88195-83-9

Upstream product

• 105243-32-1 (S)-(+)-2-acetoxyhexadecanoic acid 
• 658-78-6 1-nitro-4-trifluoroacetoxy-benzene 
• 154857-70-2 (S)-2-((S)-2-Acetoxy-2-phenyl-acetoxy)-hexadecanoic acid methyl ester 
• 16742-51-1 methyl 2-hydroxypalmitate 
• 112-39-0 hexadecanoic acid methyl ester 
• 98393-17-0 L-2-aminohexadecanoic acid 
• 78330-57-1 (2S)-2-hydroxyhexadecanoic acid methyl ester 
• 16452-52-1 (S)-2-hydroxyhexadecanoic acid 

Downstream Products

• 105369-19-5 (4E,8E,2R,3S,2'S)-N-2'-acetoxyhexadecanoyl-1-O-benzoyl-9-methyl-4,8-sphingadienine 
• 105308-55-2 (4E,8E,2R,3R,2'S)-N-2'-acetoxyhexadecanoyl-1-O-benzoyl-9-methyl-4,8-sphingadienine 
• 105308-53-0 (4E,8E,2S,3S,2'S)-N-2'-acetoxyhexadecanoyl-1-O-benzoyl-9-methyl-4,8-sphingadienine 
• 105308-54-1 (4E,8E,2S,3R,2'S)-N-2'-acetoxyhexadecanoyl-1-O-benzoyl-9-methyl-4,8-sphingadienine 

Relevant academic research and scientific papers

Sphingolipids and glycerolipids. IV. Syntheses and ionophoretic activities of several analogues of soya-cerebroside II, a calcium ionophoretic sphingoglycolipid isolated from soybean

For examination of the structure-activity relationship five analogues [(2'R)-2'-hydroxypalmitoyl (3), palmitoyl (4), (2'S)-2'-hydroxypalmitoyl (5), β-D-galactosyl (6), and 8,9-dihydro (7) relevancies] of soya-cerebroside II (2), which is a calcium ionopho

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.