Synthesis and biological evaluation of longanlactone analogues as neurotrophic agents
作者:Chada Raji Reddy、Amol Gorgile Tukaram、Siddique Z. Mohammed、Uredi Dilipkumar、Bathini Nagendra Babu、Sumana Chakravarty、Dwaipayan Bhattacharya、Pranav C. Joshi、René Grée
DOI:10.1016/j.bmcl.2018.01.020
日期:2018.2
Longanlactone analogues were synthesized using a route featuring Friedel-Crafts acylation, Sonogashira coupling and 1,3-dipolar cycloaddition reactions. Structure–activity relationships were investigated for neurotrophic activity. Compound 6 was found to have the most potent neurotrophic activity among all the synthesized analogues in Neuro2a cells as evidenced by a battery of in vitro/cell based assays
使用以Friedel-Crafts酰化,Sonogashira偶联和1,3-偶极环加成反应为特征的途径合成Longanlactone类似物。研究了结构-活动关系的神经营养活动。发现化合物6在Neuro2a细胞中所有合成的类似物中具有最强的神经营养活性,这一点已通过一系列基于神经/潜在神经营养活性的体外/细胞试验(包括神经突增生试验和实时PCR进行流行的标记物评估)得到证明。增强的神经营养活动。化合物6可以用作进一步开发高效神经营养分子的模板。