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加兰他敏磷酸酯衍生物的合成、光谱特征及生物评价。

Synthesis, spectral characterization and biological evaluation of phosphorylated derivatives of galanthamine.

机构信息

Department of Chemistry, Sri Venkateswara University, Tirupati, Andhra Pradesh 517 502, India.

出版信息

Eur J Med Chem. 2010 Jan;45(1):203-9. doi: 10.1016/j.ejmech.2009.09.045. Epub 2009 Oct 6.

Abstract

A series of novel phosphorylated derivatives of galanthamine 6-11 and 12-17 were synthesized in two step process with high yields. In the first step galanthamine 1 was reacted with bis (2-chloroethyl) phosphoramidic dichloride 2/4-nitrophenyl phosphorodichloridate 3 in presence of triethylamine (TEA) in dry tetrahydrofuran (THF) yielded the intermediates 4/5. They were further reacted with various compounds like 2-aminoethanol, ethyleneglycol, ethylenediamine, 2-aminoethanethiol, 2-hydroxyethanethiol, monopotassium dihydrogenphosphate to obtain the title compounds 6-11 and 12-17. The title compounds showed promising antimicrobial, antioxidant activities and was greatly influenced by the presence of different bioactive groups.

摘要

一系列新型的加兰他敏 6-11 和 12-17 的磷酸化衍生物通过两步法高收率合成。在第一步中,加兰他敏 1 与双(2-氯乙基)磷酰胺二氯 2/4-硝基苯基磷酰二氯 3 在三乙胺(TEA)存在下于干燥四氢呋喃(THF)中反应,生成中间体 4/5。它们进一步与各种化合物如 2-氨基乙醇、乙二醇、乙二胺、2-氨基乙硫醇、2-羟乙硫醇、磷酸二氢钾单盐反应,得到标题化合物 6-11 和 12-17。标题化合物表现出有前景的抗菌、抗氧化活性,并且受到不同生物活性基团的极大影响。

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