ID Name Structure References (top 5) Molecular Target(s)
1ID:462
AROMADENDRENE


Aldrich#:05680
Aldrich#:11067

Freqency:
in 2 ingredients:

  • 92
  • 624
  • in 47 recipes:

  • 20
  • 21
  • 22
  • 27
  • 30
  • 43
  • 49
  • 80
  • 96
  • 107
  • 110
  • 156
  • 161
  • 169
  • 173
  • 199
  • 202
  • 219
  • 233
  • 241
  • 252
  • 272
  • 274
  • 280
  • 291
  • 292
  • 301
  • 308
  • 309
  • 342
  • 346
  • 361
  • 363
  • 376
  • 381
  • 403
  • 437
  • 441
  • 446
  • 449
  • 456
  • 459
  • 469
  • 488
  • 489
  • 490
  • 520

  • Properties
    C15H24    204.35





    1:  Buchi G, Hofheinz W, Paukstelis JV.
    The total synthesis of (-)-aromadendrene.
    J Am Chem Soc.    impact factor:   5.537
    1966;  88(17): 4113-4

    2:  Knight TE, Hausen BM.
    Melaleuca oil (tea tree oil) dermatitis.
    J Am Acad Dermatol.    impact factor:   1.905
    1994;  30(3): 423-7

    3:  da Cruz Francisco J, Jarvenpaa EP, Huopalahti R, Sivik B.
    Comparison of eucalyptus camaldulensis Dehn. oils from Mozambique as obtained by hydrodistillation and supercritical carbon dioxide extraction.
    J Agric Food Chem.    impact factor:   1.56
    2001;  49(5): 2339-42

    4:  Betts TJ.
    Solid phase microextraction of volatile constituents from individual fresh Eucalyptus leaves of three species.
    Planta Med.    impact factor:   1.438
    2000;  66(2): 193-5

    5:  Kaplan MA, Pugialli HR, Lopes D, Gottlieb HE.
    The stereochemistry of ledol from Renealmia chrysotrycha: an NMR study.
    Phytochemistry.    impact factor:   1.106
    2000;  55(7): 749-53

     
    Time used: 109 milliseconds.

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