Facultat de Farmacia, Unitat de Quimica Farmaceutica (Unitat Associada al CSIC), Universitat de Barcelona, Avda. Joan XXIII, s/n, 08028 Barcelona, Spain.
J Med Chem. 2010 Jul 22;53(14):5248-55. doi: 10.1021/jm100198t.
New N-alkylaminocyclitols bearing a 1,2,3-triazole system at different positions of the alkyl chain have been prepared as potential GCase pharmacological chaperones using click chemistry approaches. Among them, compounds 1d and 1e, with the shorter spacer (n = 1) between the alkyltriazolyl system and the aminocyclitol core, were the most active ones as GCase inhibitors, revealing a determinant effect of the location of the triazole ring on the activity. Furthermore, SAR data and computational docking models indicate a correlation between lipophilicity and enzyme inhibition and suggest "extended" and "bent" potential binding modes for the compounds. In the "bent" mode, the most active compounds could establish a hydrogen-bond interaction between the triazole moiety and enzyme residue Q284. Such an interaction would be precluded in compounds with a longer spacer between the triazole and the aminocyclitol core.
新型 N-烷基氨环糖醇通过点击化学方法被制备出来,作为潜在的 GCase 药理学伴侣,其烷基链的不同位置带有 1,2,3-三唑系统。其中,化合物 1d 和 1e 具有较短的间隔基(n = 1),在烷基三唑基系统和氨环糖醇核心之间,作为 GCase 抑制剂最为活跃,表明三唑环位置对活性有决定性影响。此外,SAR 数据和计算对接模型表明亲脂性与酶抑制之间存在相关性,并表明化合物具有“扩展”和“弯曲”的潜在结合模式。在“弯曲”模式下,最活跃的化合物可以在三唑部分和酶残基 Q284 之间建立氢键相互作用。这种相互作用在三唑和氨环糖醇核心之间具有较长间隔基的化合物中是被排除的。