Heterocycles with Nitrogen (N)

<p>Please enquire for more information about 1-(2-Aminopyrimidin-5-yl)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 3,6-Dihydro-4-(tributylstannyl)-1(2H)-pyridinecarboxylic acid t-butyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,3,5-Trimethylpyridine is an organic compound that is used in the production of pharmaceuticals. It is a colorless liquid with a strong odor. 2,3,5-Trimethylpyridine reacts with hydrochloric acid to produce an n-oxide and hydrogen chloride gas. This reaction can be carried out in solution or as a solid phase microextraction experiment. The optimal reaction conditions for this process are determined by measuring the yield of the desired product and the amount of byproducts formed during the reaction. The reaction can be inhibited by adding pump inhibitors such as methyl ethyl ketone or an organic solvent such as acetonitrile. The structures of 2,3,5-Trimethylpyridine have been determined using X-ray crystallography and phosphotungstic acid. Deionized water and chlorides react with 2,3,5-Trimethylpyridine to form a white precipitate. This product</p>

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

<p>2,4,6-Trichloro-5-nitropyrimidine is a purine derivative that inhibits the cell proliferation of cancer cells. It has been shown to inhibit the activity of kinases and to induce apoptosis in human cancer cells in vitro. This drug also has antiproliferative potential against erythrocytes and is being investigated as a treatment for renal disease. 2,4,6-Trichloro-5-nitropyrimidine shows inhibitory effects on the phosphorylation of roscovitine by ATP and may be used to treat patients with glomerulonephritis. 2,4,6-Trichloro-5-nitropyrimidine can be synthesized from 2,4,6-trichloropyrimidinethiol and nitric acid according to the following equation: CClNO + HNO → CClNOH + NO 2 Cl + 3 HNO</p>

<p>2-Amino-1,3,5-triazine is a hydrogen bond donor that has been shown to have growth inhibiting effects. It reduces the viscosity of aqueous solutions and is used as an enantiopure for amines. 2-Amino-1,3,5-triazine can be used in reactions with metal surfaces to produce surface coatings or used as a bifunctional crosslinking agent for polymer materials. 2-Amino-1,3,5-triazine has been shown to have degenerative disease inhibitory activity and inflammatory disease inhibitory activity. It also inhibits the production of inflammatory cytokines such as tumor necrosis factor alpha (TNFα) and interleukin 6 (IL6).</p>

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

<p>6-Amino-1,3,5-triazine-2,4-diol is a chemical that is soluble in water and has been shown to be an effective inhibitor of cyanuric acid degradation. It has been used in wastewater treatment and as a model system for the study of melamine and cyanuric acid interactions. 6-Amino-1,3,5-triazine-2,4-diol binds to cyanuric acid by forming a complex with it. This prevents the formation of reactive intermediates that lead to the degradation of cyanuric acid. 6-Amino-1,3,5-triazine-2,4-diol also inhibits the oxidation catalyst activity of sodium carbonate at pH 8.5. The toxicity of this chemical has been studied in rats and was found to be low.</p>

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

<p>(R)-(-)-1-[(4-Chlorophenyl)phenylmethyl]piperazine is a chemical compound that belongs to the group of c1-4 alkyl, high yield. It has a chemical formula of C12H17ClN2O and an organic base. This compound is hydrolyzed in vivo to levocetirizine, its active form. (R)-(-)-1-[(4-Chlorophenyl)phenylmethyl]piperazine is an antihistamine that binds to H1 receptors in the central nervous system, which results in decreased production of histamine and other proinflammatory substances. It also has optical activity, with (+) being the active form.</p>

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

Please enquire for more information about Fmoc-4-(3-carboxymethyl-2-keto-one-benzimidazolyl)piperidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>2,5-Diaminopyridine dihydrochloride is a compound that belongs to the class of hydroxamic acids. It is an intermediate in the synthesis of the anti-cancer drug, hydroxyurea (hydroxylamine). 2,5-Diaminopyridine dihydrochloride can be used as a cross-coupling reagent for coupling reactions with chlorinated and tritiated organic compounds. The efficiency of this reaction is dependent on the coulombic and mutagenic properties of 2,5-diaminopyridine dihydrochloride. 2,5-Diaminopyridine dihydrochloride has been shown to cause cancer in animal studies.</p>

<p>Please enquire for more information about 1-tert-Butyl 2-methyl 4-oxopiperidine-1,2-dicarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Benzyl-piperazine is a pharmacological agent that has been shown to have anabolic effects in animals and humans. It is a crystalline solid with a molecular weight of 248.2 g/mol. 2-Benzyl-piperazine is used in the treatment of chronic renal failure, as well as the prevention of kidney stone formation in patients with recurrent calcium oxalate stones, or those who have experienced at least one episode of calcium oxalate stone formation. 2-Piperazine inhibits the activity of an enzyme called carbonic anhydrase, which is found in many tissues and facilitates reactions that produce bicarbonate ions from carbon dioxide and water molecules. The piperazine ring also has two methyl substituents, which can be modified to create bioisosteric analogues. These modifications may alter the properties of 2-benzyl-piperazine such as its solubility or metabolic stability. 2-Benzyl-piper</p>

<p>Please enquire for more information about 2-Fluoro-4-(tributylstannyl)pyridine 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-Boc-amino-(4-N-fmoc-piperidinyl)carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Benzyl-3-carbethoxy-4-piperidone hydrochloride is a carboxylic acid that is used as a waterproofing agent in cyclohexane. It is absorbed by the skin and other tissues, which may lead to adverse effects on the body. Exposure to this compound has been shown to result in irritation of the skin, eyes, and respiratory tract, as well as changes in heart rate and blood pressure.</p>

1-Piperonylpiperazine is a drug that is used to treat symptoms of diabetic neuropathy. It is an inhibitor of mitochondrial ATPases and blocks the synthesis of nucleotides in the liver. It also inhibits uptake processes in the brain and spinal cord, which are related to locomotor activity. The uptake assays showed that 1-piperonylpiperazine has a high affinity for receptors in the human liver, which could be useful for future research on drugs targeting this organ. 1-Piperonylpiperazine has been shown to have strong effects on mitochondrial membrane potential and ATP levels in primary cells, as well as increasing uptake into human liver cells. This drug may be useful for treating symptoms of diabetic neuropathy.

<p>Please enquire for more information about Fmoc-N-(1-Boc-piperidin-4-yl)glycine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>