ID Name Structure References (top 5) Molecular Target(s)
1ID:7332
INDIGO


NSC#:8645
Aldrich#:229296

Freqency:
in 1 ingredients:

  • 147
  • in 18 recipes:

  • 3
  • 75
  • 76
  • 98
  • 125
  • 150
  • 206
  • 228
  • 289
  • 325
  • 335
  • 378
  • 404
  • 434
  • 458
  • 496
  • 519
  • 525

  • Properties
    C16H10N2O2    262.27





    1:  Ribbe MW, Hu Y, Guo M, Schmid B, Burgess BK.
    The FeMoco-deficient MoFe protein produced by a nifH deletion strain of Azotobacter vinelandii shows unusual P-cluster features.
    J Biol Chem.    impact factor:   7.666
    2002;  277(26): 23469-76

    2:  Meyer A, Wursten M, Schmid A, Kohler HP, Witholt B.
    Hydroxylation of indole by laboratory-evolved 2-hydroxybiphenyl 3-monooxygenase.
    J Biol Chem.    impact factor:   7.666
    2002;  277(37): 34161-7

    3:  Adachi J, Mori Y, Matsui S, Takigami H, Fujino J, Kitagawa H, Miller CA 3rd, Kato T, Saeki K, Matsuda T.
    Indirubin and indigo are potent aryl hydrocarbon receptor ligands present in human urine.
    J Biol Chem.    impact factor:   7.666
    2001;  276(34): 31475-8

    4:  Sharma P, Weston AP, Topalovski M, Cherian R, Bhattacharyya A, Sampliner RE.
    Magnification chromoendoscopy for the detection of intestinal metaplasia and dysplasia in Barrett's oesophagus.
    Gut.    impact factor:   5.748
    2003;  52(1): 24-7

    5:  Gillam EM, Notley LM, Cai H, De Voss JJ, Guengerich FP.
    Oxidation of indole by cytochrome P450 enzymes.
    Biochemistry.    impact factor:   4.493
    2000;  39(45): 13817-24

     
    Time used: 469 milliseconds.

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