112758-77-7

Upstream product

• 1007-54-1 2-benzylsulfanyl-ethylamine 
• 81282-38-4 N-diphenoxymethylene benzamide 

Downstream Products

• 144153-33-3 N-Benzoyl-N'-(2-benzylsulfanyl-ethyl)-N''-[3-(5-methyl-1H-imidazol-4-yl)-propyl]-guanidine 
• 144153-35-5 N-Benzoyl-N'-(2-benzylsulfanyl-ethyl)-N''-[2-methyl-3-(5-methyl-1H-imidazol-4-yl)-propyl]-guanidine 
• 112758-60-8 N-(2-Benzylsulfanyl-ethyl)-N'-[3-(1H-imidazol-4-yl)-propyl]-guanidine; hydrochloride 
• 106668-54-6 N-Benzoyl-N'-(2-benzylsulfanyl-ethyl)-N''-[3-(1H-imidazol-4-yl)-propyl]-guanidine 
• 144284-46-8 N-(2-Benzylsulfanyl-ethyl)-N'-[3-(5-methyl-1H-imidazol-4-yl)-propyl]-guanidine; compound with picric acid 
• 144284-48-0 N-(2-Benzylsulfanyl-ethyl)-N'-[2-methyl-3-(5-methyl-1H-imidazol-4-yl)-propyl]-guanidine; hydrochloride 

Relevant academic research and scientific papers

The effect of lipophilic substituents on the H2-histaminergic activity of some close analogues of impromidine

The cimetidine-like moiety of the potent H2-agonist impromidine (9a) and three closely related guanidines (10a, 11a, and 12a) which are modified in the imidazolylpropyl portion, has been replaced by 2-[(2-pyridyl)methylthio]ethyl, 2-(benzylthio

Synthesis and pharmacological activity of arylmethylthioethylguanidines

Impromidine analogues guanidines have been prepared characterized by H2-unspecific arylmethyl groups instead of the 5-methylimidazole residue. The most potent substances proved to be about 20 times more active than histamine at the isolated spo