ID Name Structure References (top 5) Molecular Target(s)
1ID:5094
PHELLANDRENE


NSC#:1842
Aldrich#:77429
Aldrich#:77430

Freqency:
in 2 ingredients:

  • 244
  • 417
  • in 39 recipes:

  • 4
  • 37
  • 44
  • 100
  • 111
  • 142
  • 143
  • 146
  • 174
  • 181
  • 184
  • 200
  • 208
  • 229
  • 231
  • 236
  • 257
  • 268
  • 285
  • 289
  • 324
  • 339
  • 342
  • 352
  • 355
  • 361
  • 380
  • 412
  • 423
  • 430
  • 461
  • 469
  • 470
  • 472
  • 474
  • 475
  • 484
  • 502
  • 519

  • Properties
    C10H16    136.24





    1:  Savage TJ, Hatch MW, Croteau R.
    Monoterpene synthases of Pinus contorta and related conifers. A new class of terpenoid cyclase.
    J Biol Chem.    impact factor:   7.666
    1994;  269(6): 4012-20

    2:  Heyen U, Harder J.
    Geranic acid formation, an initial reaction of anaerobic monoterpene metabolism in denitrifying Alcaligenes defragrans.
    Appl Environ Microbiol.    impact factor:   3.541
    2000;  66(7): 3004-9

    3:  Harder J, Probian C.
    Microbial degradation of monoterpenes in the absence of molecular oxygen.
    Appl Environ Microbiol.    impact factor:   3.541
    1995;  61(11): 3804-8

    4:  Sklenska J, Broskovicova A, Vecera Z.
    Wet effluent diffusion denuder technique and the determination of volatile organic compounds in air. II. Monoterpenes.
    J Chromatogr A.    impact factor:   2.52
    2002;  973(1-2): 211-6

    5:  Bos R, Koulman A, Woerdenbag HJ, Quax WJ, Pras N.
    Volatile components from Anthriscus sylvestris (L.) Hoffm.
    J Chromatogr A.    impact factor:   2.52
    2002;  966(1-2): 233-8

     
    Time used: 484 milliseconds.

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