58484-76-7

Usage

Uses

Used in Pharmaceutical Industry:
N-HYDROXY-2-(4-HYDROXY-PHENYL)-ACETAMIDINE is used as a precursor in the synthesis of pharmaceutical compounds for the treatment of various medical conditions. Its unique structure allows for the development of drugs with novel mechanisms of action, potentially leading to more effective therapies.
Used in Research and Development:
In the research industry, N-HYDROXY-2-(4-HYDROXY-PHENYL)-ACETAMIDINE serves as a valuable tool for studying the properties and interactions of similar compounds. It can be utilized in the design and testing of new drug candidates, contributing to the advancement of medical science and the discovery of innovative treatments.
Used in Drug Discovery:
N-HYDROXY-2-(4-HYDROXY-PHENYL)-ACETAMIDINE is employed as a key component in drug discovery processes. Its unique properties and structural features make it an attractive target for the development of new therapeutic agents, with potential applications in a wide range of medical fields.

Upstream product

• 14191-95-8 4-cyanomethylphenol 

Downstream Products

• 1001852-28-3 p-{[(acetoxy)imino]-2-aminoethyl}phenol 
• 144797-29-5 1-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-3-[4-(5-methyl-[1,2,4]oxadiazol-3-ylmethyl)-phenoxy]-propan-2-ol 
• 144797-43-3 4-{5-[4-(2-Methoxy-phenyl)-piperazin-1-ylmethyl]-[1,2,4]oxadiazol-3-ylmethyl}-phenol 
• 144797-25-1 1-Isopropylamino-3-[4-(5-methyl-[1,2,4]oxadiazol-3-ylmethyl)-phenoxy]-propan-2-ol 
• 144797-49-9 1-(2-Methoxy-phenyl)-4-[3-(4-oxiranylmethoxy-benzyl)-[1,2,4]oxadiazol-5-ylmethyl]-piperazine 
• 144797-45-5 5-Methyl-3-(4-oxiranylmethoxy-benzyl)-[1,2,4]oxadiazole 
• 144797-39-7 4-(5-Chloromethyl-[1,2,4]oxadiazol-3-ylmethyl)-phenol 
• 144797-40-0 4-(5-Methyl-[1,2,4]oxadiazol-3-ylmethyl)-phenol 

Relevant academic research and scientific papers

N-hydroxy-substituted 2-aryl acetamide analogs: A novel class of HIV-1 integrase inhibitors

An in silico method has been used to discover N-hydroxy-substituted 2-aryl acetamide analogs as a new class of HIV-1 integrase inhibitors. Based on the molecular requirements of the binding pocket of catalytic active site, two molecules (compounds 2 and 4

A facile synthesis of p- and m-(amidinomethyl)phenyl esters derived from amino acid and tryptic hydrolysis of these synthetic inverse substrates

A facile synthetic method for p- and m-(amidinomethyl)phenyl esters derived from a variety of amino acids is presented. We analyzed the kinetic behavior of trypsin towards these synthetic esters, which are inverse substrates. The substituent (meta- and para-isomers) and isosteric effects of (amidinomethyl)phenyl esters are discussed.

New 1,2,4-oxadiazole derivatives: Synthesis and adrenergic receptors binding studies

In order to obtain derivatives with simultaneous α- and β-adrenergic blocking activity, compounds having the phenoxypropanolaminic structure of β-adrenergic blockers have been synthesised, as well as 1,2,4-oxadiazole moiety, which could imitate the imidaz