Thailand Excellence Center for Tissue Engineering and Stem Cells, Department of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
School of Traditional and Alternative Medicine, Chiang Rai Rajabhat University, Chiang Rai 57100, Thailand.
Molecules. 2021 Feb 11;26(4):949. doi: 10.3390/molecules26040949.
Unapproved ingredients included in herbal medicines and dietary supplements have been detected as adulterated synthetic drugs used for erectile dysfunction. Extraction from a dietary supplement was performed to isolate the compounds by HPLC analysis. The structural characterization was confirmed using mass spectrometry (ESI-TOF/MS and LC-MS/MS), H NMR, and C NMR spectroscopy techniques. Results identified the thus-obtained compound to be sulfoaildenafil, a thioketone analogue of sildenafil. The biological activities of this active compound have been focused for the first time by the experimental point of view performance in vitro. The results revealed that sulfoaildenafil can affect the therapeutic level of nitric oxide through the upregulation of nitric oxide synthase and phosphodiesterase type 5 (PDE5) gene expressions. This bulk material, which displays structural similarity to sildenafil, was analyzed for the presence of a PDE5 inhibitor using a theoretical calculation. These unique features of the potential activity of PDE5 protein and its inhibitors, sildenafil and sulfoaildenafil, may play a key consideration for understanding the mode of actions and predicting the biological activities of PDE5 inhibitors.
在草药和膳食补充剂中发现了未经批准的成分,这些成分被检测为用于勃起功能障碍的掺假合成药物。通过 HPLC 分析从膳食补充剂中提取化合物进行分离。使用质谱(ESI-TOF/MS 和 LC-MS/MS)、H NMR 和 C NMR 光谱技术对结构进行了表征。结果表明,所得到的化合物为磺酰基艾地那非,一种西地那非的硫酮类似物。首次从实验角度研究了这种活性化合物的生物学活性。结果表明,磺酰基艾地那非可以通过上调一氧化氮合酶和磷酸二酯酶 5(PDE5)基因表达来影响一氧化氮的治疗水平。使用理论计算分析了这种与西地那非结构相似的大块物质,以确定其是否存在 PDE5 抑制剂。这些 PDE5 蛋白及其抑制剂西地那非和磺酰基艾地那非的潜在活性的独特特征可能是理解作用模式和预测 PDE5 抑制剂生物学活性的关键考虑因素。