- Synthesis of α-D-Glcp-(1→2)-α-D-Glcp-(1→3)-α-D-Glcp-O-(CH2)8COOh3 for use in the assay of α-glucosidase I activity
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The chemical synthesis of α-D-Glcp-(1 → 2)-α-D-Glc p-(1 → 3)-α-D-Glcp-O-(CH2)8COOCH3 (9), a substrate specific for α-glucosidase I, is reported. This enzyme removes the terminal α-D-Glcp unit to produce α-D-Glcp-α-D-Glcp-(1 → 3) -α-D-Glcp-O-(CH2)8COOCH3 (10). This is the first synthetic substrate described for glucosidase I that allows kinetic evaluation of substrates and inhibitors of this enzyme. Tetramethylrhodamine was coupled to 9 through an ethylenediamine linker to produce a brilliant red derivative. Addition of this fluorescent dye did not affect enzyme binding to the substrate, as determined by a comparison of the K(m) value (1.3 mM). The fluorescent label allows visual detection of 2-3 pmol of product by TLC.
- Scaman, Christine H.,Hindsgaul, Ole,Palcic, Monica M.,Srivastava, Om P.
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p. 203 - 213
(2007/10/03)
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- ENTWICKLUNG EINES SYNTHESEBLOCKS DER 3-O-β-D-GALACTOPYRANOSYL-D-GALACTOPYRANOSE
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In the presence of trimethylsilyl triflate, 1,2,3,4,6-penta-O-acetyl-β-D-galactopyranose reacted with benzyl 4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranoside to give benzyl 2,6-di-O-benzyl-3-O-β-D-galactopyranosyl-β-D-galactopyranoside further converted i
- Paulsen, Hans,Hasenkamp, Thomas,Paal, Michael
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