
Substratos enzimáticos
Substratos enzimáticos são moléculas sobre as quais as enzimas atuam para catalisar reações químicas. O substrato liga-se ao sítio ativo da enzima, onde passa por uma transformação específica para formar o produto da reação. Os substratos enzimáticos são ferramentas essenciais na pesquisa para estudar a cinética enzimática, especificidade e mecanismo de ação. Eles também são usados em ensaios diagnósticos e estudos bioquímicos. Na CymitQuimica, oferecemos uma seleção diversificada de substratos enzimáticos de alta qualidade para apoiar suas pesquisas em enzimologia e bioquímica.
Subcategorias de "Substratos enzimáticos"
Foram encontrados 1527 produtos de "Substratos enzimáticos"
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Salmon-pal
CAS:<p>6-Chloro-1H-indol-3-yl hexadecanoate is a chromogenic substrate for an enzyme that oxidizes it to produce a blue color. It can be used in the diagnosis of bacterial infections, such as tuberculosis and leprosy. 6CHIH is a ligand for various enzymes, including lactate dehydrogenase, which catalyzes the conversion of pyruvate to lactic acid. This compound reacts with oxygen to produce light in the presence of a catalyst. 6CHIH is also used as a fluorescent tag for protein labeling and detection.<br>6CHIH has been shown to be effective in detecting bacteria in food products and water samples using bioluminescence techniques. The high purity and quality of this compound make it suitable for use in diagnostics, culture media, and environmental testing.</p>Pureza:Min. 95%Peso molecular:406 g/molChitin azure
CAS:<p>Chitin azure is a chromogenic substrate for chitinases. It is one of the few specific substrates for this enzyme that produces chito-oligosaccharides from chitin.</p>Cor e Forma:Powder4-Methylumbelliferyl-β-D-glucopyranoside
CAS:<p>Fluorogenic substrate for beta-glucosidase yielding a blue fluorescent solution. Used for the detection of beta-glucosidase as an indicator of Enterococci.</p>Fórmula:C16H18O8Pureza:Min. 99 Area-%Peso molecular:338.32 g/mol4-Methylumbelliferyl-β-L-fucopyranoside
CAS:<p>4-Methylumbelliferyl-beta-L-fucopyranoside is a fluorogenic substrate that is used in food testing. It also has uses as a chromogenic substrate and a ligand for biological studies. 4-Methylumbelliferyl-beta-L-fucopyranoside is a conjugate of 4-methylumbelliferone and beta-D-fucopyranosyl ester, which is an enzyme substrate for the detection of phosphatases. This product can be used to detect the activity of phosphatase enzymes in various media, including culture media, environmental testing, and staining. 4MUFBPY also has chemiluminescent properties that can be used for bioluminescence assays.</p>Fórmula:C16H18O7Peso molecular:322.31 g/molRef: 3D-M-5541
1gA consultar5gA consultar250mgA consultar500mgA consultar2500mgA consultar-Unit-ggA consultar1-Naphthyl a-D-galactopyranoside
CAS:<p>1-Naphthyl a-D-galactopyranoside is a chromogenic substrate use to detect alpha-galactosidase activity.</p>Fórmula:C16H18O6Pureza:Min. 95%Cor e Forma:PowderPeso molecular:306.31 g/mol4-Methylumbelliferyl-α-L-fucopyranoside
CAS:<p>Fluorogenic substrate for α-L-Fucosidase yielding a blue fluorescent solution upon cleavage.</p>Fórmula:C16H18O7Peso molecular:322.32 g/mol4-Chloro-3-Indoxyl-1,3-diacetate
CAS:<p>4-Chloro-3-indoxyl-1,3-diacetate is a fluorogenic or chromogenic substrate used in food testing. It is also an enzyme substrate that can be used to detect the presence of bioluminescence. 4-Chloro-3-indoxyl-1,3-diacetate has been shown to have high purity and high quality for use in diagnostic kits. 4-Chloro-3-indoxyl-1,3-diacetate is a ligand that is conjugated with other molecules to form complexes for use in fluorescence and chemiluminescence experiments.</p>Pureza:Min. 95%Peso molecular:251.67 g/molNaphthol AS-BI β-L-fucopyranoside
