Nitro

N-2-[(2-bromo-4,6-dinitrophenyl)azo]-5-(diethylamino)phenyl]acetamide (NBDPA) is a yellowish solid that is soluble in water. It has a molecular weight of 308.3 and chemical formula C14H21BrN2O4. NBDPA is used as an analytical reagent for the kinetic data of liver cells and in wastewater treatment. This compound has been shown to exhibit carcinogenic potential in rats, causing genetic damage to the DNA of liver cells and kidney tissue. NBDPA has also been shown to be toxic to fish embryos and larvae, with significant effects on the development of larvae at high concentrations.

<p>3-Nitropropanol is an inhibitor of the enzyme nitrite reductase, which is involved in the conversion of nitrite to nitric oxide. 3-Nitropropanol is a dietary supplement that has been shown to have a significant inhibitory effect on the growth of cancer cells and microbial metabolism. Nitrite levels were found to be reduced by 25% in mice treated with this substance. The analytical method for measuring 3-nitropropanol was developed using a type strain and fatty acid standards.</p>

<p>2-Chloro-4-nitrobenzhydrazide is a fine chemical that can be used as a versatile building block, useful intermediate, and reaction component. CAS No. 67345-78-2 is a speciality chemical that is useful in research chemicals and complex compounds. It has high quality and can be used to make reagents.</p>

<p>Please enquire for more information about 1-Methyl-4-nitro-1H-pyrazole-3-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Nitrosaccharin is a copper salt that has been shown to have cancer-causing properties in humans. It also has depressant activity, which may be due to its ability to inhibit the function of the bitter taste receptors in the mouth. 6-Nitrosaccharin is readily absorbed and excreted unchanged in urine, with only a small amount being metabolized by hydrolysis to benzoate and nitrite. 6-Nitrosaccharin is used as an industrial catalyst and an analytical reagent, but can also be found in environmental pollution caused by chlorinated compounds.</p>

<p>3-Fluoro-2-nitrobenzoic acid is an anhydrous nitrating agent that reacts with 5-fluoro-2-nitrobenzoic acid to produce 3,5-difluoronitrobenzene. This reaction mixture is introduced into a reaction vessel and heated in the presence of sulfuric acid. 3-Fluoro-2-nitrobenzoic acid is used in the production of dyes and pharmaceuticals.</p>

<p>1,3-Dinitronaphthalene is a nitrite ion and an aromatic hydrocarbon. It can be prepared by reacting 1,3-dinitrobenzene with sodium nitrite in the presence of concentrated sulfuric acid. It is used as a reagent in chromatographic analysis for the separation of amines and its derivatives. 1,3-Dinitronaphthalene has been shown to react with amines to form covalent adducts which are more polar than the parent compounds. The linear regression analysis of population growth data can be used to estimate parameters such as the rate constant or initial concentration of reactants that might not be directly measurable.</p>

<p>Please enquire for more information about 3-Nitro-4-[[(tetrahydropyran-4-yl)methyl]amino]benzenesulfonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Intermediate in the synthesis of mirabegron</p>

<p>Methyl 2-bromo-5-nitrobenzoate is a potent inhibitor of aspartyl proteases, which are enzymes that are involved in the breakdown of fibrinogen. It has been shown to inhibit the growth of Staphylococcus aureus and other bacteria. Methyl 2-bromo-5-nitrobenzoate is also a potent inhibitor of lactamase, an enzyme that catalyzes the hydrolysis of lactams. This compound has been shown to have biological properties such as antioxidant and anticancer activity. A heterocycle with two nitro groups on the methylene bridge, it is reactive.</p>

<p>4-Fluoro-3-nitrobenzyl alcohol (4FNA) is a potent, orally bioavailable, and selective inhibitor of the tyrosine kinase AXL. 4FNA binds to the ATP binding site on AXL and blocks phosphorylation of its tyrosine kinase domain. This binding leads to a conformational change in the AXL protein that prevents it from interacting with downstream signaling molecules, inhibiting T cell activation.</p>

