Dr. Reddy's Institute of Life Sciences, University of Hyderabad Campus, Gachibowli, Hyderabad 500 046, India.
Bioorg Med Chem Lett. 2013 Mar 15;23(6):1828-33. doi: 10.1016/j.bmcl.2013.01.026. Epub 2013 Jan 19.
A rapid, inexpensive and high yielding method has been developed for the synthesis of 1,8-dioxodecahydroacridines using Amberlite IR-120H as a reusable catalyst under open air. These compounds were designed as potential inhibitors of sirtuins and prepared via the MCR of 5,5-dimethyl-1,3-cyclohexanedione, (hetero)aryl aldehydes and (hetero)aromatic amines under mild conditions. Further structure elaboration of a representative compound was performed via Pd catalyzed C-C bond forming reactions. The crystal structure analysis and H-bonding patterns along with in vitro inhibitory activity against yeast Sir2 of the same compound is presented. Docking studies indicated that the compound interacts well with the yeast Sir2.
已经开发出一种使用 Amberlite IR-120H 作为可重复使用的催化剂在开放空气中快速、廉价且高产的合成 1,8-二氧代十二氢吖啶的方法。这些化合物被设计为潜在的 Sirtuins 抑制剂,并通过 5,5-二甲基-1,3-环己二酮、(杂)芳基醛和(杂)芳族胺在温和条件下的 MCR 制备。通过 Pd 催化的 C-C 键形成反应进一步对代表性化合物进行结构修饰。呈现了相同化合物的晶体结构分析和氢键模式以及对酵母 Sir2 的体外抑制活性。对接研究表明,该化合物与酵母 Sir2 相互作用良好。