ID Name Structure References (top 5) Molecular Target(s)
1ID:7589
PINANONE

Freqency:
in 1 ingredients:

  • 417
  • in 39 recipes:

  • 4
  • 37
  • 44
  • 100
  • 111
  • 142
  • 143
  • 146
  • 174
  • 181
  • 184
  • 200
  • 208
  • 229
  • 231
  • 236
  • 257
  • 268
  • 285
  • 289
  • 324
  • 339
  • 342
  • 352
  • 355
  • 361
  • 380
  • 412
  • 423
  • 430
  • 461
  • 469
  • 470
  • 472
  • 474
  • 475
  • 484
  • 502
  • 519

  • Properties
    C10H16O    152.23





    1:  Hold KM, Sirisoma NS, Sparks SE, Casida JE.
    Metabolism and mode of action of cis- and trans-3-pinanones (the active ingredients of hyssop oil).
    Xenobiotica.    impact factor:   1.335
    2002;  32(4): 251-65

    2:  Swango JH, Bhatti BS, Qureshi MM, Crooks PA.
    A novel enantioselective synthesis of (S)-(-)- and (R)-(+)-nornicotine via alkylation of a chiral 2-hydroxy-3-pinanone ketimine template.
    Chirality.    impact factor:   1.327
    1999;  11(4): 316-8

    3:  Minardi G, Bignardi G, Schenone P.
    [Synthesis and properties of 4-hydroxymethylene(-)3-pinanone and various derivatives]
    Farmaco [Sci].    impact factor:   0
    1968;  23(10): 968-82

     
    Time used: 125 milliseconds.

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