ID Name Structure References (top 5) Molecular Target(s)
1ID:5598
ROSEOSIDE

Freqency:
in 1 ingredients:

  • 13
  • in 22 recipes:

  • 20
  • 21
  • 26
  • 77
  • 78
  • 101
  • 146
  • 158
  • 232
  • 241
  • 245
  • 288
  • 291
  • 311
  • 312
  • 332
  • 363
  • 381
  • 413
  • 430
  • 452
  • 490

  • Properties
    C21H34O8    414.49





    1:  Ito H, Kobayashi E, Li SH, Hatano T, Sugita D, Kubo N, Shimura S, Itoh Y, Tokuda H, Nishino H, Yoshida T.
    Antitumor activity of compounds isolated from leaves of Eriobotrya japonica.
    J Agric Food Chem.    impact factor:   1.56
    2002;  50(8): 2400-3

    2:  Lee TH, Wang GJ, Lee CK, Kuo YH, Chou CH.
    Inhibitory effects of glycosides from the leaves of Melaleuca quinquenervia on vascular contraction of rats.
    Planta Med.    impact factor:   1.438
    2002;  68(6): 492-6

    3:  Murai Y, Kashimura S, Tamezawa S, Hashimoto T, Takaoka S, Asakawa Y, Kiguchi K, Murai F, Tagawa M.
    Absolute configuration of (6S,9S)-roseoside from Polygonum hydropiper.
    Planta Med.    impact factor:   1.438
    2001;  67(5): 480-1

    4:  Doi K, Kojima T, Makino M, Kimura Y, Fujimoto Y.
    Studies on the constituents of the leaves of Morus alba L.
    Chem Pharm Bull (Tokyo).    impact factor:   1.117
    2001;  49(2): 151-3

    5:  Abe F, Yamauchi T.
    5,11-Epoxymegastigmanes from the leaves of Asclepias fruticosa).
    Chem Pharm Bull (Tokyo).    impact factor:   1.117
    2000;  48(12): 1908-11

     
    Time used: 110 milliseconds.

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