81539-69-7

Upstream product

• 81539-66-4 4-(4-Hexyl-phenyl)-N¹-[1-phenyl-meth-(Z)-ylidene]-imidazole-1,2-diamine 
• 37592-72-6 1-(4-hexyl-phenyl)-ethanone 
• 64328-69-4 2-bromo-1-(4-hexylphenyl)ethan-1-one 
• 81539-57-3 2-Chloro-1-(4-hexyl-phenyl)-ethanone 

Downstream Products

• 81539-74-4 11-(4-Hexyl-phenyl)-9,9a,12,13-tetraaza-cyclopenta[b]triphenylene 

Relevant academic research and scientific papers

Method for inhibiting advanced glycosylation of proteins using aminosubstituted imidazoles

The present invention relates to compositions and methods for inhibiting nonenzymatic cross-linking (protein aging), Accordingly, a composition is disclosed which comprises 2-aminoimidazoles capable of inhibiting the formation of advanced glycosylation endproducts of target proteins by reacting with the carbonyl moiety of the early glycosylation product of such target proteins formed by their initial glycosylation, The method comprises contacting the target protein with the composition, Both industrial and therapeutic applications for the invention are envisioned, as food spoilage and animal protein aging can be treated.

Synthesis of 1,2-diamino imidazole derivatives by the reaction of benzaldehyde guanylhydrazone with α-haloalkyl aryl ketones

2-Amino-1-benzylideneamino-4-arylimidazoles were obtained by the reaction of benzaldehyde guanylhydrazone with 4-alkyl- and 4-aryl-Ω-haloacetophenones. Side products of this reaction were cis- and trans-1,1′-bis(benzylideneamino)-4,4′-diaryl-2,2′-azoimida