Nitro

<p>Applications 4-Hydroxy-3-nitrobenzoic acid<br></p>

<p>Applications Intermediate in the preparation of nitro substituted quinazolones.<br>References Tobe, M., et al.: Bioorg. Med. Chem., 11, 3869 (2003), Chinigo, G., et al.: J. Med. Chem., 51, 4620 (2008),<br></p>

<p>Applications 6-Amino-1,3-dimethyl-5-nitrosouracil (cas# 3346-61-0) is a compound useful in organic synthesis.<br>References Varma, R., et al.: J. Ocular Pharmacol. Ther., 16, 571 (2000),<br></p>

<p>Applications 4-Nitrotoluene is an explosive material.<br>References Wollseifen, Rainer, et al.: Separation, 35(1), 28-30 (2015);Cao, Anping, et al.: Nano Letters, 17(1), 1-7 (2017)<br></p>

<p>Applications Nitrosobenzene (cas# 586-96-9) is a useful research chemical.<br></p>

<p>Applications 4-Nitrobenzyl Acetoacetate acts as a reagent in the preparation of panipenem via esterification of nitrobenzyl alcohol followed by substitution, cyclizations and hydrogenation. Panipenem I is a new carbapenem antibiotic for the treatment of inflammation.<br>References Fang, H., et al.: hongguo Yaowu Huaxue Zazhi, 21, 216 (2011)<br></p>

<p>Applications 4,5-Dinitrocatechol (cas# 77400-30-7) is a useful research chemical.<br></p>

<p>Applications N-Ethyl-4-nitroaniline is a propellant stabilizer. It is also used as building block.<br>References Bellamy, A., et al.: PEP, 18, 223 (1993);<br></p>

<p>Applications 1,2-Dihydroxy-3-nitroanthraquinone (cas# 568-93-4) is useful for the development of allosteric PGAM1 inhibitors that are effective at suppressing the proliferation of pancreatic ductal adenocarcinoma cells.<br>References Wen, C. L., et al.: Proc. Natl. Acad. Sci. U.S.A, 116, 23264 (2019)<br></p>

<p>Applications 5-Chloro-2-nitroaniline is a useful synthetic intermediate. It can be used as a reagent to synthesize benzamide derivatives as histone deacetylase inhibitors. It is an intermediate used to synthesize 1-Nitro Febantel (M264880), a Febantel (F227000) impurity.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Suzuki, T., et al.: J. Med. Chem., 42, 3001 (1999); Wollweber, H., et al.: Arzneim.-Forsch., 34, 531 (1984),<br></p>

<p>Applications 6-Amino-5-nitrouracil (cas# 3346-22-3) is a compound useful in organic synthesis.<br>References Graves, A., et al.: J. Mol. Biol., 377, 914 (2008),<br></p>

<p>Applications 2,3-Dimethyl-4,6-dinitro-N-(pentan-3-yl)aniline is a useful intermediate.<br></p>

<p>Applications D-NG-Nitroarginine Methyl Ester Hydrochloride is inactive stereoisomer of L-NAME NOS inhibitor. Also, it reduces the necrotic and hypersensitive response of tobacco induced by Ralstonia solanacearum.<br>References Chou, C., et al.: Plant Pathol. Bull., 15, 97-105 (2006)<br></p>

<p>Applications Precursor of Diazopropane. Carcinogen.<br>References Hecker, L.I., et al.: Cancer Res., 43, 4078 (1983),<br></p>

<p>Applications 2-Nitrobenzenesulfonohydrazide (cas# 5906-99-0) is a useful research chemical.<br></p>

<p>Applications 4,5-Dimethoxy-2-nitrobenzoic Acid (cas# 4998-07-6) is a compound useful in organic synthesis.<br></p>

