Monosaccharides

Ethyl D-thioglucuronide is a modification of an oligosaccharide, carbohydrate, complex carbohydrate or sugar. It can be synthesized by custom synthesis or by synthetic methods. The product is highly pure and monosaccharide methylated. The product can be glycosylated, polysaccharide, sugar fluorinated and saccharides click modified.

1,4-Anhydro-3-deoxy-D-threo-pentitol is a custom synthesis of a monosaccharide. The structure consists of a hydrogen attached to the oxygen on the anomeric carbon which is then substituted with fluorine. The hydroxyl group on C1 is methylated and then reduced to form a hemiacetal linkage with the C6 hydroxyl group. This product can be used in glycosylation reactions to produce complex carbohydrates.

SN-38 glucuronide is a metabolite of irinotecan that inhibits the growth of cancer cells by binding to the DNA polymerase, blocking the synthesis of DNA. SN-38 glucuronide has potent antitumor activity and high values for inhibiting tumor metastasis. It is mainly excreted in urine as a conjugate with glucuronic acid, which may be why urine samples are often used to measure its concentration. SN-38 glucuronide also interacts with other drugs, including chemical inhibitors and ATP-binding cassette transporters, which can affect its pharmacological properties.

1,2-O-Isopropylidene-3-deoxy-3-fluoro-a-D-ribofuranose is a custom synthesis. It is a complex carbohydrate that has been modified by methylation and glycosylation. This molecule has been fluorinated to produce a high purity product with the desired properties. The 1,2-O-isopropylidene group provides for increased stability and solubility of the product.

b-D-Thioglucose sodium salt hydrate is a complex carbohydrate that is used as an intermediate for the synthesis of oligosaccharides and polysaccharides. It is also used in the modification of saccharide chains, such as glycosylation, and for the preparation of fluorinated carbohydrates. b-D-Thioglucose sodium salt hydrate is high purity, with no detectable impurities or degradation products. It has been modified with fluorine to form a new chemical entity that has not been previously described in the literature.

Allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside is a synthetic compound that belongs to the class of carbohydrates. It is used as a reagent in sugar chemistry and glycosylation reactions. Allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside is also used for the modification of polysaccharides and fluorination reactions. This product has been shown to be effective as a substrate for site specific methylation reactions. Allyl 2 acetamido 4,6 O benzylidene 2 deoxy b D glucopyranoside has been tested in vitro against methicillin resistant Staphylococcus aureus (MRSA) with promising results.

N-Acetyl-L-neuraminic acid is a glycosylation compound that is an important component of the cell wall of Gram negative bacteria. It is used in the synthesis of polysaccharides and in the formation of complex carbohydrates. N-Acetyl-L-neuraminic acid has been studied for its potential use as a drug delivery agent due to its ability to inhibit the activity of enzymes such as α-mannosidase, which can lead to tumor metastasis. This compound can be synthesized using methylation, fluorination, and click chemistry, or custom synthesized by ordering specific monosaccharides. N-Acetyl-L-neuraminic acid can also be modified with acetate groups to create an acetylated form for use in chemical analysis or as a substrate for enzymatic reactions.

6-O-Benzyl-D-glucose is an aglycon of 6-O-benzylglycosides, which are synthesized from glucose by alkaline hydrolysis in the presence of silver oxide. The benzyl group can be removed by a variety of methods, including treatment with hydrogen chloride gas. 6-O-Benzyl-D-glucose has been used in research to demonstrate that carbohydrates have a common structural feature that can be identified by looking at their molecular structure. This molecule has also been used to study the synthesis and reactivity of benzyl groups.

4-Deoxy-D-glucose is a sugar that is synthesized by the condensation of two molecules of erythrose. It has been shown to be an efficient donor substrate for nucleophilic attack, which can lead to the synthesis of glycosides and other natural products. 4-Deoxy-D-glucose is also a competitive inhibitor of uridine diphosphate (UDP) glucose, which is an enzyme involved in the biosynthesis of UDP sugars and glycoproteins. The concentration of 4-deoxy-D-glucose affects its catalytic mechanism, as it acts as a competitive inhibitor at high concentrations. Molecular modeling has revealed that this molecule adopts a chair conformation with significant solvent exposure.

