Heterociclos con nitrógeno (N)

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

<p>4-Chloro-2-hydroxypyridine is a chemical substance that has been shown to inhibit the replication of viruses in cell culture. It has demonstrated antiobesity effects in animal studies, but its mechanism is not well understood. This substance may be a thioxanthone derivative, which are heterocyclic compounds containing oxygen and sulfur. 4-Chloro-2-hydroxypyridine can crosslink DNA and form adducts with deoxyribose sugars. It also has affinity for sequences containing pyridones and imidazopyridines.</p>

<p>Piperidin-3-one hydrochloride is an organic solvent that belongs to the group of benzyl compounds. It is a reagent for the synthesis of sulfides, which are used in the production of dyes, pharmaceuticals, and other products. Piperidin-3-one hydrochloride can be used as a constant in calculating the shift of tetrafluoroborate ions. This compound has been shown to be assembled into planar structures with six atoms per side. The resonance frequencies of this compound depend on the solvents and its aliphatic nature. Piperidin-3-one hydrochloride can be used to generate dimethyl sulfide by reacting with methanol or methyl chloride.</p>

<p>4-Hydroxypyridine-3-sulfonic acid is the anion of 4-hydroxypyridine with sulfate. It has a pK a of 1.5 and is soluble in water, ethanol, and methanol. 4-Hydroxypyridine-3-sulfonic acid can be used as a crystallographic data collection reagent. The anion can act as an acceptor for radiation and can also be used to generate hydrogen sulfate. Hydrogen sulfate is generated by the reaction of sulfuric acid with potassium hydroxide or sodium hydroxide. Hydrogen sulfate reacts with elemental sulfur to produce hydrogen sulfide. This compound has been shown to have properties that make it useful in analytical chemistry, such as its ability to form hydrogen bonds and act as an anion. The structure of 4-hydroxypyridine-3-sulfonic acid is shown below: 4 H O 2 S</p>

<p>2-Amino-6-chloropyrazine (2ACP) is an inhibitor that binds to the active site on human protein kinase C (PKC). It has been shown to inhibit PKC by hydrogen bonding with the hydroxide ion, which blocks its catalytic activity. 2ACP has been studied for its potential use in treating cancer and for inhibiting amine oxidases, which are enzymes associated with inflammation and chronic obstructive pulmonary disease. The inhibition of these enzymes may help to reduce stenosis in the lungs or other organs. 2ACP also has been shown to have antimycobacterial activity against Mycobacterium tuberculosis, M. avium complex, and M. leprae by inhibiting DNA synthesis and RNA synthesis. 2ACP inhibits the kinase receptor on the cell membrane that phosphorylates a water molecule into a chlorine atom, which then reacts with hydrogen peroxide to form free radicals that can kill bacteria</p>

<p>Please enquire for more information about 1-[(1,5-Dimethyl-1H-pyrazol-4-yl)methyl]piperazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Chloro-4-pyrimidinecarbonitrile is a synthetic compound that belongs to the group of phenylpyrimidines. It inhibits the tyrosine kinase activity and cytokine production in cells. 2-Chloro-4-pyrimidinecarbonitrile is used as an immunomodulatory agent in the treatment of cancer, autoimmune disorders and other immune dysfunctions. This drug also has anti-inflammatory properties and can be used for the treatment of inflammatory bowel diseases, such as ulcerative colitis or Crohn's disease. 2CPCN is metabolized by deamination and demethylation, which leads to the formation of nitrite ion, a reactive nitrogen species that can cause DNA damage.</p>

<p>Iloperidone is a white to off-white crystalline powder that is soluble in water and alcohol. It is used as an antipsychotic drug and belongs to the class of benzamides. Iloperidone has been shown to be effective for schizophrenia, bipolar disorder, and major depressive disorder. The chemical name for iloperidone hydrochloride is 4-(2,4-Difluorobenzoyl)piperidine hydrochloride. This drug also has a high affinity for serotonin 5-HT2A receptors in the brain, which may contribute to its therapeutic effects.</p>

