Organic Chemistry Department, Chemistry Institute, Federal University of Bahia, Barão de Jeremoabo 147, Salvador, 40170115, Bahia, Brazil.
Institute for Research in Pharmaceuticals and Medications, Federal University of Paraíba, Campus I, João Pessoa, 58051900, Paraíba, Brazil.
Chem Biodivers. 2021 Oct;18(10):e2100493. doi: 10.1002/cbdv.202100493. Epub 2021 Sep 7.
Hundreds of millions of people worldwide are affected by Chagas' disease caused by Trypanosoma cruzi. Since the current treatment lack efficacy, specificity, and suffers from several side-effects, novel therapeutics are mandatory. Natural products from endophytic fungi have been useful sources of lead compounds. In this study, three lactones isolated from an endophytic strain culture were in silico evaluated for rational guidance of their bioassay screening. All lactones displayed in vitro activity against T. cruzi epimastigote and trypomastigote forms. Notably, the IC values of (+)-phomolactone were lower than benznidazole (0.86 vs. 30.78 μM against epimastigotes and 0.41 vs. 4.88 μM against trypomastigotes). Target-based studies suggested that lactones displayed their trypanocidal activities due to T. cruzi glyceraldehyde-3-phosphate dehydrogenase (TcGAPDH) inhibition, and the binding free energy for all three TcGAPDH-lactone complexes suggested that (+)-phomolactone has a lower score value (-3.38), corroborating with IC assays. These results highlight the potential of these lactones for further anti-T. cruzi drug development.
全世界数亿人受到克氏锥虫引起的恰加斯病的影响。由于目前的治疗方法缺乏疗效、特异性,并伴有多种副作用,因此必须开发新的疗法。内寄生真菌的天然产物是有前途的先导化合物来源。在这项研究中,从一种内生菌株的培养物中分离出的三种内酯,通过计算机模拟评估,为它们的生物测定筛选提供了合理的指导。所有内酯均显示出体外抗克氏锥虫滋养体和鞭毛体的活性。值得注意的是,(+)-phomolactone 的 IC 值低于苯并咪唑(对滋养体为 0.86 与 30.78 μM,对鞭毛体为 0.41 与 4.88 μM)。基于靶点的研究表明,内酯通过克氏锥虫甘油醛-3-磷酸脱氢酶(TcGAPDH)抑制发挥杀锥虫活性,并且三种 TcGAPDH-内酯复合物的结合自由能表明(+)-phomolactone 的得分值较低(-3.38),与 IC 测定结果相符。这些结果突出了这些内酯在进一步开发抗克氏锥虫药物方面的潜力。