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. 2024 Jun 17;14(27):19428–19445. doi: 10.1039/d4ra03404j

Comparison between the tested DMIH compound and other inhibitors in the literature.

Compound name IE (%) Reference
• α-Aminophosphonate 92.4 5
• (N,NE,N,NE)-N,N′-(Thiophene-2,5-diylbis(methanylylidene))bis(1H-benzo[d]imidazole-2-amine) 96.0 10
• Dimethyl-4,6-dihydroxyisophthalate 79.9 22
• Succinic acid 97.5 33
• 4,6-Dihydroxyisophthalaohydrazide 86.2 20
• 4(p-Tolyldiazenyl)-2-((E)-(p-tolylimino)methyl)phenol 55.0 67
• 3-(2-((4-Hydroxybenzylidene)amino)thiazole-4-yl)-2H-chromen-2-one 52.9 68
N-(Pyridine-4-ymethylene)-3,4-dihydropyridine-4-amine 88.0 69
N-(4-N,N-Dimethylaminobenzal)-p-anisidine 80.6 70
N-(4-N,N-Dimethylaminobenzal)-p-toluidine 79.1 70
N-(4-N,N-Dimethylaminobenzal)-2,4-dinitroaniline 75.9 70
• 4,6-Dimethoxyisophthalohydrazide (DMIH) 83.8 This work