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作 者:王文雪[1,2] 娄京荣 牟艳玲[2] 郑重飞[2] 李莹[2] 姚庆强[2] WANG Wen-xue;LOU Jing-rong;MU Yan-ling;ZHENG Zhong-fei;LI Ying;YAO Qing-qiang(Sehool of Medicine and Life Sciences,University of Jinan-Shandong Academy of Medical Sciences,Jinan 250200,China;Institute of Materia Medica,Shandong Academy of Medical Sciences,Key Laboratory for Biotech-Drugs Ministry of Health,Key Laboratory for Rare & Uncommon Diseases of Shandong Province,Jinan 250062,China)
机构地区:[1]济南大学-山东省医学科学院/医学与生命科学学院,山东济南250200 [2]山东省医学科学院药物研究所/国家卫生部生物技术药物重点实验室/山东省罕少见病重点实验室,山东济南250062
出 处:《中药材》2017年第12期2844-2848,共5页Journal of Chinese Medicinal Materials
基 金:山东省自主创新及成果转化专项(2014ZZCX02105)
摘 要:目的:研究金佛山雪胆块根乙酸乙酯部位的化学成分。方法:利用硅胶柱色谱、ODS反相柱色谱、HPLC制备色谱等技术分离纯化化合物,根据化合物的波谱数据分析鉴定化合物结构。结果:从金佛山雪胆块根乙酸乙酯部位中共分离鉴定了11个化合物,分别为:scandenoside R8(1)、3-O-β-D-glucopyranosyl-3β,27-dihydroxycucurbita-5,24(Z)-diene-11-one-27-O-β-D-glucopyranoside(2)、短柄雪胆苷A(3)、scandenoside R3(4)、scandenoside R4(5)、jinfushanoside J(6)、carnosiflosideⅤ(7)、carnosiflosideⅢ(8)、scandenoside R6(9)、jinfushanoside K(10)、雪胆双糖(11)。结论:其中,化合物4、5、7、9、11为首次从该植物中分离得到,并首次归属了化合物11的羟基信号。Objective: To study the chemical constituents of the ethyl acetate extract of the tubers of Hemsleya pengxianensis var. jinfushanensis. Methods: The compounds were isolated by various chromatographic techniques,including silica gel,ODS reversed phase column and preparative high-performance liquid. The structures were identified on the basis of MS and NMR data. Results: Eleven compounds were obtained from the ethyl acetate fraction of the tubers of Hemsleya pengxianensis var. jinfushanensis and identified as scandenoside R8( 1),3-O-β-D-glucopyranosyl-3β,27-dihydroxycucurbita-5,24( Z)-diene-11-one-27-O-β-D-glucopyranoside( 2),delavanoside A( 3),scandenoside R3( 4),scandenoside R4( 5),jinfushanoside J( 6),carnosifloside Ⅴ( 7),carnosifloside Ⅲ( 8),scandenoside R6( 9),jinfushanoside K( 10),amabiose( 11). Conclusion: Compounds 4,5,7,9,11 are isolated from this plant for the first time,and the hydroxyl signals of compound 11 are identified for the first time.
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