4-Aminophenyl b-D-thioglucopyranoside is a compound that belongs to the group of small molecules and has been studied for its potential use as a drug to treat brain tumours. It has been shown that 4-Aminophenyl b-D-thioglucopyranoside binds to centromeric DNA sequences in mammalian cells, which can lead to inhibition of transcription and replication. This inhibitory effect on transcription and replication is due to the inhibition of acetyltransferase enzymes by 4-Aminophenyl b-D-thioglucopyranoside.

2-Amino-2,3,5-trideoxy-3-methyl-L-arabinonic acid-gamma-lactone hydrochloride is a lipid biosynthesis inhibitor that blocks the first step of this pathway by inhibiting the enzyme d-arabinose 4,5-diphosphate aldolase. This compound inhibits bacterial growth and leads to cell lysis. It has been shown to be active against cryptococcus neoformans and Candida neopformans. 2AADL has also been shown to inhibit the production of cell wall polysaccharides in C. neoformans and other fungi. 2AADL is thought to bind to the cell membrane through its alcohol group, which may lead to changes in the redox potential of the cells.

1,2,3,5-Tetra-o-acetyl-D-xylofuranose is a fatty acid that is found in human red blood cells. It is used as a biochemical marker to diagnose the activity index of fatty acids in the red cell membrane. The activity index can be used to determine whether an individual has metabolic disorders such as hepatic steatosis or lc-ms/ms method. 1,2,3,5-Tetra-o-acetyl-D-xylofuranose also has antimicrobial effects against bacteria and fungi and can be used for the treatment of infectious diseases.

a-D-Xylopyranosyl azide is a sugar that can be synthesized from the reaction of 1,2-dichloroethane with 2,3,4,6-tetra-O-acetyl-a-D-xylopyranose. This compound has a high purity and can be custom synthesized to order. It is used in glycosylation reactions to modify saccharides and oligosaccharides. It has been shown to be useful for click modification and fluorination reactions.

Muraglitazar acyl-b-D-glucuronide is a complex carbohydrate that has been modified with fluorination. The compound is synthesized from methylation, glycosylation, and carbamylation reactions with saccharides. The saccharide modification includes the attachment of various sugars such as glucose, galactose, and mannose. Muraglitazar acyl-b-D-glucuronide can be used in the synthesis of oligosaccharides and polysaccharides. It is also used for Click modification of sugar molecules.

Fucose 2-nitrophenylhydrazone is a custom synthesis that is a modification of fucose. It has been used in methylation, click modification, and fluorination. This compound has been shown to be effective in the synthesis of oligosaccharides and polysaccharides. Fucose 2-nitrophenylhydrazone has also been used as an intermediate for the synthesis of saccharides such as monosaccharide and sugar.

4-Epi-daunosamine is a glycopeptide antibiotic that is used to treat infections caused by Gram-positive bacteria. It binds to the cell wall of these bacteria and inhibits the synthesis of new cell walls. This causes the cells to burst and die, which leads to bacterial death. 4-Epi-daunosamine has been shown to be effective against animal pathogens such as Streptococcus pneumoniae, Haemophilus influenzae, and Clostridium perfringens. 4-Epi-daunosamine also has a low level of toxicity in humans, but can cause adverse effects such as nausea and vomiting if taken in large doses.

Penta-O-acetyl-a-L-idopyranose is a monosaccharide that is synthesized from D-glucose and acetic anhydride. It has been modified with methylation, fluorination, and saccharide modification. Penta-O-acetyl-a-L-idopyranose is soluble in water, methanol, ethanol, and acetone. This compound has been shown to be useful for glycosylation reactions as well as click chemistry. CAS No. 16299-15-3.

D-Allose is a sugar that is modified with a fluorine atom at position 6. This modification can be used to trace the origin of D-allose in complex carbohydrates such as glycogen and glycosylated proteins. The addition of a 13C6 atom allows for the identification of this sugar through mass spectrometry and nuclear magnetic resonance (NMR) analysis.

