ID Name Structure References (top 5) Molecular Target(s)
1ID:3893
LINALOOL


NSC#:3789
Aldrich#:62139
Aldrich#:62140
Aldrich#:L2602

Freqency:
in 7 ingredients:

  • 467
  • 509
  • 624
  • 660
  • 726
  • 901
  • 906
  • in 18 recipes:

  • 43
  • 56
  • 64
  • 80
  • 89
  • 202
  • 219
  • 233
  • 236
  • 274
  • 289
  • 304
  • 309
  • 312
  • 342
  • 369
  • 489
  • 515

  • Properties
    C10H18O    154.25





    1:  Brown K.
    Plant genetics. Plants 'speak' using versatile volatiles.
    Science.    impact factor:   24.595
    2002;  296(5577): 2329

    2:  Liu B, Duan S, Sutterer AC, Moeller KD.
    Oxidative cyclization based on reversing the polarity of enol ethers and ketene dithioacetals. Construction of a tetrahydrofuran ring and application to the synthesis of (+)-nemorensic Acid.
    J Am Chem Soc.    impact factor:   5.537
    2002;  124(34): 10101-11

    3:  Lucker J, Bouwmeester HJ, Schwab W, Blaas J, van der Plas LH, Verhoeven HA.
    Expression of Clarkia S-linalool synthase in transgenic petunia plants results in the accumulation of S-linalyl-beta-D-glucopyranoside.
    Plant J.    impact factor:   5.09
    2001;  27(4): 315-24

    4:  Niinemets U, Reichstein M, Staudt M, Seufert G, Tenhunen JD.
    Stomatal Constraints May Affect Emission of Oxygenated Monoterpenoids from the Foliage of Pinus pinea.
    Plant Physiol.    impact factor:   4.434
    2002;  130(3): 1371-85

    5:  Lewinsohn E, Schalechet F, Wilkinson J, Matsui K, Tadmor Y, Nam KH, Amar O, Lastochkin E, Larkov O, Ravid U, Hiatt W, Gepstein S, Pichersky E.
    Enhanced levels of the aroma and flavor compound S-linalool by metabolic engineering of the terpenoid pathway in tomato fruits.
    Plant Physiol.    impact factor:   4.434
    2001;  127(3): 1256-65

     
    Time used: 125 milliseconds.

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