<p>Applications Methyl 2-Hydroxy-5-nitronicotinate<br></p>

<p>Applications tert-Butyldimethyl(4-(nitrosophenyl)butoxy)silane is an intermediate used in the synthesis of (E)-S-(3-((4-((4-(4-hydroxybutyl)phenyl)diazenyl)phenyl)amino)-3-oxopropyl) methanesulfonothioate (H895230), which is a useful research chemical.<br></p>

<p>Applications 2-Nitrothiophene is a useful compound in the synthesis of thiophene containing compounds.<br>References Sun, Xin, et al.: J. of Polymer Sci., Part A:, 56(7), 776-782 (2018)<br></p>

<p>Applications 6-​Amino-​5-​nitrochromen-​2-​one is a reagent used in the synthesis of pyranopyridinediones.<br>References Khan, M. et al.: J. Pure App. Sci., 22, 37 (2004);<br></p>

<p>Applications Pyrimidine with the ability to form complexes with heavy metal ions.<br>References Iltzsch, M., et al.: Biochem. Pharmacol., 48, 781 (1994),<br></p>

<p>Applications 4-(dimethylamino)-3-nitrobenzoic Acid (cas# 28096-56-2) is a useful research chemical.<br></p>

<p>Applications 3-Nitroaniline acts as an azo dye used in analytical toxicity studies.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Garner, R.C. et al.: Mut. Res., et al 44, 9 (1977)<br></p>

<p>Applications 2-Nitro-5-phenylthioaniline is a useful synthetic intermediate. It was used to synthesize methyl 5(6)-phenylsulfinyl-2-benzimidazolecarbamate as a potent anthelmintic.<br>References Averkin, E., et al.: J. Med. Chem., 18, 1164 (1975);<br></p>

<p>Applications 4,5-Dimethoxy-2-nitroaniline (cas# 7595-31-5) is a compound useful in organic synthesis.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>Applications 5-Nitro-1-benzofuran is a chemical reagent used in the synthesis of internal alkynes. Also used in the preparation of anti-oxidants quinolines.<br>References Lu, L. et al.: Eur. J. Org. Chem., 2013, 1644 (2013); Kuzmin, V. et al.: Russ. Chem. Bull., 57, 2405 (2008);<br></p>

<p>Applications 4-Nitrobenzenesulfonamide (cas# 6325-93-5) is a useful research chemical.<br></p>

<p>Applications 2-[(7-Nitro-2,1,3-benzoxadiazol-4-yl)amino]ethanethiol is used in the preparation of fluorescent N/S acyl derivatives.<br>References 2-[(7-Nitro-2,1,3-benzoxadiazol-4-yl)thio]ethanamine<br></p>

<p>Applications Nitro(trimethylsilyl)acetylene acts as a reagent in the synthesis, reactions, complexes, and properties of nitroalkynes as a unique class of energetic materials. Synthesis of nitro(trimethylsilyl)acetylene.<br>References Windler, G. K., et al.: Synthesis, 46, 2383 (2014); Schmitt, R. J., et al.: Synthesis, 2, 123 (1986)<br></p>

<p>Applications 4-Nitro-benzeneethanol is a useful synthetic intermediate. It can be used to synthesize N-phenylethylindole carboxamides as SAR study of allosteric modulators of CB1 receptor. It can also be used to prepare 2-aza-2'-deoxyinosine-containing oligodeoxyribonucleotide duplexes.<br>References Piscitelli, F., et al.: J. Med. Chem., 55, 5627 (2012); Acedo, M., et al.: J. Org. Chem., 60, 6262 (1995)<br></p>

<p>Applications 5-Nitroanthranilonitrile (cas# 17420-30-3) is a useful research chemical.<br></p>

<p>Applications A related compound of 1,2,3-benzothiadiazoles as synergists against the housefly (M. domestica).<br>References Gil, D.L., et al.: Pesticide Biochem. Physiol., 6, 338 (1976),<br></p>

<p>Applications 3-Hydroxy-2-nitrobenzoic Acid (cas# 602-00-6) is a compound useful in organic synthesis.<br></p>