CAS:<p>Substrate for the detection of beta-D-fucosidase</p>Fórmula:C24H24BrNO7Pureza:Min. 95%Peso molecular:518.35 g/molGlycyl-glycine 7-amido-4-methylcoumarin hydrochloride
CAS:<p>Glycyl-glycine 7-amido-4-methylcoumarin hydrochloride (Gly-Gly-AMC) is a fluorescent compound that can be used as a probe for the transfer of glycine in the brain. Gly-Gly-AMC binds to Langerhans cells and is transferred by an anterograde axonal transport mechanism from the peripheral nervous system to the central nervous system. The binding of Gly-Gly-AMC to Langerhans cells has been shown to activate them, which induces the release of inflammatory mediators into the surrounding tissue. This activity may be due to increased levels of calcium ions, which are known to induce exocytosis in these cells. Glycine is also involved in depression and other mental disorders, as well as muscle and brain activity.</p>Fórmula:C14H16ClN3O4Peso molecular:325.75 g/mol4-Methylumbelliferyl phosphate, free acid
CAS:<p>A sensitive fluorogenic substrate for fluorometric and UV-spectrophotometric assays of phosphatases. It is used for the detection of C. perfringens because acid phosphatase is a highly specific indicator for C. perfringens.</p>Fórmula:C10H9O6PPeso molecular:256.15 g/mol2-Nitrophenyl α-D-glucopyranoside
CAS:<p>2-Nitrophenyl a-D-glucopyranoside is a chromogenic substrate commonly used to assay the activity of glucosidases. Upon cleavage of the glycosidic bond by glucosidases, the released 2-nitrophenyl group yields a yellow color detectable by spectrophotometry. This substrate has high sensitivity and is widely used in a variety of applications, including drug discovery and enzyme kinetics studies.</p>Fórmula:C12H15NO8Pureza:Min. 95%Cor e Forma:White to off-white solid.Peso molecular:301.25 g/molAldol® 470 acetate, Biosynth Patent: EP 2427431 and US 8940909
CAS:Produto Controlado<p>Aldol® 470 acetate is a Fluorogenic substrate that is used in enzymatic reactions to produce a fluorescent product. Aldol® 470 acetate can be used as a ligand or a chromogenic substrate. This product is also used in diagnostic tests, such as conjugates and chemiluminescence, to detect the presence of certain enzymes or microorganisms. It can be used in culture media to measure the amount of certain enzymes, such as phosphatases or proteases, and has been shown to have high purity and quality. This product has CAS No. 1318785-37-3, 1318785-38-4, 1318785-39-5, 1318785-40-6 and 1318785-41-7.</p>Fórmula:C25H21NO5Pureza:Min. 95%Cor e Forma:PowderPeso molecular:415.44 g/molAldol® 484 α-D-glucopyranoside, Biosynth Patent: EP 2427431 and US 8940909
CAS:<p>Aldol® 484 alpha-D-glucopyranoside is a chromogenic and fluorogenic enzyme substrate for alpha-glucosidase activity (EC 3.2.1.20, alpha-1,4-glucosidase, also known as maltase). The colorless enzyme substrate is cleaved by bacteria producing this enzyme in liquid or solid media, yielding orange color. Green fluorescence is also generated if a suitable matrix is present such as: cellulose acetate filters, polypropylene tubes or microplates and polyethylene vials. Aldol® 484 alpha-D-glucopyranoside can be used under aerobic and anaerobic conditions.</p>Fórmula:C26H24ClFN2O7Pureza:Min. 95%Cor e Forma:PowderPeso molecular:530.93 g/molN,N,N',N'-Tetramethyl-p-phenylenediamine dihydrochloride
CAS:<p>Reducing co-substrate for heme peroxidases; test reagent in microbiology</p>Fórmula:C10H16N2·2HClPureza:Min. 95%Cor e Forma:White PowderPeso molecular:237.17 g/mol4-Methylumbelliferyl heptanoate
CAS:<p>Lipase targeting MOSCERDAM® substrate</p>Fórmula:C17H20O4Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:288.34 g/mol2-Naphthyl b-D-galactopyranoside
