Laboratory of Medicinal Chemistry, University of Antwerp, Antwerp, Belgium.
Antimicrob Agents Chemother. 2010 May;54(5):1900-8. doi: 10.1128/AAC.01787-09. Epub 2010 Mar 1.
In this paper, we present the biochemical and biological evaluation of N-arylmethyl-substituted iminoribitol derivatives as potential chemotherapeutic agents against trypanosomiasis. Previously, a library of 52 compounds was designed and synthesized as potent and selective inhibitors of Trypanosoma vivax inosine-adenosine-guanosine nucleoside hydrolase (IAG-NH). However, when the compounds were tested against bloodstream-form Trypanosoma brucei brucei, only one inhibitor, N-(9-deaza-adenin-9-yl)methyl-1,4-dideoxy-1,4-imino-d-ribitol (UAMC-00363), displayed significant activity (mean 50% inhibitory concentration [IC(50)] +/- standard error, 0.49 +/- 0.31 microM). Validation in an in vivo model of African trypanosomiasis showed promising results for this compound. Several experiments were performed to investigate why only UAMC-00363 showed antiparasitic activity. First, the compound library was screened against T. b. brucei IAG-NH and inosine-guanosine nucleoside hydrolase (IG-NH) to confirm the previously demonstrated inhibitory effects of the compounds on T. vivax IAG-NH. Second, to verify the uptake of these compounds by T. b. brucei, their affinities for the nucleoside P1 and nucleoside/nucleobase P2 transporters of T. b. brucei were tested. Only UAMC-00363 displayed significant affinity for the P2 transporter. It was also shown that UAMC-00363 is concentrated in the cell via at least one additional transporter, since P2 knockout mutants of T. b. brucei displayed no resistance to the compound. Consequently, no cross-resistance to the diamidine or the melaminophenyl arsenical classes of trypanocides is expected. Third, three enzymes of the purine salvage pathway of procyclic T. b. brucei (IAG-NH, IG-NH, and methylthioadenosine phosphorylase [MTAP]) were investigated using RNA interference. The findings from all these studies showed that it is probably not sufficient to target only the nucleoside hydrolase activity to block the purine salvage pathway of T. b. brucei and that, therefore, it is possible that UAMC-00363 acts on an additional target.
本文介绍了 N-芳甲基取代的异肌醇衍生物作为潜在抗锥虫病化疗药物的生化和生物学评价。先前,设计并合成了 52 种化合物库,作为锥虫 vivax 肌苷-腺嘌呤-鸟嘌呤核苷水解酶(IAG-NH)的有效且选择性抑制剂。然而,当这些化合物针对血流形式的布氏锥虫布鲁斯氏菌进行测试时,只有一种抑制剂,N-(9-脱氮腺嘌呤-9-基)甲基-1,4-二脱氧-1,4-亚氨基-D-核糖醇(UAMC-00363)表现出显著的活性(平均 50%抑制浓度[IC(50)]±标准误差,0.49±0.31 microM)。在非洲锥虫病的体内模型中进行的验证显示,该化合物具有有希望的结果。进行了几项实验以研究为什么只有 UAMC-00363 显示出抗寄生虫活性。首先,对化合物库进行了筛选,以检测 T. b. brucei IAG-NH 和肌苷-鸟苷核苷水解酶(IG-NH),以确认先前证明的化合物对 T. vivax IAG-NH 的抑制作用。其次,为了验证这些化合物被 T. b. brucei 摄取,测试了它们对 T. b. brucei 核苷 P1 和核苷/核苷碱基 P2 转运体的亲和力。只有 UAMC-00363 对 P2 转运体表现出显著的亲和力。还表明,UAMC-00363 通过至少一种额外的转运体在细胞内浓缩,因为 T. b. brucei 的 P2 敲除突变体对该化合物没有抗性。因此,预计不会对二脒或苯并脒基砷类杀锥虫剂产生交叉耐药性。第三,研究了三个 Procyclic T. b. brucei 的嘌呤补救途径酶(IAG-NH、IG-NH 和甲基硫代腺苷磷酸化酶[MTAP]),使用 RNA 干扰。所有这些研究的结果表明,可能不足以仅针对核苷水解酶活性来阻断 T. b. brucei 的嘌呤补救途径,因此,UAMC-00363 可能作用于另一个靶标。