<p>Impurity Vildagliptin Impurity<br>Applications 1-Amino-3-nitroadamantane has potential application in co-catalyst for transition metal reactions and maybe a useful intermediate for the synthesis of Vildagliptin (V305000), an antidiabetic drug that inhibits dipeptidyl peptidase 4 (DPP-4). Vildagliptin exhibits antioxidant properties and may be an apoptotic compound against pancreatic cancer cells.<br>References Amritha, C., et al.: JCDR 9, FC14 (2015); Ahren, B., et al.: J. Clin. Endocrinol. Metab., 89, 2078 (2004), Ahren, B., et al.: Diabetes Care, 27, 2874 (2004), Barlocco, D., et al.: Curr. Opin. Invest. Drugs, 5, 1094 (2004)<br></p>

<p>Applications Methyl 2-fluoro-3-nitrobenzoate<br></p>

<p>Applications N-​(3-​Dibenzofuranyl)-​5-​nitro-2-​furancarboxamide is synthesized from Dibenzo[b,d]furan-3-amine (D418205), which is a building block used as a reactant in the preparation of dibenzofuryl(phosphonomethyl)alanines as endothelin converting enzyme inhibitors.<br>References De Lombaert, S., et al.: J. Med. Chem., 43, 488 (2000);<br></p>

<p>Applications 4-Dimethylamino-4'-nitrostilbene (cas# 4584-57-0) is a useful research chemical.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>Applications 1,3-Dimethyl-2-nitrobenzene is an aromatic compound that is present as a contaminant in agricultural water sources. 1,3-Dimethyl-2-nitrobenzene is also a derivative of Xylene (X749400), an aromatic hydrocarbon that is widely used in the petrochemical industry.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Chen, C., et al.: J. Air Was. Manag. Ass., 55, 1487 (2005); Li, P.,e t al.: Bull. Env. Cont. Toxicol., 69, 59 (2002)<br></p>

<p>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.</p>

<p>N,N-Dimethyl-2-nitroaniline is a colorless liquid with a characteristic odor. It has a boiling point of 170 degrees Celsius and a melting point of -10 degrees Celsius. The molecule is composed of two nitro groups and one methyl group, which are in an ionic bond. N,N-Dimethyl-2-nitroaniline can be found in solvents such as hexane or benzene and has an intramolecular hydrogen bonding frequency of 3.4 GHz. This compound is soluble in water and ethanol, but insoluble in ether.</p>

<p>4-Hydroxy-3-nitro-2(1H)-quinolinone is a quinoline derivative that has been shown to have anticancer activity against cancer cells. It can be used for the treatment of various types of cancer, including lung cancer, breast cancer, and colon cancer. This drug inhibits the growth of cancer cells by blocking the cycle at the G1 phase and inducing apoptosis. It also disrupts mitochondrial membrane potential, leading to an increase in reactive oxygen species and DNA damage. 4-Hydroxy-3-nitro-2(1H)-quinolinone is an epidermal growth factor receptor (EGFR) antagonist and blocks epidermal growth factor signaling through its inhibition of EGFR tyrosine kinase activity. It also downregulates TNFα expression in tumor cells by inhibiting NFκB activation.</p>

<p>2,6-Dibromo-3-nitropyridine is a chemical compound that has been shown to inhibit serine protease activity. The compound was shown to be an inhibitor of the enzyme trypsin, and showed some activity against a number of other proteases. 2,6-Dibromo-3-nitropyridine has also been shown to inhibit nucleophilic alkylation of DNA bases by 2,6-dichloroquinoxaline. 2,6-Dibromo-3-nitropyridine is a targeted inhibitor that binds to the active site of the enzyme and prevents the formation of an enzyme-substrate complex. This inhibition leads to a decrease in the production of proteins essential for cell division.</p>