Glufosfamide is a cytotoxic drug that is used in the treatment of some types of cancer. It is a prodrug that requires conversion to its active form, glufosfamid, by esterase enzymes before it can exert its genotoxic effects. Glufosfamide has shown to be active against platinum-resistant ovarian cancer and solid tumours. This drug also has been shown to inhibit the growth of prostate cancer cells and miapaca-2 cells, which are derived from pancreatic cancer. Glufosfamide has been found to have low toxicity in mice, but there may be adverse reactions when combined with other drugs such as erythromycin or ketoconazole.

UDP-2-ketopropyl-a-D-galactose is a synthetic compound that belongs to the group of oligosaccharides. It is an excellent candidate for glycosylation, methylation, and click modification. The product has a CAS number, which provides high purity and custom synthesis. The product is also a complex carbohydrate with a variety of modifications.

2,4-O-Ethylidene-D-erythrose is a trimerization product of glyoxal and acetaldehyde. It is an aldehyde that can be used as a precursor to other compounds. The hydrated form of 2,4-O-ethylidene-D-erythrose has been rationalized by the mesoxalic acid and water molecules to form the trimer. This compound can be produced from the glycolaldehyde and sulfoxide in an oxidation reaction with hydrogen peroxide. The acetylation of 2,4-O-ethylidene-D-erythrose produces isoxazolidines which are stereoselective.

1,2,3,5,6-Penta-O-propanoyl-b-D-glucofuranose is a methylated sugar. It is a polysaccharide consisting of 1,2,3,5,6-penta-O-propanoyl-b-D-glucopyranosyl units linked by β-(1→4)-glycosidic bonds. This carbohydrate can be used in the synthesis of oligosaccharides and glycosylation reactions. 1,2,3,5,6-Penta-O-propanoyl b -D -glucofuranose has been fluorinated to give pentafluorobenzoyl b -D -glucofuranose which is used for click modification.

1,4:3,6-Dianhydro-2-O-methyl-D-glucitol is a modified sugar that belongs to the group of carbohydrates. It is synthesized by the modification of 1,4:3,6-dianhydro-2,5-diO-methyl D glucitol with methyl iodide and sodium methoxide. The compound is used in pharmaceuticals as an excipient and in cosmetics as a moisturizer. It has been shown to be effective against influenza A virus.

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.

2-Hydroxyimipramine b-D-glucuronide is a custom synthesis, modification, and fluorination of the drug 2-hydroxyimipramine. The methyl group from the molecule is replaced with a fluoro group. This modification leads to a new compound with improved pharmacokinetic properties. The new compound also has glycosylation sites on the sugar ring that are not present in the parent drug. This modification may lead to an increase in the therapeutic efficacy of 2-hydroxyimipramine b-D-glucuronide as it interacts with other drugs and increases their bioavailability.

3'-a-Sialyl-N-acetyllactosamine sodium salt is a high purity, custom synthesis sugar. It has been modified with fluorination, glycosylation, and methylation to provide the desired properties. This product is also available in other forms such as monosaccharide and saccharide. 3'-a-Sialyl-N-acetyllactosamine sodium salt can be used in various applications including Click modification, fluoroamination, glycosylation, carbonylation and methylation. CAS No. 350697-53-9

3,2',3',4'-Tetra-O-acetyl-6,6'-di-O-tert-butyldimethylsilyl-lactal is a glycosylation agent that can be used in the synthesis of oligosaccharides and polysaccharides. It can be fluorinated to create a reactive site for methylation and click modification. 3,2',3',4'-Tetra-O-acetyl-6,6'-di-O-tert-butyldimethylsilyl-lactal is an acetylated lactal with a silyl ether protecting group. This product has been custom synthesized and is available in high purity.

