1426224-57-8

Basic information

• Product Name: 2-(4-(6-fluorobenzo[d]isoxazol-3-yl)piperidine-1-carbonyl)-N-(4-methoxyphenyl)pyrrolidine-1-carbothioamide
• Synonyms: 2-(4-(6-fluorobenzo[d]isoxazol-3-yl)piperidine-1-carbonyl)-N-(4-methoxyphenyl)pyrrolidine-1-carbothioamide
• CAS NO: 1426224-57-8
• Molecular Weight: 482.579
• Mol File: 1426224-57-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(4-(6-fluorobenzo[d]isoxazol-3-yl)piperidine-1-carbonyl)-N-(4-methoxyphenyl)pyrrolidine-1-carbothioamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-(6-fluorobenzo[d]isoxazol-3-yl)piperidine-1-carbonyl)-N-(4-methoxyphenyl)pyrrolidine-1-carbothioamide(1426224-57-8)
• EPA Substance Registry System: 2-(4-(6-fluorobenzo[d]isoxazol-3-yl)piperidine-1-carbonyl)-N-(4-methoxyphenyl)pyrrolidine-1-carbothioamide(1426224-57-8)

Safety Data

• Hazardous Substances Data: 1426224-57-8(Hazardous Substances Data)

Upstream product

• 15761-39-4 1-(tert-butoxycarbonyl)-L-proline 
• 1426224-76-1 C₁₇H₂₀FN₃O₂*C₂HF₃O₂ 
• 2284-20-0 4-Methoxyphenyl isothiocyanate 
• 84163-13-3 6-fluoro-3-(piperidin-4-yl)benzo[d]isoxazole hydrochloride 
• 1426224-72-7 tert-butyl 2-(4-(6-fluorobenzo[d]isoxazol-3-yl)piperidin-1-carbonyl)pyrrolidine-1-carboxylate 

Relevant articles and documents

Inhibition of protein glycation by urea and thiourea derivatives of glycine/proline conjugated benzisoxazole analogue-Synthesis and structure-activity studies

Synthesis of a new series of urea/thiourea derivatives of Gly/Pro conjugated benzisoxazole has been reported. Structure of the compounds was characterized by physical and spectroscopical data and has been screened for their in vitro antiglycation activity. Several compounds showed promising activity with IC50 50 = 41.9 μM). Further, it was found that compounds containing methoxy and bromine substituents have exerted highly potent activity. Thus, the title compounds represent novel class of potent antiglycating agents.