Nitro

4-Nitro-D-phenylalanine hydrate is a cytosolic enzyme that catalyzes the conversion of phenylpropionic acid to its conjugate base, 4-nitrophenol. This reaction is important in the synthesis of antimicrobial peptides and extractants. The enzyme also has hemolytic activity and can be used as an extractant for pancreatic juice. 4-Nitro-D-phenylalanine hydrate is a catalyst for acylation reactions, which are involved in the production of various pharmaceuticals. 4-Nitro-D-phenylalanine hydrate binds to receptors on the surface of bacterial cells, making it an effective antibacterial agent.

3-Nitrobenzanthrone is a pharmacological agent that is used to induce the activation of various enzymes. It has been shown to be an effective inducer of DNA topoisomerase II, DNA gyrase, and cytochrome P450 in vivo. 3-Nitrobenzanthrone has also been shown to cause DNA adducts in hl-60 cells and dna template in vitro. These effects are observed at low doses of 3-nitrobenzanthrone and not at high doses. The carcinogenic potential of 3-nitrobenzanthrone has been studied using a rat model system and analytical methods. Low doses of nitrosamines such as 3-nitrobenzanthrone can induce cancer by forming DNA adducts, which can lead to mutations that cause uncontrolled cell growth.

1-(4-Carboxyphenyl)-2-nitroethene is a reagent that belongs to the group of speciality chemicals. It has been used as a reaction component in organic synthesis and as a building block for more complex compounds. 1-(4-Carboxyphenyl)-2-nitroethene is an effective intermediate for the synthesis of fine chemicals such as pesticides, pharmaceuticals, and herbicides. It is also used as an intermediate in the production of dyes and pigments.

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4-Nitro-3-(trifluoromethyl)aniline (FLU-1) is a molecule that has been shown to be carcinogenic in both animals and humans. This compound has an activation energy of 4.2 kcal/mol, which is a measure of the amount of energy required for a reaction to occur. FLU-1 is stable in n-dimethylformamide and reacts with acetic acid to form an ester, which can be hydrolyzed to form 4-nitro-3-(trifluoromethyl)acetic acid. FLU-1 also reacts with ammonia and boron nitride to form 4-(aminocarbonyl)-3-(trifluoromethyl)aniline. The physical properties of this compound are dependent on the solvents used in the reaction. For example, its nmr spectra are different in chloroform than they are in acetone or

1-(2-Chloro-4-fluorophenyl)-2-nitropropene is a versatile building block that can be used to produce a variety of compounds with various properties. It is a high quality, reagent grade chemical that is useful for research and development purposes. This compound has been shown to be an effective intermediate in the synthesis of complex compounds, such as pharmaceuticals and pesticides.

3,5-Dinitrosalicylic acid sodium is an inorganic compound that is used as a biochemical reagent. It can be used to measure the phosphatase activity of muscle and liver samples, as well as to determine the level of autophagy in cells. 3,5-Dinitrosalicylic acid sodium has been shown to inhibit the activity of a number of enzymes, including acid phosphatase and thiourea. When combined with chloroplast or mitochondria, it can be used to determine the rate of electron transport chain. 3,5-Dinitrosalicylic acid sodium binds to sulfhydryl groups on proteins and prevents them from being used for other purposes. This process optimization leads to engulfment followed by lysosomal degradation.

7-Nitrocoumarin is an agent that inhibits the growth of protozoa by inhibiting enzyme activities, specifically those involved in glycolysis. It has been shown to be a potent inhibitor of surface proteins and functional assays. 7-Nitrocoumarin is also active against trophozoites in vitro. The compound has been shown to be nontoxic to mammalian cells, with a constant of 0.3 μM for inhibition of resazurin reduction. The mechanism of action for 7-nitrocoumarin is not well understood, but it may involve oxidation products such as nitro groups, which are indicated by the prefix '7-'.

