ID Name Structure References (top 5) Molecular Target(s)
1ID:4920
PACHYMIC ACID


NSC#:244427

Freqency:
in 1 ingredients:

  • 185
  • in 70 recipes:

  • 3
  • 20
  • 21
  • 22
  • 27
  • 30
  • 45
  • 48
  • 49
  • 63
  • 73
  • 79
  • 85
  • 95
  • 107
  • 109
  • 110
  • 123
  • 128
  • 131
  • 133
  • 135
  • 151
  • 157
  • 160
  • 169
  • 171
  • 177
  • 180
  • 187
  • 200
  • 225
  • 227
  • 241
  • 248
  • 252
  • 255
  • 272
  • 276
  • 279
  • 280
  • 287
  • 292
  • 301
  • 309
  • 311
  • 312
  • 323
  • 338
  • 346
  • 359
  • 361
  • 375
  • 381
  • 383
  • 402
  • 403
  • 405
  • 410
  • 450
  • 484
  • 488
  • 490
  • 507
  • 510
  • 515
  • 520
  • 523
  • 524
  • 527

  • Properties
    C33H52O5    528.77





    1:  Cuella MJ, Giner RM, Recio MC, Just MJ, Manez S, Rios JL.
    Two fungal lanostane derivatives as phospholipase A2 inhibitors.
    J Nat Prod.    impact factor:   1.652
    1996;  59(10): 977-9

    2:  Giner EM, Manez S, Recio MC, Giner RM, Cerda-Nicolas M, Rios JL.
    In vivo studies on the anti-inflammatory activity of pachymic and dehydrotumulosic acids.
    Planta Med.    impact factor:   1.438
    2000;  66(3): 221-7

    3:  Keller AC, Maillard MP, Hostettmann K.
    Antimicrobial steroids from the fungus Fomitopsis pinicola.
    Phytochemistry.    impact factor:   1.106
    1996;  41(4): 1041-6

    4:  Kaminaga T, Yasukawa K, Kanno H, Tai T, Nunoura Y, Takido M.
    Inhibitory effects of lanostane-type triterpene acids, the components of Poria cocos, on tumor promotion by 12-O-tetradecanoylphorbol-13-acetate in two-stage carcinogenesis in mouse skin.
    Oncology.    impact factor:   0
    1996;  53(5): 382-5

     
    Time used: 110 milliseconds.

    Webpage designed by Dr. Xueliang Fang, last updated on 3/10/2005