3-Pyridinylmethylbeta-D-glucopyranoside is a sugar that can be custom synthesized. It is a white to off-white crystalline powder with an odorless taste and is soluble in water. 3-Pyridinylmethylbeta-D-glucopyranoside is used in the synthesis of glycosides, saccharides, oligosaccharides, and monosaccharides. This compound can also be modified with fluorination or methylation reactions. The use of this product has been shown to produce high purity compounds for use in pharmaceuticals, agrochemicals, and other chemical industries.

5-(β-D-Galactopyranosyloxy)-DL-lysine is a custom synthesized compound that has been modified with 5-(β-D-galactopyranosyloxy) groups. It is an oligosaccharide, polysaccharide, and saccharide that belongs to the category of carbohydrates. This product is available for purchase in high purity and has been fluorinated. The CAS number for this product is 35910-05-5.

3-O-Triisopropylsilyl-D-glucal is a modified carbohydrate, which is a saccharide that has been modified by the addition of three isopropyl groups. This modification can be used to synthesize oligosaccharides and polysaccharides in order to obtain desired properties. 3-O-Triisopropylsilyl-D-glucal can also be used as a fluorinating agent in synthesis reactions. The compound is also custom synthesized and can be synthesized with high purity (>98%) or with methylation or glycosylation. 3-O-Triisopropylsilyl-D-glucal will react with nucleophiles like amines and alcohols to form adducts, which are then hydrolyzed to release the product.

2,3,4-Tri-O-acetyl-b-D-xylopyranosyl azide is a compound that has a linear range of 10 to 500 μM. It has been shown to inhibit the growth of bacteria such as C. perfringens and S. aureus. This compound inhibits the production of toxins in these bacteria by binding to the ribosomes and inhibiting protein synthesis. In addition, this compound has been shown to have high activity at salinity levels up to 15% NaCl and diffraction data was obtained from 2,3,4-tri-O-acetyl-b-D-xylopyranosyl azide crystals using XRD in order to quantify its molecular structure.

Clofibric acid acyl-b-D-glucuronide is a reactive chemical species that has been shown to have genotoxic effects. It binds to DNA and forms covalent adducts, leading to mutations in the DNA sequence. Clofibric acid acyl-b-D-glucuronide is a metabolite of clofibrate, which is used for the treatment of hyperlipidemia and atherosclerosis. This metabolite can be detected in human blood, serum, and liver samples by GC/MS, with a limit of detection of 0.1 ng/mL (0.0003 µg/L).

Anthracycline antibiotic with potent anti-tumoral activity. The compound interferes with DNA replication and RNA transcription since it intercalates between the base pairs of nucleic acids. It also inhibits the topoisomerase II, proteasome and generates free radicals, which leads to cell death of treated cells. Moreover, daunorubicin triggers apoptosis trough the stimulation of ceramide synthesis. It has been used as chemotherapy agent for the treatment of myeloid leukaemia (AML) and acute lymphocytic leukaemia (ALL).

Methyl L-rhamnopyranoside is a sugar that is the product of the reaction between l-rhamnose and acetone. This compound has been used as a chiral building block for the synthesis of other sugars, such as D-arabinose and D-lyxose. The yield of this reaction depends on the concentration of potassium thioacetate and temperature. This compound can be obtained in two forms: (1) anomeric form, which is an intermediate in the synthesis of carbohydrates and (2) crystalline form, which is a white solid with melting point at 157.3°C. The anomeric form has a stereogenic center at carbon atom 3, whereas the crystalline form does not have any stereogenic centers. Methyl L-rhamnopyranoside also reacts with chlorination reagents to produce chlorinated derivatives, such as 2-chloro-3-(3′,4′-dimeth

Pantothenic acid 2,4-di-O-b-D-galactopyranoside is a custom synthesis of Methylated Pantothenic Acid 2,4-Di-O-b-D-Galactopyranoside. The compound is an oligosaccharide composed of two glucose molecules and one galactose molecule. It contains a fluorine atom at the 4th position of the sugar chain. This modification was made to increase the solubility in water. Pantothenic acid 2,4-di-O-b-D-galactopyranoside can be used in industry as a food additive or pharmaceutical intermediate.