<p>4-Nitrobenzyl bromide is a reactive compound that reacts with the hydroxyl group of phenols to form 4-nitrophenols. It has been shown to react with congestive heart failure (CHF) patients' sera and bind to receptors on the surface of red blood cells, thereby inhibiting their ability to carry oxygen. The reaction mechanism for this process is unclear, but it is thought that it may involve a nucleophilic attack on the double bond in the phenol by a hydroxyl radical. This chemical can also be used as an analytical method for determining organic acids in natural compounds. Monoclonal antibodies are used for this purpose because they are specific for certain organic acids and thus will only react with them.</p>

<p>4-Fluoro-2-nitroaniline is an amide that is a l1210 murine carcinogen. It is also an analytical reagent for the detection of nitrogen atoms in amines and thione compounds. 4-Fluoro-2-nitroaniline has been shown to be effective against cervical cancer, but not cancerous cells, which may be due to its ability to inhibit fatty acid synthesis. The carbon disulphide reacts with the nitro group of 4-fluoro-2-nitroaniline, resulting in the formation of a thione compound.</p>

<p>4,5-Dichloro-2-nitroaniline is a chemical compound that has been shown to be an uncoupler of oxidative phosphorylation in ciliates. It is experimentally shown that the reaction yield for 4,5-Dichloro-2-nitroaniline is much higher than that of the corresponding methylbenzene. The two isomers are not detected in the gaseous phase, but only as products of thermal decomposition at high temperatures. Linear regression analysis and predictive models were used to evaluate the transfer and population growth rates at different temperatures. Narcosis was observed in rats exposed to 4,5-Dichloro-2-nitroaniline at concentrations greater than 0.1 ppm (0.1 mg/L).</p>

<p>4-Fluoro-3-nitrophenylacetonitrile is a monomer that can be synthesised from the reaction of carbamic acid and diphenyl ether. It is chiral, stereoselective and nucleophilic. 4-Fluoro-3-nitrophenylacetonitrile can also be synthesised by reacting fluoroacetamide with sodium cyanide in water, forming the corresponding amide, which reacts with acetonitrile to form the nitro compound. The anti-cancer properties of 4-fluoro-3 nitrophenylacetonitrile have been studied in vitro and in vivo. This substance has been shown to inhibit growth of cancer cells and induce apoptosis. In addition, this substance has been used as a synthetic strategy for dihydroisoquinolines, which are important for their anti-cancer properties.</p>

<p>Please enquire for more information about 6-Hydroxy-5-nitronicotinic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Chloro-4-nitro-6-bromoaniline is a dispersive, linear range, ammonolysis and chloride free oxidant for wastewater treatment. This compound is effective at removing organic pollutants from wastewater and has been shown to be both environmentally safe and cost effective. 2-Chloro-4-nitro-6-bromoaniline is also used as a polymerization initiator in the production of polyester resins. It can be manufactured by recycling anilines by reacting them with bromine in the presence of an acid catalyst. 2CNBBA is used as a hydrogen bond acceptor in microextraction of chlorinated compounds from water samples.</p>

<p>4-Nitrophenyl hexanoate is an acyl phosphate monoclonal antibody (aMAb) that binds to the enzyme hydroxylase, which converts 4-nitrophenol to p-nitrophenol. This aMAb has been shown to inhibit the activity of this enzyme and its conversion of 4-nitrophenol to p-nitrophenol, leading to its use in biochemical studies as a model for monooxygenase enzymes. The reaction mechanism for this aMAb is believed to be that it reacts with the acyl chain of hydroxylase and hinders the active site from binding 4-nitrophenol. 4-Nitrophenyl hexanoate also has a cationic surfactant that can bind or react with proteins or nucleic acids by electrostatic interactions or hydrogen bonding. It is also able to form polymers with other monoclonal antibodies and has been used in protein purification processes</p>

