Table 1

Summary of biological activity based on secondary increases in Isc

CompoundRIaIC50 (μM)Activity
Reference compounds
 Aminoguanidine1.00.11Active
N-methyl hydroxylamine2100.1221.56Inactive
Aliphatic hydroxylamines
O-1-allyl, 12.20.23Active
O-1-pentyl, 23.30.35Active
O-2-butyl, 36.60.70Active
O-1-hexyl, 411.11.17Active
O-1-pent-4-ynyl, 523.32.46Active
O-1-(2-methyl)propyl, 635.63.76Active
O-1-octyl, 764.66.82Marginal
O-1-decyl, 8115.612.20Negative
O-1-(3-methyl)butyl, 9147.515.56Marginal
Benzylic hydroxylamines
O-1-E-Cinnamyl, 1010.81.14Marginal
O-p-hydroxybenzyl, 1112.61.33Active
O-p-hydroxy-m-bromobenzyl, 1214.81.56Marginal
O-m-methoxybenzyl, 1320.62.17Marginal
O-p-methoxybenzyl, 1436.23.82Marginal
O-p-bromobenzyl, 1552.65.55Marginal
O-benzyl, 16161.717.06Negative
  • a Relative Inhibition (RI) ratios were obtained by dividing the IC50 value for each compound by the IC50 value for the reference compound aminoguanidine (0.11 μM).