ID Name Structure References (top 5) Molecular Target(s)
1ID:370
ANISALDEHYDE


NSC#:5590
Aldrich#:10440
Aldrich#:A0519
Aldrich#:A88107

Freqency:
in 4 ingredients:

  • 4
  • 27
  • 302
  • 639
  • in 6 recipes:

  • 134
  • 188
  • 190
  • 212
  • 233
  • 247

  • Properties
    C8H8O2    136.15





    1:  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

    2:  Tien M, Ma D.
    Oxidation of 4-methoxymandelic acid by lignin peroxidase. Mediation by veratryl alcohol.
    J Biol Chem.    impact factor:   7.666
    1997;  272(14): 8912-7

    3:  Blackwell JM, Piers WE, McDonald R.
    Mechanistic studies on the B(C(6)F(5))(3) catalyzed allylstannation of aromatic aldehydes with ortho donor substituents.
    J Am Chem Soc.    impact factor:   5.537
    2002;  124(7): 1295-306

    4:  Huang Y, Rawal VH.
    Hydrogen-bond-promoted hetero-Diels-Alder reactions of unactivated ketones.
    J Am Chem Soc.    impact factor:   5.537
    2002;  124(33): 9662-3

    5:  Sartorius C, Gerber M, Zeppezauer M, Dunn MF.
    Active-site cobalt(II)-substituted horse liver alcohol dehydrogenase: characterization of intermediates in the oxidation and reduction processes as a function of pH.
    Biochemistry.    impact factor:   4.493
    1987;  26(3): 871-82

    BAS
    MET
    PEST
    STEP
     
    Time used: 94 milliseconds.

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