Inhibitors of glycolic acid oxidase. 4-Substituted-2,4-dioxobutanoic acid derivatives

H. W. R. WILLIAMS, Eva Eichler, William C. Randall, C. S. ROONEY, E. J. Cragoe, K. B. STREETER, Harvey Schwam, Stuart R. Michelson, A. A. PATCHETT, D. Taub

Journal of Medicinal Chemistry · 1983 · 26 citations · 0 references

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Abstract

Fourteen new 4-substituted 2,4-dioxobutanoic acids have been synthesized. These compounds, all of which contain lipophilic 4-substituents, are potent inhibitors in vitro of porcine liver glycolic acid oxidase. The I50 value of the two most potent representatives, 4-(4'-bromo[1,1'-biphenyl]-4-yl)-2, 4-dioxobutanoic acid (8) and 4-[4'-[[(3,4-dihydro-3-hydroxy-2H-1, 5-benzodioxepin-3-yl)methyl]thio][1,1'-biphenyl]-4-yl]-2, 4-dioxobutanoic acid (13) is 6 X 10(-8)M.