Glycosyl compounds
Aobchem (4-Chlorophenyl)(4-nitrophenyl)sulfane | ≥95% | CAS 21969-11-9 | C12H8ClNO2S | 25g
(4-Chlorophenyl)(4-nitrophenyl)sulfane | ≥95% | CAS 21969-11-9 | C12H8ClNO2S | 25g
Aobchem 2-Nitrophenyl acetate | ≥97% | CAS 610-69-5 | C8H7NO4 | 10g
2-Nitrophenyl acetate | ≥97% | CAS 610-69-5 | C8H7NO4 | 10g
Aobchem (4-Chlorophenyl)(4-nitrophenyl)sulfane | ≥95% | CAS 21969-11-9 | C12H8ClNO2S | 10g
(4-Chlorophenyl)(4-nitrophenyl)sulfane | ≥95% | CAS 21969-11-9 | C12H8ClNO2S | 10g
Aobchem Isopropyl(2-nitrophenyl)sulfane | ≥97% | CAS 70415-85-9 | C9H11NO2S | 1g
Isopropyl(2-nitrophenyl)sulfane | ≥97% | CAS 70415-85-9 | C9H11NO2S | 1g
Cayman Chemical 9Nitrooleate Fatty Acids and D
A novel endogenous lipid signaling molecule; nitration product of oleic acid in vivo mediated by peroxynitrite, acidified nitrite, or myeloperoxidase (in the presence of H2O2 and nitrite)
Aobchem Methyl(2-nitrophenyl)sulfane | ≥97% | CAS 3058-47-7 | C7H7NO2S | 1g
Methyl(2-nitrophenyl)sulfane | ≥97% | CAS 3058-47-7 | C7H7NO2S | 1g
Sigma Aldrich Fine Chemicals Biosciences beta-Lactoglobulin from bo1G
Milk from dairy cows contains the protein -lactoglobulin (BLG). It naturally occurs in a number of genetic variants and the most prevalent bovine variants are BLG A and BLG B.
Medchemexpress LLC 4 6-O-Benzylidene-D- 5g | 30688-66-5 | 5 G
4,6-O-Benzylidene-D-glucose is a benzaldehyde-protected D-glucose derivative used as a synthetic intermediate and research reagent. It protects the 4- and 6-hydroxyl groups as a benzylidene acetal, enabling selective transformations in carbohydrate chemistry and has reported anticancer activity.
- Protects 4 and 6 hydroxyl groups as a benzylidene acetal
- Useful intermediate for selective carbohydrate synthesis
- Solid research-grade material suitable for laboratory use
- Available in small, research-scale packages (e.g., 5 g)
- CAS number 30688-66-5 and molecular weight 268.26 g·mol-1
Alkali Scientific 4 Nitrophenyl 2 acetamido 2 deoxy β D glucopyranoside, 250 Mg
4-Nitrophenyl 2-acetamido-2-deoxy-β-D-glucopyranoside (250 mg) is a chemical reagent used in enzyme assays to study β-D-glucosidase activity. This compound serves as a substrate for the enzyme, where the cleavage of the glucosidic bond produces p-nitrophenol, which can be quantified spectrophotometrically. The compound's acetamido and deoxy groups enhance its specificity for particular enzymatic processes. This reagent is used primarily in glycoside hydrolase studies, which are vital for understanding cell wall biosynthesis, carbohydrate metabolism, and certain metabolic disorders. It is a critical tool for glycoscience and enzymology research.
Aobchem (3-Bromo-5-nitrophenyl)(thiomorpholino)methanone | ≥95% | CAS 2432848-90-1 | C11H11BrN2O3S | 5g
(3-Bromo-5-nitrophenyl)(thiomorpholino)methanone | ≥95% | CAS 2432848-90-1 | C11H11BrN2O3S | 5g
Alkali Scientific 2 Nitrophenyl β D Glucopyranoside, 10 G
2-Nitrophenyl β-D Glucopyranoside, 10g, is a highly useful reagent in studying β-glucosidase enzyme activity. This compound is utilized in colorimetric assays where β-glucosidase cleaves the β-glucopyranoside bond, releasing a yellow product, allowing researchers to visually track enzyme activity. This reagent is essential for enzyme kinetics studies, particularly in microbiology and genetic research, where it helps in assessing enzyme functions and metabolism. The 10g quantity is ideal for large-scale experiments and routine testing in research laboratories, offering an efficient and cost-effective means to measure β-glucosidase activity and enzyme reaction rates in various research applications.
Alkali Scientific 4 Nitrophenyl α L Arabinopyranoside, 500 Mg
4 Nitrophenyl α-L Arabinopyranoside (500 mg) is a potent substrate used to study the activity of α-L-arabinosidases in biochemical assays. The compound, upon hydrolysis by the enzyme, releases a yellow color, providing an easy-to-detect indicator of enzyme activity. It is widely used in glycobiology and carbohydrate chemistry to study the breakdown of arabinose-containing polysaccharides, such as hemicelluloses. This reagent is commonly applied in enzyme research, high-throughput screening, and the development of novel α-L-arabinosidase inhibitors. It is also valuable in exploring the role of arabinose in various cellular processes, including metabolism and signaling.
Alkali Scientific p Nitrophenyl β D fucopyranoside, 1 G
p Nitrophenyl β-D fucopyranoside (1 g) is a high-purity reagent designed for use in enzymatic assays where fucosidases are involved. This reagent is commonly utilized in biochemical studies to detect and measure the activity of β-D-fucosidases through colorimetric analysis. Upon hydrolysis, the nitrophenyl group releases a yellow color, enabling precise measurement of enzyme activity. The compound is ideal for high-throughput assays, carbohydrate research, and studies involving glycoside hydrolases. It plays a key role in understanding the breakdown of fucosidic linkages in glycoproteins, a process important in cellular communication and immune response.