ID Name Structure References (top 5) Molecular Target(s)
1ID:6586
VANILLIC ACID


NSC#:3987
NSC#:407800
NSC#:674322
Aldrich#:94770
Aldrich#:H36001
Aldrich#:V2250

Freqency:
in 6 ingredients:

  • 5
  • 27
  • 88
  • 214
  • 238
  • 430
  • in 77 recipes:

  • 8
  • 20
  • 21
  • 22
  • 27
  • 30
  • 32
  • 49
  • 63
  • 73
  • 87
  • 101
  • 107
  • 131
  • 155
  • 156
  • 158
  • 161
  • 170
  • 188
  • 189
  • 190
  • 212
  • 227
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  • 238
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  • 241
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  • 247
  • 252
  • 259
  • 263
  • 272
  • 278
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  • 288
  • 289
  • 291
  • 292
  • 293
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  • 301
  • 305
  • 308
  • 311
  • 323
  • 324
  • 327
  • 338
  • 346
  • 351
  • 359
  • 361
  • 363
  • 367
  • 381
  • 403
  • 410
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  • 441
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  • 448
  • 449
  • 456
  • 459
  • 485
  • 488
  • 490
  • 507
  • 515
  • 516
  • 519
  • 527

  • Properties
    C8H8O4    168.15





    1:  Mayer MJ, Narbad A, Parr AJ, Parker ML, Walton NJ, Mellon FA, Michael AJ.
    Rerouting the plant phenylpropanoid pathway by expression of a novel bacterial enoyl-CoA hydratase/lyase enzyme function.
    Plant Cell.    impact factor:   10.463
    2001;  13(7): 1669-82

    2:  Shimoni E, Baasov T, Ravid U, Shoham Y.
    The trans-anethole degradation pathway in an Arthrobacter sp.
    J Biol Chem.    impact factor:   7.666
    2002;  277(14): 11866-72

    3:  Meyermans H, Morreel K, Lapierre C, Pollet B, De Bruyn A, Busson R, Herdewijn P, Devreese B, Van Beeumen J, Marita JM, Ralph J, Chen C, Burggraeve B, Van Montagu M, Messens E, Boerjan W.
    Modifications in lignin and accumulation of phenolic glucosides in poplar xylem upon down-regulation of caffeoyl-coenzyme A O-methyltransferase, an enzyme involved in lignin biosynthesis.
    J Biol Chem.    impact factor:   7.666
    2000;  275(47): 36899-909

    4:  Rechner AR, Spencer JP, Kuhnle G, Hahn U, Rice-Evans CA.
    Novel biomarkers of the metabolism of caffeic acid derivatives in vivo.
    Free Radic Biol Med.    impact factor:   4.116
    2001;  30(11): 1213-22

    5:  Appendino G, Minassi A, Morello AS, De Petrocellis L, Di Marzo V.
    N-Acylvanillamides: development of an expeditious synthesis and discovery of new acyl templates for powerful activation of the vanilloid receptor.
    J Med Chem.    impact factor:   4.079
    2002;  45(17): 3739-45

     
    Time used: 78 milliseconds.

    Webpage designed by Dr. Xueliang Fang, last updated on 3/10/2005