16452-52-1

Upstream product

• 52485-05-9 (S)-2-acetoxybutanedioic acid 1-ethyl ester 
• 544-63-8 n-tetradecanoic acid 
• 16742-51-1 methyl (R)-2-hydroxyhexadecanoate 
• 78330-57-1 (2S)-2-hydroxyhexadecanoic acid methyl ester 
• 112-39-0 hexadecanoic acid methyl ester 
• 16742-51-1 methyl 2-hydroxypalmitate 
• 16452-51-0 (R)-(-)-2-hydroxyhexadecanoic acid 
• 112-71-0 1-Bromotetradecane 
• 193885-58-4 2-(2-Chloro-acetylamino)-hexadecanoic acid 
• 105243-32-1 (S)-(+)-2-acetoxyhexadecanoic acid 
• 98393-18-1 D-2-chloroacetamidohexadecanoic acid 
• 7769-79-1 2-aminohexadecanoic acid 
• 98393-17-0 L-2-aminohexadecanoic acid 
• 154857-70-2 (S)-2-((S)-2-Acetoxy-2-phenyl-acetoxy)-hexadecanoic acid methyl ester 

Downstream Products

• 88195-83-9 p-nitrophenyl (S)-2-acetoxyhexadecanoate 
• 105308-54-1 (4E,8E,2S,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 
• 105308-55-2 (4E,8E,2R,3R,2'S)-N-2'-acetoxyhexadecanoyl-1-O-benzoyl-9-methyl-4,8-sphingadienine 
• 105369-19-5 (4E,8E,2R,3S,2'S)-N-2'-acetoxyhexadecanoyl-1-O-benzoyl-9-methyl-4,8-sphingadienine 
• 115648-55-0 Acetic acid (S)-1-((3E,7Z)-(1S,2R)-2-hydroxy-1-trityloxymethyl-heptadeca-3,7-dienylcarbamoyl)-pentadecyl ester 
• 115523-77-8 Acetic acid (R)-1-((3E,7Z)-(1S,2R)-2-hydroxy-1-trityloxymethyl-heptadeca-3,7-dienylcarbamoyl)-pentadecyl ester 
• 115648-56-1 Acetic acid (S)-1-((3E,7Z)-(1R,2S)-2-hydroxy-1-trityloxymethyl-heptadeca-3,7-dienylcarbamoyl)-pentadecyl ester 
• 115589-64-5 Acetic acid (R)-1-((3E,7Z)-(1R,2S)-2-hydroxy-1-trityloxymethyl-heptadeca-3,7-dienylcarbamoyl)-pentadecyl ester 
• 115648-58-3 Benzoic acid (2E,6Z)-(S)-1-[(R)-1-((S)-2-acetoxy-hexadecanoylamino)-2-hydroxy-ethyl]-hexadeca-2,6-dienyl ester 
• 115648-52-7 Benzoic acid (2E,6Z)-(S)-1-[(R)-1-((R)-2-acetoxy-hexadecanoylamino)-2-hydroxy-ethyl]-hexadeca-2,6-dienyl ester 
• 115648-57-2 Benzoic acid (2E,6Z)-(R)-1-[(S)-1-((S)-2-acetoxy-hexadecanoylamino)-2-hydroxy-ethyl]-hexadeca-2,6-dienyl ester 
• 115538-45-9 Benzoic acid (2E,6Z)-(R)-1-[(S)-1-((R)-2-acetoxy-hexadecanoylamino)-2-hydroxy-ethyl]-hexadeca-2,6-dienyl ester 

Relevant academic research and scientific papers

ENZYMATIC FORMATION OF (2R)-HYDROXY- AND 2-OXO-HEXADECANOIC ACID IN ULVA PERTUSA AND PORPHYRA SP.

(2R)-Hydroxy-hexadecanoic acid and 2-oxo-hexadecanoic acid have been isolated for the first time from marine algae (Ulva pertusa and Porphyra sp.).The two acids were shown to be formed enzymatically from palmitic acid (16:0) using palmitic acid.

Spicamycin derivatives and their use as anticancer agents

Spicamycin derivative represented by the formula (I) or a salt thereof: STR1 wherein R represents specific diverse substituents, for example, a linear alkadienyl having from 11 to 13 carbon atoms, and R1 and R2 respectively represent H or OH. Examples of specific compounds are 6-[4'-N-(N'-trans,trans 2,4-tridecadienoylglycyl)spicaminyl-amino]purine, and 6-[4'-N-(N'-trans,trans-2,4 dodecadienyoly glycyl) spicaminyl-amino]purine. Comopunds according to this invention are useful as a pharmaceutical for inhibition of a tumor, for example, human colon cancer.

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.

SYNTHESIS 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, AND ITS (2R,3S)-ISOMER

A synthesis of the natural enantiomer as well as its diastereomer of the title compound was accomplished, confirming the structure proposed for the fruiting-inducing cerebroside of Schizophyllum commune.