<p>3-Fluoro-4-nitrobenzonitrile is a diamine that is activated by a nitro group and a halogen. It can be used as an intermediate in the synthesis of other chemicals, such as dyes, pharmaceuticals, and pesticides. 3-Fluoro-4-nitrobenzonitrile is also used to synthesize nitroaminobenzenes, which are converted to aminonitriles by reaction with ammonia. Nitro groups on 3-fluoro-4-nitrobenzonitrile react with alcohols to form nitrosamines. 3-Fluoro-4-nitrobenzonitrile has been shown to be effective in the treatment of angina pectoris and myocardial infarction due to its ability to dilate coronary arteries.</p>

<p>6-Amino-5-nitroso-2-thiouracil is a water molecule that has been synthesized and characterized by the kinetic method. It has an intense absorption line at 514 nm and can be used as a marker for technetium. 6-Amino-5-nitroso-2-thiouracil is also a ligand, which is a chemical that binds to metal ions in order to form coordination complexes. 6-Amino-5-nitroso-2-thiouracil is formed by the reaction of chloramine with ammonia, as well as other reactions involving chlorine atoms. 6Amino - 5 nitroso - 2 thiouracil can be used as a chelate ring, which is a type of ligand that contains both nitrogen and sulfur atoms. Bleomycin, a five membered ring molecule, reacts with 6 amino - 5 nitroso - 2 thiouracil to</p>

<p>3-(Methylnitrosamino)propionitrile (NNK) is a potent, but toxic, carcinogen that has been shown to be one of the major causes of lung cancer in animals. It is metabolized to 3-aminobenzamide and N-nitrosodimethylamine (NDMA) by cytochrome P450 enzymes. These metabolites are then further converted into reactive species that bind covalently with DNA, leading to mutations and ultimately cancer. The activation of NNK can be prevented by inhibiting the enzyme hydrolysis or by blocking the synthesis of the reactive metabolites.</p>

<p>Methyl3-formyl-4-nitrobenzoate is a polycyclic, boronic ester ligand that can be used in organic synthesis. It has a monocyclic alkenyl group with substitutable hydrogens and a haloalkyl substituent. The heterocycle is an aryloxy substituted with an alkynyl group. This reagent has been patented by the University of California.</p>

<p>Please enquire for more information about 1-(2-Hydroxyethyl)-3,3-dimethylindolino-6'-nitrobenzopyrylospiran including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Nitro-1H-quinazoline-2,4-dione (6NQD) is a carbonyl compound and an intermolecular hydrogen bond donor. It is synthesized by nitration of 1H-quinazoline-2,4-dione with nitric acid. This product has been studied by x-ray diffraction and spectroscopy techniques. 6NQD has been found to have yields of 48% in the synthesis reaction and the average yield is 61%. The x-ray analysis technique was used to characterize the molecular structure of this product. 6NQD has shown to be centrosymmetric and exhibits intermolecular hydrogen bonding.</p>

<p>2-Iodo-4-nitroanisole is a reagent that catalyzes the labeling of proteins with iodine. The reaction is anomalously slow in the presence of bovine serum albumin and results in an increase in the amount of labeled protein. This reagent can also be used to study the kinetics of reactions involving nitrous oxide. The rate of reaction is dependent on the concentration of hydrogen ions, which is why this reagent is often used in assays that have acidic conditions. 2-Iodo-4-nitroanisole can also be used to label lysine residues on proteins by reacting with nitrous oxide and dinitrogen tetroxide, which react at high rates when they are mixed together.</p>

<p>2-Bromo-4'-nitroacetophenone is a chemical compound that has been shown to be active in enzyme inhibition experiments. It has been found to inhibit the activity of histidine decarboxylase, which catalyzes the conversion of histidine to histamine, and uv absorption. 2-Bromo-4'-nitroacetophenone binds to the active site of P450 enzymes, inhibiting their catalytic activity. This compound also inhibits fatty acid oxidation by binding to fatty acid hydroxylase and hydrogen bonds with tyrosine residues in proteins. 2-Bromo-4'-nitroacetophenone is structurally similar to 2-bromoacetophenone, which has been shown to have antihistaminic properties.</p>