Phenyl a-L-thiorhamnopyranoside is a monosaccharide that is synthesized by the methylation of alpha-D-glucose. It is a custom synthesis that is used in the synthesis of oligosaccharides, polysaccharides, and sugar drugs. Phenyl a-L-thiorhamnopyranoside can be fluorinated to create an active form that has antibacterial activity. This compound has shown no signs of toxicity in animal studies and has been used as a food additive.

1,2,3,4-Tetra-O-acetyl-D-fucopyranose is a glycosylation agent that can be used in the synthesis of complex carbohydrates or in the modification of natural polysaccharides. It can be fluorinated to produce 1,2,3,4-tetra-O-fluoro-D-fucopyranose or modified with a click reagent to produce 1,2,3,4-tetra-[5-(N'-diethylamino)pentyl]-D-fucopyranose. The CAS number for this product is 109712-63-7. This product is available for custom synthesis and is sold at a purity of >99%.

1,2,3,6-Tetra-O-benzoyl-5-thio-D-glucopyranose is a monosaccharide that can be synthesized by the methylation of 1,2,3,6-tetra-O-(benzoyl) D-glucopyranose. The synthesis of this compound is accomplished by a click modification and the use of a fluoroquinolone to modify the sugar at C1. This compound has been shown to be an excellent substrate for polysaccharide and saccharide synthesis as well as fluorination. Purity levels are high with this product.

Thiamine galactoside is a custom synthesis of a monosaccharide. It is modified with fluorination, methylation and saccharide. The resulting product has a molecular weight of 578.08 g/mol and the chemical formula C24H34N6O18S2.

4,6-O-Benzylidene-a-D-galactopyranoside is an artificial sweetener that has a high purity and can be custom synthesized. This compound is also known as an oligosaccharide or complex carbohydrate. It is a member of the saccharide family, which includes monosaccharides and disaccharides. 4,6-O-Benzylidene-a-D-galactopyranoside is a sugar that has been modified by glycosylation and methylation. This product has CAS No. 57783-86-5 and can be found in the Glycosides section of the Chemical Directory.

1,2,3,4-Tetra-O-acetyl-D-xylopyranose is a molecule that is derived from D-xylose. It has been shown to inhibit the growth of fungi such as T. rubrum and L. candidum by acetylation of l-threonine at the C2 position. This molecule can be recycled and its inhibitory activity can be increased through acetylation of the hydroxymethyl group on the C4 position. The mechanism of inhibition is not known but it may be due to steric hindrance or peracylation.

5-Deoxy-L-lyxono-1,4-lactone is a crystalline solid that belongs to the class of hydroxamic acids. This compound has been shown to react with hydroxylamine in an aldonic reaction and to inhibit the enzyme xanthin oxidase. The monoclinic crystal structure of 5-Deoxy-L-lyxono-1,4-lactone was determined by XRD analysis. This compound is synthesized from glyoxylate and malonitrile in an efficient manner. It also inhibits glucose oxidation and can be used as an additive for food products.

Methyl 1-(5-fluoro-1H-2-oxopyrimidin-4-yl)-b-D-glucopyranuronate is an anticancer drug that inhibits β-glucuronidase. Methyl 1-(5-fluoro-1H-2-oxopyrimidin-4-yl)-b-D-glucopyranuronate is a colorless solid that has been recrystallized, purified, and analyzed for its chloride content. The function of this compound has been tested in vitro using tissue cultures and animal models. The reaction vessel used for the test was an acetonitrile solution with a pH between 7 and 8. The methylester form of methyl 1-(5-fluoro-1H--2--oxopyrimidin 4--yl)-b--D--glucopyranuronate reacts with sulphite to produce a green product with a colorimetric method

3,4,5,6-Tetra-O-acetyl-D-myo-inositol is a carbohydrate that can be used as a monosaccharide or an oligosaccharide. It is produced by the modification of inositol with acetate and fluoride. The compound has been shown to have anti-inflammatory properties and can be used as a drug target for treating inflammation. 3,4,5,6-Tetra-O-acetyl-D-myo-inositol is also methylated and glycosylated.

