ID Name Structure References (top 5) Molecular Target(s)
1ID:2921
HEDERAGENIN


NSC#:24954
NSC#:87530

Freqency:
in 5 ingredients:

  • 44
  • 225
  • 267
  • 384
  • 512
  • in 35 recipes:

  • 19
  • 32
  • 43
  • 47
  • 51
  • 61
  • 74
  • 77
  • 88
  • 90
  • 122
  • 126
  • 130
  • 223
  • 236
  • 260
  • 263
  • 272
  • 274
  • 278
  • 285
  • 289
  • 291
  • 297
  • 299
  • 324
  • 337
  • 338
  • 368
  • 370
  • 401
  • 405
  • 409
  • 515
  • 522

  • Properties
    C30H48O4    472.71





    1:  Nishino H, Nishino A, Takayasu J, Hasegawa T, Iwashima A, Hirabayashi K, Iwata S, Shibata S.
    Inhibition of the tumor-promoting action of 12-O-tetradecanoylphorbol-13-acetate by some oleanane-type triterpenoid compounds.
    Cancer Res.    impact factor:   8.614
    1988;  48(18): 5210-5

    2:  Suzuki H, Achnine L, Xu R, Matsuda SP, Dixon RA.
    A genomics approach to the early stages of triterpene saponin biosynthesis in Medicago truncatula.
    Plant J.    impact factor:   5.09
    2002;  32(6): 1033-48

    3:  Ying QL, Rinehart AR, Simon SR, Cheronis JC.
    Inhibition of human leucocyte elastase by ursolic acid. Evidence for a binding site for pentacyclic triterpenes.
    Biochem J.    impact factor:   4.349
    1991;  277 ( Pt 2): 521-6

    4:  Bomford R, Stapleton M, Winsor S, Beesley JE, Jessup EA, Price KR, Fenwick GR.
    Adjuvanticity and ISCOM formation by structurally diverse saponins.
    Vaccine.    impact factor:   3.173
    1992;  10(9): 572-7

    5:  Shinoda T, Nagao T, Nakayama M, Serizawa H, Koshioka M, Okabe H, Kawai A.
    Identification of a triterpenoid saponin from a crucifer, Barbarea vulgaris, as a feeding deterrent to the diamondback moth, Plutella xylostella.
    J Chem Ecol.    impact factor:   1.653
    2002;  28(3): 587-99

     
    Time used: 172 milliseconds.

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