<p>1,3,5-Triacryloylhexahydro-1,3,5-triazine (TTH) is a particle that absorbs UV light. It is a reactive chemical with a high thermal stability and low reactivity to air. TTH has been used as a cross-linker in polymer films and as a microsphere filler. The absorption of UV light by TTH may be due to the presence of hydroxyl groups or nitrogen atoms. The nmr spectra show that TTH contains trimethylolpropane groups.</p>

<p>5-Cyanopyridine-2-carboxylic acid is a small molecule that has been found to have significant biological activity in a number of different areas, including neurotherapeutics. It is the result of a scalable synthesis and is soluble in water. The molecule has two chiral centers and can exist as four different stereoisomers (enantiomers). In vitro studies show that 5-cyanopyridine-2-carboxylic acid inhibits fatty acid uptake by blocking the proton pump, which transports lipids into cells. This compound also binds to the cytosolic protein pyrazine 2-carboxylic acid receptor 1 (PYZR1), which may provide an explanation for its effects on fatty acid uptake.</p>

<p>2,3,3-Trimethyl-4,5-benzo-3H-indole is a fine chemical that is used as a versatile building block for research chemicals and speciality chemicals. It can be used to synthesize drugs. 2,3,3-Trimethyl-4,5-benzo-3H-indole is also a reaction component in the synthesis of complex compounds with high quality.</p>

<p>5-Amino-2-chloropyridine-4-carboxylic acid is a potent tyrosine kinase inhibitor. It inhibits the activation of EGFR, which may be due to its binding to the ATP-binding pocket in EGFR. 5-Amino-2-chloropyridine-4-carboxylic acid has been shown to inhibit cancer cell growth and induce apoptosis in vitro. This drug has also been shown to have potent anticancer activity in vivo, as well as inhibitory effect on tumor growth in xenograft models of human cancer cells. In addition, it inhibits the production of formamidine acetate, a precursor for histamine synthesis. 5-Amino-2-chloropyridine-4-carboxylic acid binds to formamide and formamidine acetate with high affinity and therefore inhibits histamine synthesis.</p>

<p>2-Chloro-3-iodopyridine is an efficient method for the synthesis of various 2-chloro-3-iodopyridines. The reaction is catalyzed by triphosgene, a reagent that is also used in the synthesis of other important heterocycles. In this process, triphosgene reacts with a broad range of primary amines to form chloronitroso derivatives. These compounds are then used to synthesize 2-chloro-3-iodopyridines by reaction with pyridine. The reaction can be run at temperatures as low as -78°C, which has led to its use in bladder cancer research and some other reactions involving aminations or furopyridines.</p>

<p>2,6-Dichloro-5-nitropyrimidin-4-amine is a chlorinating agent that reacts with aliphatic and aromatic amines to form substituted pyrimidines. The substitution pattern of the product depends on the regioselectivity of the reaction. 2,6-Dichloro-5-nitropyrimidin-4-amine is one of the few chlorinating agents that react with propylamine. Substitution at position 2 of the purine ring has been found to be more selective than substitution at position 6. The 2,6-dichloropyrimidine can also be used as a nitro group source in chemical synthesis or as an intermediate in production of other compounds.</p>

<p>Pyridine-2,5-diol is a bacterial metabolite that is the product of the enzyme pyridoxal 5'-phosphate oxidase. This enzyme has been shown to be involved in microbial metabolism and enzymatic reactions, such as the conversion of picolinic acid to pyridine-2,5-diol. Pyridine-2,5-diol has been found to be expressed in wild type strains but not in mutant strains. The gene product for this enzyme has also been identified as maleate dehydrogenase.</p>