<p>4-Bromo-3-nitrobenzoicacid is a fluorogenic substrate for the labeling of d-serine. It reacts with picric acid to form a fluorescent product, which can be detected by fluorescence spectroscopy. 4BnBA has been used in immobilized enzyme studies to determine the catalysis of chloride and the fluorescence response of chloride. The hydrolysis of 4BnBA by esterases produces 3-nitroaniline, which has been shown to be an intermediate for the synthesis of flavin mononucleotide (FMN). FMN is an essential cofactor for catalytic reactions involving ribonucleotides and ATP. The subunits of FMN are flavin adenine dinucleotide (FAD) and nicotinamide adenine dinucleotide (NAD). 4BnBA has also been analysed using synthetic techniques and functional theory to determine its role in biomolecular processes.</p>

<p>5-Nitropseudocumene (5NPC) is a molecule that belongs to the group of methylbenzenes. It is a precursor to dyes such as nitrobenzene, which are used in the production of nylon. 5NPC is also an intermediate in the synthesis of trifluoroacetic acid, which is used as an industrial solvent and chemical reagent. The acetoxylation of 5NPC with acetic acid yields methylbenzoate. This reaction requires two molecules of acetic acid for each molecule of 5NPC. Desorption from the catalyst can be achieved by treatment with methyl groups or nitrous acid. Naphthalene reacts with 5NPC to form biphenyl and nitric oxide gas, which are released into the atmosphere. The inorganic residue can be removed by filtration.</p>

<p>2-Chloro-3,5-dinitrobenzotrifluoride is a chemical compound that is used as an intermediate in the synthesis of dyes and pharmaceuticals. It reacts with nitrous acid to form 2-chloro-3,5-dinitrobenzoic acid. The hydrogen bond between the hydroxyl group and the chlorine atom in this compound is weak, which leads to a constant value for its spectrometer. This chemical compound has photophysical properties that are dependent on the concentration of solutes. When it is mixed with other solutes such as potassium ion or sulfoxide, it can produce isomers. This chemical compound can be refluxed in a neutral pH environment to form anilines and acetonitrile, two compounds that are important for organic synthesis.</p>

<p>Boc-L-Nitroarginine is a nitric oxide synthase inhibitor that belongs to the class of drugs called nitric oxide inhibitors. It is a potent inhibitor of nitric oxide synthase, preventing the production of nitric oxide from arginine. The drug has been shown to have therapeutic effects in the treatment of cancer, diabetes mellitus, and other diseases. Boc-L-Nitroarginine inhibits tumor angiogenesis by blocking endothelial cell proliferation and migration. It also inhibits insulin secretion, leading to an improved glycemic control in diabetic patients. Boc-L-Nitroarginine can be used as a hydrogenation reducing agent for the synthesis of imatinib and palladium catalysts for hydrogenation reactions.</p>

<p>Dehydronitroso nifedipine is an antibiotic-resistant drug that is used to treat infectious diseases. It is a carboxylate, which can react with water to form a reactive intermediate. This reactive intermediate reacts with various functional groups, including amines and amino acids, leading to the formation of products such as trimers and tetramers. Dehydronitroso nifedipine has been shown to have physiological activities in muscle cells and tissues. Dehydronitroso nifedipine has two structural analogs: nitrosobenzene and nitrosophenol. Nitrosobenzene is used as an analytical reagent in the detection of beta-lactamase inhibitors. Nitrosophenol can be used as a linker for the synthesis of triazines.br&gt;br&gt; END&gt;&gt;</p>

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<p>2-Nitro-9H-carbazole is a nitro aromatic compound that is used in the synthesis of other organic compounds. It has shown mutagenic and carcinogenic properties, as well as toxicity to the liver and kidney. 2-Nitro-9H-carbazole is metabolized by a number of metabolic transformations, including activation by cytochrome P450 enzymes and conjugation with glucuronic acid. The liver enzyme S9 also catalyzes the conversion of 2-nitro-9H-carbazole to its ultimate metabolite, 3-methylcholanthrene, which is cytotoxic to both cultured hepatocytes and lung cells.</p>

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