1,4-Dideoxy-1,4-imino-D-xylitol HCl (DDX) is a potent inhibitor of the enzyme carboxypeptidase A2. DDX has been shown to inhibit the growth of HIV in vitro and in vivo. DDX also inhibits the production of proinflammatory cytokines and neurotrophic factors from HL60 cells. It has been shown to be a potential drug target for the treatment of infectious diseases such as alphaviruses, which produce a severe neuroinvasive disease in humans. DDX binds to dna with high affinity and specificity, but does not bind to RNA or proteins. DDX inhibits mitochondrial membrane potential by binding to ATP synthase and blocking the synthesis of ATP. DDX has also been shown to have an anti-oxidative injury effect on mitochondria, which may contribute to its inhibition of viral replication.

Methyl 2,3-di-O-benzoyl-4,6-O-benzylidene-b-D-galactopyranoside is a custom synthesis that belongs to the class of complex carbohydrates. This compound is an oligosaccharide or a polysaccharide that has been modified by methylation and glycosylation. The modification of this saccharide with methyl groups allows for fluorination which is a click modification. Methyl 2,3-di-O-benzoyl-4,6-O-benzylidene b -D galactopyranoside is synthesized via glycosylation followed by fluorination. This product can be used as a research chemical or in other applications.

3-Azido-5-O-benzoyl-3-deoxy-1,2-O-isopropylidene a D-ribofuranose (3ABI) is a synthetic monosaccharide that can be synthesized via a custom synthesis. 3ABI is an oligosaccharide that has the ability to modify glycosylation and polysaccharide synthesis. The fluorination of this sugar provides it with high purity and stability. 3ABI has been shown to have a CAS number of 44793-23-2.

D-ribulose-5-phosphate sodium is a nucleotide sugar that is one of the ribonucleotides, which are fundamental components of RNA. D-ribulose 5-phosphate sodium has been shown to be an intermediate in the metabolism of ribulose and catalyzes the oxidation of d-arabinose. This enzyme also catalyses the synthesis of fatty acids and participates in reactions involving glycerolipids and phospholipids. The reaction mechanism involves a double displacement with simultaneous attack by a water molecule on C2' and C3'. When deuterium is present, it affects the rate of these reactions in a way that depends on the orientation of the substrate to the enzyme.

Phenyl 2,3,6-tri-O-benzyl-b-D-thioglucopyranoside is a high purity, custom synthesis sugar that has been modified with Click modification, fluorination and glycosylation. It is a synthetic compound in the form of an oligosaccharide and monosaccharide. Phenyl 2,3,6-tri-O-benzyl-b-D-thioglucopyranoside has CAS No. 97974-20-4 and can be found under Modification.

Remdesivir impurity

1,2,3,4-Tetra-O-acetyl-6-deoxy-6-fluoro-a-D-glucopyranose is a synthetic sugar that contains four acetyl groups and one fluorine atom. It can be used for the synthesis of oligosaccharides and glycosylations. This product is custom synthesized according to customers' requirements, with high purity and good quality.

1,2,3,4-Tetra-O-acetyl-D-glucuronide methyl ester is a lactone that can be used as a precursor for the synthesis of various types of compounds. The chemical structure was determined by high-resolution x-ray diffraction to be a planar molecule with two conformations: one where the four acetyl groups are on different sides and another where they are all on the same side. The latter conformation is more stable due to the dihedral angle between the hydroxyl group and carbonyl group. This compound is an intermediate in synthesizing 2-(4'-hydroxybenzoyl)-1,2,3,4-tetra-O-acetyl-.alpha.-D-.beta.-D glucopyranoside methyl ester by reacting with 3-(3'-azido)benzaldehyde. The single crystal x-ray diffraction study revealed that this compound has a conformation

