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Solid-Phase and Solution-Phase Synthesis of Glycosylphosphatidylinositol Glycans

a glycosylphosphatidylinositol and solution-phase technology, which is applied in the direction of antibody medical ingredients, carrier-bound antigen/hapten ingredients, immunological disorders, etc., can solve the problem of no solid-phase or automated synthesis reports

Inactive Publication Date: 2012-01-05
MASSACHUSETTS INST OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Further, despite the tremendous amount of work on the synthesis of GPIs, there have been no solid-phase or automated syntheses reported.

Method used

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  • Solid-Phase and Solution-Phase Synthesis of Glycosylphosphatidylinositol Glycans
  • Solid-Phase and Solution-Phase Synthesis of Glycosylphosphatidylinositol Glycans
  • Solid-Phase and Solution-Phase Synthesis of Glycosylphosphatidylinositol Glycans

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0151]

[0152]Ethyl-4-O-acetyl-2-azido-3,6-di-O-benzyl-2-deoxy-thio-β-D-glucopyranoside 5. [α]24D: −43.5° (c 1.07, CH2Cl2); IR (thin film) 2916, 2108, 1743, 1222, 1047 cm−1; 1H NMR (500 MHz, CDCl3) δ 7.40-7.29 (m, 10H), 5.06-5.02 (m, 1H), 4.86 (d, J=11.3 Hz, 1H), 4.68 (d, J=11.3 Hz, 1H), 4.52 (s, 2H), 4.34 (d, J=9.5 Hz, 1H), 3.59-3.48 (m, 6H), 2.83-2.73 (m, 2H), 1.87 (s, 3H), 1.35 (t, J=7.3 Hz, 3H); 13C-NMR (125 MHz, CDCl3) δ 169.9, 138.0, 137.8, 128.8, 128.6, 128.3, 128.1, 128.0, 84.5, 82.8, 77.9, 75.9, 73.8, 71.1, 69.9, 66.0, 25.0, 21.0, 15.4; FAB MS m / z (M+Na)+ calcd 494.1726, found 494.1716.

example 2

[0153]

[0154]6-O-Acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranose trichloroacetimidate 6. [α]24D: +34.4° (c 2.18, CH2Cl2); IR (thin film) 2938, 2880, 1707, 1683, 1220 cm−1; 1H NMR (500 MHz, CDCl3) δ 8.53 (s, 1H), 7.38-7.21 (m, 14H), 6.29 (d, J=2.1 Hz, 1H), 4.91 (d, J=10.7 Hz, 1H), 4.73 (s, 2H), 4.61-4.55 (m, 3H), 4.33 (dd, J=2.1, 12.2 Hz, 1H), 4.24 (dd, J=4.3, 11.9 Hz, 1H), 4.00-3.90 (m, 4H), 3.84-3.83 (m, 1H), 2.00 (s, 3H); 13C-NMR (125 MHz, CDCl3) δ 170.8, 160.3, 137.8, 137.8, 137.7, 128.5, 128.4, 128.3, 128.3, 128.0, 127.8, 127.8, 95.6, 78.8, 75.3, 73.6, 73.2, 72.7, 72.5, 72.2, 63.0, 20.8; FAB MS m / z (M+Na)+ calcd 658.1137, found 658.1123.

example 3

[0155]

[0156]2-O-Acetyl-3,4-di-O-benzyl-6-O-triisopropylsilyl-α-D-mannopyranose trichloroacetimidate 8. [α]24D: +43.4° (c 2.20, CH2Cl2); IR (thin film) 2940, 2865, 1752, 1674, 1229 cm−1; 1H NMR (500 MHz, CDCl3) δ 8.63 (s, 1H), 7.38-7.26 (m, 10H), 6.26 (d, J=1.8 Hz, 1H), 5.46 (dd, J=2.1, 3.1 Hz, 1H), 4.93 (d, J=10.4 Hz, 1H), 4.75 (d, J=11.3 Hz, 1H), 4.71 (d, J=10.7 Hz, 1H), 4.62-4.57 (m, 1H), 4.17 (t, J=9.8 Hz, 1H), 4.09-4.05 (m, 2H), 3.95 (d, J=11.3 Hz, 1H), 3.85 (dd, J=1.5, 9.8 Hz, 1H), 2.16 (s, 3H), 1.15-1.05 (m, 22H); 13C-NMR (125 MHz, CDCl3) δ 170.8, 160.7, 139.1, 138.3, 129.1, 129.1, 129.0, 128.8, 128.6, 128.5, 96.2, 91.6, 77.9, 76.3, 74.0, 72.8, 68.1, 62.8, 21.6, 18.7, 18.6, 12.8; FAB MS m / z (M+Na)+ calcd 724.2007, found 724.2006.

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Abstract

One aspect of the present invention relates to solution-phase approaches to GPI synthesis. Another aspect of the present invention relates to key building blocks, and syntheses thereof, useful for GPI assembly. Yet another aspect of the invention relates to an automated method for the synthesis of GPIs and fragments thereof.

Description

RELATED APPLICATIONS[0001]This application is a continuation of U.S. patent application Ser. No. 10 / 520,963, accorded a 371(c) date of Aug. 26, 2005, which is a U.S. National Stage of Patent Cooperation Treaty Application serial number PCT / US03 / 21564, filed Jul. 10, 2003; which claims the benefit of priority to U.S. Provisional Patent Application Ser. No. 60 / 394,794, filed Jul. 10, 2002.BACKGROUND OF THE INVENTION[0002]Glycosylphosphatidylinositol (GPI) structures are ubiquitous in nature—they occur in almost all organisms except eubacteria, and roughly 0.5% of all proteins are expected, based on genomic analysis, to be linked to the cell surface via GPI anchors.1 Many organisms, especially protozoa, also express non-protein-linked GPI-type glycans on their cell surfaces; these are often essential for virulence, immune evasion, and other important properties.2 In addition to their structural functions, GPI molecules serve as intermediate messengers in signal-transduction pathways in...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K39/385A61P37/04A61P33/02C07H15/207C07K17/10
CPCC07H15/203C08B37/006C07H15/207A61P33/02A61P37/04
Inventor SEEBERGER, PETER H.HEWITT, MICHAEL C.SNYDER, DANIEL
Owner MASSACHUSETTS INST OF TECH
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