Eterocicli con azoto (N)

<p>Please enquire for more information about 4-Bromo-3-(trifluoromethoxy)pyridine hydrobromide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,5-Diaminopyridine is an organic compound that is expressed in the human body. It has been shown to inhibit the growth of cells in culture by binding to their DNA and preventing the production of hydrogen bonds. 2,5-Diaminopyridine has also been used clinically to treat inflammatory diseases such as rheumatoid arthritis. The hydrogen bond formation and inhibition of cell growth occurs at a low concentration of 2,5-Diaminopyridine. This drug may have potential as a therapeutic agent for cancer treatment because it inhibits the transcription factor CXCR4.</p>

<p>Please enquire for more information about 6-Bromo-4-hydroxypyrazolo[1,5-a]pyridine-3-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(4,4'-Difluorobenzhydry)piperazine (1-DFBP) is a potential antitumor agent that has been shown to inhibit the growth of leukemia cells. It may be an inhibitor of apoptotic cell death, as it has been shown to induce hydrogen bond formation with coumarin derivatives. 1-DFBP has also been shown to have inhibitory activities against leukemia HL-60 cells, and is a competitive inhibitor of cinnarizine. The catalytic mechanism for 1-DFBP is not known, although kinetic data suggest that it involves hydrogen bonding and/or pi stacking interactions.</p>

<p>Desloratadine N-hydroxypiperidine is a drug that is used to treat allergic rhinitis and urticaria. It belongs to the class of antihistamines, which block the activity of histamine in the body. Desloratadine N-hydroxypiperidine is a prodrug that has a piperidine moiety attached to its side chain. This prodrug is metabolized into desloratadine, its active form, by esterase enzymes in the liver and blood plasma. The onset of action is rapid after oral administration and the duration of action is 12 hours or more. Desloratadine N-hydroxypiperidine has shown linearity over a wide range of pH values (pH 1 to 10) and ionic strengths (0.1 M to 0.5 M). Optimization was achieved by adjusting elution time, ion-pairing agent, mobile phase composition, organic modifier concentration and column particle</p>

<p>Ligand used to prepare ruthenium complexes for asymmetric catalysis</p>

<p>3-(Boc-amino)pyridine is a glycine derivative with a trigonal, chelate ring. It can be hydrolyzed by acid to form 3-aminopyridine. 3-(Boc-amino)pyridine has been shown to react with trimethyltin chloride to form an intramolecular complex in the presence of alkyllithiums. This reaction proceeds through lithiation and methylation of the carboxyl group of 3-(Boc-amino)pyridine. The interaction between 3-(Boc-amino)pyridine and trimethyltin chloride forms an antiaromatic six membered ring that resembles a benzene molecule.</p>

<p>Please enquire for more information about 3-Amino-5-chloropyrazine-2-carbonitrile 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 4,6-Dichloro-pyridin-3-ylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Methylenepiperidine hydrochloride is a synthetic, ethylene oxide derivative that is used as an antifungal drug. It is also used in the synthesis of other compounds and as a reagent in organic chemistry. 4-Methylenepiperidine hydrochloride can be synthesized by reacting ethylene with an alkoxide, followed by adding a metal halide such as organolithium reagents to form the desired product. The yield rate of this reaction is high and it is easy to perform on a large scale.</p>

<p>Please enquire for more information about 3-Bromo-6-methylpicolinic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Imidazole methyl carboxylate is a drug that inhibits the activity of dehydrogenases and other enzymes. It has been shown to be an inhibitor of the enzyme catalase in vitro and in vivo, which may be due to its ability to bind bidentately with the active site. 4-Imidazole methyl carboxylate is effective when administered orally, and it has been shown to improve symptoms of neurodegenerative diseases such as Alzheimer's disease. This drug also has a trifunctional chemical structure that contains a macrocyclic ring system with an imidazole group and a carboxylic acid group. The redox potential of this molecule makes it suitable for use as an antioxidant.</p>