1-(3-Bromophenyl)-2-nitropropane is a fine chemical that is used as a building block in the synthesis of complex organic compounds. It can be used as a reagent and speciality chemical with high quality. 1-(3-Bromophenyl)-2-nitropropane is versatile for use in reactions, such as coupling reactions, because it can be used as an intermediate or scaffold to create many different compounds. CAS No.: 155988-18-4

2,4,6-Trinitrobenzenesulfonic acid, also known as TNBS, TNSBA or picrylsulfonic acid, is a strongly oxidising organic acid that has long been used as a reagent to determine the presence of free primary amine groups. TNBS reacts rapidly with primary amines to form highly coloured N-trinitrophenyl products which can then be analysed by colorimetry. Competing hydrolysis of the TNBS reagent may influence the assay result. The amine can be regenerated by treatment with hydrazine. This analytical technique can also be applied to thiols and hydrazides.
As is common with nitrated aromatic compounds, there is a risk of explosion and TNBS is typically commercially available as a solution. We also supply the 5% aqueous solution.

5-Chloro-2-nitrotoluene is an anti-cancer drug that has been shown to be effective against a variety of cancer cell lines, including carcinoma and pancreatic cancer cell lines. 5-Chloro-2-nitrotoluene inhibits the growth of cancer cells by binding to sulfhydryl groups in cellular membranes, which prevents the release of essential building blocks for the synthesis of proteins, nucleic acids, and lipids. This compound also inhibits the activity of enzymes that are involved in the synthesis of these compounds. It has been shown to have chemopreventive effects in animal studies.

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4-Nitrobenzenesulfonamide is an organic compound that consists of a nitro group, a sulfonamide group, and an amine. It is the active analog of 4-dimethylaminobenzoic acid, which is used as an inhibitor of histamine release in the treatment of allergic reactions. The molecule has been shown to bind to copper ions and triflic acid and has been used as a catalyst for aziridination.

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3-Nitroformanilide is an organic molecule that is synthesized by the reaction of formamide and nitroethane. It can be used as a precursor for the synthesis of other molecules with pharmaceutical properties, such as imines, sulfoxides, and nucleophilic anions. 3-Nitroformanilide has shown high reactivity with sulfoxide and nucleophilic anions in organic solvents. The reaction yield of the reaction between 3-nitroformanilide and sulfoxide increases when it is carried out in inorganic solvents. This reaction produces a nucleophilic anion, which can then be used to synthesize other molecules with pharmaceutical properties.

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Nitrosobis(2-hydroxyethyl)amine (NBEA) is an inhibitor of nitrite reductase, an enzyme that catalyzes the reduction of nitrite to ammonia. Nitrite reductase is used in wastewater treatment and is also involved in the metabolism of some carcinogens. NBEA has been shown to inhibit the activity of nitrite reductase by binding to its active site, preventing the enzyme from reducing nitrite to ammonia. NBEA has genotoxic effects on E. coli K-12 cells and increases DNA damage with prolonged exposure, which may be due to the production of reactive oxygen species such as superoxide radical anion and hydrogen peroxide.

2,4-Dinitrobenzenesulfonyl chloride is a chemical reagent that is used in analytical chemistry. It reacts with pyrazole rings to form 2-aminopyridine derivatives. The reaction can be enhanced by adding metal ions such as copper(II) or zinc(II). 2,4-Dinitrobenzenesulfonyl chloride is also used in the solid-phase synthesis of heterocycles and in the synthesis of pharmaceuticals. The compound has been shown to react with human serum and form an unstable intermediate that undergoes hydrolysis to produce sulfate ion and trifluoroacetic acid. This reaction mechanism can be applied to other nucleophilic compounds such as bromide ion. 2,4-Dinitrobenzenesulfonyl chloride reacts with the amine group of proteins using the S N 1 mechanism. The resulting product is a chlorinated amino acid derivative which exhibits fluorescence properties when reacted with

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4-Chloro-2-nitroaniline (4CNA) is a chemical that is used for wastewater treatment. 4CNA reacts with phosphorus pentachloride or phosphorus pentoxide to form phosphoric acid, which can be used as a pH buffer in water treatment applications. It is also used as an antidepressant treatment in pharmaceutical dosage and has been shown to have signal properties. 4CNA is also used in the production of monoclonal antibodies, n-dimethyl formamide and intracranial haemorrhage treatments. It can be produced by reacting hydrochloric acid with membrane systems at low energy.

