Han Young Taek, Kim Kyeojin, Choi Gyeong-In, An Hongchan, Son Dohyun, Kim Hee, Ha Hee-Jin, Son Jun-Hyeng, Chung Suk-Jae, Park Hyun-Ju, Lee Jeewoo, Suh Young-Ger
College of Pharmacy, Woosuk University, Wanju 565-701, Republic of Korea.
College of Pharmacy, Seoul National University, 599 Gwanak-ro, Gwanak-gu, Seoul 151-742, Republic of Korea.
Eur J Med Chem. 2014 May 22;79:128-42. doi: 10.1016/j.ejmech.2014.03.072. Epub 2014 Mar 26.
In an effort to develop novel inhibitors of receptor for advanced glycation end products (RAGE) for the treatment of Alzheimer's disease, a series of pyrazole-5-carboxamides were designed, synthesized and biologically evaluated. Analyses of the extensive structure-activity relationship (SAR) led us to identify a 4-fluorophenoxy analog (40) that exhibited improved in vitro RAGE inhibitory activity and more favorable aqueous solubility than the parent 2-aminopyrimidine, 1. Surface plasmon resonance (SPR) and molecular docking study strongly supported the RAGE inhibitory activity of pyrazole-5-carboxamides. The brain Aβ-lowering effect of 40 is also described.
为了开发用于治疗阿尔茨海默病的新型晚期糖基化终产物受体(RAGE)抑制剂,设计、合成并对一系列吡唑-5-甲酰胺进行了生物学评估。通过广泛的构效关系(SAR)分析,我们确定了一种4-氟苯氧基类似物(40),它比母体2-氨基嘧啶1表现出更好的体外RAGE抑制活性和更有利的水溶性。表面等离子体共振(SPR)和分子对接研究有力地支持了吡唑-5-甲酰胺的RAGE抑制活性。还描述了化合物40降低大脑中β淀粉样蛋白(Aβ)的作用。