ID Name Structure References (top 5) Molecular Target(s)
1ID:3090
HUMULENE


Aldrich#:53675
Aldrich#:H5887

Freqency:
in 8 ingredients:

  • 5
  • 80
  • 119
  • 177
  • 419
  • 531
  • 624
  • 901
  • in 59 recipes:

  • 4
  • 8
  • 13
  • 37
  • 43
  • 81
  • 83
  • 89
  • 98
  • 100
  • 107
  • 109
  • 123
  • 136
  • 138
  • 166
  • 176
  • 202
  • 206
  • 208
  • 212
  • 218
  • 219
  • 223
  • 228
  • 233
  • 234
  • 274
  • 308
  • 309
  • 316
  • 335
  • 339
  • 341
  • 342
  • 343
  • 344
  • 345
  • 349
  • 351
  • 352
  • 353
  • 354
  • 364
  • 378
  • 380
  • 387
  • 402
  • 412
  • 415
  • 416
  • 420
  • 425
  • 465
  • 469
  • 478
  • 489
  • 492
  • 519

  • Properties
    C15H24    204.35





    1:  van Der Hoeven RS, Monforte AJ, Breeden D, Tanksley SD, Steffens JC.
    Genetic control and evolution of sesquiterpene biosynthesis in Lycopersicon esculentum and L. hirsutum.
    Plant Cell.    impact factor:   10.463
    2000;  12(11): 2283-94

    2:  Steele CL, Crock J, Bohlmann J, Croteau R.
    Sesquiterpene synthases from grand fir (Abies grandis). Comparison of constitutive and wound-induced activities, and cDNA isolation, characterization, and bacterial expression of delta-selinene synthase and gamma-humulene synthase.
    J Biol Chem.    impact factor:   7.666
    1998;  273(4): 2078-89

    3:  Murakami A, Takahashi D, Kinoshita T, Koshimizu K, Kim HW, Yoshihiro A, Nakamura Y, Jiwajinda S, Terao J, Ohigashi H.
    Zerumbone, a Southeast Asian ginger sesquiterpene, markedly suppresses free radical generation, proinflammatory protein production, and cancer cell proliferation accompanied by apoptosis: the alpha,beta-unsaturated carbonyl group is a prerequisite.
    Carcinogenesis.    impact factor:   4.118
    2002;  23(5): 795-802

    4:  Hu T, Corey EJ.
    Short syntheses of (+/-)-delta-araneosene and humulene utilizing a combination of four-component assembly and palladium-mediated cyclization.
    Org Lett.    impact factor:   3.367
    2002;  4(14): 2441-3

    5:  Adlington RM, Baldwin JE, Mayweg AV, Pritchard GJ.
    Biomimetic cycloaddition approach to tropolone natural products via a tropolone ortho-quinone methide.
    Org Lett.    impact factor:   3.367
    2002;  4(17): 3009-11

     
    Time used: 437 milliseconds.

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