132832-52-1Relevant academic research and scientific papers
Synthesis of lipid A type carboxymethyl derivatives with ether chains instead of ester chains and their LPS-antagonistic activities
Watanabe, Yukiko,Miura, Kumiko,Shiozaki, Masao,Kanai, Saori,Kurakata, Shin-Ichi,Nishijima, Masahiro
, p. 47 - 54 (2007/10/03)
Synthesis of lipid A type carboxymethyl derivatives having ether chains at both the C-3 and C-3′ positions and their LPS-antagonistic activities toward human U937 cells are described.
Synthesis of 2-deoxy-2-[(3R)-3-hydroxytetradecanamido]-3-O-[(3R)-3-hydroxytetradecan yl]-α-D-glucopyranosyl dihydrogen phosphate and 2-deoxy-2-[(3R)-3-hydroxy-tetradecanamido]-3-O-[(3R)-3-hydoxytetradecan yl]-4-O-phosphono-D-glucopyranose
Shiozaki,Kobayashi,Ishida,Arai,Hiraoka,Nishijima,Kuge,Otsuka,Akamatsu
, p. 57 - 68 (2007/10/02)
Both a 3-O-alkyl lipid X analogue and its 4-O-phosphono isomer were synthesized from allyl 2-deoxy-4,6-O-isopropylidene-2-trifluoroacetamido-α-D-glucopyranoside. Both a 3-O-alkyl lipid X analogue and its 4-O-phosphono isomer were synthesized from allyl 2-deoxy-4,6-O-isopropylidene-2- trifluoroacetamido-α-D- glucopyranoside.
