ID Name Structure References (top 5) Molecular Target(s)
1ID:1084
CINNAMIC ACID


NSC#:9189
NSC#:30118
NSC#:44010
NSC#:174025
NSC#:623441
Aldrich#:133760
Aldrich#:96340
Aldrich#:C4415
Aldrich#:C80857

Freqency:
in 5 ingredients:

  • 27
  • 114
  • 124
  • 216
  • 555
  • in 59 recipes:

  • 5
  • 7
  • 23
  • 41
  • 43
  • 57
  • 61
  • 80
  • 89
  • 102
  • 136
  • 145
  • 157
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  • 526

  • Properties
    C9H8O2    148.16





    1:  Xiang L, Moore BS.
    Inactivation, complementation, and heterologous expression of encP, a novel bacterial phenylalanine ammonia-lyase gene.
    J Biol Chem.    impact factor:   7.666
    2002;  277(36): 32505-9

    2:  Schoch GA, Nikov GN, Alworth WL, Werck-Reichhart D.
    Chemical inactivation of the cinnamate 4-hydroxylase allows for the accumulation of salicylic acid in elicited cells.
    Plant Physiol.    impact factor:   4.434
    2002;  130(2): 1022-31

    3:  Ro DK, Mah N, Ellis BE, Douglas CJ.
    Functional characterization and subcellular localization of poplar (Populus trichocarpa x Populus deltoides) cinnamate 4-hydroxylase.
    Plant Physiol.    impact factor:   4.434
    2001;  126(1): 317-29

    4:  Silverman P, Seskar M, Kanter D, Schweizer P, Metraux JP, Raskin I.
    Salicylic Acid in Rice (Biosynthesis, Conjugation, and Possible Role).
    Plant Physiol.    impact factor:   4.434
    1995;  108(2): 633-639

    5:  Orr JD, Edwards R, Dixon RA.
    Stress Responses in Alfalfa (Medicago sativa L.) (XIV. Changes in the Levels of Phenylpropanoid Pathway Intermediates in Relation to Regulation of L-Phenylalanine Ammonia-Lyase in Elicitor-Treated Cell-Suspension Cultures).
    Plant Physiol.    impact factor:   4.434
    1993;  101(3): 847-856

     
    Time used: 156 milliseconds.

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