ICPAL, Université Lille Nord de France , EA4481, IFR114, 3 Rue du Pr. Laguesse, BP 83, F-59006 Lille Cedex, France.
J Med Chem. 2012 Oct 25;55(20):8948-52. doi: 10.1021/jm3008568. Epub 2012 Oct 12.
Further on to our earlier work on the 4-oxo-1,4-dihydropyridine, we describe herein our strategy to get access to potent selective CB₂ receptor agonists. Thus, we designed and synthesized 29 compounds, evaluated on both hCB₁ and hCB₂ cannabinoid receptors, and assessed 11 of them in the TNBS-induced colitis model in mice. Compound 48 was found to be the most efficient of our series, exhibiting an exquisite protection against experimental colitis, superior to the one observed after treatment with Pentasa.
继我们早期关于 4-氧代-1,4-二氢吡啶的工作之后,本文描述了我们获得有效选择性 CB₂ 受体激动剂的策略。为此,我们设计并合成了 29 种化合物,对 hCB₁ 和 hCB₂ 大麻素受体进行了评估,并在小鼠 TNBS 诱导的结肠炎模型中评估了其中的 11 种化合物。发现化合物 48 是我们系列中最有效的一种,对实验性结肠炎具有极好的保护作用,优于 Pentasa 治疗后观察到的效果。