Glycom A/s

Glycom Aps

István Bajza

Gyula Dekany

Markus Jondelius Hederos

Lars Kröger

Károly Ágoston

Christoph Röhrig

Marie Bøjstrup

Markus Hederos

Andreas Schroven

Julien Boutet

Piroska Kovács-Pénzes

Ferenc Horváth

Ioannis Vrasidas

Christian Risinger

Ágnes Ágoston

Péter Trinka

Sándor Demkó

Gergely Pipa

Ignacio Pérez Figueroa

Johan Olsson

László Kalmár

Ignacio Figueroa Pérez

Ignacio Figuero-Pérez

Irme Kovács

Gábor Kádár

Ignacio Figueroa-Pérez

Paulo Vital

Erzsébet Czinege

Ignacio Fegueroa Pérez

Karoly Agoston

Gyula DÉKANY

Imre Kovács

The present invention relates to a method for preparation of the trisaccharide 6'-O-sialyllactose (formula (I)) or salts thereof as well as intermediates in the synthesis and for the use of 6&#x2032;-O-sialyllactose salts in pharmaceutical or nutritional compositions. 

Production of 6'-O-sialyllactose and intermediates

The present invention relates to a method for preparation of the tetrasaccharide lacto-N-neotetraose (LNnt, formula (I)) especially in large scale, as well as intermediates in the synthesis, a new crystal form (polymorph) of LNnt, and the use thereof in pharmaceutical or nutritional compositions. 

Method for preparation of the tetrasaccharide lacto-N-neotetraose (LNnt) containing N-acetyllactosamine

The present invention relates to novel polymorphs of the trisaccharide 2'-O-fucosyllactose (2-FL) of formula (1), methods for producing said polymorphs and their use in pharmaceutical or nutritional compositions. 

Polymorphs of 2'-O-fucosyllactose and producing thereof

A 1,2-dideoxy-1,2-diamino oligosaccharide or polysaccharide in its free base, salt or metal-complex form as shown in General Formula 1 and derivative thereof is described. R, Rand Rare each independently selected from the group consisting of H and a carbohydrate moiety, with the proviso that at least one of the groups R, Ror Ris a carbohydrate moiety; Ris selected from the group consisting of: H, optionally substituted C-alkyl, optionally substituted heteroalkyl, optionally substituted C-alkenyl, optionally substituted C-alkynyl, optionally substituted C-cycloalkyl, optionally substituted heterocyclyl, optionally substituted aryl, and optionally substituted heteroaryl.

1,2-dideoxy-1,2-diamino oligosaccharides and polysaccharides and derivatives thereof

&#x3b1;-Lactosamine hydrochloride, substantially free of &#x3b2;-lactosamine hydrochloride; a method of preparing &#x3b1;-lactosamine hydrochloride monohydrate from an anomeric mixture of lactosamine hydrochloride, including: preparing a solution including the anomeric mixture of lactosamine hydrochloride, water and at least one water-miscible organic solvent at a temperature of 0-100&#xb0; C., and cooling the solution to cause crystallization of &#x3b1;-lactosamine hydrochloride monohydrate; a method of preparing anhydrous &#x3b1;-lactosamine hydrochloride; and use of &#x3b1;-lactosamine hydrochloride as a food supplement or intermediate in synthesis.

Crystalline carbohydrate derivative

The present application discloses novel glycoproteins and a related glycosylcarbamoylation methodology suitable for the preparation of glycopeptides (in particular glycoproteins and glycosylated cells), as well as the use of such glycoproteins in medicine, e.g. as pharmaceuticals and diagnostics or in diagnostic kits. A method for the preparation of a carbohydrate-peptide conjugate includes reacting a cyclic carbamate with a peptide which has at least one primary amino group.

Glycoproteins and glycosylated cells and a method for the preparation of the same

Lactosamine derivatives and related methods suitable for the preparation, including large-scale production, of N-acetyllactosamine, lactosamine, numerous lactosamine salts and a number of lactosamine-containing oligosaccharides are provided.

Lactosamine derivatives

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Debrecen, Hungary

István Bajza