ID Name Structure References (top 5) Molecular Target(s)
1ID:1086
CINNAMIC ALDEHYDE


NSC#:16935
NSC#:40346
Aldrich#:239968
Aldrich#:96320
Aldrich#:C80687

Freqency:
in 2 ingredients:

  • 114
  • 690
  • in 40 recipes:

  • 4
  • 37
  • 44
  • 80
  • 100
  • 102
  • 111
  • 157
  • 174
  • 181
  • 184
  • 200
  • 208
  • 229
  • 231
  • 233
  • 257
  • 268
  • 285
  • 289
  • 339
  • 341
  • 342
  • 352
  • 355
  • 361
  • 380
  • 382
  • 412
  • 446
  • 461
  • 469
  • 470
  • 472
  • 474
  • 475
  • 484
  • 497
  • 502
  • 519

  • Properties
    C9H8O    132.16





    1:  Kohli RM, Massey V.
    The oxidative half-reaction of Old Yellow Enzyme. The role of tyrosine 196.
    J Biol Chem.    impact factor:   7.666
    1998;  273(49): 32763-70

    2:  Paras NA, MacMillan DW.
    New strategies in organic catalysis: the first enantioselective organocatalytic Friedel-Crafts alkylation.
    J Am Chem Soc.    impact factor:   5.537
    2001;  123(18): 4370-1

    3:  Fu H, Park J, Pei D.
    Peptidyl aldehydes as reversible covalent inhibitors of protein tyrosine phosphatases.
    Biochemistry.    impact factor:   4.493
    2002;  41(34): 10700-9

    4:  Vaz AD, Chakraborty S, Massey V.
    Old Yellow enzyme: aromatization of cyclic enones and the mechanism of a novel dismutation reaction.
    Biochemistry.    impact factor:   4.493
    1995;  34(13): 4246-56

    5:  Prakash GK, Mandal M, Schweizer S, Petasis NA, Olah GA.
    A facile stereocontrolled synthesis of anti-alpha-(trifluoromethyl)-beta-amino alcohols.
    Org Lett.    impact factor:   3.367
    2000;  2(20): 3173-6

     
    Time used: 94 milliseconds.

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