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药西瓜中3个新的葫芦烷型三萜苷及其抗炎活性研究 被引量:2

Three new cucurbitane-type triterpenoid glycosides from Citrullus colocynthis and their anti-inflammatory activity
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摘要 综合运用多种色谱技术从药西瓜乙酸乙酯提取物中分离得到3个新的葫芦烷型三萜苷。利用核磁、高分辨质谱等技术及对照文献鉴定其结构为colocynthenin E(1)、colocynthenin G(2)、colocynthenin H(3)。通过LPS诱导的RAW264.7巨噬细胞炎症模型对新化合物1~3进行了抗炎活性的测定,结果表明,与阳性对照dexamethasone(IC_(50)=7.57μmol·L-1)相比,化合物2和3显示出微弱的抗炎活性,IC50分别为48.21、40.11μmol·L^(-1)。 Three new cucurbitane-type triterpenoid glycosides were separated from the ethyl acetate extract of Citrullus colocynthis by a variety of chromatographic techniques.According to the data of NMR,HR-ESI-MS,and/or comparison with the reported data,the three novel cucurbitane-type triterpenoid glycosides were identified as colocynthenin E(1),colocynthenin G(2),and colocynthenin H(3).The cell inflammation model was established with RAW264.7 macrophages exposed to lipopolysaccharide and then used to determine the anti-inflammatory activities of the three compounds.Compounds 2 and 3 showed mild anti-inflammatory activities with the IC_(50)of 48.21 and 40.11μmol·L^(-1),respectively,compared with that(IC_(50)=7.57μmol·L~(-1))of the positive control dexamethasone.
作者 吴俊凌 刘玉霜 赵曦 袁涛 WU Jun-ling;LIU Yu-shuang;ZHAO Xi;YUAN Tao(College of Life Sciences,Jiangxi Normal University,Nanchang 330022,China;Xinjiang Technical Institute of Physics and Chemistry,Chinese Academy of Sciences,Urumqi 83001l,China)
出处 《中国中药杂志》 CAS CSCD 北大核心 2023年第15期4124-4129,共6页 China Journal of Chinese Materia Medica
基金 江西省“双千计划”项目(jxsq2018101008)。
关键词 药西瓜 化学成分 葫芦烷型三萜苷 抗炎活性 Citrullus colocynthis chemical constituents cucurbitane-type triterpenoid glycosides anti-inflammatory activity
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  • 1余爱琴.什么是糖尿病?糖尿病有危害吗?[J].临床医学工程,1997,10(4):28-28. 被引量:1
  • 2王雪芬,卢文杰,陈家源,龚敏阳,李宇红,卢多,吕杨,郑启泰.罗汉果根化学成分的研究(Ⅰ)[J].中草药,1996,27(9):515-518. 被引量:23
  • 3新疆甜瓜西瓜资源调查组.新疆甜瓜西瓜志[M].乌鲁木齐:新疆人民出版社,1985.
  • 4Podlasek CA, Wu J, Stripe WA, et al. [^13C] Enriched methyl aldopyranosides: structural interpretations of ^13C-^1H spin-coupling constants and ^1H chemical shifts [J]. J Am Chem Soc, 1995, 117: 8635-8644.
  • 5Shashkov AS. ^13C NMR spectra of parent hexopyranoses [J]. Russ Chem Bull, 1983, 32: 1200-1207.
  • 6Yu DQ, Yang JS. Analytical Chemistry Handbook(分析化学手册).Analysis of Nuclear Magnetic Resonance Spectroscopy(核磁共振波谱解析)[M].Beijing: Chemical Industry Press,2002: 492.
  • 7Snyder JR, Serianni AS. D-Idose: a one- and two-dimensional NMR investigation of solution composition and conformation [J]. J Org Chem, 1986, 51: 2694-2702.
  • 8Bock K, Pedersen C. Carbon-13 nuclear magnetic resonance spectroscopy of monosaccharides [J]. Adv Carbohydr Chem Biochem, 1983, 41: 27-66.
  • 9Gong YH, Ding LS. ^13C NMR Analysis of Natural Products(天然产物核磁共振碳谱分析)[M].Kunming: Yurman Science and Technology Press, 2006: 856.
  • 10King-Morris MJ, Serianni AS. ^13C NMR studies of [1-^13C] aldoses: empirical rules correlating pyranose ring configuration and conformation with ^13C chemical shifts and ^13C-^13C spin couplings [J]. J Am Chem Soc, 1987, 109: 3501-3508.

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