<p>1-(2-Methoxyphenyl)piperazine is a drug that has been shown to have locomotor activity, antihypertensive activity, and inhibitory properties. It also acts as a matrix effect and receptor activity. 1-(2-Methoxyphenyl)piperazine has been shown to have inhibitory effects on 5-ht7 receptors, which are mainly found in the brain. This drug binds to the 5-ht2 receptor, which is a type of serotonin receptor in the brain. The binding of 1-(2-methoxyphenyl)piperazine to the 5-ht2 receptor inhibits the release of dopamine from neurons and leads to necrotic cell death. This drug can also be used as an analytical tool for measuring 5-ht1a receptors, which is a type of serotonin receptor found in the brain.</p>

<p>Please enquire for more information about 2-(tert-Butylamino)-4,6-dichloro-1,3,5-triazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Kinetin is a chemical compound that is used in research as a reagent, useful scaffold, and an intermediate. It has been shown to be an effective building block for the synthesis of complex compounds. Kinetin is also a versatile building block that can be used to synthesize many different types of compounds. Kinetin has a CAS number 525-79-1 and is classified as a speciality chemical.</p>

<p>Please enquire for more information about 5-Chloro-2-(ethylsulfonyl)pyrimidine-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(3-Chlorophenyl)-4-(3-chloropropyl)piperazine Hydrochloride is an antidepressant that belongs to the class of nefazodone. It is a prodrug, which is hydrolyzed to nefazodone in the liver. It has been shown to have a high affinity for serotonin receptors and as such may be useful for the treatment of depression. 1-(3-Chlorophenyl)-4-(3-chloropropyl)piperazine Hydrochloride also has anticonvulsant properties, which may be due to its inhibition of neuronal excitability by blocking sodium channels in the brain.</p>

<p>Pyridine-3-carboxaldehyde is a heterocyclic compound that is structurally related to nicotinic acid and picolinic acid. It has been shown to have anti-tumor activity, with hl-60 cells as the model system. Pyridine-3-carboxaldehyde has also been shown to be toxic to bacteria in biological studies. The chemical stability of this compound was studied by Langmuir adsorption isotherm and electrochemical impedance spectroscopy. It was found that pyridine-3-carboxaldehyde is stable at a pH range of 7 to 8 and at temperatures up to 60 degrees Celsius.</p>

<p>Please enquire for more information about 4-(Piperazinomethyl)benzoic acid, dihydrochloride 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 5-Bromo-1-methyl-1H-1,2,3-triazole including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Prasugrel is a pharmaceutical compound that belongs to the class of thienopyridines. It has been shown to inhibit platelet aggregation and is used for the prevention of blood clots in patients with coronary artery disease. Prasugrel binds to the P2Y12 receptor on the surface of platelets, which prevents ADP from binding, thereby inhibiting platelet aggregation. Prasugrel is a crystalline solid that is soluble in water.</p>

<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>

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<p>5,5-Dipropylpyrimidine-2,4,6(1H,3H,5H)-trione is a molecule that is used as a food additive. It has been shown to inhibit the growth of cancer cells in heart tissue. The optimum concentration for this compound is 0.02% (w/v) and it has been found to be effective at concentrations up to 0.1%. The protonation of 5,5-dipropylpyrimidine-2,4,6(1H,3H,5H)-trione depends on its pH value and it can be protonated by potassium ions or sodium ions. The polycarboxylic acid form of 5,5-dipropylpyrimidine-2,4,6(1H,3H,5H)-trione is more stable than its free acid form. This molecule has also been shown to have properties similar to those of</p>

<p>Indole is a heterocyclic aromatic organic compound. It is a colorless solid that has a strong, unpleasant odor. Indole is classified as a nitrogenous base and is found in many natural products such as the amino acid tryptophan and the alkaloid caffeine. Indole can also be used as a building block for complex molecules, such as pharmaceuticals, herbicides, and pesticides. Indole is soluble in water, but insoluble in most organic solvents. It can be used to synthesize other compounds through reactions with other chemicals or by heating it with different reagents.</p>