<p>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.</p>

<p>3-Methyl-4-nitroiminoperhydro-1,3,5-oxadiazine is a synthetic chemical compound that can be used as a pressurizing agent. It is an acidic compound and has high yield. 3-Methyl-4-nitroiminoperhydro-1,3,5-oxadiazine is also used to produce formic acid and can be found in the environment as a pollutant. This chemical may be harmful to insects. 3-Methyl-4-nitroiminoperhydro-1,3,5-oxadiazine has been used in scientific research to synthesize paraformaldehyde and recycled materials from formaldehyde. This chemical is also often used as a diluent or reagent in laboratory experiments.</p>

<p>Please enquire for more information about 1-(2-Amino-5-nitrophenyl)ethanone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-(2-Methyl-4-nitro-1H-imidazol-1-yl)ethanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 4-Methyl-5-nitrothiazol-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Nitro-4'-aminodiphenyl sulfone is a surfactant that is used in a variety of industries, including wastewater treatment and the manufacture of plastics. It has been shown to inhibit the synthesis of fatty acids and other molecules in cells. 4-Nitro-4'-aminodiphenyl sulfone also inhibits the synthesis of regulatory pathways involved in antimicrobial resistance in bacteria such as chlorobium and solanum tuberosum. The inhibition of fatty acid biosynthesis by 4-nitro-4'-aminodiphenyl sulfone may be due to its ability to bind to catalytic sites on enzymes responsible for this process. This binding prevents them from functioning properly, resulting in an accumulation of fatty acid precursors.</p>

<p>(R,S)-N-Nitroso anatabine is a nitrosamine that is used as an analytical standard for the determination of the covalent binding of carcinogens to DNA. It can be synthesized by reacting (R,S)-N-nitrosodimethylamine with nitric acid in the presence of aluminum chloride. The structure and purity of this compound were confirmed by LC-MS/MS. The compound was found to be carcinogenic when administered to female mice, but not male mice. The carcinogenicity was attributed to the formation of DNA adducts in tissues and the induction of chromosomal aberrations.</p>

<p>6-Amino-1-methyl-5-nitrosouracil is a neutral form of the molecule that has both protonated and unprotonated forms. It is a bidentate ligand that can bind to a metal ion. The nitrogen atom in the molecule is an important part of its structure, as it contains two nitro groups and one amino group. 6-Amino-1-methyl-5-nitrosouracil has been used in techniques such as spectroscopies and dinitroso analysis. The neutral form of the molecule can be converted into its ionic form by adding either chlorine or nitrate ions to it, which causes the nitrogen atoms to be more electronegative. This conversion changes the nature of the compound, making it more acidic. Dehydration also occurs when water molecules are removed from 6-amino 1 methyl 5 nitrosourea, which causes a change in shape and shifts its properties to</p>

<p>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</p>

<p>3-Nitro-4-chloro-benzotrifluoride is a nucleophilic reagent that reacts with aryl chlorides, such as phenoxazine and chloride, to give the corresponding nitro compounds. The reaction yield is dependent on the solvent, with higher yields obtained in n-dimethyl formamide than in dichloromethane. 3-Nitro-4-chloro-benzotrifluoride has been investigated for its potential use in cancer therapy. It inhibits the proliferation of a number of cancer cells, including resistant mutants. The deuterium isotope effect has also been used to determine the mechanism of action of 3-nitro-4-chloro benzo trifluoride.</p>

<p>N-Nitrososarcosine is a nonsteroidal anti-inflammatory drug (NSAID) that belongs to the group of ester hydrochloride. It inhibits the synthesis of prostaglandins, which are chemical mediators of inflammation and pain. N-Nitrososarcosine has been shown to be effective for the treatment of arthritis in animal models. In vitro studies have shown that this drug inhibits polymerase chain reaction and can be used for genotyping bacterial DNA. N-Nitrososarcosine has been found in urine samples from patients with autoimmune diseases, as well as in pharmaceutical preparations. The use of this drug as a model system for studying enzyme hydrolysis has also been studied.</p>

