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菲并吲哚里西啶生物碱及其衍生物的合成与抗病毒活性。

Synthesis and antiviral activities of phenanthroindolizidine alkaloids and their derivatives.

机构信息

State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, People's Republic of China.

出版信息

J Agric Food Chem. 2010 Mar 10;58(5):2703-9. doi: 10.1021/jf902543r.

Abstract

Racemic phenanthroindolizidine alkaloids tylophorine, antofine, and deoxytylophorinine, and optically pure alkaloids S-(+)-tylophorine and R-(-)-tylophorine were synthesized and evaluated for their antiviral activities against tobacco mosaic virus (TMV). Further salinization modifications based on tylophorine increased stability and water solubility and improved the antiviral activity in application. The bioassay results showed that most of these synthesized compounds showed higher antiviral activity against TMV in vitro and in vivo than commercial Ningnanmycin. Especially, tylophorine salt derivatives 10, 11, 13, 17, and 22 emerged as potential inhibitors of plant virus. These findings demonstrate that these phenanthroindolizidine alkaloids and their salt derivatives represent a new template for antiviral studies and could be considered for novel therapy against plant virus infection.

摘要

消旋菲并吲哚里西啶生物碱千里光菲灵碱、阿多芬和脱氧千里光菲灵碱,以及光学纯生物碱 S-(+)-千里光菲灵碱和 R-(-)-千里光菲灵碱被合成并评估了它们对烟草花叶病毒 (TMV) 的抗病毒活性。基于千里光的进一步盐化修饰提高了稳定性和水溶性,并提高了应用中的抗病毒活性。生物测定结果表明,这些合成化合物中的大多数对 TMV 的体外和体内抗病毒活性均高于商业宁南霉素。特别是千里光碱盐衍生物 10、11、13、17 和 22 表现出作为植物病毒抑制剂的潜力。这些发现表明这些菲并吲哚里西啶生物碱及其盐衍生物代表了抗病毒研究的新模板,可考虑用于新型植物病毒感染治疗。

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