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Home > Biochemical Engineering > Saccharides (Find 2380 items)

2,5-Dideoxy-2,5-imino-D-mannitol

(59920-31-9)
Many pyrrolidines are powerful inhibitors of glycohydrolases, enzymes responsible forcleavage of glycosidic bonds, glycoprotein processing and the gastrointestinal breakdown of dietary carbohydrates.These compounds are charged at physiological pH and are believed to associate with acidic amino acids at the active site.Inhibition of glycohydrolases could be of therapeutic value for the treatment of viral infections, cancer, diabetes, and obesity.

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D-Mannono-1,4-lactone

(26301-79-1)
D-Mannono-1,4-lactone acts as an inhibitor to β-galactosidase of Escherichia coli providing proof that the furanose form of this sugar was contributory to its efficacy.

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5'-DEOXYTHYMIDINE

(3458-14-8)
The pyrimidine thymidine consists of thymine combined with deoxyribose. Prior to polymerization into DNA, thymidine must be phosphorylated at the hydroxyl group on carbon 5 of the ribose moiety. 5'-Deoxythymidine is a form of thymidine in which the hydroxyl group on carbon 5 of ribose has been replaced with hydrogen. As a result, this compound cannot be phosphorylated and used by DNA polymerase in the synthesis of DNA. 5'-Deoxythymidine is readily imported by cellular nucleoside importers and co

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Pirlimycin

(79548-73-5)
Pirlimycin is a semi-synthetic lincosamide prepared from clindamycin by hydrolysing the propyl N-methylproline and re-annealing a 4-ethylpipecolic acid. Pirlimycin is more hydrophobic than clindamycin and is more potent against a number of important pathogens. Like other members of the lincosamide family, pirlimycin is a broad spectrum antibiotic with activity against anaerobic bacteria and protozoans. Pirlimycin acts by binding to the 23S ribosomal subunit, blocking protein synthesis. Pirlimyci

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Agarose, 2-hydroxyethyl ether

(39346-81-1)
The gel has good transparency, and is particularly suitable for preparing medium containing heat-resistant substances. Recommended for the preparation of agarose microspheres.

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GLYCOPROTEIN, ALPHA1-ACID HUMAN

(66455-27-4)
α1-Acid glycoprotein was used to study nonviral gene delivery to the lung with copolymer-protected and transferrin-modified polyethylenimine.

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Saccharides, also called sodium saccharin, is the oldest sweetener. Saccharides was discovered by American scientists in 1878 and was quickly accepted by the food industry and consumers. The sweetness of saccharin is 300 to 500 times that of sucrose. It is not metabolized and absorbed by the human body and is stable in the production of various foods.

Frequently Asked Questions

What are saccharides and how are they classified?

Saccharides, also known as carbohydrates, are organic compounds composed of carbon, hydrogen, and oxygen. They are classified based on the number of sugar units: monosaccharides (e.g., glucose, fructose), disaccharides (e.g., sucrose, lactose), oligosaccharides (3–10 units), and polysaccharides (e.g., starch, cellulose). Understanding saccharide classification is essential for applications in food, pharmaceuticals, and biotechnology.

What are the common industrial uses of saccharides?

Saccharides are widely used across multiple industries:1. In food and beverage production as sweeteners, thickeners, and stabilizers.2. In pharmaceuticals as excipients, drug delivery agents, or active ingredients.3. In cosmetics for moisturizing and skin-conditioning properties.4. In biotechnology as fermentation substrates for producing biofuels and enzymes.Their versatility makes them critical raw materials in many manufacturing processes.

How do I choose a reliable saccharide supplier for industrial use?

Selecting a reliable saccharide supplier involves evaluating several key factors:1. Compliance with international quality standards such as ISO, GMP, or FCC.2. Purity and consistency of the saccharide products offered.3. Certifications for food-grade, pharmaceutical-grade, or technical-grade materials as needed.4. Supply chain reliability, including packaging, logistics, and scalability.5. Technical support and documentation (e.g., COA, MSDS).Partnering with a certified and experienced supplier ensures product safety and process efficiency.

What is the difference between reducing and non-reducing saccharides?

Reducing saccharides have a free aldehyde or ketone group that can act as a reducing agent in chemical reactions—common examples include glucose and maltose. Non-reducing saccharides, like sucrose, lack a free reactive group because their anomeric carbons are involved in glycosidic bonds. This distinction affects their reactivity in analytical tests (e.g., Benedict’s test) and their behavior in food processing or pharmaceutical formulations.

Are natural and synthetic saccharides interchangeable in formulations?

Natural and synthetic saccharides may not always be interchangeable due to differences in purity, stereochemistry, regulatory status, and functional performance. For example, naturally derived lactose is commonly used in tablets as a filler, while synthetic alternatives might not meet pharmacopeial standards. Always verify compatibility with your application requirements, regulatory guidelines (e.g., USP, EP), and end-user safety before substitution.

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