ID Name Structure References (top 5) Molecular Target(s)
1ID:6954
ALPHA-IONONE


NSC#:34560
Aldrich#:58170
Aldrich#:I12409
Aldrich#:I3384

Freqency:
in 1 ingredients:

  • 43
  • in 48 recipes:

  • 19
  • 20
  • 21
  • 22
  • 23
  • 24
  • 29
  • 30
  • 41
  • 43
  • 48
  • 122
  • 123
  • 124
  • 150
  • 169
  • 221
  • 223
  • 229
  • 233
  • 236
  • 241
  • 242
  • 243
  • 247
  • 248
  • 252
  • 258
  • 260
  • 272
  • 274
  • 279
  • 283
  • 288
  • 294
  • 297
  • 311
  • 401
  • 402
  • 403
  • 434
  • 487
  • 490
  • 497
  • 500
  • 505
  • 513
  • 521

  • Properties
    C13H20O    192.3





    1:  Lutz-Wahl S, Fischer P, Schmidt-Dannert C, Wohlleben W, Hauer B, Schmid RD.
    Stereo- and regioselective hydroxylation of alpha-ionone by Streptomyces strains.
    Appl Environ Microbiol.    impact factor:   3.541
    1998;  64(10): 3878-81

    2:  Ng SC, Ong TT, Fu P, Ching CB.
    Enantiomer separation of flavour and fragrance compounds by liquid chromatography using novel urea-covalent bonded methylated beta-cyclodextrins on silica.
    J Chromatogr A.    impact factor:   2.52
    2002;  968(1-2): 31-40

    3:  Quattrini F, Biressi G, Juza M, Mazzotti M, Fuganti C, Morbidelli M.
    Enantiomer separation of alpha-ionone using gas chromatography with cyclodextrin derivatives as chiral stationary phases.
    J Chromatogr A.    impact factor:   2.52
    1999;  865(1-2): 201-10

    4:  Polak EH, Fombon AM, Tilquin C, Punter PH.
    Sensory evidence for olfactory receptors with opposite chiral selectivity.
    Behav Brain Res.    impact factor:   2.318
    1989;  31(3): 199-206

    5:  Hartman DA, Pontones ME, Kloss VF, Curley RW Jr, Robertson LW.
    Models of retinoid metabolism: microbial biotransformation of alpha-ionone and beta-ionone.
    J Nat Prod.    impact factor:   1.652
    1988;  51(5): 947-53

     
    Time used: 109 milliseconds.

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