Glycosaminoglycans 6 sulfate

Brand Name(s) Hep-Lock, Hep-Pak CVC Chemical Class Glycosaminoglycan, sulfated... 

Chemical Class Glycosaminoglycan, sulfated heparin derivative Clinical Pharmacology ... 

Panin G, Naia S, DallA Amico R, Chiandetti L, Zachello F, Catassi C, Felici, L, Coppa GV (1986) Simple spectrophotometric quantification of urinary, excretion of glycosaminoglycan sulfates. Clin Chem 32 2073-2076... 

There are other glycosaminoglycans. Hyaluronic acid [9004-61-9] occurs both free and in noncovalent association with proteoglycan molecules. Heparin [9005-49-6] and heparan sulfate [39403-40-2] also known as heparitin sulfate [9050-30-0] occur in mast cells and in the aorta, Hver, and lungs. 

Danaparoid (Orgaran mean MW, 6,000 Da) is a mixture of nonheparin glycosaminoglycans derived from pig gut (dermatan sulfate, heparan sulfate, chondroitin sulfate). Die anti-Xa/anti-IIa ratio (22 1) is even greater than seen with LMWH. Die anti-IIa effect may be mediated in part by dermatan sulfate, which catalyzes thrombin inhibition by heparin cofactor II. 

Some alcohols, arylamines, and phenols are sulfated. The sulfate donor in these and other biologic sulfation reactions (eg, sulfation of steroids, glycosaminoglycans, glycolipids, and glycoproteins) is adenosine 3 -phos-phate-S -phosphosulfate (PAPS) (Chapter 24) this compound is called active sulfate. ... 

Fig. 34.—Circular Dichroism of Glycosaminoglycans (a) Hyaluronic Acid (b) Heparan Sulfate from Normal Mammalian Tissue (c) Chondroitin 4-Sulfate (d) Dermatan Sulfate ...

Contamination from other L-iduronic acid-containing glycosaminoglycans (dermatan sulfate and heparan sulfate species) cannot usually be lowered below the 1-2% level, unless repeated precipitations or treatments with resin are made. As will be discussed in Section VIII, extensive... 

Infrared spectra are commonly used for characterizing glycosaminoglycans, especially solid samples thereof. However, being dominated by strong and broad bands due to polar and ionized groups (OH, C02 , and S03 ), the i.r. spectrum of heparin often contains concealed bands from contaminants.77 More-reproducible spectra, obtainable for solutions in H20 (Ref. 79) and D20 (Ref. 80) provide a better characterization, as well as quantitative information about such functional groups as carboxyl, acetamido, and sulfate groups. 

A classical, and still most useful, physicochemical parameter for characterizing glycosaminoglycans is their specific optical rotation. For pure heparins from common sources, [a]80 = + 45 to + 53 ° (see Table II). The actual value depends on the relative proportions of monosaccharide constituents (that is, the L-idosyluronic acid residues make a less positive contribution than the n-glucosyluronic residues), and on the degree of sulfation of the preparation (that is, although sulfate groups may have little direct influence on the molecular rotation, they lower the value by acting as diluents ). 

Periodate oxidation was used in early work for obtaining information on the substitution pattern of heparin.1,100 102 In fully N-substituted (N-sulfated or N-acetylated, or both) glycosaminoglycans, the only bond susceptible to splitting by periodate is C-2-C-3 of unsubstituted uronic acid residues. As illustrated in Scheme 4 for heparin, only nonsulfated D-glucuronic acid and L-iduronic acid residues are split by periodate. 

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