Monossacáridos

2-Deoxy-2-trifluoroacetamido-D-glucose (dTFA) is an acetal that is formed from the reaction of trifluoroacetic acid with 2-deoxy-2-trifluoroacetamido-D-glucose. This compound yields aldehydes, and can be used to form glycosidic bonds. It also has the ability to react with amino groups on peptides and proteins, forming acetals. 2-Deoxy-2-trifluoroacetamido-D-glucose has been shown to have a variety of functions including being a carbohydrate, an acetal, and an inhibitor of peptide bond formation.

D-Galacturonic acid benzyl ester is a donor of d-galacturonic acid that is used to regulate the growth of bacterial cells. It has been shown to be an acceptor for oligosaccharides, which are substrates for glycosidases. D-Galacturonic acid benzyl ester has been shown to have anti-inflammatory effects in animal models and may be useful in the treatment of heart diseases, such as cardiac hypertrophy.

5-Keto-D-gluconic acid is an intermediate in the synthetic pathway of glucose. The enzyme 5-keto-D-gluconate dehydrogenase catalyzes the conversion of 5-keto-D-gluconate to D-glucono-1,5-lactone. This reaction is important for plant physiology and is used industrially for the production of citric acid. In order to synthesize 5-keto-D-gluconic acid, a p. pastoris strain was engineered with an increased expression of 5KGDH, which led to an increase in the production of this compound. This synthesis took place through a dinucleotide phosphate intermediate that was formed by two molecules of malonic acid. Citric acid was also synthesized from this intermediate.
The enzyme activity levels were measured using a bacterial strain that contained a wild type gene sequence (WT) and a mutant gene sequence (

Conduritol D (CD) is a natural product that has been isolated from the pancreas of rats. It is homochiral, and it has been shown to be active in the treatment of diabetic patients. CD has a hydroxy group at C-4' and an alcohol group at C-5'. The functional groups are acetylated at C-3', which may make this compound more potent than other similar compounds with different functional groups. It is also synthesized stereoselectively, making it a selective molecule. CD has been shown to have pharmacokinetic properties that may be beneficial for treating diabetes.

D-Arabonic acid-1,4-lactone is a synthetic sugar that is modified to produce a variety of carbohydrates. This product can be used in the synthesis of oligosaccharides and monosaccharides. It is also used as a carbohydrate in the production of saccharide-based polymers, such as polysaccharides or polyols. This product has CAS number 2782-09-4 and a purity level of ≥99%.

D-Arabinose is a dinucleotide phosphate that is an important metabolic intermediate in the pentose phosphate pathway. It has been shown to have pharmacological effects, such as enzyme inhibition and binding to DNA. D-Arabinose has been used in biochemical studies of energy metabolism and related areas. D-Arabinose is converted to ribitol by ribitol dehydrogenase, which can be oxidized to ribulose 5-phosphate by ribulose 5-phosphate dehydrogenase. The conversion of D-arabinose to ribitol requires NAD(P)H, which provides the reducing power for this reaction. The conversion of ribitol to ribulose 5-phosphate also requires NAD(P)H, but does not produce any reducing power. A redox potential measurement was used to determine the relative reduction potentials of the two reactions and found that they are equal at -0.5 volts (V).

Used as source of carbon in culture medium.

N-acetyl D-glucosamine (GlcNAc) is an aldohexose (2-acetamido-2-deoxyglucose) in which the hydroxyl group at position 2 is replaced by NHAc (Collins, 2006). N-acetyl D-glucosamine forms the exoskeletons of molluscs and insects as the building block of the polysaccharide chitin (Rudrapatnam, 2003). N-acetyl D-glucosamine is a key component of N- and O-linked glycans, present in glycolipids and the glycosaminoglycan hyaluronic acid (Fallacara, 2018). A recent study has suggested that N-acetyl D-glucosamine may have therapeutic potential for COVID-19 as it affects the spike protein-ACE2 receptor interaction during the infection with SARS-CoV-2 virus (Baysal, 2021).

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3-C-Methyl-1-deoxy-psicose is a sugar that is used in the synthesis of complex carbohydrates. This synthetic sugar is synthesized by the click modification of 3,4-dihydroxybenzaldehyde with 1,2,3,4-tetraacetylated benzyl chloride. The compound has a molecular weight of 228.22 and an empirical formula of C6H8O6F2. It's CAS number is 52714-32-0 and it's Oligosaccharide number is 976.

Corn Cob Syrup is a custom synthesis of polysaccharides, which are complex carbohydrates. This syrup is made from corn cobs and has been modified with fluorine and methyl groups. The monosaccharides in this syrup have been modified with a click modification and the oligosaccharides have been modified with glycosylation. This product contains sugar that has been modified by glycosylation.

Substrate for UDP-3-O-acyl-N-acetylglucosamine deacetylase (LpxC)

a-D-Glucuronic acid-1-phosphate is a substrate for alkaline phosphatase. It hydrolyzes phosphate esters and modifies inorganic phosphate, including pyrophosphate. It also catalyzes the hydrolysis of nucleotide monophosphates such as NADPH and UDPglucose to their respective diphosphates. This enzyme is not inhibited by inorganic phosphate, phosphatase, NADP+, or UDP-.

2-Iodoethyl a-L-fucopyranoside is an organic compound that belongs to the group of fluorinated saccharides. It is used in the synthesis of oligosaccharides, polysaccharides, and complex carbohydrates. 2-Iodoethyl a-L-fucopyranoside can be modified with click chemistry at the C4 position for the synthesis of monosaccharides or sugar derivatives. This modification leads to high purity and chemical stability.

The compound 1,4-dideoxy-1,4-imino-L-altritol is a synthetic carbohydrate that is made of a monosaccharide and an oligosaccharide. The monosaccharide is a simple sugar with the chemical formula C5H10O5. The oligosaccharide has the chemical formula C2n+1(C3H3O3)n. The monosaccharide has four carbons and one oxygen molecule. The oligosaccharide also has five carbon atoms, but it also has three oxygen molecules. The two sugars are linked by a glycosidic linkage.
The compound was created to be used in the synthesis of complex carbohydrates. It can be modified to have fluorine atoms added to it, methyl groups added to it, or both. It can also be modified to make it into an ester or an amide. It is soluble in water and alcohol

N-2,4-Dinitrophenyl-deoxynojirimycin (DNPDNJ) is a methylated derivative of deoxynojirimycin. It is an inhibitor of glycosylation that can be used to study the structure and function of carbohydrates. DNPDNJ is a synthetic saccharide that can be custom synthesized. Click modification and modification with Oligosaccharides are common modifications for DNPDNJ. DNPDNJ is available in high purity and has been fluorinated for use in fluorescence studies.

Methyl 2-deoxy-a-D-ribopyranoside is a sugar molecule that is used in the synthesis of glycosides, saccharides, oligosaccharides, and polysaccharides. It has been shown to be an effective reagent for the fluorination of saccharides and sugars. Methyl 2-deoxy-a-D-ribopyranoside is also used for modification of complex carbohydrates and other organic molecules.

3,4-O-Isopropylidene-D-arabinose is a synthetic compound that has been used as an active analogue for the study of nucleophile reactions. 3,4-O-Isopropylidene-D-arabinose undergoes nucleophilic addition with potassium azide to form a thiazolidine intermediate. The stereospecificity of this reaction was shown by the chemists and biochemists who synthesized it. It has also been shown to react with an anion in a similar manner. This chemical is used in the synthesis of d-arabinose, which can be used for the production of other compounds.