(114,116) After that, the acyl-hydrazide dissociates or gets further deacylated to the free hydrazide, but none of these species show as high potency, selectivity, or τ as the original DFMO.
Very long-chain acyl-CoA dehydrogenase deficiency (VLCAD), a rare inherited genetic condition, is caused by mutations in the ACADVL gene. It is associated with a disorder in fatty acid metabolism ...
WE have found that isonicotinic acid hydrazide, a widely used drug 1, is a potent inhibitor of the crosslinking of fibrin. This reaction constitutes the terminal step in normal blood coagulation ...