ID Name Structure References (top 5) Molecular Target(s)
1ID:603
BENZYL ACETONE


NSC#:813
NSC#:44829
Aldrich#:13150
Aldrich#:B16003

Freqency:
in 1 ingredients:

  • 396
  • in 11 recipes:

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

  • Properties
    C10H12O    148.2





    1:  Lee M, Ishizaki H, Brady JF, Yang CS.
    Substrate specificity and alkyl group selectivity in the metabolism of N-nitrosodialkylamines.
    Cancer Res.    impact factor:   8.614
    1989;  49(6): 1470-4

    2:  Fan JQ, Quesenberry MS, Takegawa K, Iwahara S, Kondo A, Kato I, Lee YC.
    Synthesis of neoglycoconjugates by transglycosylation with Arthrobacter protophormiae endo-beta-N-acetylglucosaminidase. Demonstration of a macro-cluster effect for mannose-binding proteins.
    J Biol Chem.    impact factor:   7.666
    1995;  270(30): 17730-5

    3:  Wykle RL, Plantadosi C, Snyder F.
    The role of acyldihydroxyacetone phosphate, reduced nicotinamide adenine dinucleotide, and reduced nicotinamide adenine dinucleotide phosphate in the biosynthesis of O-alkyl glycerolipids by microsomal enzymes of Ehrlich ascites tumor.
    J Biol Chem.    impact factor:   7.666
    1972;  247(9): 2944-8

    4:  Crich D, Smith M.
    Solid-phase synthesis of beta-mannosides.
    J Am Chem Soc.    impact factor:   5.537
    2002;  124(30): 8867-9

    5:  Taki M, Teramae S, Nagatomo S, Tachi Y, Kitagawa T, Itoh S, Fukuzumi S.
    Fine-tuning of copper(I)-dioxygen reactivity by 2-(2-pyridyl)ethylamine bidentate ligands.
    J Am Chem Soc.    impact factor:   5.537
    2002;  124(22): 6367-77

    ARG
    LC
    MET
    P450
    STEP
     
    Time used: 703 milliseconds.

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