Kim D S, Kim J Y
The Program for Collaborative Research in Pharmaceutical Science and the Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois at Chicago, 833 South Wood Street, Chicago, IL 60612, USA.
Bioorg Med Chem Lett. 2001 Sep 17;11(18):2541-3. doi: 10.1016/s0960-894x(01)00489-9.
A total synthesis of Calebin-A (1), a novel curcuminoid isolated from turmeric (Curcuma longa, Zingiberaceae) that has been demonstrated to protect neuronal cells from beta-amyloid insult, was successfully achieved in four steps. Elaborating on this synthetic route, 13 analogues were prepared for a structure-activity relationship (SAR) study. It was found that the parent compound 1 and derivatives 21, 28, and 30 protect PC12 rat pheocromocytoma and IMR-32 human neuroblastoma cells from beta-amyloid(25-35) insult. These results suggest that hydroxy group at para-position is most critical for the expression of biological activity.
从姜黄(姜科姜黄属)中分离出的新型姜黄素类化合物Calebin-A(1)已被证明可保护神经元细胞免受β-淀粉样蛋白损伤,通过四步反应成功实现了其全合成。基于此合成路线,制备了13种类似物用于构效关系(SAR)研究。发现母体化合物1以及衍生物21、28和30可保护PC12大鼠嗜铬细胞瘤细胞和IMR-32人神经母细胞瘤细胞免受β-淀粉样蛋白(25-35)损伤。这些结果表明对位羟基对于生物活性的表达最为关键。