<p>3-Bromopyridine is a colorless liquid that is soluble in water and methanol. It has a chemical ionization mass spectrum with hydrogen bonding interactions, which are shown by the nitrogen atoms. 3-Bromopyridine reacts with amines to form nitroso compounds and has transport properties that are dependent on pH. 3-Bromopyridine has been shown to be a metastable substance, which means it can be isolated in a yield of greater than 50%. 3-Bromopyridine is soluble in alkaline solutions, but decomposes at high temperatures. The solution turns red when phosphotungstic acid is added and it gives an orange precipitate when hydrochloric acid is added. The solution turns yellow when sodium hydroxide is added. 3-Bromopyridine can be detected by its nmr spectra and kinetic energy measurements.</p>

<p>4-[(4-Chlorophenyl)phenylmethyl]-1-piperazineethanol dihydrochloride is a cholinergic drug that is used to treat allergic rhinitis in children and adults. It has been shown to be well tolerated in pediatric patients and geriatric patients, as well as being an innovative, labile, and biopharmaceutical compound. 4-[(4-Chlorophenyl)phenylmethyl]-1-piperazineethanol dihydrochloride is not metabolized by the liver and does not have significant side effects. It has a low potential for abuse because of its low solubility in water. It is an antihistamine that blocks the action of histamine at H1 receptors on smooth muscle cells in the nose, which helps reduce nasal congestion and sneezing.</p>

<p>3-Fluoro-4-(tributylstannyl)pyridine is a high affinity, selective, and membrane permeable ligand of the A2B adenosine receptor. It has been shown to be a potent antagonist of A2B receptors in vitro. This compound has also been shown to have a lower affinity for A1, A3, and A4 receptors. 3-Fluoro-4-(tributylstannyl)pyridine has been shown to have high brain uptake in vivo studies. 3-Fluoro-4-(tributylstannyl)pyridine binds to the x-ray structure of the adenosine receptor with high affinity and penetrability. The binding site is proposed to be located on the extracellular side of the receptor near the interface with the second transmembrane domain. In vivo studies have shown that 3-fluoro-4-(tributylstannyl)p</p>

<p>2,5-Dichloropyrazine is a ligand that binds to the bromodomain of a protein and causes it to deform. The bromodomain contains a metal ion at its core and is an important component of many proteins that regulate gene expression. 2,5-Dichloropyrazine has been shown to bind to the metal ion in the bromodomain of some proteins and cause them to deform. This deformation results in changes in the shape of the protein's DNA-binding site, which can alter the way it regulates gene expression. 2,5-Dichloropyrazine also interacts with hexamethylenetetramine (HMT) to form anions and chlorinating agents. These interactions may be responsible for 2,5-dichloropyrazine's high yield.</p>

<p>5-Bromopyridine-2-carbaldehyde is a water soluble organic molecule that has been shown to inhibit the mitochondrial respiratory chain. It is a structural analog of the natural substrate for mitochondrial cytochrome c oxidase, 5-aminolevulinic acid. This compound has been shown to be selective against cancer cells and has anti-viral properties. The photophysical properties of 5-bromopyridine-2-carbaldehyde have been studied extensively. The fluorescence quantum yield of this molecule in aqueous solution is 0.06%.</p>

<p>Gamma-oxo-3-pyridinebutyric acid (GOBA) is a non-protein amino acid that has been shown to be involved in the development of cancer. GOBA was found to be present in urine samples from patients with liver cancer and breast cancer, as well as in healthy individuals. GOBA is also present in rat liver microsomes and human liver, where it is converted into gamma-aminobutyric acid (GABA). This conversion may be due to GOBA's hydroxy group that can be oxidized by cytochrome P450 enzymes. The biological activity of GOBA appears to depend on its carboxyl group, which can form a complex with molybdenum. This complex inhibits the activity of the protein polymerase chain reaction, leading to a decrease in transcriptional regulation. In animal experiments, GOBA has been shown to inhibit tumor growth and induce cell cycle arrest by inhibiting the expression of cyclin D1 at the</p>

