BW A4C and other hydroxamic acids are potent inhibitors of linoleic acid 8R-dioxygenase of the fungus Gaeumannomyces graminis

This publication has 17 references indexed in Scilit:

• Biosynthesis of 8R-hydroperoxylinoleic acid by the fungus Laetisaria arvalis
  Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1993
• Criteria for the identification of non-redox inhibitors of 5-lipoxygenase
  Biochemical Pharmacology, 1993
• Metabolism of 18:2(n − 6), 18:3(n − 3), 20:4(n − 6) and 20:5(n − 3) by the fungus Gaeumannomyces graminis: Identification of metabolites formed by 8-hydroxylation and by w2 and w3 oxygenation
  Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1992
• Recent investigations into the lipoxygenase pathway of plants
  Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1991
• [22] Precipitation techniques
  Published by Elsevier ,1990
• Inhibition of tolbutamide metabolism by substituted imidazole drugs in vivo: evidence for a structure‐activity relationship
  British Journal of Pharmacology, 1985
• The mechanism of inactivation of lipoxygenases by acetylenic fatty acids
  European Journal of Biochemistry, 1984
• Rationally designed, potent competitive inhibitors of leukotriene biosynthesis
  Journal of the American Chemical Society, 1984
• A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
  Analytical Biochemistry, 1976
• The Complex between Hydroxamic Acids and Ferric Ions, and the Use of the Complex for Quantitative Determination of Hydroxamic Acids, Acylderivatives, and Ferric Salts.
  Acta Chemica Scandinavica, 1957