Chromogenic Substrates

p-Nitrophenylphosphorylcholine is a substrate molecule for enzymes that catalyze phospholipid biosynthesis. It is the most common substrate used to study the enzyme activity of phosphatidylcholine synthase and phospholipase A2 in human serum. The reaction mechanism is not well understood, but it appears to involve autocatalysis and an initial nucleophilic attack by p-nitrophenolate on the carbonyl carbon atom of the choline moiety. p-Nitrophenylphosphorylcholine has been shown to exhibit receptor activity on cells, which may be due to its ability to bind with basic proteins. This compound can also inhibit meiosis in Drosophila melanogaster and increase levels of natriuretic peptides in rats, as well as cause cell lysis and polymerase chain reactions in mammalian cells.

4-Nitrophenyl b-D-cellopentaoside hexadecaacetate is a fluorogenic substrate that is used to study the activity of various enzymes. It reacts with hydrolytic enzymes in the presence of hydrogen peroxide to produce light, and it can be used for food testing, environmental testing, and diagnostics. 4-Nitrophenyl b-D-cellopentaoside hexadecaacetate is a conjugate of 4-nitrophenol and cellobiose pentaacetate that has a high purity and high quality. The CAS number for this compound is 129411-66-1.

<p>4-Nitrophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside is an extracellular nucleic acid molecule that is produced by the bacterium Corynebacterium glutamicum. This compound has been shown to inhibit cancer cells by blocking the transport of glucose through the cell membrane and may be a potential drug target for cancer treatment. 4NPTAPG has also been shown to have diagnostic properties and can identify corynebacterium glutamicum strains. It is a fluorescent molecule that can be used to detect the presence of this bacterium in culture media.</p>

<p>4-Nitrophenyl 2-acetamido-2-deoxy-3,6-di-O-benzoyl-b-D-galactopyranoside is an advanced pNP-based enzyme substrate designed for the detection and measurement of glycosidase activity in biological samples. This synthetic compound offers high specificity and sensitivity for b-galactosidase enzymes, enabling accurate determination of enzymatic hydrolysis rates in a variety of research applications, including diagnostics, drug development, and discovery of novel enzymes. Its chromogenic properties ensure easy analysis of the results and make it suitable for high-throughput screening.</p>

<p>4-Nitrophenyl 2-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-b-D-glucopyranoside is a state-of-the-art chromogenic substrate designed for rapid and sensitive enzyme activity detection. As a versatile pNP substrate, it produces a noticeable color change upon enzyme-catalyzed hydrolysis, facilitating easy monitoring and quantification of enzyme levels in research and diagnostic applications. The substrate's acetylated glucose moiety ensures specificity and stability, allowing for precise and reliable results across a range of experimental conditions.</p>

<p>5-Bromo-6-chloro-1H-indol-3-yl-a-D-mannopyranoside is a chromogenic substrate that yields a magenta-colored product after cleavage. The chromophore 5-bromo-6-chloro-indoxyl is released, generating the observable color. It is used in lysosomal storage disorder screening.</p>

<p>Jalapeno green-Gal (Jalapeno green-beta-D-galactopyranoside) is a chromogenic indicator for beta-galactosidase activity. The colorless product is cleaved by lactose-utilizing bacteria in liquid media or on agar plates and yields a Jalapeno green colored precipitate. Jalapeno green-Gal can also be used as detecting agent for beta-galactosidase activity in reporter gene assays or for identification of positive transformants on agar plates when using the α-complementation approach.</p>

<p>2-Nitrophenyl hexyl ether is a chromogenic substrate commonly used to assay the activity of esterases. Upon cleavage of the ester bond by esterases, the released 2-nitrophenyl group yields a yellow color detectable by spectrophotometry. This substrate has been used in a variety of applications, including environmental monitoring and studies of insecticide resistance. It is particularly useful for screening large numbers of samples because of its rapid reaction rate and high sensitivity. However, it should be noted that some non-specific hydrolysis may occur with this substrate, particularly at high concentrations or in the presence of strong nucleophiles.</p>

<p>2-Nitrophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside is a chromogenic substrate used to detect and measure the activity of glycosidase enzymes. Glycosidases are enzymes that hydrolyze glycosidic bonds in carbohydrates, and are produced by many organisms. The substrate is cleaved by glycosidase to release a chromophore, which can be quantified via spectrophotometry analysis. 2-Nitrophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside is widely used in various applications, including enzyme kinetics studies, inhibitor screening, and the detection of NAGase activity in biological samples, such as serum, urine, and cell lysates. It is also used for the identification and characterization of glycosidases in microorganisms and the study of glycosylation-related processes in cells and tissues.</p>

chromogenic substrate for beta-glucuronidase

<p>2-Chloro-4-nitrophenyl b-D-xylobioside is a chemiluminescent substrate that is used as a diagnostic agent. It has been used in the identification of gram positive and gram negative bacteria, which are differentiated by the color of the reaction. This substrate has also been used to detect the presence of certain enzymes produced by bacteria. 2-Chloro-4-nitrophenyl b-D-xylobioside has shown to be an effective enzyme substrate for detecting bacterial growth in culture media and is often used as a fluorogenic substrate in food testing.</p>

