ID Name Structure References (top 5) Molecular Target(s)
1ID:2418
FRIEDELIN


NSC#:55141
Aldrich#:855022
Aldrich#:R221716

Freqency:
in 5 ingredients:

  • 214
  • 254
  • 267
  • 419
  • 856
  • in 68 recipes:

  • 20
  • 21
  • 22
  • 27
  • 30
  • 32
  • 49
  • 61
  • 63
  • 65
  • 73
  • 87
  • 101
  • 130
  • 131
  • 155
  • 156
  • 158
  • 170
  • 188
  • 189
  • 227
  • 232
  • 238
  • 241
  • 244
  • 247
  • 252
  • 259
  • 263
  • 272
  • 276
  • 278
  • 280
  • 288
  • 291
  • 293
  • 294
  • 301
  • 311
  • 314
  • 323
  • 324
  • 327
  • 346
  • 359
  • 361
  • 363
  • 367
  • 381
  • 403
  • 409
  • 410
  • 441
  • 443
  • 444
  • 446
  • 448
  • 449
  • 459
  • 485
  • 488
  • 490
  • 507
  • 515
  • 516
  • 519
  • 527

  • Properties
    C30H50O    426.72





    1:  Miura N, Matsumoto Y, Miyairi S, Nishiyama S, Naganuma A.
    Protective effects of triterpene compounds against the cytotoxicity of cadmium in HepG2 cells.
    Mol Pharmacol.    impact factor:   5.465
    1999;  56(6): 1324-8

    2:  Moiteiro C, Justino F, Tavares R, Marcelo-Curto MJ, Florencio MH, Nascimento MS, Pedro M, Cerqueira F, Pinto MM.
    Synthetic secofriedelane and friedelane derivatives as inhibitors of human lymphocyte proliferation and growth of human cancer cell lines in vitro.
    J Nat Prod.    impact factor:   1.652
    2001;  64(10): 1273-7

    3:  Chang CW, Wu TS, Hsieh YS, Kuo SC, Chao PD.
    Terpenoids of Syzygium formosanum.
    J Nat Prod.    impact factor:   1.652
    1999;  62(2): 327-8

    4:  Chavez H, Estevez-Braun A, Ravelo AG, Gonzalez AG.
    Friedelane triterpenoids from Maytenus macrocarpa.
    J Nat Prod.    impact factor:   1.652
    1998;  61(1): 82-5

    5:  Gunasekera SP, Cordell GA, Farnsworth NR.
    3 beta-hydroxy-28-P-coumaroyloxy-lup-20(29)-en-27-oic acid from Caraipa densifolia.
    J Nat Prod.    impact factor:   1.652
    1983;  46(1): 118-22

     
    Time used: 141 milliseconds.

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