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机构地区:[1]黑龙江中医药大学药学院,黑龙江哈尔滨150040 [2]哈药集团制药六厂,黑龙江哈尔滨150056
出 处:《中草药》2010年第1期11-14,共4页Chinese Traditional and Herbal Drugs
基 金:黑龙江省研究生创新科研项目(YJSCX2007-0177HLJ)
摘 要:目的研究抗肿瘤中药青龙衣的化学成分。方法近年大量的药理实验及临床研究表明青龙衣CHCl3及EtOAc部分具有显著的抗肿瘤作用,且毒性较小。本实验利用硅胶柱色谱和大孔吸附树脂分离化合物,并利用1D-NMR及2D-NMR光谱数据确定了化合物的结构。结果从青龙衣的CHCl3活性部位中分得8个化合物,并分别确定为20(S)-原人参二醇-3-酮(1)、达玛烷-20,24-二烯-3β-醇(2)、茸毛香杨梅酮(galeon)(3)、胡桃宁A(juglanin A)(4)、2a,3β,23-三羟基-12-烯-28-齐墩果酸(5)、2a,3β—23-三羟基-12-烯-28-熊果酸(6)、齐墩果酸(7)、熊果酸(8)。结论化合物1为首次从天然资源中分离得到的新天然产物;化合物2及5~8均为首次从胡桃属植物中分离得到,此前未见该属三萜类化合物的报道;化合物3为首次从青龙衣中分离得到。Objective To study the chemical components from the pericarps of Juglans mandshurica with anti-tumor activity. Methods It showed that pericarps of J. mandshurica had a good performance in treating cancer and low toxicity from CHC13 and EtOAc portions by a lot of pharmacological experiments and modern clinical application in the past. Compounds were isolated by chromatography on silica gel columns and AB-8 macroporous resin. On the basis of spectral evidences including 1D-NMR and 2D-NMR,the structures of these compounds were determined. Results These compounds from CHC13 portion were identified as 20(S)-protopanaxadiol-3-one (1), dammara-20, 24-dien-317-ol (2), galeon (3), juglanin A (4), 2a, 3β, 23-trihydroxy olean-12-en-28-oic acid (5), 2α, 3β, 23-trihydroxy urs-12-en-28-oic acid (6), oleanolic acid (7), ursolic acid (8). Conclusion Compound 1 is a new natural product. Compounds 2 and 5-8 are isolated firstly from the plants of Juglans L. which are due to pentacyclic triterpane. Compound 3 is isolated from the pericarps of J. mandshurica for the first time.
关 键 词:青龙衣 20(S)-原人参二醇-3-酮 抗肿瘤活性
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