ID Name Structure References (top 5) Molecular Target(s)
1ID:1942
DIOSCIN


NSC#:115920

Freqency:
in 5 ingredients:

  • 197
  • 530
  • 654
  • 823
  • 854
  • in 59 recipes:

  • 1
  • 31
  • 53
  • 61
  • 64
  • 65
  • 68
  • 79
  • 82
  • 84
  • 115
  • 140
  • 149
  • 154
  • 159
  • 160
  • 171
  • 175
  • 176
  • 182
  • 190
  • 192
  • 203
  • 204
  • 230
  • 262
  • 272
  • 278
  • 280
  • 285
  • 289
  • 293
  • 301
  • 309
  • 312
  • 314
  • 318
  • 338
  • 340
  • 341
  • 344
  • 346
  • 392
  • 406
  • 409
  • 421
  • 433
  • 437
  • 439
  • 442
  • 443
  • 453
  • 471
  • 473
  • 493
  • 507
  • 512
  • 514
  • 520

  • Properties
    C45H72O16    869.05





    1:  Tal B, Tamir I, Rokem JS, Goldberg I.
    Isolation and characterization of an intermediate steroid metabolite in diosgenin biosynthesis in suspension cultures of Dioscorea deltoidea cells.
    Biochem J.    impact factor:   4.349
    1984;  219(2): 619-24

    2:  Yu B, Tao H.
    Glycosyl trifluoroacetimidates. 2. Synthesis of dioscin and xiebai saponin I.
    J Org Chem.    impact factor:   3.44
    2002;  67(25): 9099-102

    3:  Squibb RE Jr, Squibb RL.
    Effect of food toxicants on voluntary wheel running in rats.
    J Nutr.    impact factor:   2.15
    1979;  109(5): 767-72

    4:  Aquino R, Conti C, De Simone F, Orsi N, Pizza C, Stein ML.
    Antiviral activity of constituents of Tamus communis.
    J Chemother.    impact factor:   2.081
    1991;  3(5): 305-9

    5:  Mi Q, Lantvit D, Reyes-Lim E, Chai H, Zhao W, Lee IS, Peraza-Sanchez S, Ngassapa O, Kardono LB, Riswan S, Hollingshead MG, Mayo JG, Farnsworth NR, Cordell GA, Kinghorn AD, Pezzuto JM.
    Evaluation of the potential cancer chemotherapeutic efficacy of natural product isolates employing in vivo hollow fiber tests.
    J Nat Prod.    impact factor:   1.652
    2002;  65(6): 842-50

     
    Time used: 125 milliseconds.

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