Heterocycles with Nitrogen (N)

<p>Please enquire for more information about (3R,4R)-3-[(6-Amino-4-pyrimidinyl)methylamino]-4-methyl-β-oxo-1-piperidinepropanenitrile 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 tert-Butyl 6-amino-3-azabicyclo[3.1.0]hexane-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>Pyrimidine nucleobase; component of nucleic acids</p>

<p>6-Chloro-2-fluoropurine is an analytical reagent with a monoclonal antibody that binds to the nucleic acid of HL-60 cells and can be used for optical analysis. 6-Chloro-2-fluoropurine has been shown to have significant cytotoxicity against HL-60 cells, which may be due to its ability to bind to intracellular targets. 6-Chloro-2-fluoropurine has also been shown to inhibit the growth of HL-60 cells in a fluorescein angiography study and is used as a diagnostic agent for diagnosis of cancer.</p>

<p>2-Chloropyridine-4-boronic acid is a nicotinic acetylcholine receptor antagonist that has been shown to be effective against trypanosomiasis. It blocks the binding of acetylcholine to its receptor, which prevents the propagation of an action potential in the postsynaptic cell. 2-Chloropyridine-4-boronic acid inhibits the enzymes cyclooxygenase and prostaglandin synthase, which are involved in inflammation. 2-Chloropyridine-4-boronic acid is potent and selective for nicotinic acetylcholine receptors, but it also binds to other sites on the enzyme. The molecular modeling studies have shown that this compound has a pharmacophore that can be used as a guide for drug design.</p>

<p>Pyrrole-2-carboxylic acid is a polycyclic aromatic compound that can be found in coal tar. It has been shown to have anti-inflammatory, antiallergic, and antifungal properties. Pyrrole-2-carboxylic acid is produced by the human body as an intermediate in the metabolism of tryptophan. This compound can also be synthesized and used to treat chronic bronchitis, which is caused by excessive mucus production and inflammation of the airways. The reaction mechanism for pyrrole-2-carboxylic acid is similar to that of other drugs that are used in respiratory therapy, such as aminophylline or acetylcysteine.</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>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>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.</p>

<p>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&gt; 1-(4-Nitrophenyl)piper</p>

<p>4-Hydroxy-6-mercaptopyrazolo[3,4-d]pyrimidine is a pyrimidine compound that is a competitive inhibitor of xanthine oxidase (XO) with an IC50 of 0.5 μM. It binds reversibly to the XO enzyme and reverses the effect of the enzyme, thereby inhibiting the production of uric acid. 4-Hydroxy-6-mercaptopyrazolo[3,4-d]pyrimidine does not bind to any other enzymes in the body or affect serum protein levels, which makes it an ideal drug for patients with gout who are at risk for developing renal failure. The drug has been shown to be effective in animal models and is currently undergoing clinical trials in humans.</p>

<p>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.</p>

<p>Please enquire for more information about Domperidone N-oxide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Piperazinoacetic acid anilide dihydrochloride is a high quality, reagent compound which can be used as a useful intermediate or a speciality chemical. Piperazinoacetic acid anilide dihydrochloride is a complex compound that has been shown to have a number of useful properties, such as being an effective building block for the synthesis of other compounds. It can also be used as a reaction component in the preparation of fine chemicals and research chemicals. This product is also versatile, allowing it to be built into different scaffolds to create new compounds.</p>

<p>2-Hydroxypyrimidine HCl is a compound that is soluble in water and has an appearance of white crystals. It can be used as a metal ion chelator, as well as an inhibitor of aldehyde oxidase. 2-Hydroxypyrimidine HCl has been shown to be effective in the treatment of solid tumours and may also be used for the treatment of neoplastic diseases such as leukemia. The compound is cytotoxic and inhibits DNA synthesis, which may lead to cell death. 2-Hydroxypyrimidine HCl also has functional groups that are responsible for its ability to inhibit aldehyde oxidase and 5-aminouracil (5AU).</p>

<p>2-Amino-5-methoxypyridine (2AM5MP) is a synthetic compound that is used to study the nicotinic acetylcholine receptor. It has been shown that 2AM5MP can be used as an agonist for the nicotinic acetylcholine receptor, which may be due to its ability to act as a substrate for amine oxidase. This compound has been shown to have anti-cancer properties and fluoresce when exposed to positron emission tomography (PET) scans. The anti-cancer effects of 2AM5MP are thought to be due to its ability to inhibit cancer cell proliferation and induce cancer cell apoptosis.</p>

<p>2-Bromo-6-methylpyridine-3-carboxaldehyde (BMPCA) is a pharmacological agent that belongs to the group of antagonists. It has been shown to be a potent antagonist at the NMDA receptor and may be used for treating neuropathic pain. BMPCA also has been shown to have competitive inhibition at the naphthyridine receptor, which may allow it to act as an antagonist or an agonist depending on its binding site. The regioisomeric analogs of BMPCA are 2-(2,5-dichloropyridyl)-6-methylpyridine-3-carboxaldehyde and 2-(2,5-dimethylpyridyl)-6-methylpyridine-3-carboxaldehyde. These analogs have been shown to inhibit the growth of tumor cells in vitro and in vivo.</p>

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<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>