Heterociclos com Nitrogénio (N)

<p>4-Azido-2,2,6,6-tetramethyl-1-piperidinyloxy is a fine chemical that is a versatile building block useful in research and synthesis. It has been used as a reaction component in the preparation of other compounds. This compound is also an intermediate for the production of other chemicals.</p>

<p>2-Mercaptopyridine is a quinone that has been used as an inhibitor of the HIV reverse transcriptase enzyme. It binds to the active site of the enzyme and inhibits its activity by forming a stable covalent bond with two cysteine residues in the enzyme. The molecule is stabilized by two adjacent sulfide bonds, which form a six-membered ring with three nitrogen atoms and one oxygen atom. This ring coordinates to the zinc ion in the active site of the enzyme. 2-Mercaptopyridine has also been found to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Mycobacterium tuberculosis. 2-Mercaptopyridine binds to DNA at positions where it is complementary to guanine or adenine nucleotides, thus preventing RNA synthesis and replication.</p>

<p>Intermediate in the synthesis of tofacitinib</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>Please enquire for more information about 2-Bromo-5-methylpyrimidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Boc-4-piperidineacetaldehyde is a chiral, stable, and readily available aldehyde. It has been used in the synthesis of various biologically active molecules including imidazolidinones, which are important for their use as catalysts in organic chemistry. The synthesis of this molecule by the condensation of 4-piperidineacetic acid with acetaldehyde followed by reduction with sodium borohydride is an example of this type of reaction. N-Boc-4-piperidineacetaldehyde can be used to synthesize imines and linkers that are covalently bonded to the protein backbone. This molecule also has conformational stability and is not susceptible to oxidation or radiation damage.</p>

<p>Ligand used to prepare ruthenium complexes for asymmetric catalysis</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>2,5-Dibromopyridine is a chemical compound that can be used as a coupling agent in palladium-catalyzed cross-coupling reactions. It is used on the surface of metal particles to increase the efficiency of the reaction, and has been shown to react with substrates such as sodium hydroxide solution, sodium carbonate, halides and hydroxides. 2,5-Dibromopyridine also reacts with benzoate to form a palladium complex. 2,5-Dibromopyridine can be used as an oxidant or reductant depending on the type of reaction it is being used in. It has redox potentials at -0.6 volts for oxidation and +0.6 volts for reduction.</p>

<p>3-Hydroxy-5-methylpyridine (3HMP) is a chemical substance that has been classified as an amine. It is a product of the metabolism of purines, which are nitrogenous bases found in DNA and RNA. 3HMP is produced by aerogenic bacteria (such as Enterobacter), and can be used to estimate the number of these bacteria present in water samples. 3HMP has been shown to have antiviral properties against influenza virus, and can be used as a biomarker for the presence of other viruses in animals. 3HMP also has mineralization properties, which have been studied extensively, particularly with regards to pancreatic disease.</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>2-Amino-4-hydroxypyridine (2AH) is a synthetic, isomeric compound that has been synthesized in two different forms: 3-bromo-5-hydroxypyridine and hydroxy group. 2AH has been shown to be chemically stable at room temperature and pH levels of less than 7. It also withstands the loss of membrane fluidity induced by amides, such as 3-amino-2-bromopyridine. 2AH can be used to synthesize oxindole derivatives, which are found in natural gas, and piperidines. This chemical can also be used for aminations with pyrrole or 2 amino 4 hydroxypyridine.</p>

<p>Please enquire for more information about 3-Bromo-2-methyl-5-nitropyridine 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 1-(5-Bromopyrimidin-2-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 6-Chloro-pyridazine hydrochloride 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 RC-3095 trifluoroacetate 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 1-Boc-4-Iodomethyl-Piperidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Piperazine-2-carboxylic acid dihydrochloride (PZC) is an aminopyrimidine antibiotic that binds to the amine groups of plasma proteins and hydroxyapatite. It has been shown to have a specific interaction with Gram-negative bacteria, such as Escherichia coli and Salmonella typhimurium, as well as cancer cells. PZC can be used as a modifier in the treatment of staphylococcal infections and has been shown to inhibit protein synthesis in mammalian cells. PZC interacts with histidine residues on the surface of bacterial cells and inhibits their growth by binding to sites on DNA called triplexes. This drug also specifically binds to primary amines and reacts with other molecules containing amines such as polyamines, amides, or thiols.</p>

<p>Sulfamethoxypyridazine is a sulfa drug that inhibits bacterial growth by inhibiting the synthesis of folic acid, which is essential for DNA and RNA production. It has been shown to be effective in the treatment of urinary infections and infectious diseases. Sulfamethoxypyridazine interacts with other drugs, such as oral contraceptives, to increase their blood levels. This drug also has a matrix effect on urine samples, which can be used to detect the presence of bacteria. The matrix effect is due to its hydrophobic nature and ability to form aggregates with other compounds. Sulfamethoxypyridazine is used in wastewater treatment plants as an analytical method for nitrogen atoms.</p>

<p>1,1'-Carbonimidoylbis-1H-imidazole is a ligand that binds to amines and isosteres. It can be activated with electrophilic reagents to form an activated linker. This ligand has been shown to inhibit the growth of xenograft tumor cells in mice by binding to functional groups on the cell surface. This drug also has been shown to bind to the receptor for advanced glycation end products (RAGE) and inhibit its function. 1,1'-Carbonimidoylbis-1H-imidazole has also been evaluated as a cancer therapeutic agent in animal models.</p>