Hétérocycles azotés (N)

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1-(4-Nitrophenyl)piperazine is a nitro compound with a molecular weight of 147.2. It is soluble in DMSO and ethanol, but not in water. 1-(4-Nitrophenyl)piperazine has the ability to absorb ultraviolet radiation (UV) and it can be used as a UV-absorbing agent in plastics. 1-(4-Nitrophenyl)piperazine can also be used as an intermediate for the synthesis of triazole antifungal agents. The molecule has been shown to have high values at magnetic resonance spectroscopy (NMR). The crystal structure of 1-(4-nitrophenyl)piperazine was determined by x-ray diffraction data and molecular modeling techniques. This molecule's melting point was determined by titration calorimetry, which showed that its melting point is around 195 degrees Celsius.br> 1-(4-Nitrophenyl)piper

2,4-Dibromopyridine is a brominated derivative of pyridine. It is synthesized through the substitution of two bromine atoms for two hydrogens on the pyridine ring. This synthesis can be achieved by disubstitution or cross-coupling reactions. The reaction products are nucleophilic and react with electrophiles to produce substitution products. The reaction mechanism is thought to involve a six-membered transition state, which has been observed using X-ray absorption spectroscopy.

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4-Hydroxypiperidine is a molecule with a carbonyl group. It is the most active and selective CCR5 receptor antagonist that has been studied to date. 4-Hydroxypiperidine inhibits HIV infection by preventing the binding of HIV to its receptor on the surface of white blood cells, thereby preventing it from entering these cells. 4-Hydroxypiperidine also acts as an anti-inflammatory agent in chronic bronchitis patients, due to its ability to inhibit prostaglandin synthesis. The chemical ionization mass spectra of this molecule show peaks for methyl ethyl, malic acid, and hydroxyl groups. These properties make 4-hydroxypiperidine a useful candidate for drug development against inflammatory diseases and several cancers.

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8-Chloro-3,7-dihydro-1H-purine-2,6-dione is a reactive molecule that binds to the active site of bacterial cyclic nucleotide phosphodiesterases and inhibits their activity. This inhibition prevents the breakdown of cAMP and cGMP, which are important second messengers in eukaryotic cells. 8-Chloro-3,7-dihydro-1H-purine-2,6-dione is also a potent inhibitor of protein synthesis and has been used in research studies on wheat leaves.

2-(Hydroxymethyl)pyridine N-oxide is a model system that was originally synthesized to study the mechanism of perchlorate and amine degradation in vivo. It has been shown to be an excellent model for studying the oxidative decomposition of n-oxides with metal ions, as well as their transformation into monomers. 2-(Hydroxymethyl)pyridine N-oxide reacts with chloride ion to form 2-(hydroxymethyl)pyridine N-oxide chloride. The reaction of 2-(hydroxymethyl)pyridine N-oxide with a sulfoxide produces an adduct that can be used to study hydrogen bonding. 2-(Hydroxymethyl)pyridine N-oxide has biological properties and is a potential drug candidate for the treatment of cancer.

1-Acetylpiperazine is a growth factor that has been shown to stimulate the proliferation of keratinocytes and dermal fibroblasts. It also inhibits the production of proinflammatory cytokines, such as tumor necrosis factor alpha (TNF-α) and interleukin-1 beta (IL-1β), in immune cells. 1-Acetylpiperazine has been shown to have antimicrobial properties against Gram-positive bacteria, including methicillin resistant Staphylococcus aureus and Clostridium perfringens. The compound binds to the receptor for epidermal growth factor in cancer cells, which may be responsible for its anticancer effects. 1-Acetylpiperazine has also been shown to inhibit the binding of imatinib to its receptor, which may be responsible for its anticancer effects.

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