Monosaccharides

Glycosylation is the process of adding glycosyl groups to a molecule. This process is essential for the synthesis of complex carbohydrates, which are essential in cell membranes and other biological structures. Methylation is the addition of one or more CH3 groups to a compound. Click chemistry is a type of chemical reaction that is used when an orthogonal protection strategy is required. Polysaccharides are long chains of sugar molecules linked together by glycosidic bonds. Fluorination is the introduction of fluorine into organic molecules to modify their properties. Saccharide refers to any sugar, especially monosaccharides and oligosaccharides. Modification refers to the altering of a molecule by adding or removing functional groups, such as methyl groups or glycosyl groups. Sugar refers to any carbohydrate that contains two hydroxyl (OH) groups on adjacent carbons and includes monosaccharides and oligosaccharides. Synthetic means artificially made by humans

<p>1,6-Di-O-benzyl-a-D-glucopyranoside is an oligosaccharide that has been synthesized by the Click chemistry method. It is a polysaccharide with a high purity and an excellent yield. The product contains a single monosaccharide unit of D-glucose with a 1,6 glycosylation pattern. The product has undergone methylation and fluorination to produce the desired structure. 1,6-Di-O-benzyl-a-D-glucopyranoside has been shown to have antihypertensive effects in rats and is thought to be due to its ability to inhibit angiotensin II receptor activity.</p>

<p>Octyl 4-O-acetyl-2,3-O-isopropylidene-a-L-rhamnopyranoside is a monosaccharide that is synthesized from the glycosylation of octyl β-D-glucopyranoside and L-rhamnose by means of an acetal exchange reaction. The product is a complex carbohydrate with a molecular weight of 578. This compound can be fluorinated at the hydroxyl group to produce octyl 4-[4-(trifluoromethoxy)phenyl]butanoate, which has been shown to have significant antiinflammatory activities in animal models.</p>

<p>Phenyl 2-O-benzoyl-4,6-O-benzylidene-3-O-(4-methoxybenzyl)-a-D-thiomannopyranoside is a custom synthesis. It is a polysaccharide that can be modified with methylation, glycosylation, click modification and fluorination. This compound is a white powder that has high purity and is suitable for use in the production of oligosaccharides or polysaccharides.</p>

Erigeside C is a flavonoid derivative that has been shown to be effective in treating allergic symptoms. Erigeside C inhibits the production of various pro-inflammatory cytokines, such as IL-6 and TNF-α, by inhibiting the activity of protein kinase C (PKC). The compound also inhibits the production of prostaglandin E2 by inhibiting cyclooxygenase-2. In addition, Erigeside C is able to inhibit the release of histamine from mast cells. This antihistamine effect is due to its ability to inhibit oxidation reactions in the cell membrane and block cellular calcium channels.

Coumaroyl L-arabinofuranoside is a glycosylation agent that has been used in the synthesis of complex carbohydrates, polysaccharides, and oligosaccharides. The compound can be fluorinated to give p-coumaroylfluoride. It is also possible to methylate the compound with methanol and methyl iodide. The compound can be modified by Click chemistry reactions to form a reactive ester or an amine. Coumaroyl L-arabinofuranoside is available as a CAS number and can be custom synthesized. It is available at high purity. !--

<p>1,2,3,4-Tetra-O-acetyl-L-xylopyranose is a custom synthesis product. It is a sugar that is found in glycosaminoglycans and proteoglycans. This product can be customized through the modification of the sugar with fluorination, methylation, acetylation or other modifications. This product has a CAS number of 142130-89-0 and can be synthesized from sucrose using Click chemistry. The chemical name for this compound is 1,2,3,4-Tetra-O-[(trimethylsilyl)acetyl]-L-xylopyranose.</p>

<p>Methyl 2,3-O-isopropylidene-5-O-(4-toluenesulfonyl)-b-D-ribofuranoside is a nucleoside derivative. It is a deprotected nucleoside that can be used as an alkylation agent. Methyl 2,3-O-isopropylidene-5-O-(4-toluenesulfonyl)-b-D-ribofuranoside is the sodium salt of 5'-O-(4-(methylsulfonyl)benzenesulfonate) -2'-deoxyadenosine. This compound is used in the preparation of other nucleosides, including 5'-O-(4-(methylsulfonyl)benzenesulfonate) -2'-deoxycytidine and 5'-O-(4-(methylsulfonyl)benzenesulfonate) -2'-</p>

<p>2-(L-Fuco-tetrahydroxypentyl)-4(R)-1,3-thiazolidine-4-carboxylic acid is a high purity custom synthesis sugar. It has been synthesized by click modification and fluorination of 2-(L-fuco-tetrahydroxypentyl)-4(R)-1,3-thiazolidine-4-carboxylic acid methyl ester. This compound can be used in glycosylation with oligosaccharides, monosaccharides, saccharides and complex carbohydrates.</p>

1,2-Dideoxy-2'-dimethylamino-a-D-glucopyranoso-[2,1-d]-2'-thiazoline is a synthetic sugar that is used in the synthesis of complex carbohydrates. It can be used to modify polysaccharides and glycosyls with methyl groups. This product has high purity and custom synthesis.