3-Chloro-4-nitropyridine 1-oxide is the condensation product of 2-chloro-3-nitropyridine and nitric acid. 3-Chloro-4-nitropyridine 1-oxide has an isomeric nature and can be purified by recrystallization from water. The compound has a molecular weight of 286.1 g/mol and a monoclinic crystal structure. It has two n-oxides, which are isomers of each other, with nmr spectra that differ by the shift in the chemical shifts of the protons on the aromatic ring. 3-Chloro-4-nitropyridine 1-oxide condenses with lanthanides to form lanthanide complexes, such as Eu(III)(3,5'-ClO 4 ) 2 . This compound is also used in the synthesis of phenoxathiine derivatives that have antihypertensive activity.

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2,6-Dichloro-5-nitropyrimidin-4-amine is a chlorinating agent that reacts with aliphatic and aromatic amines to form substituted pyrimidines. The substitution pattern of the product depends on the regioselectivity of the reaction. 2,6-Dichloro-5-nitropyrimidin-4-amine is one of the few chlorinating agents that react with propylamine. Substitution at position 2 of the purine ring has been found to be more selective than substitution at position 6. The 2,6-dichloropyrimidine can also be used as a nitro group source in chemical synthesis or as an intermediate in production of other compounds.

Intermediate in the synthesis of nintedanib

N-Nitrosodiethylamine (NDEA) is a genotoxic carcinogen that is formed as an intermediate in the industrial production of nitric acid. It has been shown to be a potent inhibitor of DNA polymerase and topoisomerase II, which are involved in DNA replication and repair. NDEA has been detected in human blood samples and has been shown to induce squamous cell carcinoma in animal models. This chemical can also cause inflammation by binding to toll-like receptor 4, which activates the inflammatory response. The biocompatible polymer used for this product is not known to produce any genotoxic or mutagenic effects.

1-Nitronaphthalene is a nitrobenzene derivative that has been used as an intermediate in the synthesis of pharmaceuticals, dyes, and other organic compounds. 1-Nitronaphthalene is classified as a hazardous substance due to its carcinogenicity and toxicity. In particular, it can cause irritation and burns on skin contact and may be fatal if swallowed. The toxicity profile of 1-nitronaphthalene has been studied in rats, mice, guinea pigs, rabbits, hamsters, and dogs. It was found to have moderate acute oral toxicity in rats but no significant acute toxicity in mice or dogs. 1-Nitronaphthalene also had little effect on p450 activity or enzyme activities in rats.

4-Nitrobenzotrifluoride is a chemical with the formula C6H3N3O2F3. It is a white solid that is soluble in organic solvents and insoluble in water. The compound has been used as a precursor to other compounds, including 4-nitrobenzoic acid, 4-nitrophenol, and 2,4-dinitrobenzenesulfonic acid. The nitro group of this compound can be reduced to an amine by reaction with hydroxide solution. This reaction is exothermic and produces hydrogen gas as a byproduct. Further reactions involving the nitro group can be performed in the presence of aryl chlorides or alkali metals such as potassium or sodium hydroxide. These reactions yield products that have the functional groups RNH2, RCOOH, and RN=C=O. The product of these reactions can be identified using nuclear magnetic resonance spectroscopy

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N-Nitroso guvacoline is a nitrosated guvacoline analog that is used to induce cancer in animals and as an experimental tool for studying the role of acetylcholine in lung cancer. N-Nitroso guvacoline has been shown to inhibit the growth of bacteria such as typhimurium and nadph-cytochrome p450 in the presence of fatty acids, suggesting that it may be genotoxic. The carcinogenic effects of N-nitrosoguvacolin were studied using Sprague-Dawley rats exposed to this agent by inhalation. The rats were found to have increased levels of urinary nitrite and nitrate, which are products from the metabolism of N-nitrosoguvacolin.

