维加利辛C和D,是由Apiospora sp.生产的新型普拉玛尼辛类似物. 在FKI-805858中使用
So-Ichiro Kimura1, Yoshihiro Watanabe1,2, Yudai Mikasa3
1Graduate School of Infection Control Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.
The Journal of antibiotics
|February 1, 2024
概括
从Apiospora sp.中鉴定出了两种新的普拉玛尼辛类似物,即维加利辛C和D. 这些化合物表现出适度的抗疟疾和细胞毒性作用,需要进一步调查.
科学领域:
- 自然产品化学 自然产品化学
- 微生物学 微生物学
- 药理学 药理学是指药理学的学科.
背景情况:
- 藻类物种是已知的生物活性二次代谢产物的来源.
- 普拉曼尼辛的类似物已经表现出各种生物活性.
- 由于药物耐药性,对新的抗疟疾药物的需求至关重要.
研究的目的:
- 发现和描述来自Apiospora sp.的新化合物. 在FKI-8058.8.上使用.
- 评估分离化合物的抗疟疾和细胞毒性潜力.
主要方法:
- 静态培养的Apiospora sp.的物理化学选 在FKI-8058.8.上使用.
- 使用质谱 (MS) 和核磁共振 (NMR) 分析进行结构阐明.
- 用于结构确认的化学衍生.
主要成果:
- 两种新的普拉玛尼辛类似物,维加利辛C (1) 和D (2) 被分离和鉴定出来.
- 化合物1和2显示了中度的抗疟疾活性.
- 对维加利素C和D都观察到细胞毒性.
结论:
- 维尔加里辛C和D代表了普拉马尼辛类化合物的新增.
- 这些已识别的化合物具有初步的抗疟疾和细胞毒性.
- 建议进行进一步的研究,以探索它们的治疗潜力和作用机制.
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