南京中医药大学学报
南京中醫藥大學學報
남경중의약대학학보
JOURNAL OF NANJING UNIVERSITY OF TRADITIONAL CHINESE MEDICINE
2010年
2期
126-129,Ⅲ,Ⅳ
,共6页
陈东军%王磊%祖晓冬%王超磊%徐进宜
陳東軍%王磊%祖曉鼕%王超磊%徐進宜
진동군%왕뢰%조효동%왕초뢰%서진의
大黄素%提取%NMR%结构测定
大黃素%提取%NMR%結構測定
대황소%제취%NMR%결구측정
Emodin%extract%NMR%structure analysis
目的通过NMR定性研究大黄素的结构以及大黄素结构中的活泼性部位,为大黄素的化学结构修饰提供依据.方法从虎杖中高效提取了蒽醌类化合物大黄素,采用1D和2D-NMR的分析方法对大黄素结构进行鉴定,通过NMR变温技术及NOESY技术研究活泼性部位.结果以DMSO为溶剂、TMS作内标,采用~1HNMR,~(13)CNMR,DEPF,~1H-~1H COSY,NOESY,HSQC,HMBC等多种核磁共振方法对大黄素氢谱、碳谱进行完整归属,并通过NMR变温技术及NOESY的研究确定了其结构的活泼性部位.结论大黄素的3位羟基为其活泼性部位,该信息为大黄素的结构修饰以及衍生物的设计与抗肿瘤活性研究提供了物质基础.
目的通過NMR定性研究大黃素的結構以及大黃素結構中的活潑性部位,為大黃素的化學結構脩飾提供依據.方法從虎杖中高效提取瞭蒽醌類化閤物大黃素,採用1D和2D-NMR的分析方法對大黃素結構進行鑒定,通過NMR變溫技術及NOESY技術研究活潑性部位.結果以DMSO為溶劑、TMS作內標,採用~1HNMR,~(13)CNMR,DEPF,~1H-~1H COSY,NOESY,HSQC,HMBC等多種覈磁共振方法對大黃素氫譜、碳譜進行完整歸屬,併通過NMR變溫技術及NOESY的研究確定瞭其結構的活潑性部位.結論大黃素的3位羥基為其活潑性部位,該信息為大黃素的結構脩飾以及衍生物的設計與抗腫瘤活性研究提供瞭物質基礎.
목적통과NMR정성연구대황소적결구이급대황소결구중적활발성부위,위대황소적화학결구수식제공의거.방법종호장중고효제취료은곤류화합물대황소,채용1D화2D-NMR적분석방법대대황소결구진행감정,통과NMR변온기술급NOESY기술연구활발성부위.결과이DMSO위용제、TMS작내표,채용~1HNMR,~(13)CNMR,DEPF,~1H-~1H COSY,NOESY,HSQC,HMBC등다충핵자공진방법대대황소경보、탄보진행완정귀속,병통과NMR변온기술급NOESY적연구학정료기결구적활발성부위.결론대황소적3위간기위기활발성부위,해신식위대황소적결구수식이급연생물적설계여항종류활성연구제공료물질기출.
OBJECTIVE In order to develop novel anti - tumor agents by modify the structure of Emodin, Studies on the extraction of Emodin and the analysis of structure by NMR were conducted.METHOD The process of extracting Emodin from Polyonum cupida-tum Sieb. Et Zucc was optimized and some changes have been developed with improved overall yield. The structure of Emodin was analyzed by NMR 1D and 2D spectra. By changing temperature technique and NOSEY technique in NMR, the active site of Emodin structure was investigated. RESULT The Proton and 13Carbon spectra of Emodin were assigned completely by 1HNMR, 13CNMR, DEPT, COSY , HSQC, HMBC and NOESY methods. The active site of Emodin structure was verified by changing temperature technique and NOSEY technique in NMR, then structure modifications were performed. CONCLUSION 3-Hydroxy of Emodin is the active site of structure and this information will supply a material basis for anti - tumor activity research of Emodin derivatives.