ID Name Structure References (top 5) Molecular Target(s)
1ID:6729
XANTHOTOXOL


NSC#:401269

Freqency:
in 2 ingredients:

  • 85
  • 733
  • in 31 recipes:

  • 22
  • 37
  • 51
  • 55
  • 61
  • 63
  • 73
  • 77
  • 83
  • 158
  • 161
  • 193
  • 203
  • 229
  • 268
  • 292
  • 299
  • 301
  • 303
  • 309
  • 313
  • 315
  • 339
  • 342
  • 345
  • 352
  • 359
  • 438
  • 452
  • 456
  • 504

  • Properties
    C11H6O4    202.16





    1:  Wang Z, Wang X, Rana TM.
    Protein orientation in the Tat-TAR complex determined by psoralen photocross-linking.
    J Biol Chem.    impact factor:   7.666
    1996;  271(29): 16995-8

    2:  Chatterjee DK, Sen K.
    New syntheses of xanthotoxol and xanthotoxin.
    Tetrahedron Lett.    impact factor:   2.4
    1969;  59: 5223-4

    3:  Ng TB, Liu F, Wang ZT.
    Antioxidative activity of natural products from plants.
    Life Sci.    impact factor:   1.774
    2000;  66(8): 709-23

    4:  Chen IS, Chang CT, Sheen WS, Teng CM, Tsai IL, Duh CY, Ko FN.
    Coumarins and antiplatelet aggregation constituents from Formosan Peucedanum japonicum.
    Phytochemistry.    impact factor:   1.106
    1996;  41(2): 525-30

    5:  Sharma SK, Garrett JM, Brown SA.
    Separation of the S-adenosylmethionine: 5- and 8-hydroxyfuranocoumarin O-methyltransferases of Ruta graveolens L. by general ligand affinity chromatography.
    Z Naturforsch [C].    impact factor:   .709
    1979;  34C(5-6): 387-91

     
    Time used: 125 milliseconds.

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