1197856-33-9

Upstream product

• 1197856-24-8 methyl 2-(4-methoxybenzyl)-8-(naphthalen-1-ylmethyl)-6-oxo-9-(3-(trifluoromethyl)phenyl)-3,4-dihydro-2H,6H-pyrido[1,2-e][1,2,5]thiadiazine-4-carboxylate 1,1-dioxide 
• 288270-18-8 5-[1-hydroxy-2-(nalphthalen-1-yl)ethylidene]-2,2-dimethyl[1,3]dioxane-4,6-dione 
• 864365-18-4 (4R)-2-(3-(trifluoromethyl)benzyl)-4,5-dihydrothiazole-4-carboxylic acid methyl ester 
• 86-87-3 naphth-1-yl acetic acid 
• 2338-76-3 3-trifluoromethylphenylacetonitrile 
• 1024869-14-4 C₁₁H₁₂F₃NO 

Downstream Products

• 1197856-34-0 8-(naphthalen-1-ylmethyl)-6-oxo-9-(3-(trifluoromethyl)phenyl)-3,4-dihydro-2H,6H-pyrido[1,2-e][1,2,5]thiadiazine-4-carboxylic acid 1,1-dioxide 

Relevant academic research and scientific papers

INHIBITORS OF MICROBIALLY INDUCED AMYLOID

The present disclosure provides compounds useful for the prevention of amyloid formation and the treatment of amyloid related disorders, including synucleopathies such as Parkinson's Disease.

A novel heterocyclic scaffold formed by ring expansion of a cyclic sulfone to sulfonamides

"Chemical Equation Presented" A novel heterocyclic scaffold with a peptidomimetlc backbone structure has been synthesized. The scaffold is formed by insertion of primary amines into a cyclic sulfone to give the corresponding ring-expanded sulfonamides. By