I. Lederman

发表

Synthesis of heparin fragments: A methyl α-pentaoside with high affinity for antithrombin III☆

G. Torri, M. Petitou, J. Choay, 1987 .

Biologically active heparin-like fragments with a “non-glycosamino”glycan structure. Part 1: a pentasaccharide containing a 3-O-methyl iduronic acid unit.

M. Petitou, C. V. Boeckel, J. Basten, 1992 .

Total synthesis of a heparin pentasaccharide fragment having high affinity for antithrombin III

G. Torri, M. Petitou, J. Choay, 1984 .

Synthesis of heparin fragments. A chemical synthesis of the trisaccharide O-(2-deoxy-2-sulfamido-3,6-di-O-sulfo-α-d-glucopyranosyl)-(1→4)-O-(2-O-sulfo-α-l-idopyranosyluronic acid)-(1→4)-2-deoxy-2-sulfamido-6-O-sulfo-d-glucopyranose heptasodium salt

G. Torri, M. Petitou, J. Choay, 1984 .

Total synthesis of a heparin pentasaccharide fragment having high affinity for antithrombin III

G. Torri, M. Petitou, J. Choay, 1984 .

Synthesis of N-acetyl-muramyl-L-alanyl-D-isoglutamine, an adjuvant of the immune response, and of some n-acetyl-muramyl-peptide analogs.

J. Choay, M. Derrien, I. Lederman, 2009, International journal of peptide and protein research.

Synthesis of heparin fragments: a methyl alpha-pentaoside with high affinity for antithrombin III.

G. Torri, M. Petitou, J. Choay, 1987, Carbohydrate research.

Synthesis and pharmacological properties of a close analogue of an antithrombotic pentasaccharide (SR 90107A/ORG 31540).

J. Herbert, J. Hérault, M. Petitou, 1997, Journal of medicinal chemistry.

Identification of a hexasaccharide sequence able to inhibit thrombin and suitable for 'polymerisation'.

J. Herbert, M. Petitou, P. Duchaussoy, 1999, Carbohydrate research.

Assessment through chemical synthesis of the size of the heparin sequence involved in thrombin inhibition.

J. Herbert, M. Petitou, M. Ceccato, 1999, Carbohydrate research.

Binding of heparin to antithrombin III: a chemical proof of the critical role played by a 3-sulfated 2-amino-2-deoxy-D-glucose residue.

M. Petitou, J. Choay, P. Duchaussoy, 1988, Carbohydrate research.

Synthesis of heparin fragments. A chemical synthesis of the pentasaccharide O-(2-deoxy-2-sulfamido-6-O-sulfo-alpha-D-glucopyranosyl)-(1-4 )-O-(beta-D-glucopyranosyluronic acid)-(1-4)-O-(2-deoxy-2-sulfamido-3,6-di-O-sulfo-alpha-D-glu copyranosyl)-(1-4)-O-(2-O-sulfo-alpha-L-idopyranosyluronic acid)-(1

G. Torri, M. Petitou, J. Choay, 1986, Carbohydrate research.

Synthesis of Heparin Fragments. A Chemical Synthesis of the Pentasaccharide O-(2-Deoxy-2-sulfamido-6-O-sulfo-α-D-glucopyranosyl)-(l->4)-O-(β-glucopyranosyluronic acid)-(1->4)-O-(2-deoxy-2-sulfamido-3,6-di-O- sulfo-α-D-glucopyranosyl)-

G. Torri, M. Petitou, J. Choay, 1986 .

Synthesis of some new analogs of the immunoadjuvant glycopeptide MDP (N-acetyl-muramyl-L-alanyl-D-isoglutamine).

E. Lederer, J. Choay, M. Derrien, 2009, International journal of peptide and protein research.

SYNTHESIS OF SOME NEW ANALOGS OF THE IMMUNOADJUVANT GLYCOPEPTIDE MDP (N-ACETYL-MURAMYL-L-ALANYL-D-ISOGLUTAMINE)

E. Lederer, J. Choay, M. Derrien, 1978 .