8,9-Dideoxy-28,29-dihydro-7,10-dihydroxy-35-O-(2,6-dideoxy-L-ribo-hexopyranosyl)amphotericin B is an antifungal drug that belongs to the class of polyene macrolides. It is a potent inhibitor of Candida albicans and Candida glabrata. This compound has been shown to have synergistic effects when used in combination with nystatin against C. albicans. 8,9-Dideoxy-28,29-dihydro-7,10-dihydroxy-35O-(2,6 - dideoxy - L - ribo - hexopyranosyl)amphotericin B also inhibits toll like receptor 4 (TLR4), which is responsible for the induction of inflammatory cytokines such as IL1B and IL8

Please enquire for more information about Glucosamine L-5-methyltetrahydrofolate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Methyl b-D-fructofuranoside is a chemical compound that is used in the production of esters and fatty acids. Methyl b-D-fructofuranoside is produced by a dehydration reaction between two molecules of acetone. The product of this reaction, methyl b-D-fructopyranoside, can be broken down into two molecules of acetone and one molecule each of methyl alcohol and carbon dioxide. This process is called alkylation. Furanocoumarin derivatives are often found in plants such as asperulosidic acid and quinquefasciatus. These compounds are found in many species of plant, but they are most concentrated in the roots of these plants because they are more metabolically active there than other parts of the plant. Environmental pollution can lead to high concentrations of furanocoumarins in plants, which can have toxic effects on organisms that come into contact with them.

D-Sedoheptulose is a sugar that is a member of the pentoses. It has been shown to have a ph optimum of 4.5 and oxidizing potential of -0.18 V. It is also an important intermediate in carbohydrate metabolism and can be used as an energy source by cells. D-Sedoheptulose plays a role in transcriptional regulation and cellular physiology, as well as being involved in the production of acyl chains and disulfide bonds for proteins. D-Sedoheptulose has also been found to have synergic effects with other sugars such as glucose, sucrose, or fructose, which may be due to its ability to act as an inducer of reductive enzymes such as glucose-6-phosphate dehydrogenase (G6PD).

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Decyl D-glucopyranoside is a sodium salt of decyl D-glucopyranoside that is used as a detergent additive in cleaning compositions. Decyl D-glucopyranoside has shown antimicrobial activity against both Gram-positive and Gram-negative bacteria, including methicillin resistant Staphylococcus aureus (MRSA) and Clostridium perfringens. Decyl D-glucopyranoside has also been shown to have chemical stability at high temperatures, making it useful in the manufacture of lacrimal gland preparations and cationic surfactants.

D-Gluconic acid potassium salt is a glycol ether with biochemical properties that can be used to synthesize covalent linkages. It has been shown to have antimicrobial properties in wild-type strains of Escherichia coli and Salmonella typhimurium. D-Gluconic acid potassium salt has been shown to exhibit inhibitory effects on the synthesis of DNA, RNA, and protein, as well as enzyme activities. The matrix effect is an analytical method that measures the inhibition of bacterial growth in agar plates. Electrochemical impedance spectroscopy (EIS) is a technique that measures changes in electrical resistance when bacteria are placed on an electrode surface. This technique has been used to show that D-gluconic acid potassium salt exhibits inhibitory effects against group P2 enzymes, such as polymerase chain reaction (PCR), which is used for DNA replication and amplification.

Lectins are carbohydrate-binding proteins that can be classified into different types based on their specificities for glycan structures. One of the most common types is the N-acetyl-D-glucosamine (NAG) lectin, which binds to oligomers of NAG and related sugars. Lectins are used to activate cells and induce cell death. The dodecyl NAG lectin has been shown to bind to glucocerebrosides in a reductively irreversible manner and has been used as a model for such interactions. This lectin is also inexpensively produced from a synthetic benzylidene acetal, which can be made from commercially available materials. It has been shown that this lectin binds to polyacrylamide gels in an SDS-polyacrylamide gel electrophoresis, with a pH optimum at 7.0 and an amino acid composition that includes glutamic acid, glutamine, asparagine, ser

Benzyl 2,3-O-isopropylidene-a-D-mannofuranoside is a fluorinated monosaccharide that is synthesized using glycosylation and polysaccharide modification. This product has a CAS number of 20689-03-6 and can be used for complex carbohydrate synthesis. It has been shown to have high purity.

