Heparin Disaccharides

Heparin Disaccharides

Heparin consists of repeating disaccharide units primarily composed of 2-O-sulfated L-iduronic acid (IdoA(2S)) α(1→4)-linked to N-sulfated, 6-O-sulfated D-glucosamine (GlcNS(6S)). This produces the trisulfated IdoA(2S)-GlcNS(6S) motif, which accounts for approximately 75–85% of porcine or bovine heparin chains. These structural units derive from linear polymers of uronic acids (GlcA or IdoA) and glucosamine, exhibiting an average sulfation level of about 2.7 groups per disaccharide—significantly higher than that of heparan sulfate. Enzymatic depolymerization produces unsaturated ΔUA-containing disaccharides, such as ΔUA(2S)-GlcNS(6S) (heparin disaccharide I-S), commonly used for analytical profiling.

Biosynthesis and Variability

Heparin biosynthesis begins with GlcA β(1→4) N-acetylglucosamine repeating units that undergo sequential modifications, including C5-epimerization to IdoA, N-deacetylation/N-sulfation, and O-sulfation at positions 2, 6, and 3. These steps generate extensive microheterogeneity with domains of high sulfation. Major resulting disaccharides include ΔUA-GlcNAc, ΔUA-GlcNS, ΔUA(2S)-GlcNS, and ΔUA(2S)-GlcNS(6S), with compositional patterns dependent on tissue origin. These structures are typically analyzed using chromatographic methods. As a nontemplate-driven process, biosynthesis produces chains ranging from 3–30 kDa, where IdoA residues predominate over GlcA in mature heparin.

Biological Functions and Analysis

Heparin disaccharides underpin its anticoagulant activity by enabling high-affinity binding to antithrombin, particularly through the IdoA(2S)-GlcNS(6S)-containing pentasaccharide sequence. Beyond anticoagulation, structural diversity among disaccharides supports roles in inflammation, cell signaling, and extracellular matrix interactions. Detailed mapping of disaccharide composition is essential for pharmaceutical quality control and batch consistency. Variants such as heparin disaccharide IV-H (ΔUA-GlcNAc) are characteristic of less sulfated regions and affect enzymatic susceptibility and biological interactions.

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