ID Name Structure References (top 5) Molecular Target(s)
1ID:4538
MYRCENE


NSC#:406264
Aldrich#:70049
Aldrich#:M0382
Aldrich#:M100005

Freqency:
in 8 ingredients:

  • 169
  • 177
  • 501
  • 536
  • 584
  • 715
  • 901
  • 906
  • in 72 recipes:

  • 2
  • 6
  • 8
  • 10
  • 22
  • 23
  • 29
  • 39
  • 42
  • 43
  • 51
  • 57
  • 62
  • 67
  • 87
  • 109
  • 111
  • 115
  • 123
  • 124
  • 181
  • 205
  • 210
  • 212
  • 215
  • 219
  • 223
  • 227
  • 232
  • 233
  • 241
  • 242
  • 247
  • 248
  • 254
  • 255
  • 258
  • 259
  • 269
  • 271
  • 272
  • 273
  • 274
  • 287
  • 288
  • 291
  • 292
  • 294
  • 299
  • 300
  • 305
  • 309
  • 310
  • 312
  • 313
  • 315
  • 317
  • 324
  • 334
  • 340
  • 363
  • 367
  • 383
  • 392
  • 399
  • 402
  • 403
  • 412
  • 472
  • 488
  • 507
  • 515

  • Properties
    C10H16    136.24





    1:  Wise ML, Savage TJ, Katahira E, Croteau R.
    Monoterpene synthases from common sage (Salvia officinalis). cDNA isolation, characterization, and functional expression of (+)-sabinene synthase, 1,8-cineole synthase, and (+)-bornyl diphosphate synthase.
    J Biol Chem.    impact factor:   7.666
    1998;  273(24): 14891-9

    2:  Bohlmann J, Steele CL, Croteau R.
    Monoterpene synthases from grand fir (Abies grandis). cDNA isolation, characterization, and functional expression of myrcene synthase, (-)-(4S)-limonene synthase, and (-)-(1S,5S)-pinene synthase.
    J Biol Chem.    impact factor:   7.666
    1997;  272(35): 21784-92

    3:  Colby SM, Alonso WR, Katahira EJ, McGarvey DJ, Croteau R.
    4S-limonene synthase from the oil glands of spearmint (Mentha spicata). cDNA isolation, characterization, and bacterial expression of the catalytically active monoterpene cyclase.
    J Biol Chem.    impact factor:   7.666
    1993;  268(31): 23016-24

    4:  Svatos A, Attygalle AB.
    Characterization of vinyl-substituted, carbon-carbon double bonds by GC/FT-IR analysis.
    Anal Chem.    impact factor:   4.555
    1997;  69(10): 1827-36

    5:  Heyen U, Harder J.
    Geranic acid formation, an initial reaction of anaerobic monoterpene metabolism in denitrifying Alcaligenes defragrans.
    Appl Environ Microbiol.    impact factor:   3.541
    2000;  66(7): 3004-9

     
    Time used: 516 milliseconds.

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