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Development of Serine Protease Inhibitors Displaying a Multicentered Short (<2.3 Å) Hydrogen Bond Binding Mode: Inhibitors of Urokinase-Type Plasminogen Activator and Factor Xa

Journal of medicinal chemistry, 2001-08, Vol.44 (17), p.2753-2771

2001

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Substrate specificities and structure-activity relationships for acylation of antibiotics catalyzed by kanamycin acetyltransferase

Biochemistry (Easton), 1984-10, Vol.23 (22), p.5118-5122

1984

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UDP-N-acetylglucosamine acyltransferase of Escherichia coli. The first step of endotoxin biosynthesis is thermodynamically unfavorable

The Journal of biological chemistry, 1993-09, Vol.268 (26), p.19858-19865

1993

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2-(2-Hydroxy-3-alkoxyphenyl)-1H-benzimidazole-5-carboxamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors

Bioorganic & medicinal chemistry letters, 2002-08, Vol.12 (15), p.2019-2022

2002

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2-(2-Hydroxy-3-alkoxyphenyl)-1 H-benzimidazole-5-carboxamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors

Bioorganic & medicinal chemistry letters, 2002, Vol.12 (15), p.2019-2022

2002

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Anti-Immune Complex Antibodies Enhance Affinity and Specificity of Primary Antibodies

Proceedings of the National Academy of Sciences - PNAS, 1993-02, Vol.90 (4), p.1184-1189

1993

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Expression, Purification, and Characterization of Deglycosylated Human Pro-Prostate-Specific Antigen

Protein expression and purification, 2000-12, Vol.20 (3), p.405-413

2000

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A new kinetic diagnostic for enzymatic mechanisms using alternative substrates

Analytical biochemistry, 1984-01, Vol.141 (2), p.413-417

1984

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PURIFICATION AND KINETIC CHARACTERISATION OF KANAMYCIN ACETYLTRANSFERASE IV

RADIKA, KESAVAN

1982

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Purification of two forms of kanamycin acetyltransferase from Escherichia coli

Archives of biochemistry and biophysics, 1984-08, Vol.233 (1), p.272-285

1984

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Structural basis for selectivity of a small molecule, S1-binding, submicromolar inhibitor of urokinase-type plasminogen activator

Chemistry & biology, 2000-04, Vol.7 (4), p.299-312

2000

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Substrate specificites and structure-activity relationships for acylation of antibiotics catalyzed by kanamycin acetyltransferase

Biochemistry (Easton), 1984-10, Vol.23 (22), p.5118-5122

1984

Volltextzugriff (PDF)

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Development of Serine Protease Inhibitors Displaying a Multicentered Short (<2.3 Å) Hydrogen Bond Binding Mode: Inhibitors of Urokinase-Type Plasminogen Activator and Factor Xa

Substrate specificities and structure-activity relationships for acylation of antibiotics catalyzed by kanamycin acetyltransferase

UDP-N-acetylglucosamine acyltransferase of Escherichia coli. The first step of endotoxin biosynthesis is thermodynamically unfavorable

2-(2-Hydroxy-3-alkoxyphenyl)-1H-benzimidazole-5-carboxamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors

2-(2-Hydroxy-3-alkoxyphenyl)-1 H-benzimidazole-5-carboxamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors

Anti-Immune Complex Antibodies Enhance Affinity and Specificity of Primary Antibodies

Expression, Purification, and Characterization of Deglycosylated Human Pro-Prostate-Specific Antigen

A new kinetic diagnostic for enzymatic mechanisms using alternative substrates

PURIFICATION AND KINETIC CHARACTERISATION OF KANAMYCIN ACETYLTRANSFERASE IV

Purification of two forms of kanamycin acetyltransferase from Escherichia coli

Structural basis for selectivity of a small molecule, S1-binding, submicromolar inhibitor of urokinase-type plasminogen activator

Substrate specificites and structure-activity relationships for acylation of antibiotics catalyzed by kanamycin acetyltransferase

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