ID Name Structure References (top 5) Molecular Target(s)
1ID:371
ANISIC ACID


NSC#:7926
NSC#:32742
NSC#:83523
Aldrich#:10550
Aldrich#:117390
Aldrich#:491578
Aldrich#:A0631

Freqency:
in 1 ingredients:

  • 396
  • in 11 recipes:

  • 3
  • 8
  • 13
  • 206
  • 212
  • 218
  • 233
  • 236
  • 492
  • 495
  • 496

  • Properties
    C8H8O3    152.15





    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:  Waldman AS, Waldman BC.
    Stimulation of intrachromosomal homologous recombination in mammalian cells by an inhibitor of poly(ADP-ribosylation).
    Nucleic Acids Res.    impact factor:   5.748
    1991;  19(21): 5943-7

    3:  Xiao P, Staubli U, Kessler M, Lynch G.
    Selective effects of aniracetam across receptor types and forms of synaptic facilitation in hippocampus.
    Hippocampus.    impact factor:   4.979
    1991;  1(4): 373-80

    4:  Lynas J, Walker B.
    Peptidyl inverse esters of p-methoxybenzoic acid: a novel class of potent inactivator of the serine proteases.
    Biochem J.    impact factor:   4.349
    1997;  325 ( Pt 3): 609-16

    5:  Shirane M, Nakamura K.
    Group II metabotropic glutamate receptors are a common target of N-anisoyl-GABA and 1S,3R-ACPD in enhancing ACh release in the prefrontal cortex of freely moving SHRSP.
    Neuropharmacology.    impact factor:   4.176
    2000;  39(5): 866-72

    C-AMP
    LTK
    MET
    P450
    STEP
    THYMIDINE KINASE
    PKC
     
    Time used: 484 milliseconds.

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