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High-throughput identification of fucosyltransferase inhibitors using carbohydrate microarrays

Bioorganic & medicinal chemistry letters, 2004-06, Vol.14 (12), p.3185-3188

2004

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Towards new antibiotics targeting bacterial transglycosylase: Synthesis of a Lipid II analog as stable transition-state mimic inhibitor

Bioorganic & medicinal chemistry letters, 2018-09, Vol.28 (16), p.2708-2712

2018

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Development of bacterial transglycosylase inhibitors as new antibiotics: Moenomycin A treatment for drug-resistant Helicobacter pylori

Bioorganic & medicinal chemistry letters, 2014-06, Vol.24 (11), p.2412-2414

2014

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Acceptor substrate-based selective inhibition of galactosyltransferases

Bioorganic & medicinal chemistry letters, 1998-12, Vol.8 (23), p.3359-3364

1998

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Synthesis of C2-symmetrical polyhydroxyazepanes as inhibitors of glycosidases

Bioorganic & medicinal chemistry letters, 1996-05, Vol.6 (10), p.1117-1122

1996

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Protein microarray using α-amino acids as metal tags on chips

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (5), p.1413-1416

2005

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Facile synthesis of metal-chelating peptides on chip for protein array

Bioorganic & medicinal chemistry letters, 2004-04, Vol.14 (8), p.1987-1990

2004

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Chemoenzymatic synthesis of iminocyclitol derivatives: A useful library strategy for the development of selective fucosyltransfer enzymes inhibitors

Bioorganic & medicinal chemistry letters, 1998-12, Vol.8 (23), p.3353-3358

1998

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Synthesis of sialyl Lewis X mimetics using the Ugi four-component reaction

Bioorganic & medicinal chemistry letters, 1998-09, Vol.8 (17), p.2333-2338

1998

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Design, synthesis, and biological evaluation of HIV/FIV protease inhibitors incorporating a conformationally constrained macrocycle with a small P3' residue

Bioorganic & medicinal chemistry letters, 2001-01, Vol.11 (2), p.219-222

2001

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Design and synthesis of an α-mannosyl terpenoid as selective inhibitor of P-selectin

Bioorganic & medicinal chemistry letters, 1997-10, Vol.7 (19), p.2485-2490

1997

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Synthesis of lactosamine derivatives using β- d-galactosidase from Bacillus circulans

Bioorganic & medicinal chemistry letters, 1996-05, Vol.6 (10), p.1123-1126

1996

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Liposome-like fucopeptides as sialyl lewis X mimetics

Bioorganic & medicinal chemistry letters, 1996-11, Vol.6 (22), p.2755-2760

1996

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Toward a transition state analog inhibitor of N-acetylglucosaminyl transferase V

Bioorganic & medicinal chemistry letters, 1997-11, Vol.7 (21), p.2809-2812

1997

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Azasugar and glycal inhibitors of α-L-fucosidase

Bioorganic & medicinal chemistry letters, 1992, Vol.2 (1), p.33-36

1992

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Probing the inhibition of leukotriene A4 hydrolase based on its aminopeptidase activity

Bioorganic & medicinal chemistry letters, 1991-01, Vol.1 (10), p.551-556

1991

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Probing the inhibition of leukotriene A 4 hydrolase based on its aminopeptidase activity

Bioorganic & medicinal chemistry letters, 1991, Vol.1 (10), p.551-556

1991

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Enzymatic synthesis of sialyl Le x and derivatives based on a recombinant fucosyltransferase

Bioorganic & medicinal chemistry letters, 1991, Vol.1 (8), p.425-428

1991

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Enzymatic synthesis of sialyl Lex and derivatives based on a recombinant fucosyltransferase

Bioorganic & medicinal chemistry letters, 1991-01, Vol.1 (8), p.425-428

1991

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High-throughput identification of fucosyltransferase inhibitors using carbohydrate microarrays

Towards new antibiotics targeting bacterial transglycosylase: Synthesis of a Lipid II analog as stable transition-state mimic inhibitor

Development of bacterial transglycosylase inhibitors as new antibiotics: Moenomycin A treatment for drug-resistant Helicobacter pylori

Acceptor substrate-based selective inhibition of galactosyltransferases

Synthesis of C2-symmetrical polyhydroxyazepanes as inhibitors of glycosidases

Protein microarray using α-amino acids as metal tags on chips

Facile synthesis of metal-chelating peptides on chip for protein array

Chemoenzymatic synthesis of iminocyclitol derivatives: A useful library strategy for the development of selective fucosyltransfer enzymes inhibitors

Synthesis of sialyl Lewis X mimetics using the Ugi four-component reaction

Design, synthesis, and biological evaluation of HIV/FIV protease inhibitors incorporating a conformationally constrained macrocycle with a small P3' residue

Design and synthesis of an α-mannosyl terpenoid as selective inhibitor of P-selectin

Synthesis of lactosamine derivatives using β- d-galactosidase from Bacillus circulans

Liposome-like fucopeptides as sialyl lewis X mimetics

Toward a transition state analog inhibitor of N-acetylglucosaminyl transferase V

Azasugar and glycal inhibitors of α-L-fucosidase

Probing the inhibition of leukotriene A4 hydrolase based on its aminopeptidase activity

Probing the inhibition of leukotriene A 4 hydrolase based on its aminopeptidase activity

Enzymatic synthesis of sialyl Le x and derivatives based on a recombinant fucosyltransferase

Enzymatic synthesis of sialyl Lex and derivatives based on a recombinant fucosyltransferase

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