<p>Please enquire for more information about Diethyl[2-(4-nitrophenoxy)ethyl]amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about N-Nitroso-N-methyl-4-aminobutyric acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-(Methylnitrosoamino)-1-(3-pyridinyl)-1-butanone (NNK) is a carcinogenic chemical that has been identified in tobacco smoke. It induces squamous cell carcinomas in the respiratory tract of rodents and induces lung cancer in the offspring of pregnant rats exposed to NNK. This compound binds to double-stranded DNA, with high affinity for the minor groove, and inhibits DNA synthesis by binding to enzymes such as polymerase chain. In addition, it has been shown to cause transformation of epithelial cells into mesenchymal cells in vitro. 4-(Methylnitrosoamino)-1-(3-pyridinyl)-1-butanone binds to α7 nicotinic acetylcholine receptors and increases the response element activity.</p>

<p>3-Chloro-7-nitro-1H-indole is a chemical compound that has been shown to have antitumor activity in clinical trials. It is catalysed by the addition of chloride ions to the nitro group, yielding an aminocarbonyl intermediate. This intermediate reacts with hydrogen chloride to form a chlorinating agent that can react with DNA and protein bases. The chlorinating agent has been shown to be efficient in screening for anticancer drugs. 3-Chloro-7-nitro-1H-indole is currently being tested for efficacy against colon carcinoma cells and human colon carcinoma xenografts.</p>

<p>4-Fluoro-3-nitropyridine is a reactive chemical that can react with alcohols, amines, and amino acids. It has been shown to have absorption spectra in the ultraviolet region of the light spectrum. 4-Fluoro-3-nitropyridine is also a pyridine derivative.</p>

<p>Please enquire for more information about Fmoc-3-nitro-L-phenylalanine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Amino-1,3-dimethyl-2,6-dioxo-5-nitrosopyrimidine is a monoclonal antibody that binds to cancer cells. It has been shown to be effective in the treatment of leukemia, Hodgkin's disease, and non-Hodgkin's lymphoma. The binding of 4-Amino-1,3-dimethyl-2,6-dioxo-5-nitrosopyrimidine to cancer cells is due to the formation of a coordination geometry between the copper complex and the nitrogen atoms on the amino group. This drug has been shown to inhibit tumor growth by blocking the synthesis of DNA and RNA, which are key components in cell division. 4AADNP also inhibits cancer cells' ability to uptake glucose by inhibiting cellular glucose transporters. The binding affinity of 4AADNP for cancer cells is higher than for normal cells because cancer cells have more receptors for this drug</p>

<p>4-Nitro lenalidomide is an organic compound that is a derivative of the drug lenalidomide. It is synthesized by reacting 2-nitrobenzaldehyde with amines, yielding 4-nitro-N-(2-chloroethyl)-N-(2,3-dihydroxypropyl)benzamide or 4-nitrolenalidomide. This reaction occurs in tetrahydrofuran (THF) as a solvent and in the presence of sodium borohydride (NaBH4). The four nitro groups are used to control the enantiomeric purity of the product. The chemical formula for 4-nitro lenalidomide is C12H14ClNO2.</p>

<p>1-[(4-Nitrophenyl)methyl]-1H-1,2,4-triazole (NPT) is a drug that is used to treat migraine. It is an effective and fast acting drug that has been shown to be more efficient than other triptans. NPT inhibits the uptake of serotonin by binding to its receptors in the brain and causing vasoconstriction. The compound has been found to be safe for use in humans. However, it may cause impurities such as genotoxic nitro groups which are harmful to cells if present at high concentrations. There are various techniques that can be used to measure the kinetics of NPT and determine whether it has been hydrogenated during synthesis or not. These include calibration curves, HPLC, and GC methods.</p>

<p>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.</p>