Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, CS, Italy.
CNR-NANOTEC, SS Rende (CS), Department of Physics, University of Calabria, Via Pietro Bucci, 87036 Rende, CS, Italy.
Int J Mol Sci. 2023 Dec 28;25(1):435. doi: 10.3390/ijms25010435.
Arylalkane-derived prodrugs of arylacetic acids are a small group of substances that have long been known for their anti-inflammatory action. Despite their ease of synthesis and good potential for the development of new potent and safe anti-inflammatory agents, this group of substances has not received much attention from researchers so far. Therefore, representative arylalkane derivatives were investigated through molecular docking techniques to verify the possible hepatic activation mode toward active metabolites by CYP1A2. In this regard, arylalkanoic acid prodrugs were docked with a crystallographic structure of human CYP1A2, in which the enzyme is co-crystallized with the selective competitive inhibitor α-naphthoflavone BHF. Of note, all the examined compounds proved capable of interacting with the enzyme active site in a manner similar to Nabumetone, thus confirming that a productive metabolic transformation is feasible. On the basis of these findings, it is possible to argue that subtle differences in the way CYP1A2 accommodates the ligands depend on the fine details of their molecular structures. Overall, these data suggest that compounds simply formed by an aromatic moiety bearing an appropriate alkane-derived chain could lead to innovative anti-inflammatory agents.
芳基烷酸的芳基烷衍生前药是一组已知具有抗炎作用的物质。尽管它们易于合成,并且具有开发新型有效且安全的抗炎剂的良好潜力,但到目前为止,这组物质并没有引起研究人员的太多关注。因此,通过分子对接技术研究了代表性的芳基烷衍生物,以验证 CYP1A2 对活性代谢物可能的肝活化模式。在这方面,芳基烷酸前药与人类 CYP1A2 的晶体结构对接,其中酶与选择性竞争性抑制剂 α-萘黄酮 BHF 共结晶。值得注意的是,所有检查的化合物都被证明能够以类似于萘丁美酮的方式与酶活性位点相互作用,从而证实可行的生产代谢转化。基于这些发现,可以说 CYP1A2 容纳配体的方式的细微差异取决于其分子结构的细微差别。总的来说,这些数据表明,简单地由带有适当烷衍生链的芳基部分形成的化合物可能会导致创新的抗炎剂。