New antimicrobial pregnane glycosides from the stem of Ecdysanthera rosea.

Phytochemical investigation on the stem of Ecdysanthera rosea led to the isolation of eight new C-21 pregnane glycoside ecdysosides A–H ( 1 – 8 ), together with one known pregnane glycoside ecdysantheroside A ( 9 ). Their structures were elucidated based on extensive spectroscopic data (MS, IR, 1D a...

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Publicado en:Fitoterapia Vol. 99; pp. 267 - 276
Autores principales: Song, Chang-Wei, Lunga, Paul-Keilah, Qin, Xu-Jie, Cheng, Gui-Guang, Gu, Jian-Long, Liu, Ya-Ping, Luo, Xiao-Dong
Formato: Journal Article
Publicado: Elsevier B.V. Dec2014
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Dec2014
      vid: 99
      pid: 467
      pub: Elsevier B.V.
      place: New York, New York
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        10.1016/j.fitote.2014.10.008
        99919208
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        atl: New antimicrobial pregnane glycosides from the stem of Ecdysanthera rosea.
      aug:
        au:
          Song, Chang-Wei
          Lunga, Paul-Keilah
          Qin, Xu-Jie
          Cheng, Gui-Guang
          Gu, Jian-Long
          Liu, Ya-Ping
          Luo, Xiao-Dong
        affil: State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, People's Republic of China
      sug:
        subj:
          Plants, Medicinal
          Plant Stems
          Plant Extracts Analysis
          Plant Extracts Pharmacodynamics
          Antiinfective Agents Pharmacodynamics
          Glycosides Analysis
          Alternative Therapies
          In Vitro Studies
          Microbial Culture and Sensitivity Tests
          Magnetic Resonance Spectroscopy
          Mass Spectrometry
          Enterococcus
          Cryptococcus
          Dose-Response Relationship, Drug
          Descriptive Statistics
          Chemistry, Physical
      ab: Phytochemical investigation on the stem of Ecdysanthera rosea led to the isolation of eight new C-21 pregnane glycoside ecdysosides A–H ( 1 – 8 ), together with one known pregnane glycoside ecdysantheroside A ( 9 ). Their structures were elucidated based on extensive spectroscopic data (MS, IR, 1D and 2D NMR) analysis, as well as comparison with the reported literature data. Antimicrobial activities of all the compounds were evaluated against bacteria and yeasts. Compounds 1 , 9 , 3 and 5 exhibited moderate antibacterial activities against respective Enterococcus faecalis and Providensia smartii , with MIC value of 12.5 μg/mL. Compound 8 showed significant anti-yeast activity against Cryptococcus neoformans with MIC value of 12.5 μg/mL.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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