<p>Please enquire for more information about 4-[(4-chlorophenyl)-2-pyridinylmethoxy]-1-piperidinecarboxylic acid ethylester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Methyloxy-phenyl)-piperazin-1-yl]-phenylamine is an organic compound that has a reactive silicon group. It contains two phenyl groups, one of which is attached to the silicon. This compound exhibits phase equilibrium in water and can be used as a monomer for fabricating inorganic materials with orderly patterns, such as glass and metal oxides. This product also has impurities and can be grown at different rates depending on the conditions, such as temperature. The optical properties of 4-methyloxy-phenyl)-piperazin-1-yl]-phenylamine are dependent on its environment and it has been shown to have exothermic properties when reacting with iron powder.</p>

<p>3-(Chloromethyl)-5-methylpyridine hydrochloride (3CMPH) is a chemical compound that is synthesized from chlorine and methylpyridine. 3CMPH can be produced by the reaction of chlorination with toluene or hydrogen chloride. The synthesis of 3CMPH is done in two steps: first, reacting toluene with chlorine gas at high temperature and pressure in the presence of sulfuric acid, followed by the addition of sulfuric acid to the resulting product. In the second step, hydrogen chloride reacts with methylpyridine in an alkaline solution, yielding 3-(chloromethyl)-5-methylpyridine hydrochloride as a white solid. 3CMPH has been shown to have antihistamine effects and can be used for treating allergies. It can also be used as a skin protectant against uv light and rupatadine.</p>

<p>4,4'-Dimethyl-2,2'-bipyridine is a molecule that belongs to the group of p2 metal complexes. It has been shown to have synergistic effects with ruthenium complexes in analytical chemistry and electrochemical studies. Theoretical calculations have been performed for 4,4'-dimethyl-2,2'-bipyridine and its derivatives. These calculations show that the molecule is planar and that it can be considered as a diazonium salt. The photochemical properties of 4,4'-dimethyl-2,2'-bipyridine have also been studied in detail. This substance emits light when excited by ultraviolet light or visible light, which makes it an excellent candidate for use as a luminescent material in optical displays.</p>

<p>Please enquire for more information about 1-Pyridin-2-ylmethylpiperidine-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethyl 3-(pyridin-2-ylamino)propanoate is a thrombin inhibitor that can be used for the treatment of cancer. Ethyl 3-(pyridin-2-ylamino)propanoate is a reactive, profile compound with electrons and hydrogen bonds. It has been shown to have anticancer activity in vitro and in vivo, inhibiting tumor cell growth by inhibiting DNA synthesis. This molecule also has anti-inflammatory properties, which may be due to its ability to inhibit platelet aggregation.</p>

<p>5-Amino-2-methoxy-4-methylpyridine is a small molecule that inhibits bromodomains. Bromodomains are protein domains that bind to acetylated lysine residues on histones. 5-Amino-2-methoxy-4-methylpyridine binds to the bromodomain, preventing the acetylated lysine residues from binding with other proteins and inhibiting transcription. This drug has been shown to be effective in treating prostate cancer by interacting with the androgen receptor. 5-Amino-2-methoxy-4-methylpyridine also interacts with ATPase, which may lead to increased levels of ATP production, and has been shown to have antitumor effects in vitro.</p>

<p>4-(tert-Butyldimethylsilyloxymethyl)pyridine is a reagent that is used to prepare stoichiometric quantities of triethyloxonium ions in the presence of catalytic amounts of palladium. 4-(tert-Butyldimethylsilyloxymethyl)pyridine is also used as an anticancer agent, which may be due to its ability to inhibit cell proliferation and induce apoptosis. This compound has been shown to prevent the growth of micellar structures and reduce the rate of ester hydrolysis. It also has the ability to convert into two enantiomers, one with a hydroxyl group on the methylene carbon at position 4 and another with an alcohol group on this same carbon.</p>