<p>4-Nitrophenyl 3-O-(2,3,4,6-tetra-O-acetyl-a-D-mannopyranosyl)-4,6-O-cyclohexylidene-b-D-mannopyranoside is a chromogenic pNP enzyme substrate, which features a cyclohexylidene-protected mannopyranosyl core. Upon enzymatic hydrolysis by glycosidases or other related enzymes, it releases a yellow-colored product, 4-nitrophenol, that can be easily detected spectrophotometrically. This substrate is useful for studying enzyme specificity, kinetics, and inhibition, as well as for the screening of enzyme inhibitors, the identification of glycosidase-producing organisms, and the development of new analytical methods.</p>

4-Nitrophenyl 2-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-4,6-O-benzylidene-b-D-glucopyranoside is a compound that is used in gene expression profiling. It has been shown to be an effective inhibitor of glutamicum and corynebacterium glutamicum. 4NPBG can inhibit the production of acid molecules by blocking the activity of cytochrome P450 enzymes in the cells of these bacteria. The compound also inhibits cellular transport and membrane transport genes in these species. This inhibition prevents the synthesis of nucleic acid molecules such as RNA and DNA.

<p>2-Nitrophenyl 2-acetamido-2-deoxy-b-D-galactopyranoside is a carboxymethyl derivative of the natural substrate of β-galactosidase, which is used as a substrate for the production of recombinant proteins in the corynebacterium glutamicum. The enzyme β-galactosidase hydrolyzes this substrate to produce an acid molecule and a sugar molecule. This product can be used in biotechnological processes for the production of recombinant proteins or other bioactive molecules. It can also be used in the isolation of nucleic acid from bacteria or fungi, or to study bacterial membrane transport systems. 2NPGAG can be expressed as a recombinant protein with expression vectors such as pET21a and pET24a. It has been shown that this product inhibits transport through membranes by binding to cellulose, which may be useful for studies on cellulose biosynthesis</p>

<p>4-Nitrophenyl b-D-glucuronide sodium salt is a high-quality chromogenic substrate specifically designed for the colorimetric detection and measurement of β-glucuronidase activity. Upon enzymatic cleavage, it releases the yellow 4-nitrophenol, enabling quantitative analysis via spectroscopy. This compound is conveniently provided as a sodium salt to ensure enhanced solubility, stability, and shelf life. It is an ideal choice for biochemical, research, and diagnostic applications requiring a reliable and efficient b-D-glucuronide substrate.</p>

<p>4-Nitrophenyl 2-O-(α-D-glucopyranosyl)-α-D-glucopyranoside is a specialized chromogenic pNP substrate featuring dual glucose-linked moieties, designed for accurate detection and quantification of specific glycosidase enzymes. Upon cleavage by target enzymes, this substrate releases 4-Nitrophenol, which can be easily monitored spectrophotometrically as a yellow color change. This advanced substrate offers enhanced specificity and sensitivity in enzyme assays, facilitating cutting-edge research in biochemistry, enzymology, and other related fields.</p>

1-Naphthyl a-D-glucopyranoside is a chromogenic substrate used to detect the presence of enzymes that catalyze the hydrolysis of glycosidic bonds, such as alpha-glucosidase. When the substrate is cleaved by the enzyme, it produces a colored product that can be visualized and quantified.

2-Nitrophenyl 2,3,4-tri-O-acetyl-beta-D-xylopyranoside is a chromogenic substrate used to detect the enzymatic activity of xylosidase. After cleavage, the nitrophenyl moiety is released exhibiting a light yellowish color. 2-Nitrophenyl 2,3,4-tri-O-acetyl-beta-D-xylopyranoside is used in bacterial hemicellulose metabolism assays.

5-Bromo-3-indolyl decanoate (BID) is a chromogenic enzyme substrate often used for the detection of lipase activity. It is hydrolyzed by lipase to produce a blue-violet product, which can be detected visually or by spectrophotometry. BID is particularly useful for the detection of microbial lipases in food and environmental samples. It is commonly used in a wide range of biochemical, biological, and environmental testing applications that require precise lipase enzyme analysis.

4-Nitrophenyl hepta-O-acetyl-1-thio-b-lactoside is an inorganic molecule that binds to the surface of bacteria. It has been used as a fingerprinting tool for a variety of organisms, including corynebacterium glutamicum. The molecule can be used to measure the metabolic activity of corynebacterium glutamicum with a technique called incremental acidification. This technique is based on the observation that the concentration of 4-nitrophenol decreases by one unit for each glucose metabolized by corynebacterium glutamicum. The use of 4NPHTBL and other primers can also be useful in diagnosing patients with autoimmune diseases such as celiac disease and inflammatory bowel disease.