143393-84-4

Upstream product

• 140195-49-9 1L-1,2:3,4-di-O-cyclohexylidene-5-O-methyl-6-O-(trifluoromethylsulfonyl)-chiro-inositol 
• 6848-53-9 L-3,4:5.6-di-O-cyclohexylidene-2-O-methyl-(-)-chiro-inositol 
• 744209-88-9 O¹,O²;O³,O⁴-diisopropyliden-5,6-anhydro-allo-inositol 
• 58769-23-6 1L-3,4,:5,6-di-O-isopropylidene-2-O-methyl-chiro-inositol 
• 642-38-6 quebrachitol 

Downstream Products

• 160712-71-0 Phosphoric acid dibenzyl ester (1S,2S,3R,4S,5S,6S)-2-benzyloxy-3,4-bis-(bis-benzyloxy-phosphoryloxy)-5-chloro-6-(1-ethoxy-ethoxy)-cyclohexyl ester 
• 160712-66-3 C₃₈H₃₇ClO₉ 
• 160712-68-5 C₃₀H₂₉ClO₇ 

Relevant academic research and scientific papers

Synthesis and biological activity of the D-3-deoxy-3-fluoro and D-3-chloro-3-deoxy analogues of phosphatidylinositol

The naturally occurring inositol derivative, L-quebrachitol (1), serves as starting material for the synthesis of D-3-deoxy-3-fluoro- and D-3-chloro-3-deoxy-myo-inositol (4, 28). Their transformation into the title compounds 22 and 40 (abbreviated as FPI

Synthesis and evaluation of 3-modified 1D-myo-inositols as inhibitors and substrates of phosphatidylinositol synthase and inhibitors of myo-inositol uptake by cells

A number of 3-substituted 1D-myo-inositols were synthesized and evaluated as substrates for phosphatidylinositol synthase and uptake by intact cells. 1D-3-Amino-, -3-chloro-, and -3-(acetylthio)-3-deoxy-myo-inositols were all synthesized by nucleophilic d