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Biological properties of synthetic glycoconjugate mimics of heparin comprising different molecular spacers

Bioorganic & medicinal chemistry letters, 1998-08, Vol.8 (16), p.2081-2086

1998

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In vitro evaluation of synthetic heparin-like conjugates comprising different thrombin binding domains

Bioorganic & medicinal chemistry letters, 1998-05, Vol.8 (10), p.1201-1206

1998

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Synthesis of heparin-like antithrombotics having perphosphorylated thrombin binding domains

Bioorganic & medicinal chemistry, 1999-09, Vol.7 (9), p.1881-1890

1999

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Polymer-supported solution synthesis of heparan sulphate-like oligomers

Bioorganic & medicinal chemistry letters, 1997-05, Vol.7 (9), p.1175-1180

1997

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Solid-phase synthesis of an RNA nucleopeptide fragment from the nucleoprotein of poliovirus

Nucleic acids research, 1992-05, Vol.20 (10), p.2435-2439

1992

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Synthesis of the nucleopeptides H-Phe-Tyr(pGC)-NH2 and H-Phe-Ser(pGC)-Ala-OH via a phosphotriester approach

Nucleic acids research, 1989-04, Vol.17 (8), p.2897-2905

1989

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Solid-phase synthesis of the nucleopeptide fragment H-Asp-Ser[pAAGTAAGCC]-Glu-OH from the nucleoprotein of Bacillus Subtilis phage ø29

Nucleic acids research, 1992-08, Vol.20 (15), p.4015-4020

1992

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A new protected acyl protecting group for exocyclic amino functions of nucleobases

Tetrahedron letters, 1990, Vol.31 (3), p.427-430

1990

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Synthesis of a peptidyldimannosyl phosphate: fragment of the variant-specific surface glycoprotein membrane anchor from trypanosoma brucei

Tetrahedron letters, 1991-11, Vol.32 (45), p.6637-6640

1991

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Synthesis of seryl threonyl phosphate. A model compound designed to study the spectroscopic and chemical features of a phosphodiester linkage similar to the one proposed to exist in Azotobacter flavodoxin

Journal of the American Chemical Society, 1989-08, Vol.111 (16), p.6470-6471

1989

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Glutathione analogues as novel inhibitors of rat and human glutathione S-transferase isoenzymes, as well as of glutathione conjugation in isolated rat hepatocytes and in the rat in vivo

Biochemical journal, 1995-05, Vol.308 ( Pt 1) (1), p.283-290

1995

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Conformational Aspects of an Uncharged Phosphate Analogon Built In at the Branch-point of a DNA Four-way Junction

Journal of molecular biology, 1996-09, Vol.262 (3), p.349-357

1996

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ChemInform Abstract: A Convenient Approach Towards the Conversion of H-Phosphonate and H-Phosphonothioate Diesters into Phosphoro(di)thioate Derivatives

ChemInform, 1991-01, Vol.22 (2), p.no-no

1991

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ChemInform Abstract: Synthesis and Phosphorylating Properties of Hydroxy Amino Acid Phosphoramidites

ChemInform, 1993-06, Vol.24 (23), p.no-no

1993

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An expeditious in situ preparation of benzyl (S)-2-aziridinecarboxylate

Recueil des Travaux Chimiques des Pays-Bas, 1989, Vol.108 (9), p.314-316

1989

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Solid-phase synthesis of RNA via a silyl-protecting-group strategy

Recueil des Travaux Chimiques des Pays-Bas, 1991, Vol.110 (9), p.378-383

1991

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The action of serpins and heparin as leads in drug discovery

Pharmacochemistry Library, 1997, Vol.28, p.477-486

1997

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Solid-phase synthesis of the nucleopeptide fragment H-Asp-Ser[pAAAGTAAGCC]-Glu-OH from the nucleoprotein of Bacillus subtilis phage phi 29

Nucleic acids research, 1992-08, Vol.20 (15), p.4015-4020

1992

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Solid-phase synthesis of H-Phe-Tyr-(pATAT)-NH2: a nucleopeptide fragment from the nucleoprotein of bacteriophage phi X174

Nucleic acids research, 1990-11, Vol.18 (22), p.6491-6495

1990

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A Convenient Approach Towards the Conversion of H-Phosphonate and H-Phosphonothioate Diesters into Phosphoro(di)thioate Derivatives

