ID Name Structure References (top 5) Molecular Target(s)
1ID:4099
MANDELONITRILE


NSC#:77668
Aldrich#:116025
Aldrich#:12023
Aldrich#:469653

Freqency:
in 1 ingredients:

  • 153
  • in 4 recipes:

  • 8
  • 61
  • 292
  • 309

  • Properties
    C8H7NO    133.15





    1:  Fenselau C, Pallante S, Batzinger RP, Benson WR, Barron RP, Sheinin EB, Maienthal M.
    Mandelonitrile beta-glucuronide: synthesis and characterization.
    Science.    impact factor:   24.595
    1977;  198(4317): 625-7

    2:  Cicek M, Blanchard D, Bevan DR, Esen A.
    The aglycone specificity-determining sites are different in 2, 4-dihydroxy-7-methoxy-1,4-benzoxazin-3-one (DIMBOA)-glucosidase (Maize beta -glucosidase) and dhurrinase (Sorghum beta -glucosidase).
    J Biol Chem.    impact factor:   7.666
    2000;  275(26): 20002-11

    3:  Jones PR, Moller BL, Hoj PB.
    The UDP-glucose:p-hydroxymandelonitrile-O-glucosyltransferase that catalyzes the last step in synthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor. Isolation, cloning, heterologous expression, and substrate specificity.
    J Biol Chem.    impact factor:   7.666
    1999;  274(50): 35483-91

    4:  Gopalan V, Pastuszyn A, Galey WR Jr, Glew RH.
    Exolytic hydrolysis of toxic plant glucosides by guinea pig liver cytosolic beta-glucosidase.
    J Biol Chem.    impact factor:   7.666
    1992;  267(20): 14027-32

    5:  Colombo G, Giedroc DP, Rajashekhar B, Villafranca JJ.
    Alternate substrates of dopamine beta-hydroxylase. II. Inhibition by benzyl cyanides and reactivation of inhibited enzyme.
    J Biol Chem.    impact factor:   7.666
    1984;  259(3): 1601-6

     
    Time used: 110 milliseconds.

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