Nitro

Nitroxoline is a compound that inhibits the formation of iron-containing proteins and has been shown to be effective in reducing tumor growth. It has also been shown to reduce the development of resistant mutants in bacteria, as well as inhibiting the production of epithelial mesenchymal markers. Nitroxoline inhibits the polymerase chain reaction (PCR) by blocking DNA synthesis and is being studied for its potential to treat cancer. Nitroxoline was found to inhibit the proliferation of carcinoma cell lines and showed anticancer activity when combined with temozolomide treatment. Nitroxoline is not active against Gram-positive bacteria such as Staphylococcus aureus or Enterococcus faecalis, but it does have antimicrobial effects against Gram-negative bacteria such as Escherichia coli, Pseudomonas aeruginosa, Haemophilus influenzae, and Klebsiella pneumoniae. Nitroxoline can be used to clean wounds infected with

Please enquire for more information about 5-Chloro-6-nitro-1,3-dihydro-2H-benzimidazol-2-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Chloro-6-fluoronitrobenzene is an aromatic compound that has been used as a versatile building block in the synthesis of complex compounds. It is also used as a research chemical, reaction component, and speciality chemical. This compound has been shown to be useful for the preparation of pharmaceuticals, agrochemicals, and other organic compounds. 2-Chloro-6-fluoronitrobenzene is a colorless liquid with a boiling point of 130 degrees Celsius at atmospheric pressure. It has many uses in research and industry due to its versatility and high quality.

The 6-tert-butyl-4-methyl-2-(4-chloro-2-nitrophenyl) azo phenol (CAS: 126633-00-1) is a benzene with the nitro group in the para position. The electron delocalization of this molecule has been calculated to be 0.30, which is higher than that of benzene; this is due to the nitro group and the electron acceptor sites. This molecule also has a dihedral angle of 36 degrees, which means that it can rotate freely about its central axis. The benzene ring is not planar and contains two different types of bonds: donor atoms are represented by hydrogen bonds and acceptor atoms are represented by the bond with the nitro group.

Please enquire for more information about Methyl 2-methyl-3-(5-methyl-3-nitro-1H-pyrazol-1-yl)propanoate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Ethyl 2-methyl-5-nitro-3-pyridinecarboxylate is an anticoccidial agent that has been shown to be effective against the coccidia of poultry. It is a potent analogue for ethyl pyridinecarboxylate, and its mechanism of action is not well understood. The optimal concentration for this drug has been determined at 3 ppm in feed. It has been shown to inhibit the growth of tenella, a parasitic roundworm, in mice and chickens. Ethyl 2-methyl-5-nitro-3-pyridinecarboxylate dechlorinates when heated to 100°C in chloroform, but it is not activated by light or by oxygen.

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3,5-Bis(Trifluoromethyl)nitrobenzene is a hydroxamic acid that can be used as an additive. It has the ability to form complexes with anions due to its affinity for them. These complexes are often used as additives in organic chemicals, such as dimethylformamide and nitroarenes. The complexation of 3,5-Bis(Trifluoromethyl)nitrobenzene with anions can be observed using the dipole moment and transition state theory. This product has been shown to have high yield in reactions involving hydroxamic acids and boronic acids.

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Trans-3-Nitrocinnamic acid is a white solid that can be obtained by the nitration of cinnamic acid. Trans-3-Nitrocinnamic acid is an isoenzyme as it has different chemical properties than cis-3-nitrocinnamic acid. The intermolecular hydrogen bonding and vibrational frequencies are different in trans-3-nitrocinnamic acid, which causes the dipole to change and increases the solubility in water. The genotoxic activity of trans-3-nitrocinnamic acid was evaluated using the Ames test, which showed that it is not mutagenic. However, there were some genotoxic effects observed in rats after applying trans-3-nitrocinnamic acid on skin.

Please enquire for more information about Ethyl 4-(5-methyl-3-nitro-1H-pyrazol-1-yl)butanoate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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. References Windler, G. K., et al.: Synthesis, 46, 2383 (2014); Schmitt, R. J., et al.: Synthesis, 2, 123 (1986)

3-Nitro-benzamidine is a chemical compound that is used as an inhibitor for xanthine oxidase and nitroreductases. It also has the ability to inhibit mammalian cell growth, which may be due to its inhibition of allopurinol, an acceptor of electron transfer. 3-Nitro-benzamidine inhibits nitroaromatic compounds by binding with one or more electrons. This chemical has been shown to be a sensitizer in humans and can cause allergic reactions.

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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.