检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:曾志[1,2] 谢润乾[1] 张涛[2,3] 谭丽贤[1] 庾秀英[1]
机构地区:[1]华南师范大学化学与环境学院,广东广州510631 [2]Faculty of Bioresource Sciences,Akita Prefectural University,Akita 010-0195,Japan [3]华南师范大学光电材料与技术研究所,广东广州510631
出 处:《质谱学报》2011年第5期293-300,共8页Journal of Chinese Mass Spectrometry Society
基 金:广东省科技计划重大专项(No.A301020101);广东省自然科学基金(No.01142)资助
摘 要:质谱学在中药药效物质的结构确定中起至关重要的作用,对每一个化合物质谱的确切解释需要对每一个质谱的关键裂解过程具有足够的了解。本研究报道了川芎中具有不饱和侧链与饱和侧链内酯类化合物的质谱学规律。质谱特征峰[M+-29]和[M+-42]表明了从这些内酯类化合物的分子离子分别失去不饱和侧链上的末端烷基-C2H5和-C3H6基团,这是川芎中具有不饱和侧链内酯类化合物(如(Z)-藁本内酯、(E)-藁本内酯、丁烯基酞内酯和川芎内酯I)的典型质谱特征;质谱特征峰[M+-57]显示了从这些内酯类化合物的分子离子失去饱和侧链-C4H9基团,这是川芎中具有饱和侧链内酯类化合物(如丁基酞内酯和川芎内酯A)的典型质谱特征。Mass spectrometry plays a crucial role in the structure elucidation of those effec- tive substances from traditional Chinese medicine. Secure interpretation of the mass spec- trum of each compound requires an adequate understanding of the key fragmentation process of the mass spectrum. In this paper, the regular patterns of mass spectrometry of lactones with unsaturated side chain and with saturated side chain from Ligusticum chuanxiong Hort. were reported. The diagnostic peaks at [M+ --29-] and [M+ --42] show the molecular ion of the lactones losses a --Cz H5 group and a --Ca H6 group, respectively, the terminalalkyl groups from the unsaturated side chain. They are typical characteristm ot the mass spectra of the lactones with unsaturated side chain from Ligusticum chuanxiong Hort. , such as (Z)-ligustilide, (E)-ligustilide, butylidene phthalide and senkyunolide I. The char- acteristic peak at [M+ --57] displays the molecular ion of the lactones losses a -C4H9 group from the saturated side chain. This is typical characteristic of the mass spectra of the lactones with saturated side chain from Ligusticum chuanxiong Hort., such as bu- tylphthalide and senkyunolide A.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.51