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蛇床子和白芷中香豆素类化合物抑制磷酸二酯酶5活性的研究
引用本文:尉小慧,张树军,夏广新,付收,王伟,沈敬山,嵇汝运.蛇床子和白芷中香豆素类化合物抑制磷酸二酯酶5活性的研究[J].中国药学杂志,2006,41(2):100-101.
作者姓名:尉小慧  张树军  夏广新  付收  王伟  沈敬山  嵇汝运
作者单位:1. 中国科学院上海生命科学研究院上海药物研究所,上海,201203
2. 河南天方药业股份有限公司,河南,驻马店,463000
摘    要: 目的研究香豆素类化合物的PDE5抑制活性。方法用体积分数为95%乙醇和氯仿分别提取蛇床子及白芷中总香豆素类化合物,并通过柱色谱和HPLC进行分离,结构鉴定后进行PDE5抑制活性研究。结果分离得到8个化合物,结构修饰4 个化合物,并测得其PDE5抑制活性数据。结论蛇床子素具有较强的PDE5抑制剂。

关 键 词:蛇床子  白芷  香豆素类  PDE5抑制剂
文章编号:1001-2494(2005)16-0100-03
收稿时间:2005-01-16
修稿时间:2005-01-16

Inhibitation of Coumarins in Cnidium monnieri Cusson and Angelian dahuricn on PDE5
WEI Xiao-hui,ZHANG Shu-jun,XIA Guang-xin,FU Shou,WANG Wei,SHEN Jing-shan,JI Ru-yun.Inhibitation of Coumarins in Cnidium monnieri Cusson and Angelian dahuricn on PDE5[J].Chinese Pharmaceutical Journal,2006,41(2):100-101.
Authors:WEI Xiao-hui  ZHANG Shu-jun  XIA Guang-xin  FU Shou  WANG Wei  SHEN Jing-shan  JI Ru-yun
Institution:1. Shanghai Institute of Materia Medica , Shanghai Institutes for Biological Sciences , Chinese Academy of Sciences , Shanghai 201203, China ; 2. Topfond Pharmaceutical Inc , Zhumodian 463000, China
Abstract:OBJECTIVE To study the activity of coumarins as PDE5 inhibitor.METHODS The coumarins were extracted with 95% alcohol from Cnidium monnieri(L.) Cusson and with CHCl3 from Angelica dahurica Benth.et Hook.,and then isolated via column chromatog-raphy and HPLC. After structure identification, the inhibition of compounds on PDE5 was investigated according to the existing methods. RESULTS 8 compounds were isolated and identified, and 4 compounds were obtained by structure modification. The activities data as PDE5 inhibitors were tested. CONCLUSION Osthol showes the potent inhibitation on PDE5.
Keywords:Cnidium monnieri(L  ) Cusson  Angelica dahurica Benth  et Hook    coumarins  PDE5 inhibitor  
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