,显著减少了镇静作用.
结论:
- 麦克洛纳泽的类似物可以设计为具有改善的治疗指数,用于治疗杆菌病.
- 二胺环的C3位置是进一步结构优化的关键位置.
- 这项研究为开发更安全,更有效的治疗方案提供了概念验证.
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