ID Name Structure References (top 5) Molecular Target(s)
1ID:823
CAMPHENE


NSC#:4165
Aldrich#:21290
Aldrich#:310425
Aldrich#:456055
Aldrich#:C301

Freqency:
in 10 ingredients:

  • 12
  • 177
  • 288
  • 458
  • 501
  • 509
  • 584
  • 715
  • 726
  • 906
  • in 32 recipes:

  • 6
  • 39
  • 67
  • 80
  • 89
  • 96
  • 109
  • 111
  • 145
  • 147
  • 173
  • 181
  • 210
  • 223
  • 236
  • 269
  • 270
  • 287
  • 292
  • 312
  • 317
  • 324
  • 332
  • 334
  • 342
  • 369
  • 376
  • 428
  • 469
  • 472
  • 485
  • 507

  • Properties
    C10H16    136.24





    1:  Wise ML, Savage TJ, Katahira E, Croteau R.
    Monoterpene synthases from common sage (Salvia officinalis). cDNA isolation, characterization, and functional expression of (+)-sabinene synthase, 1,8-cineole synthase, and (+)-bornyl diphosphate synthase.
    J Biol Chem.    impact factor:   7.666
    1998;  273(24): 14891-9

    2:  Croteau R, Satterwhite DM.
    Biosynthesis of monoterpenes. Stereochemical implications of acyclic and monocyclic olefin formation by (+)- and (-)-pinene cyclases from sage.
    J Biol Chem.    impact factor:   7.666
    1989;  264(26): 15309-15

    3:  Croteau R, Satterwhite DM, Cane DE, Chang CC.
    Biosynthesis of monoterpenes. Enantioselectivity in the enzymatic cyclization of (+)- and (-)-linalyl pyrophosphate to (+)- and (-)-pinene and (+)- and (-)-camphene.
    J Biol Chem.    impact factor:   7.666
    1988;  263(21): 10063-71

    4:  Gambliel H, Croteau R.
    Pinene cyclases I and II. Two enzymes from sage (Salvia officinalis) which catalyze stereospecific cyclizations of geranyl pyrophosphate to monoterpene olefins of opposite configuration.
    J Biol Chem.    impact factor:   7.666
    1984;  259(2): 740-8

    5:  Smith WB.
    A DFT Study of the Camphene Hydrochloride Rearrangement.
    J Org Chem.    impact factor:   3.44
    1999;  64(1): 60-64

    P450
    STEP
     
    Time used: 547 milliseconds.

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