Synthesis of 6-(5-cholesten-3β-yloxy)hexyl 4-O-(6-deoxy-β-d-galactopyranosyl)-1-thio-β-d-glucopyranoside and derivatives thereof for in vivo liposome studies
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Add time:09/02/2019 Source:sciencedirect.com
6-(5-Cholesten-3β-yloxy)hexyl 4-O-(6-deoxy- and 3,6-anhydro-β-d-galactopyranosyl)-1-thio-β-d-glucopyranoside were prepared from benzyl 4-O-β-d-galactopyranosyl-β-d-glucopyranoside, and incorporated into phospholipid vesicles. When injected intravenously into rats, these disaccharide-modified liposomes were found to be taken up mainly by liver cells.
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Prev:Synthesis of benzyl O-(2-O-methyl-β-d-galactopyranosyl)-(1→3)-2-acetamido-2-deoxy-β-d-glucopyranoside [benzyl 2′-O-methyllacto-N-bioside I], and its higher saccharide containing an O-(2-O-methyl-β-d-galactopyranosyl)-(1→3)-2-acetamido-2-deoxy-β-d-glucopyranosyl group as a potential substrate for (1→4)-α-l-fucosyltransferase☆
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