ID Name Structure References (top 5) Molecular Target(s)
1ID:7061
BUTENOLIDE A

Freqency:
in 2 ingredients:

  • 92
  • 385
  • in 41 recipes:

  • 20
  • 21
  • 22
  • 27
  • 30
  • 49
  • 80
  • 96
  • 107
  • 110
  • 156
  • 161
  • 169
  • 173
  • 199
  • 241
  • 252
  • 272
  • 280
  • 291
  • 292
  • 301
  • 308
  • 309
  • 342
  • 346
  • 361
  • 363
  • 376
  • 381
  • 403
  • 437
  • 441
  • 446
  • 449
  • 456
  • 459
  • 469
  • 488
  • 490
  • 520

  • Properties
    C23H24O10    460.43





    1:  Zhang YY, Dennis EA.
    Purification and characterization of a lysophospholipase from a macrophage-like cell line P388D1.
    J Biol Chem.    impact factor:   7.666
    1988;  263(20): 9965-72

    2:  Trost BM, Crawley ML.
    4-Aryloxybutenolides as "chiral aldehyde" equivalents: an efficient enantioselective synthesis of (+)-brefeldin a.
    J Am Chem Soc.    impact factor:   5.537
    2002;  124(32): 9328-9

    3:  Ma S, Duan D, Wang Y.
    Palladium(0)-catalyzed coupling-cyclization reaction of polymer-supported aryl iodides with 1,2-allenyl carboxylic acids. Solid-phase parallel synthesis of butenolides.
    J Comb Chem.    impact factor:   5.23
    2002;  4(3): 239-47

    4:  Makita H, Tanaka T, Ohnishi M, Tamai Y, Torihara M, Yamahara J, Mori H, Satoh K, Hara A.
    Inhibition of 4-nitroquinoline-1-oxide-induced rat oral carcinogenesis by dietary exposure of a new retinoidal butenolide, KYN-54, during the initiation and post-initiation phases.
    Carcinogenesis.    impact factor:   4.118
    1995;  16(9): 2171-6

    5:  Kawamori T, Tanaka T, Suzui M, Okamoto K, Tamai Y, Torihara M, Yamahara J, Mori H.
    Chemoprevention of azoxymethane-induced intestinal carcinogenesis by a novel synthesized retinoidal butenolide, 5-hydroxy-4-(2-phenyl-(E)-ethenyl)-2(5H)-furanone, in rats.
    Carcinogenesis.    impact factor:   4.118
    1995;  16(4): 795-800

     
    Time used: 93 milliseconds.

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