Synthesis of bridged catechol-homocysteine derivatives as potential inhibitors of catechol O-methyltransferase
Catechol derivatives, covalently joined to homocysteine by sulfide or sulfonium linkages, were synthesized as potential catechol O-methyl-transferase inhibitors which might bridge the enzymatic binding sites for the catechol substrate and the amino acid p
Lever Jr.,Hyman,White
p. 1241 - 1244
(2007/10/02)
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