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Carbohydrates biological activities

Triiodothyronine (3, 5,3-L-triiodothyronine, T3) is a thyroid hormone. It is producedby outer ring deiodination of thyroxine (T4) in peripheral tissues. The biologic activity of T3 is 3-8 times higher than that of T4. T3 is 99.7% protein-bound and is effective in its free non-protein-bound form. The half-life of triiodothyronine is about 19 h. The daily tur nover of T3 is 75%. Triiodothyronine acts via nuclear receptor binding with subsequent induction of protein synthesis. Effects of thyroid hormones are apparent in almost all organ systems. They include effects on the basal metabolic rate and the metabolisms of proteins, lipids and carbohydrates. [Pg.1243]

Synthesis and Biological Activities of Compounds Containing Fluorinated Carbohydrates. 186... [Pg.91]

Table II. Carbohydrate compositions (weight percentage) of individual oligomer peaks purified (QAE-Sephadex or HPLC ion-exchange separation, respectively) from mixtures of citrus pectin oligomers or B fruit extracts Compositions shown are for peaks whose biological activity is described in Figure 4. Uronic acid values are based on colorimetric assay. Proportions of neutral sugars were determined by GC and adjusted so that totals equal 100%. In fact, some oligomers (G7 peaks 8, 9 and 10. B extract peak 10) produced small (less than 1 % of the total integrated area), unknown peaks in the GC chromatograms. Table II. Carbohydrate compositions (weight percentage) of individual oligomer peaks purified (QAE-Sephadex or HPLC ion-exchange separation, respectively) from mixtures of citrus pectin oligomers or B fruit extracts Compositions shown are for peaks whose biological activity is described in Figure 4. Uronic acid values are based on colorimetric assay. Proportions of neutral sugars were determined by GC and adjusted so that totals equal 100%. In fact, some oligomers (G7 peaks 8, 9 and 10. B extract peak 10) produced small (less than 1 % of the total integrated area), unknown peaks in the GC chromatograms.
The preparation of nucleosides by reaction between carbohydrates and heterocyclic bases is fundamental to the study of the important biological activity... [Pg.286]

Haase C, Seitz O (2007) Chemical Synthesis of Glycopeptides. 267 1-36 Hahn F, Schepers U (2007) Solid Phase Chemistry for the Directed Synthesis of Biologically Active Polyamine Analogs, Derivatives, and Conjugates. 278 135-208 Hansen SG, Skrydstrup T (2006) Modification of Amino Acids, Peptides, and Carbohydrates through Radical Chemistry. 264 135-162... [Pg.259]

In addition to terpenes (as described above), carbohydrates have also been used as substrates in domino metathesis reactions, the aim being to synthesize enan-tiopure polyhydroxylated carbocyclic rings. These structures are components of several biologically active compounds such as aminoglycoside antibiotics [254], inositol phosphates [255], and carbanucleosides [256]. An efficient entry to this skeleton was developed by Madsen s group using a domino RCM/CM of the carbohy-... [Pg.448]

Chamow, S.M., Kogan, T.P., Peers, D.H., Hastings, R.C., Byrn, R.A., and Ashkenazi, A. (1992) Conjugation of soluble CD4 without loss of biological activity via a novel carbohydrate-directed cross-linking reagent. Biol. Ghem. 267, 15916-15922. [Pg.1053]

Biological activity The carbohydrate side chain of gonadotrophins is essential to the activation of gonadotrophin signal transduction... [Pg.31]

Mammalian cell culture is more technically complex and more expensive than microbial cell fermentation. Therefore, it is usually only used in the manufacture of therapeutic proteins that show extensive and essential post-translational modifications. In practice, this usually refers to glycosylation, and the use of animal cell culture would be appropriate where the carbohydrate content and pattern are essential to the protein s biological activity, its stability or serum half-life. Therapeutic proteins falling into this category include EPO (Chapter 10), the gonadotrophins (Chapter 11), some cytokines (Chapters 8-10) and intact monoclonal antibodies (Chapter 13). [Pg.127]

Most of the LPS biological activity (pyrogenicity) is associated with its lipid A moiety. This usually consists of six or more fatty acids attached directly to sugars such as glucosamine. Again, as is the case in relation to the carbohydrate component, lipid A moieties of LPS isolated from different bacteria can vary somewhat. The structure of E coli s lipid A has been studied in the greatest detail its exact structure has been elucidated and it can be chemically synthesized. [Pg.191]

Human TNF-a is initially synthesized as a 233 amino acid polypeptide that is anchored in the plasma membrane by a single membrane-spanning sequence. This TNF pro-peptide, which itself displays biological activity, is usually proteolytically processed by a specific extracellular metallo-protease. Proteolytic cleavage occurs between residues 76 (Ala) and 77 (Val), yielding the mature (soluble) 157 amino acid TNF-a polypeptide. Mature human TNF-a appears to be devoid of a carbohydrate component, and contains a single disulfide bond. [Pg.255]

Fig. 5. Structure and biological activities of Kiessling s initial carbohydrate-substituted polymers generated by ROMP. Relative inhibitory potency the saccharide residue concentration needed to inhibit the agglutination of red blood cells mediated by the protein concana-valin A... [Pg.216]

Fig. 6. Comparison of the biological activities of monovalent glucose and mannose derivatives, multivalent carbohydrate-substituted polymer with two saccharide epitopes per repeat unit, and the less sterically congested carbohydrate-substituted polymer with a single recognition element per repeat unit. All polymers were generated by ROMP using RuC13... Fig. 6. Comparison of the biological activities of monovalent glucose and mannose derivatives, multivalent carbohydrate-substituted polymer with two saccharide epitopes per repeat unit, and the less sterically congested carbohydrate-substituted polymer with a single recognition element per repeat unit. All polymers were generated by ROMP using RuC13...
Fig. 15. Mixed copolymers were generated to examine the effect of changing the recognition epitope density for a biologically active series of carbohydrate-substituted polymers. Note n and m represent ratios of mannose and galactose residues, respectively. Fig. 15. Mixed copolymers were generated to examine the effect of changing the recognition epitope density for a biologically active series of carbohydrate-substituted polymers. Note n and m represent ratios of mannose and galactose residues, respectively.
Fig.16. A ruthenium initiator was used to create block copolymers to investigate the relationship between biological activity and the spacing of carbohydrates on the polymer backbone... Fig.16. A ruthenium initiator was used to create block copolymers to investigate the relationship between biological activity and the spacing of carbohydrates on the polymer backbone...

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See also in sourсe #XX -- [ Pg.209 ]




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