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作 者:符伟玉[1] 张建和[1] 罗辉[1] 佘戟[1] 梁念慈[1]
机构地区:[1]广东医学院,广东湛江524023
出 处:《时珍国医国药》2006年第6期921-922,共2页Lishizhen Medicine and Materia Medica Research
基 金:广东省湛江市科委资助项目(No.42)
摘 要:目的制备水溶性高良姜素衍生物,提高高良姜素的生物利用度。方法采用过量的L-精氨酸与高良姜素在乙醇中回流反应,反应混合物经柱层析分离纯化,得3个水溶性化合物B,C,D。结果经TLC,UV,IR谱初步分析,确定B,C,D分别为:高良姜素一精氨酸酯、高良姜素二精氨酸酯、高良姜素三精氨酸酯。高良姜素,B,C,D抑制红白血病K562细胞生长的IC50(μg/m l)值分别为:26.2,40.4,47.9,60.5。结论此高良姜素水溶性衍生物的制备反应为一酯化过程;但高良姜素结构中羟基封闭不利于其生物活性的保持。Objective To prepare the water solubte galangin-arginine derivative and improve the bioavailability of galangin (Ga). Methods Overdosly L-arginine and Ga were refluxed in alcohol. Reaction compounds were isolated on silica gel column chromatography and their structures were identified by spectral and chemical analysis. Results Three water solube compounds were isolated and identified as galangin-monoargininate( B), galangin-diargininate (C) and galangin - triargininate (D). Ga, B, C and D inhibited the growth of erythroleukoemia K562 cells, and the inhibited IC50 (μg/ml) values were 26.2, 40.4, 47.9 and 60.5. Conclusion The above preparation of the water soluble Galangin-arginine derivative were esterification process ,but the blocking of Hydroxyl in Ga structure was disadvantageous to keep its bioavailability.
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