6236-22-2

Upstream product

• 56552-80-8 (R)-3-benzyloxy-1,2-propanediol 
• 112-76-5 Stearoyl chloride 
• 111-63-7 vinyl stearate 
• 57-11-4 stearic acid 
• 13071-59-5 3-benzyloxypropan-1,2-diol 
• 14618-80-5 (R)-benzyl glycidol 
• 100-44-7 benzyl chloride 
• 16495-03-7 (S)-4-(benzyloxymethyl)-2,2-dimethyl-1,3-dioxolane 
• 100-39-0 benzyl bromide 

Downstream Products

• 83526-65-2 2-O-Acetyl-3-O-benzyl-1-O-octadecanoyl-sn-glycerin 
• 219996-61-9 Octadecanoic acid (S)-3-benzyloxy-2-butyryloxy-propyl ester 
• 282532-75-6 Octadecanoic acid (S)-3-benzyloxy-2-dodecanoyloxy-propyl ester 
• 56586-08-4 3-O-benzyl-1,2-dioctadecanoyl-sn-glycerol 
• 282532-76-7 3-O-benzyl-2-O-hexadecanoyl-1-O-octadecanoyl-sn-glycerol 
• 79549-26-1 2-O-Acetyl-1-O-octadecanoyl-sn-glyceryl-3-phosphorylcholin 
• 22610-61-3 (S)-2,3-dihydroxypropyl n-octadecanoate 
• 3269-63-4 Glycerin-1-benzylether-3-stearat-2-(9,10,12,13-tetrabrom-stearat) 
• 1346691-02-8 C₆₀H₁₀₁O₁₅P 
• 1346691-01-7 1-O-(2,3,4,6-tetra-O-methoxyacetyl-α-D-mannopyranosyl)-3-O-benzyl-2-O-(((S)-2-O-hexadecanoyloxy-3-O-octadecanoyloxypropyl)(benzyl)phosphoryl)-DL-glycerol 
• 219996-62-0 1-O-stearoyl-2-O-octanoyl-3-O-benzyl-sn-glycerol 
• 106348-51-0 Octadecanoic acid (S)-2-dodecanoyloxy-3-hydroxy-propyl ester 
• 228406-23-3 O-benzyl O-(2R)-2-hexadecanoyloxy-3-octadecanoyloxypropyl-N,N-diisopropyl phosphoramidite 
• 228406-22-2 Octadecanoic acid (R)-3-(benzyloxy-diisopropylamino-phosphanyloxy)-2-dodecanoyloxy-propyl ester 

Relevant academic research and scientific papers

Total synthesis and mass spectrometric analysis of a: Mycobacterium tuberculosis phosphatidylglycerol featuring a two-step synthesis of (R)-tuberculostearic acid

We report the total synthesis of (R)-tuberculostearic acid-containing Mycobacterium tuberculosis phosphatidylglycerol (PG). The approach features a two-step synthesis of (R)-tuberculostearic acid, involving an (S)-citronellyl bromide linchpin, and the pho

Phosphatidyl myo-inositol mannosides mimics built on an acyclic or heterocyclic core: Synthesis and anti-inflammatory properties

Phosphatidyl myo-inositol mannosides (PIMs) are constituents of the mycobacterial cell wall and possess immunomodulatory activities. Certain PIM derivatives have immunoprotective activity and are of interest as anti-inflammatory agents. In order to identi

SYNTHETIC ANALOGUES OF PHOSPHATIDYL-MYO-INOSITOL MANNOSIDES WITH AN INHIBITORY ACTIVITY OF THE INFLAMMATORY RESPONSE

The present invention relates to novel synthetic analogues of phosphatidyl-myo-inositol mannosides (hereinafter referred to as PIMs) of general formula (I): or a pharmaceutically acceptable salt thereof, to the method for preparing same and to the use thereof in the prevention or treatment of a disease associated with the overexpression of cytokines or of chemokines, in particular of TNF and/or of IL-12. The invention also relates to a pharmaceutical composition comprising at least one synthetic derivative of PIM.

Chemoenzymatic synthesis of enantiopure structured triacylglycerols

A highly efficient chemoenzymatic method for the synthesis of enantiopure ABC-type asymmetrically structured triacylglycerols has been developed starting from enantiopure (S)-solketal and involving two lipase steps. Georg Thieme Verlag Stuttgart.

Phosphorylation of unnatural phosphatidylinositols with phosphatidylinositol 3-kinase

Phosphatidylinositol analogs (PI(C2)-PI(C18)) having a series of saturated fatty acid (C2-C18) at sn-2 position were synthesized and subjected to the phosphorylation reaction with phosphatidylinositol 3-kinase (PI 3- kinase). The reactivity of Pica with PI 3-kinase turned out to be comparable to that of natural PI, although PI(C18) was not phosphorylated under the same condition. The chirality of sn-2 center was not responsible for the phosphorylation reaction. (C) 2000 Elsevier Science Ltd.

Synthesis of diacylglycerol analogs of phosphatidylinositol 3,4,5- trisphosphate

Phosphatidylinositol 3,4,5-trisphosphate analogs with saturated diacylglycerol substructure have been designed, focusing on their reactivity with PIP3 5-phosphatase. Dephosphorylation of native PIP3 was competitively inhibited in the presence of synthetic PIP3(C2) and PIP3(C4), respectively.