ID Name Structure References (top 5) Molecular Target(s)
1ID:7590
PINORESINOL


NSC#:35444

Freqency:
in 2 ingredients:

  • 6
  • 669
  • in 27 recipes:

  • 58
  • 72
  • 74
  • 91
  • 108
  • 114
  • 121
  • 139
  • 152
  • 167
  • 226
  • 230
  • 306
  • 315
  • 322
  • 324
  • 327
  • 343
  • 359
  • 360
  • 371
  • 391
  • 398
  • 418
  • 436
  • 459
  • 466

  • Properties
    C20H22O6    358.39





    1:  Davin LB, Wang HB, Crowell AL, Bedgar DL, Martin DM, Sarkanen S, Lewis NG.
    Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center.
    Science.    impact factor:   24.595
    1997;  275(5298): 362-6

    2:  Gang DR, Kasahara H, Xia ZQ, Vander Mijnsbrugge K, Bauw G, Boerjan W, Van Montagu M, Davin LB, Lewis NG.
    Evolution of plant defense mechanisms. Relationships of phenylcoumaran benzylic ether reductases to pinoresinol-lariciresinol and isoflavone reductases.
    J Biol Chem.    impact factor:   7.666
    1999;  274(11): 7516-27

    3:  Fujita M, Gang DR, Davin LB, Lewis NG.
    Recombinant pinoresinol-lariciresinol reductases from western red cedar (Thuja plicata) catalyze opposite enantiospecific conversions.
    J Biol Chem.    impact factor:   7.666
    1999;  274(2): 618-27

    4:  Dinkova-Kostova AT, Gang DR, Davin LB, Bedgar DL, Chu A, Lewis NG.
    (+)-Pinoresinol/(+)-lariciresinol reductase from Forsythia intermedia. Protein purification, cDNA cloning, heterologous expression and comparison to isoflavone reductase.
    J Biol Chem.    impact factor:   7.666
    1996;  271(46): 29473-82

    5:  Eberhardt TL, Bernards MA, He L, Davin LB, Wooten JB, Lewis NG.
    Lignification in cell suspension cultures of Pinus taeda. In situ characterization of a gymnosperm lignin.
    J Biol Chem.    impact factor:   7.666
    1993;  268(28): 21088-96

     
    Time used: 125 milliseconds.

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