D-Galacturono-6,3-lactone is a fatty acid that is part of the glucuronolactone family and has been shown to have anti-obesity effects in vitro. D-Galacturono-6,3-lactone has been synthesized from sodium citrate and hydrochloric acid in the presence of magnesium salt, and the product was purified by crystallization. It has also been shown to inhibit aminotransferase activity and increase locomotor activity. D-Galacturono-6,3-lactone has a ph optimum of 4.5, which can be determined by an analytical method involving the measurement of hydrogen ion concentration.

2,4-O-Benzylidene-L-xylose is a white crystalline powder with a melting point of about 125°C. It is an acetate salt that can be used in the synthesis of many natural products. It has been shown to inhibit HMG-CoA reductase and is used in the treatment of hypercholesterolemia. The reaction mechanism for this compound is not well understood, but it is believed to involve an acid catalyst and an organic solvent. The yield for this compound is low and it requires a long reaction time due to its high reactivity.

N-Acetylneuraminic acid 9-phosphate is a sugar phosphate

(-)-2,3-O-Isopropylidene-D-threitol is a chiral compound with two stereoisomers. It is a crystalline solid that melts at 71°C and has a population of 50%. (-)-2,3-O-Isopropylidene-D-threitol is an important intermediate for the synthesis of polyethers with chiral centers. The catalytic asymmetric synthesis of (-)-2,3-O-isopropylidene-D-threitol is achieved by alkylation of (+)-2,3-(dimethoxyphosphinyl)propane with isopropanol. This reaction can be used to produce polyethers with chiral centers in high yields and enantioselectivity.

D-[6-13C]Galacturonic acid potassium salt is a synthetic, water-soluble complex carbohydrate with a molecular weight of 744.2. It is used as a fluorescence probe in magnetic resonance imaging (MRI) and also has applications in the synthesis of oligosaccharides and polysaccharides. D-[6-13C]Galacturonic acid potassium salt is soluble in water and has an average pH of 5.0. This compound is available for custom synthesis with high purity and can be found under CAS number 144561-27-4.

Isosaccharinic acid is a bacterial strain that produces isosaccharinic acid as its main fatty acid. The thermodynamic data for the reaction mechanism of the conversion of glucose to isosaccharinic acid has been determined. Isosaccharinic acid formation is catalyzed by an enzyme called glycosyl-glycerate dehydrogenase, which converts glycerate to 3-hydroxypropanoic acid and then to 3-oxopropanoate before it undergoes decarboxylation and reduction to form isosaccharinic acid. Radionuclides such as TcO4 are used in chemical ionization mass spectrometry for the detection of this compound in samples. Neutral pH, high activation energies, and low binding constants are all factors that affect the stability of this molecule.

5-Thio-N-acetylglucosamine is a microtubule inhibitor that binds to o-glcnac, a posttranslational modification of proteins that regulates the morphology and cycling of stem cells. 5-Thio-N-acetylglucosamine has been shown to inhibit the transcriptional activity of o-glcnacase, an enzyme that catalyzes the conversion of o-glcnac to glucosamine. This drug also inhibits the metabolic activity of neural progenitor cells, which may be due to its ability to regulate subpopulations with concomitant expression of markers such as Oct4 and Sox2.

Daunorubicin-d3 is a fluorinated, monosaccharide, synthetic, oligosaccharide and complex carbohydrate. Custom synthesis of Daunorubicin-d3 is available with glycosylation, methylation and other modifications. Daunorubicin-d3 has CAS No. 1614-68-8 and purity >99%.

ADP-L-glycero-b-D-manno-heptose is a synthetic, fluorinated oligosaccharide that is custom synthesized and modified. It has a high purity level and CAS No., as well as being a complex carbohydrate that can be modified with methylation or click modification to generate desired properties. ADP-L-glycero-b-D-manno-heptose is an Oligosaccharide with a glycosylation and methylation. This compound can be used in the synthesis of saccharides, polysaccharides, or other complex carbohydrates.