Glycosciences

3-O-Acetyl-1,2-O-isopropylidene-a-D-galactofuranose is a modification of the carbohydrate structure galactofuranose. It has been custom synthesized and is available in high purity with a monosaccharide content of >99%. 3-O-Acetyl-1,2-O-isopropylidene-a-D-galactofuranose can be methylated or glycosylated and is used as a building block for the synthesis of complex carbohydrates. 3-O-Acetyl-1,2,3,4,6,7,8,-octahydrobenzo[b]naphtho[2,1b][1]benzopyran (CAS No. 109680) is also known as 3-(acetamido)-1,2:3',4'-diisopropyl

(R)-Naproxen acyl-b-D-glucuronide benzyl ester is a custom-synthesized molecule. The synthesis of this compound is accomplished by the modification of naproxen, which is a commercially available drug. The fluorination and methylation steps are accomplished to provide a more potent drug. This compound exhibits anti-inflammatory properties that may be due to its inhibition of prostaglandin synthesis.

Allyl 4,6-O-benzylidene-b-L-glucopyranoside is a carbohydrate that is synthesized from allyl alcohol and glucose. It is a complex carbohydrate made up of two different saccharides. This product can be custom synthesized to meet your needs. Allyl 4,6-O-benzylidene-b-L-glucopyranoside has been modified by fluorination, methylation and glycosylation. It has the CAS number 133394-02-0 and can be synthesized at high purity levels.

1,2,3,4-Tetra-O-acetyl-beta-D-glucuronic acid methyl ester is a phosphatidylinositol (PtdIns) synthesis inhibitor. It inhibits the activation of the PtdIns 3 kinase enzyme by binding to its C2 domain. This inhibitor blocks the synthesis of PtdIns 3,4,5P3 and reduces the activity of protein kinases such as Akt and PKC. The structural analysis of this compound has been done on wild type virus and mouse tumor cells in vitro. One study showed that 1,2,3,4-Tetra-O-acetyl-beta-D-glucuronic acid methyl ester can inhibit hematopoietic progenitor cells and suppress wild type virus growth in vivo.1,2,3,4 Tetra-O-acetyl beta D glucuronic acid methyl ester may have potential as

4,7,8,9-Tetra-O-acetyl-N-acetyl-D-neuraminic acid methyl ester is a modified form of sialic acid. This compound is a glycosylation product that has been modified with methyl groups and fluorine atoms. The fluorination of the molecule increases its stability and prevents it from being hydrolyzed by enzymes such as β-galactosidase. 4,7,8,9-Tetra-O-acetyl-N-acetyl-D-neuraminic acid methyl ester is often used in the synthesis of polysaccharides and oligosaccharides for medical purposes. This compound can be custom synthesized for research purposes or to meet special requirements.

Momordicoside I aglycone is a compound that has been extracted from the roots of Momordica grosvenori. It is a potent inhibitor of the enzyme cyclooxygenase and has been shown to have analgesic, anti-inflammatory, and antipyretic activities in mice.

Allyl 6-o-allyl-α-D-galactopyranoside is a medicinal compound with potential anticancer properties. It is an analog of α-D-galactopyranoside and has been shown to inhibit the activity of protein kinases, which are enzymes involved in cell signaling and regulation. This inhibition can lead to apoptosis, or programmed cell death, in cancer cells. Allyl 6-o-allyl-α-D-galactopyranoside has been studied extensively in Chinese medicine as a potential inhibitor of tumor growth and has also been found in human urine. This compound holds great promise as a natural alternative for cancer treatment and warrants further investigation into its therapeutic potential.

1,2:3,5-Di-O-isopropylidene-a-D-apiose is a monosaccharide that is synthesized from D-apiose by methylation of the C1 hydroxyl group with formaldehyde and sodium methoxide in methanol. This carbohydrate has been shown to be a good substrate for glycosylation reactions and click chemistry.
1,2:3,5-Di-O-isopropylidene-a-D-apiose is a white powder that can be dissolved in water or ethanol. It has no odor and is stable at pH 2 to pH 10. The compound does not react with other carbohydrates or proteins under normal conditions.