CAS:<p>2-Naphthyl beta-D-galactopyranoside is a glycoside that is found in the flowers of the plant Eschscholzia californica. It is used as a localizer for bacterial strains and can be hydrolyzed by enzymes to release naphthalene. 2-Naphthyl beta-D-galactopyranoside has been shown to inhibit the growth of corynebacterium and diazonium salt, which may be due to its ability to bind to DNA and disrupt protein synthesis. The potential use of this molecule is for its insolubility, which prevents it from being absorbed by skin cells.</p>Fórmula:C16H18O6Pureza:Min. 99 Area-%Cor e Forma:PowderPeso molecular:306.31 g/mol7-((4'-L-Alaninamido)-rac-3'-hydroxybutyloxy) coumarin hydrochloride
<p>This Clips-O substrate 7-((4'-L-Alaninamido)-rac-3'-hydroxybutyloxy) coumarin allows the detection of single and dual enzymatic activity (L-alanine aminopetidase and oxidation of 4-amino-3-hydroxybutyloxy spacer either enzymatically or by exposure to sodium periodate) with a single substrate resulting in a fluorescent signal. The main virtues of Clips-O substrates are an increased stability towards non-enzymatic hydrolysis that results in a reduced background and high sensitivity.</p>Fórmula:C16H21ClN2O5Pureza:Min. 95%Cor e Forma:PowderPeso molecular:356.8 g/mol4-Methylumbelliferyl-α-L-rhamnopyranoside
CAS:<p>4-Methylumbelliferyl-alpha-L-rhamnopyranoside is a fluorogenic substrate for alpha-L-rhamnosidase. After enzymatic cleaveage, free 4-methylumbelliferone (also known as hymecromone) is released, exhibiting blue fluorescence upon excitation with UV light. The strongest fluorescence of 4-methylumbelliferone requires deprotonation of the hydroxyl group (thus requires alkaline pH), with a maximal fluorescence intensity obtained with excitation at 350 to 370 nm and emission at 440 to 470 nm. The use of 4-methylumbelliferyl-alpha-L-rhamnopyranosideas a substrate for measuring the alpha-L-rhamnosidase activity is used for detection of bacterial infection.</p>Fórmula:C16H18O7Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:322.32 g/molNucleic Acid Dye Green I, 10,000X in DMSO
CAS:<p>Green I is a nucleic acid dye that has been shown to have antioxidative properties. It inhibits protein synthesis in mammalian cells by binding to the DNA and blocking transcription. Green I has also been shown to inhibit the growth of tumor cells and to cause cell death by oxidative damage. Green I is not genotoxic, but it can cause false positive results in genotoxicity tests. Green I has also been shown to be a potential biomarker for renal cell cancer, as well as a prognostic marker for this cancer. This dye enhances polymerase chain reaction (PCR) and is used in biological research because of its ability to bind with proteins and form complexes with DNA.</p>Fórmula:C32H37N4SPeso molecular:509.27 g/molAquaSpark® 510 Calibration Probe, Ramot at Tel-Aviv University Ltd. Patent family WO 2017/130191
CAS:<p>AquaSpark® Calibration Probe is a water-soluble dioxetane-based chemiluminescent probe. Deprotonation of the free phenol group of the calibration probe under mild basic conditions results in an emissive decomposition process. No addition of enhancer or sensitizing agent is required to produce the bright green light emission in aqueous solutions.<br>AquaSpark® Calibration Probe is used for:<br><br>Demonstration experiment susing only the probe and an aqueous solution or water;<br>Evaluation of the AquaSpark® maximum light emission;<br>Functional tests of luminometers, plate readers and cameras;<br>Comparison with other probes bearing an enzyme labile group in order to build concentration/response curves;<br>Validation and comparison between different AquaSpark® probes.</p>Fórmula:C21H23ClO6Pureza:Min. 95%Cor e Forma:PowderPeso molecular:406.12 g/mol