N-Methyl-2,4-dinitroaniline is an organic compound that is used as a chemical intermediate. It is produced by the oxidation of N-methyl-2,4-dinitrophenylhydrazine with trifluoroacetic acid in the presence of amines and acetonitrile. It can be analyzed by gas chromatography for its oxidation products such as aldehydes and acetaldehyde. The sensitivity of this compound is insensitive to temperature and humidity, making it suitable for use in analytical chemistry.

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4-Nitrophenyl anthranilate is a potent inhibitor of serine protease. It is synthesized by reacting an anthranilate with an hydroxyl group in the presence of ultraviolet light, and can be used as a fluorescent probe. 4-Nitrophenyl anthranilate binds to the active site of serine protease, and prevents the hydrolysis of proteins by blocking the cleavage of peptide bonds at the carboxylic acid termini. This compound has been shown to inhibit human serum albumin and cell nuclei in vitro. The reaction mechanism for this compound is unknown, but it is believed that it may involve a photo-induced electron transfer mechanism.

4-(4-Nitrophenoxy)aniline is a synthetic drug that is used as a substrate for the cytochrome P450 system. It has been shown to be metabolized by the liver in two steps, forming reduction products and interacting with thiourea. This drug also has functional groups which are active in the group p2 of the periodic table, such as diphenyl ethers and aminophenols. 4-(4-Nitrophenoxy)aniline can be used to probe the interaction between an enzyme and its substrate.

4-Chloronitrobenzene is a type strain of the bacterium Nitrosomonas europaea. It has been shown to be toxic to cells in both aerobic and anaerobic culture. 4-Chloronitrobenzene inhibits the activity of hydrogenase enzymes, which are required for the reduction of molecular oxygen to water. The toxicity of 4-chloronitrobenzene is due to its ability to inhibit enzyme activity, leading to cell death. This bacterium also has the ability to use chlorinated hydrocarbons as a carbon source and cause chlorination of other biological molecules. In addition, it can reduce metal hydroxides and form metal complexes with palladium and platinum metals. 4-Chloronitrobenzene is found in soil samples that have high concentrations of chloride ions or neutral pH values. Its phase equilibrium diagram shows that this compound exists mainly in liquid form when it is at low temperature, but becomes more

4-Fluoro-3-nitroaniline is a chemical that can be used for industrial preparation. It is an efficient method for the production of 4-fluoroaniline, which is used in the manufacture of dyes and pharmaceuticals. The chemical ionization technique has been shown to be a good way to determine the presence of 4-fluoro-3 nitroaniline in animals. It has also been found to be active against infections caused by bacteria such as Salmonella enterica, Escherichia coli, and Klebsiella pneumoniae. This chemical may have adverse effects on testicular function and hematocrit levels in animals.

H-Phe-Gly-His-p-nitro-Phe-Phe-Ala-Phe-OMe is a protonated amino acid. It has been shown to have a high affinity for the histidine subsite of human thrombin. This compound has been found to have a kinetic rate of hydrolysis that is competitive with that of aspartic acid, but slower than that of valine. H-Phe-Gly-His-p-nitro-Phe--Phe--Ala--Phe--OMe also functions as an anticoagulant and inhibits clotting by inhibiting the conversion of fibrinogen to fibrin.

N'-Nitrosopentyl-(3-picolyl)amine is a research chemical that can be used as a reaction component, reagent, or intermediate. It is a high quality and versatile building block for the synthesis of complex compounds. N'-Nitrosopentyl-(3-picolyl)amine has been shown to be useful as an intermediate in the synthesis of drugs such as pentoxifylline and lodoxamide, which are used to treat respiratory diseases. This chemical is also used to synthesize other compounds that have speciality applications such as pharmaceuticals and rubber additives.