105308-55-2

Upstream product

• 16452-52-1 (S)-2-hydroxyhexadecanoic acid 
• 78330-57-1 (2S)-2-hydroxyhexadecanoic acid methyl ester 
• 105308-52-9 (R)-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester 
• 825-60-5 benzimidic acid ethyl ester 
• 105243-29-6 (2'E,6'E,4R,1'R)-4-(1'-hydroxy-7'-methyl-2',6'-hexadecadienyl)-2-phenyl-1,3-oxazolin-2-ene 
• 105243-21-8 (R)-4-formyl-2-phenyl-1,3-oxazolin-2-ene 
• 105243-32-1 (S)-(+)-2-acetoxyhexadecanoic acid 
• 98393-17-0 L-2-aminohexadecanoic acid 
• 88195-83-9 p-nitrophenyl (S)-2-acetoxyhexadecanoate 

Relevant academic research and scientific papers

Synthesis and Biological Activity of the Isomers and Analogs of (4E,8E,2S,3R,2'R)-N-2'-Hydroxyhexadecanoyl-9-methyl-4,8-sphingadienine, the Ceramide Portion of the Fruiting-inducing Cerebroside in a Basidiomycete Schizophyllum commune

The title compounds were synthesized by employing 2-aminohexadecanoic acid and serine as the chiral sources, and served for an assay of fruiting-inducing activity on Schizophyllum commune.The structure-bioactivity relationship among closely related synthetic ceramides is discussed.