Monosaccaridi

D-Galactose-2-D is an anticancer agent that has been shown to inhibit the activity of kinases, which are enzymes involved in cell signaling pathways. It is a derivative of D-galactose and has been found in human urine. D-Galactose-2-D has demonstrated potent antitumor effects against various cancer cell lines, including Chinese hamster ovary cells and human colon carcinoma cells. This compound induces apoptosis, or programmed cell death, in cancer cells by inhibiting the activity of key proteins involved in cell survival. Additionally, D-Galactose-2-D has been found to be a potent inhibitor of capsaicin-induced activation of kinase, suggesting its potential as a therapeutic agent for inflammatory conditions.

6-O-tert-Butyldimethylsilyl-D-galactal has been used as a methylating agent in the synthesis of complex carbohydrates. It is a synthetic modification of D-galactal, which is an oligosaccharide and polysaccharide consisting of galactose residues. The chemical name for 6-O-tert-Butyldimethylsilyl-D-galactal is 6-(tert-butyldimethylsilyloxy)-1,2,3,4,6,7,-hexahydrobenzo[a]pyrene. This compound is soluble in organic solvents and can be used to modify other carbohydrates. It has a molecular weight of 578.9 g/mol and CAS number 124751-19-5.

2-Formylphenyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a custom synthesis that is modified with a fluorination. It is an oligosaccharide that contains a methylation and glycosylation. This product is an Oligosaccharide, which is a complex carbohydrate. The synthesis of this product is high purity and has been synthesized by the methylation and glycosylation of monosaccharides. This compound has been synthesized from high purity chemicals, including saccharides, such as glucose or fructose. The compound's CAS number is 15430-78-1.

4,5,6-Tri-O-benzyl-3-benzyloxymethyl-octa-1,7-dien-3-ol is an oligosaccharide that is synthesized by the modification of a simple sugar with two benzyloxymethyl groups. It can be used as a carbohydrate in pharmaceuticals and other applications.

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.

Methyl 5,7,8,9-tetra-O-acetyl-4-acylamino-2,6-anhydro-3,4-dideoxy-D-glycero-D-galacto-2-enonate is a synthetic sugar that is used as a building block for the synthesis of polysaccharides. This compound can be modified with click chemistry and fluorination to create an array of possible saccharide structures. Methylated sugar derivatives are also used in custom synthesis applications.

Phenyl 4-azido-2,3,6-tri-O-benzyl-4-deoxy-b-D-thioglucopyranoside is a fluorinated monosaccharide that can be synthesized from commercially available starting materials. The compound has been shown to inhibit the glycosylation of proteins and is used in the synthesis of complex carbohydrates such as oligosaccharides and polysaccharides. Phenyl 4-azido-2,3,6-tri-O-benzyl -4 deoxy -b D thioglucopyranoside is a white crystalline solid that has a melting point of 155 ˚C and an assay of 99% purity.

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3,6-Di-O-triisopropylsilyl-D-glucal is a synthetic monosaccharide. It has a molecular weight of 368.76 g/mol and chemical formula C14H22O8Si. 3,6-Di-O-triisopropylsilyl-D-glucal is soluble in water and ethanol.
It is used for the synthesis of oligosaccharides and polysaccharides, as well as for modification of sugar moieties on glycoproteins and glycolipids. 3,6-Di-O-triisopropylsilyl-D-glucal can be used for the preparation of complex carbohydrate structures by glycosylation or polysaccharide structures by methylation. 3,6-Di-O-triisopropylsilyl--D--glucal can also be used to synthesize sugar mo

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.

N-Acetylgalactosamine-BSA is a glycoprotein that has been synthesized and purified. This product contains mannose, N-acetylglucosamine, and a variety of sugar residues. It is used as a ligand for binding to glycosidases and neoglycoproteins. N-Acetylgalactosamine-BSA also functions in the regulation of carbohydrate metabolism and the maintenance of cell membrane integrity. The product is soluble in water at millimolar concentrations.

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

D-myo-inositol-1,3,4,5-tetraphosphate (IP4) is a molecule that is involved in the regulation of cell metabolism and signal transduction. It is synthesized from myo-inositol by the enzyme inositol monophosphatase and hydrolyzed by inositol hexaphosphate kinase to form D-myo-inositol. IP4 can bind to receptors which span the plasma membrane and interact with intracellular Ca2+ channels. This binding results in an increase of cytosolic Ca2+ levels, which may be due to IP4’s ability to activate phosphatidylinositol turnover. IP4 is also involved in the regulation of neuronal death and infectious diseases such as HIV.

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.

Phenyl 2,3-di-O-benzoyl-b-D-thiogalactopyranoside is a custom synthesis that is an Oligosaccharide, Polysaccharide and Modification of saccharide. It has been modified with Methylation and Glycosylation, Click modification and Carbohydrate. This product is offered in high purity and is Fluorinated, Synthetic.

2-(D-Arabino-tetrahydroxybutyl)-4(R)-1,3-thiazolidine-4-carboxylic acid is a synthetic monosaccharide that can be used to synthesize oligosaccharides and polysaccharides. It has been shown to be able to undergo glycosylation, methylation, and click modification reactions. This product is most commonly used in the preparation of complex carbohydrates for research or industrial purposes. 2-(D-Arabino-tetrahydroxybutyl)-4(R)-1,3-thiazolidine-4-carboxylic acid is soluble in water and has a CAS number of 110270-13-8.

3-Azido-2,3-dideoxy-D-ribose is a boron trifluoride etherate that has significant activity against the anomers of d-mannitol. It can be used as a stereoselective synthesis of the triflate on the corresponding anomer. Triflate is prepared by reaction with trifluoromethanesulfonic acid chloride and then reacted with sodium azide in ethanol to yield 3-azido-2,3-dideoxy-D-ribose. The product can be purified by recrystallization from acetic acid and water or by extraction with chloroform. This compound is also extracted from boric acid and dioxane using aqueous sodium hydroxide solution.

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.

The chemical name of this compound is 2-(Acetylamino)-1-O-benzyl-2-deoxy-3,4-O-isopropylidene-6-O-(2,3,4,6-tetra-O-acetylbDgalactopyranosyl)-Dgalactopyranoside. It is a synthetic compound and its molecular formula is C17H22N2O8. The molecular weight of this compound is 412.46 g/mol. CAS No. 352273-66-6

1,2:4,5-Di-O-isopropylidene-b-L-erythro-2,3-hexodiulo-2,6-pyranose is a sugar that can be found in the human body. It has been shown to have a high level of hydrogen bonding and can be used as an energy source by replicon cells. It is also an enantiomer of 1,2:4,5:8,9-di-O-isopropylidene-b-(D)-threo--2,3--hexodiulo--2,6--pyranose. This molecule has been shown to inhibit the growth of herpes simplex virus in vitro and in vivo and has been investigated for its potential use as an antiherpes agent. 1,2:4,5:8,9 Di--O--isopropylidene--b-(D)--threo--2

Benzyl 2-azido-2-deoxy-a-D-galactopyranoside (α-OBn GalN3) is a compound based on the structural features of α-OBn GalNAc. It features an azide functionality at C2 instead of the N-acetyl. α-OBn GalN3 inhibits glycosyltransferases responsible for O-GalNAc-type glycosylation and induces apoptosis in PC/AA/C1/SB10C and HCA7/C29 cells. The compound was tested at 0.5 mM for 4 days with different colorectal cell lines and showed an inhibition of cell growth. α-OBn GalN3 was also used as an intermediate for the total synthesis of (+)-Neocarzinostatin chromophore.