<p>2,4:3,5-Di-O-benzylidene-aldehydo-D-ribose hydrate is a complex carbohydrate that contains a glycosylation site. The CAS number for this product is 32580-00-0. This product can be modified by methylation, fluorination, and saccharide modification. It is also available in custom synthesis or high purity.</p>

<p>D-Arabinopyranosyl thiosemicarbazide is a synthetic compound. It has been shown to be effective in the synthesis of oligosaccharides and sugars, as well as glycosylation reactions. This product can be used in fluorination, methylation, and other custom synthesis reactions. D-Arabinopyranosyl thiosemicarbazide is also useful for click modification of complex carbohydrates. The purity of this product is high and it can be modified with various functional groups.</p>

<p>3,4,6-Tri-O-acetyl-1,2-O-ethoxyethylidene-a-D-fructopyranose is a modified carbohydrate with the chemical formula C 12 H 20 O 8 . It is a white crystalline solid that is soluble in water. 3,4,6-Tri-O-acetyl-1,2-O-ethoxyethylidene-a-Dfructopyranose can be used as a monosaccharide or an oligosaccharide. This compound has been synthesized by methylation and glycosylation of glucose.</p>

<p>Myo-inositol-d6 is a stable isotope of myo-inositol. It is used to monitor the biosynthesis of myo-inositol in yeast cells. Myo-inositol is a carbohydrate that has regulatory functions in yeast cells. Myo-inositol-d6 can be used as an extracellular bioassay for determining the uptake and intracellular distribution of myo-inositol in mammalian cells.</p>

Benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-methyl-aDglucopyranoside is a synthetic oligosaccharide with a complex carbohydrate structure. It is custom synthesized by glycosylation and polysaccharide modification to produce a high purity product. Click chemistry modifications, methylations, and fluorination are used for the synthesis of benzyl 2-acetamido-4,6-Obenzylidene -2deoxy -3OmethylaDglucopyranoside. The CAS number for this product is 116696–66–3.

<p>Dihydrozeatin-9-glucoside is a conjugate of the natural product dihydrozeatin and glucose. The glucoside has been found to inhibit the growth of plants, which may be due to its ability to bind to polyclonal antibodies. Dihydrozeatin-9-glucoside is also an immunogen that has been shown to produce monoclonal antibodies in tissue culture. It has been used for immunoaffinity chromatography and as a biochemical marker for plant tissue cultures. Dihydrozeatin-9-glucoside binds to wheat leaf cells and inhibits their growth, making it a potential tool for the study of plant cell death.</p>

Ethyl 2,3,4-tri-O-benzyl-L-fucopyranoside is a polysaccharide that is modified by the addition of benzyl groups to the hydroxyl group at C2. This modification increases the resistance of this compound to degradation by glycosidases and also prevents any undesired reactions with other saccharides. Ethyl 2,3,4-tri-O-benzyl-L-fucopyranoside is a custom synthesis that can be made in high purity and with high carbohydrate content. The CAS number for this compound is 61721–76–8.

<p>D-Ribulose 5-phosphate is a phosphorylated sugar, which is a key intermediate in the pentose phosphate pathway, derived from the enzymatic phosphorylation of D-ribulose. This pathway is crucial in cells for the generation of NADPH and the synthesis of ribose-5-phosphate, which is essential for nucleotide biosynthesis. The compound is produced from ribulose via the action of ribose-phosphate isomerase, a crucial enzyme in cellular metabolism.D-Ribulose 5-phosphate primarily functions as a precursor in the biosynthesis of nucleotides and nucleic acids. It acts within the cellular context to balance the supply of ribose-5-phosphate for nucleotide production, while its role in the oxidative branch of the pentose phosphate pathway helps maintain redox homeostasis through NADPH production.The primary application of D-Ribulose 5-phosphate is in biochemical research and metabolic engineering, where it is vital for studies focusing on metabolic flux analysis and the elucidation of biosynthetic pathways. Understanding its pathway and regulation can lead to insights into metabolic disorders and the development of therapeutic strategies targeting nucleotide synthesis abnormalities.</p>

<p>4-O-Benzyl-D-galactal is a benzylated Oligosaccharide. It can be custom synthesized and modified according to your requirements. 4-O-Benzyl-D-galactal can be used as a raw material for the synthesis of polysaccharides and saccharides. This product has high purity with low impurities, and can be used for the synthesis of highly functional polysaccharides and saccharides.</p>

3-Deoxy-D-arabinose is a sugar that is synthesized by the biochemical process of de novo synthesis. It is a structural component of glycoproteins and lipopolysaccharides, which are essential for bacterial growth. 3-Deoxy-D-arabinose is also used in the regulation of gene expression. The efficient method for its production was discovered by enzymatic dehydrogenation of glucose with the enzyme dehydrogenase, which is encoded by corynebacterium glutamicum. This discovery has led to an unraveling of the wild-type strain's metabolic pathways.