ID Name Structure References (top 5) Molecular Target(s)


in 2 ingredients:

  • 6
  • 488

  • Properties
    C20H22O7    374.39

    1:  Sefkow M.
    Enantioselective synthesis of (-)-wikstromol using a new approach via malic acid.
    J Org Chem.    impact factor:   3.44
    2001;  66(7): 2343-9

    2:  Yesilada E, Taninaka H, Takaishi Y, Honda G, Sezik E, Momota H, Ohmoto Y, Taki T.
    In vitro inhibitory effects of Daphne oleoides ssp. oleoides on inflammatory cytokines and activity-guided isolation of active constituents.
    Cytokine.    impact factor:   2.291
    2001;  13(6): 359-64

    3:  Torrance SJ, Hoffmann JJ, Cole JR.
    Wikstromol, antitumor lignan from Wikstroemia foetida var. oahuensis Gray and Wikstroemia uva-ursi Gray (Thymelaeaceae).
    J Pharm Sci.    impact factor:   2.27
    1979;  68(5): 664-5

    4:  Belletire JL, Ho DM, Fry DF.
    Stereoselectivity questions in the synthesis of wikstromol.
    J Nat Prod.    impact factor:   1.652
    1990;  53(6): 1587-92

    5:  Lee KH, Tagahara K, Suzuki H, Wu RY, Haruna M, Hall IH, Huang HC, Ito K, Iida T, Lai JS.
    Antitumor agents. 49 tricin, kaempferol-3-O-beta-D-glucopyranoside and (+)-nortrachelogenin, antileukemic principles from Wikstroemia indica.
    J Nat Prod.    impact factor:   1.652
    1981;  44(5): 530-5

    Time used: 94 milliseconds.

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