Synlett, 1990-08, Vol.1990 (8), p.481-483

1990

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Synthesis and Phosphorylating Properties of Hydroxyamino Acid Phosphoramidites

Synthesis (Stuttgart), 1992, Vol.1992 (12), p.1269-1272

1992

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Synthesis and phsophorylating properties of hydroxyamino acid phosphoramidites

Synthesis (Stuttgart), 1992 (12), p.1269-1272

1992

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Synthesis of the nucleopeptides H-Phe-Tyr(pGC)-NH sub(2) and H-Phe-Ser(pGC)-Ala-OH via a phosphotriester approach

Nucleic acids research, 1989-01, Vol.17 (8), p.2897-2906

1989

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Solid-phase synthesis of H-Phe-Tyr-pATAT-NH2 : a nucleopeptide fragment from the nucleoprotein of bacteriophage ØX174

Nucleic acids research, 1990, Vol.18 (22), p.6491-6495

1990

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Solid-phase synthesis of H-Phe-Tyr(pATAT)-NH sub(2): A nucleopeptide fragment from the nucleoprotein of bacteriophage Phi X174

Nucleic acids research, 1990-01, Vol.18 (33), p.6491-6495

1990

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Biological properties of synthetic glycoconjugate mimics of heparin comprising different molecular spacers

In vitro evaluation of synthetic heparin-like conjugates comprising different thrombin binding domains

Synthesis of heparin-like antithrombotics having perphosphorylated thrombin binding domains

Polymer-supported solution synthesis of heparan sulphate-like oligomers

Solid-phase synthesis of an RNA nucleopeptide fragment from the nucleoprotein of poliovirus

Synthesis of the nucleopeptides H-Phe-Tyr(pGC)-NH2 and H-Phe-Ser(pGC)-Ala-OH via a phosphotriester approach

Solid-phase synthesis of the nucleopeptide fragment H-Asp-Ser[pAAGTAAGCC]-Glu-OH from the nucleoprotein of Bacillus Subtilis phage ø29

A new protected acyl protecting group for exocyclic amino functions of nucleobases

Synthesis of a peptidyldimannosyl phosphate: fragment of the variant-specific surface glycoprotein membrane anchor from trypanosoma brucei

Synthesis of seryl threonyl phosphate. A model compound designed to study the spectroscopic and chemical features of a phosphodiester linkage similar to the one proposed to exist in Azotobacter flavodoxin

Glutathione analogues as novel inhibitors of rat and human glutathione S-transferase isoenzymes, as well as of glutathione conjugation in isolated rat hepatocytes and in the rat in vivo

Conformational Aspects of an Uncharged Phosphate Analogon Built In at the Branch-point of a DNA Four-way Junction

ChemInform Abstract: A Convenient Approach Towards the Conversion of H-Phosphonate and H-Phosphonothioate Diesters into Phosphoro(di)thioate Derivatives

ChemInform Abstract: Synthesis and Phosphorylating Properties of Hydroxy Amino Acid Phosphoramidites

An expeditious in situ preparation of benzyl (S)-2-aziridinecarboxylate

Solid-phase synthesis of RNA via a silyl-protecting-group strategy

The action of serpins and heparin as leads in drug discovery

Solid-phase synthesis of the nucleopeptide fragment H-Asp-Ser[pAAAGTAAGCC]-Glu-OH from the nucleoprotein of Bacillus subtilis phage phi 29

Solid-phase synthesis of H-Phe-Tyr-(pATAT)-NH2: a nucleopeptide fragment from the nucleoprotein of bacteriophage phi X174

A Convenient Approach Towards the Conversion of H-Phosphonate and H-Phosphonothioate Diesters into Phosphoro(di)thioate Derivatives

Synthesis and Phosphorylating Properties of Hydroxyamino Acid Phosphoramidites

Synthesis and phsophorylating properties of hydroxyamino acid phosphoramidites

Synthesis of the nucleopeptides H-Phe-Tyr(pGC)-NH sub(2) and H-Phe-Ser(pGC)-Ala-OH via a phosphotriester approach

Solid-phase synthesis of H-Phe-Tyr-pATAT-NH2 : a nucleopeptide fragment from the nucleoprotein of bacteriophage ØX174

Solid-phase synthesis of H-Phe-Tyr(pATAT)-NH sub(2): A nucleopeptide fragment from the nucleoprotein of bacteriophage Phi X174

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