Orenes Lorente Silvia, Gómez Rosario, Jiménez Carmen, Cammerer Simon, Yardley Vanessa, de Luca-Fradley Kate, Croft Simon L, Ruiz Perez Luis M, Urbina Julio, Gonzalez Pacanowska Dolores, Gilbert Ian H
Welsh School of Pharmacy, Cardiff University, Redwood Building, King Edward VII Avenue, Cardiff CF10 3XF, UK.
Bioorg Med Chem. 2005 May 16;13(10):3519-29. doi: 10.1016/j.bmc.2005.02.060.
In this paper we describe the preparation of some biphenylquinuclidine derivatives and their evaluation as inhibitors of squalene synthase in order to explore their potential in the treatment of the parasitic diseases leishmaniasis and Chagas disease. The compounds were screened against recombinant Leishmania major squalene synthase and against Leishmania mexicana promastigotes, Leishmania donovani intracellular amastigotes and Trypanosoma cruzi intracellular amastigotes. Compounds that inhibited the enzyme, also reduced the levels of steroids and caused growth inhibition of L. mexicana promastigotes. However there was a lower correlation between inhibition of the enzyme and growth inhibition of the intracellular parasites, possibly due to delivery problems. Some compounds also showed growth inhibition of T. brucei rhodesiense trypomastigotes, although in this case alternative modes of action other than inhibition of SQS are probably involved.
在本文中,我们描述了一些联苯喹核碱衍生物的制备及其作为角鲨烯合酶抑制剂的评估,以探索它们在治疗寄生虫病利什曼病和恰加斯病方面的潜力。这些化合物针对重组硕大利什曼原虫角鲨烯合酶、墨西哥利什曼原虫前鞭毛体、杜氏利什曼原虫细胞内无鞭毛体和克氏锥虫细胞内无鞭毛体进行了筛选。抑制该酶的化合物也降低了类固醇水平,并导致墨西哥利什曼原虫前鞭毛体的生长受到抑制。然而,酶抑制与细胞内寄生虫生长抑制之间的相关性较低,这可能是由于递送问题所致。一些化合物也显示出对罗德西亚布氏锥虫锥鞭毛体的生长抑制作用,不过在这种情况下,可能涉及除抑制角鲨烯合酶之外的其他作用方式。