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Rhamnolipids are a class of biosurfactants which contain rhamnose as the sugar moiety linked to β-hydroxylated fatty acid chains. Rhamnolipids can be widely applied in many industries including; petroleum, food, agriculture and bioremediation etc.

Undecyl b-D-maltopyranoside is a cell culture reagent that belongs to the group of monomers. It is used in the synthesis of dodecyl maltoside and is also used as a substrate for bacterial enzymes. Undecyl b-D-maltopyranoside has been shown to inhibit the activity of leukotriene A4 hydrolase, an enzyme involved in the metabolism of leukotrienes. This product has been shown to be effective in chromatographic separation of metal ions from other components. Undecyl b-D-maltopyranoside can also be used for solubilizing peptides and proteins, including those that are neutral or have a low pH. This product is also used as a substrate for recombinant monoclonal antibodies and viral coat proteins.

3,4,2',3',6'-Penta-O-acetylsucrose is a deuterated analog of sucrose. It can be synthesized by reacting sucrose with acetyl chloride in the presence of a base. The transesterification reaction yields the desired product in an overall yield of about 20%. This process is similar to that used for the synthesis of fatty acid esters, but 3,4,2',3',6'-Penta-O-acetylsucrose does not exist in nature and cannot be found as a natural product. The X-ray crystallography studies show that 3,4,2',3',6'-Penta-O-acetylsucrose has a conformation different from that of 6-phosphate sucrose.

b-Sitosterol b-D-glucuronide methyl ester is a carbohydrate that is a modification of saccharides. It is a sugar with the molecular formula C23H36O11 and molecular weight of 594.71. It has CAS No. 64432-41-7 and was first synthesized in the laboratory by custom synthesis in 2007. This compound is highly pure and has been shown to have high purity. It has been modified using fluorination, glycosylation, and methylation reactions. The carbohydrate has been shown to have anti-inflammatory activities, which may be due to its ability to inhibit prostaglandin synthesis.

Hydroxy pioglitazone (M-VII) b-D-glucuronide is a synthetic, fluorinated glucuronide of hydroxy pioglitazone. It has been shown to inhibit the activity of bacterial dna gyrase and topoisomerase IV enzymes.

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.

UDP-6-Amino-6-deoxyglucose is a fluorinated monosaccharide that can be used as a glycosylation or polysaccharide modification reagent. It is also used to produce complex carbohydrates, such as glycosylated proteins and glycoconjugates. The synthesis of this product involves the use of Click chemistry, which allows for the selective attachment of any molecule with an amine group. This product has been shown to have high purity and is ideal for use in pharmaceuticals, agrochemicals, food additives, and other applications.

Methyl 2-O-(methyl 4-O-methyl-α-D-glucopyranosyluronate)-β-D-xylopyranoside is a methyl glycoside disaccharide

Ethyl 3-O-benzyl-b-D-thioglucopyranoside is a modification of the sugar D-thioglucose. It is synthesized by the methylation of D-thioglucose with ethyl iodide in aqueous sulfuric acid, followed by glycosylation with benzaldehyde and sodium hydroxide. This product has been used for polymerization reactions, as well as for synthesis of oligosaccharides and polysaccharides. The molecular weight of this product is 434.2 g/mol.

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Solasodine 3-glucoside is a sugar that belongs to the group of oligosaccharides. It has been synthetically modified by fluorination, methylation, and click chemistry. Solasodine 3-glucoside is synthesized from sucrose in a glycosylation reaction with glucuronic acid and an aminoglycoside antibiotic. The sugar analogs are then converted to the desired saccharide structure by monosaccharide synthesis or polysaccharide synthesis. This product is custom synthesized to order for customers and can be modified to suit their needs with click chemistry and other modifications.

a-D-Fucose-1-phosphate is a complex carbohydrate. It is an Oligosaccharide with CAS No. that can be modified by methylation, glycosylation, or click modification. Carbohydrates are saccharides that can be modified by fluorination or synthesis. a-D-Fucose-1-phosphate has high purity and a custom synthesis can be ordered from the company.

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.

Mycophenolic acid phenolic b-D-glucoside is a high purity custom synthesis that can be modified to suit customer requirements. It is a complex carbohydrate with a methyl group, fluorine atom, and glycosylation. The chemical name for Mycophenolic acid phenolic b-D-glucoside is CAS No. 55533-52-3. This product is also known as Glycosylation, Oligosaccharide, sugar, Synthetic, Fluorination, Custom synthesis, Methylation, Monosaccharide, Polysaccharide, saccharide. Click modification or Modification.

Astragaloside II is a natural compound that has been shown to have anti-inflammatory effects in vitro and in vivo. Astragaloside II inhibits the production of inflammatory mediators by inhibiting phosphodiesterase and cyclooxygenase pathways. It also has a matrix effect on the cells, which may be due to its ability to activate protein kinase C. This compound also has an analytical method, which consists of HPLC with UV detection at 210 nm.

Glcnacβ(1-2)man-α-ethylazide is a modified oligosaccharide that has been synthesized from the sugar GlcNAcβ(1-2)mannose. It is a complex carbohydrate with a high purity, which can be used as a custom synthesis. The synthesis of this product involves fluorination and saccharide methylation. The CAS number for this product is 1858224-15-3.

2-Acetamido-1,3,6-tri-O-benzyl-2-deoxy-a-D-glucopyranoside is a carbohydrate that is composed of four sugar units. It is an antigenic determinant found on the surface of human erythrocytes. The chemical synthesis of this substance begins with the condensation reaction between D-glucose and 2,4,6,-trinitrophenylacetic acid followed by benzylation and acetylation. This compound belongs to the group of substances known as carbohydrates which are chains of monosaccharides that form glycosidic bonds with other sugars. These chains are classified according to their length and the number of sugar units they contain: trioses (three sugar units), tetroses (four sugar units), pentoses (five sugar units), hexoses (six sugar units) or heptoses (seven sugar).

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.

GQ1b ganglioside (ammonium salt) has a core tetrasaccharide structure (Galβ1,3GalNAcβ1,4Galβ1,4Glc) with two sialic acids (NeuAc) linked α2,3/α2,8 to the inner galactose residue, two sialic acids (NeuAc) linked α2,3/α2,8 to the terminal galactose residue, and ceramide linked β to position 1 on the reducing terminal glucose residue (Ledeen, 2009). Anti-GQ1b ganglioside antibody is associated with Miller Fisher syndrome and is also found in patients with related conditions that may share the same pathogenic mechanism, such as, Bickerstaff brainstem encephalitis. Thus, the measurement of anti-GQ1b antibody in suspected cases of Miller Fisher syndrome is a useful diagnostic marker (Paparounas, 2004). It has been found that GQ1b ganglioside contributes to synaptic transmissions and synapse formation. Low concentrations of GQ1b ganglioside, evoked dopamine (DA) release from laboratory tissues (Chen, 2018).