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In tell as the HaberWeiss reaction (Hermetter et al., 2012

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Compound 3 , ( E )2(3,4dihydroxy5nitrobenzylidene) N phenylhydrazine1carbothioamide, was potent in the order of nM, with an IC 50 value of 0.0437 M, being 734 times more potent than its analog 3,4dihydroxy5nitrobenzaldehyde (DHNB) and 173 times more potent than the drug allopurinol, demonstrating its excellent inhibitory activity (Figure 4)

Integration with Diabetes Management Protocols Combining high-dose B12 with diabetes care improves results