1289562-91-9

Upstream product

• 1078-19-9 6-methoxy-3,4-dihydro-1(2H)-naphthalenone 
• 98-80-6 phenylboronic acid 
• 53567-96-7 1,2,3,4-tetrahydro-6-n-hydroxynaphthalene-2-carboxylic acid 
• 2473-19-0 methyl 1,2,3,4-tetrahydro-6-methoxynaphthalene-2-carboxylate 
• 40153-87-5 methyl 6-methoxy-1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate 
• 1289562-75-9 2-((tert-butyldimethylsilyloxy)(6-phenyl-1,2,3,4-tetrahydronaphthalen-2-yl)methyl)oxazole 
• 1289562-73-7 oxazol-2-yl(6-phenyl-1,2,3,4-tetrahydronaphthalen-2-yl)methanol 
• 1289562-71-5 6-phenyl-1,2,3,4-tetrahydronaphthalene-2-carboxaldehyde 
• 1289562-69-1 (6-phenyl-1,2,3,4-tetrahydronaphthalen-2-yl)methanol 
• 1289562-67-9 methyl 6-phenyl-1,2,3,4-tetrahydronaphthalene-2-carboxylate 
• 1289562-65-7 methyl 6-(trifluoromethanesulfonyloxy)-1,2,3,4-tetrahydronaphthalene-2-carboxylate 
• 65844-44-2 methyl 6-hydroxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate 

Downstream Products

• 1289561-41-6 methyl 6-(2-(6-phenyl-1,2,3,4-tetrahydronaphthalene-2-carbonyl)oxazol-5-yl)picolinate 
• 1289561-43-8 6-(2-(6-phenyl-1,2,3,4-tetrahydronaphthalene-2-carbonyl)oxazol-5-yl)picolinic acid 
• 1289561-45-0 6-(2-(6-phenyl-1,2,3,4-tetrahydronaphthalene-2-carbonyl)oxazol-5-yl)picolinic acid 
• 1289560-84-4 methyl 6-(2-(6-phenyl-1,2,3,4-tetrahydronaphthalene-2-carbonyl)oxazol-5-yl)picolinate 
• 1289560-87-7 6-(2-(6-phenyl-1,2,3,4-tetrahydronaphthalene-2-carbonyl)oxazol-5-yl)picolinic acid 
• 1289562-93-1 methyl 6-(2-(hydroxy(6-phenyl-1,2,3,4-tetrahydronaphthalen-2-yl)methyl)oxazol-5-yl)picolinate 
• 1289561-39-2 methyl 6-(2-(6-phenyl-1,2,3,4-tetrahydronaphthalene-2-carbonyl)oxazol-5-yl)picolinate 

Relevant academic research and scientific papers

Reversible competitive α-ketoheterocycle inhibitors of fatty acid amide hydrolase containing additional conformational constraints in the acyl side chain: Orally active, long-acting analgesics

A series of α-ketooxazoles containing conformational constraints in the C2 acyl side chain of 2 (OL-135) were examined as inhibitors of fatty acid amide hydrolase (FAAH). Only one of the two possible enantiomers displayed potent FAAH inhibition (S vs R en