<p>3-Nitropyridine is a nitro compound that is used in the preparation of pharmaceuticals. It has been shown to have an inhibitory effect on HIV and other viruses, which may be due to its ability to react with nucleophilic groups. 3-Nitropyridine has also been shown to have an inhibitory effect on the human immunodeficiency virus (HIV) by reacting with the acidic group of the virus. This reaction prevents the virus from binding to cells and entering them. 3-Nitropyridine is also used as a solvent for organic reactions.</p>

<p>4-Chloropyrimidine HCl is a covalent molecule that contains 4-chloropyridine and hydrogen chloride. It exists as two tautomers, the enol form and the keto form. The protonation of the proton on nitrogen will determine which tautomer it will exist in. When there is no proton present, the molecule will exist in its enol form. Resonance is also an important factor with this molecule because it can have a variety of resonance forms. Resonance spectrometry has been used to identify 4-chloropyrimidine HCl because it produces a specific resonance pattern when exposed to magnetic fields. 4-Chloropyridinium trifluoroacetate is another name for this compound that is formed when the chlorine atom bonds with trifluoroacetic acid. This chemical does not have any interactions with azide but can react with tetrazole to produce a stable compound, which can be easily</p>

<p>Piperazine-2-carboxylic acid methyl ester (PPCM) is a chemical compound that is used as an intermediate in the production of ethylenediamine and piperazine-2-carboxylic acid dihydrochloride. It is a white crystalline solid that can be synthesized by reacting ethylene diamine with piperazine-2-carboxylic acid. PPCM has been shown to inhibit the growth of bacteria, yeast, and fungi by inhibiting protein synthesis. This chemical also inhibits the production of proteins essential for respiration and cell wall formation.</p>

<p>Please enquire for more information about 1-Acetyl-4-(2,4-difluorobenzyl)piperazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Aminoorotic acid is an antimicrobial agent that has been shown to have anticancer activity. It has a nitrogen atom and two oxygen atoms in the molecule. The chemical structure of 5-aminoorotic acid can be determined using NMR spectroscopy and its biological properties are dependent on hydrogen bonding interactions with other molecules. 5-Aminoorotic acid is a chelate ring, which means it can bind to metal ions such as lanthanum (La3+). 5-Aminoorotic acid has been shown to inhibit the glycol oxidation reaction and may also be able to inhibit other enzymatic reactions. This drug is stable for use in model systems and may also be used for cancer treatment.</p>

<p>Please enquire for more information about N-Methyl-2-[[3-[(1e)-2-(2-pyridinyl)ethenyl]-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]thio]benzamide 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 Haloperidol nonanoate 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-(Benzyloxy)-6-oxo-1,6-dihydropyridine-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(3,4-Dichlorobenzyl)piperazine is an amine that is used as a reagent in organic synthesis. It is a buffered, acidic compound that emits fluorescence under UV light. It has been shown to be an electron donor and electron acceptor. 1-(3,4-Dichlorobenzyl)piperazine reacts with phenylpiperazines in the presence of acid to form a mixture of phenylpiperazines with different aliphatic chains. The reaction is characterized by emission of fluorescence that can be measured using spectroscopy techniques.</p>

<p>4-(Tributylstannyl)pyridazine is a heterocycle that can be used as an analog for pyridazine. It has been shown to have antimicrobial activity against bacteria and fungi, but not against viruses. 4-(Tributylstannyl)pyridazine is also a phosphoinositide analog, which has been shown to inhibit the synthesis of nucleic acids in cancer cells. This compound binds to the enzyme hydrazide reductase and inhibits energy metabolism through its inhibition of oxidative phosphorylation. 4-(Tributylstannyl)pyridazine also has a nitrogen atom, which may be responsible for its agrochemical properties.</p>

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

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<p>Please enquire for more information about 3-Ethyl haloperidol decanoate 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-(Pyridin-3-ylmethyl)piperazinetrihydrochloride 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-Isopropyl carvedilol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,6-Di(1H-pyrazol-1-yl)pyridine is a stable, crystalline compound that has been synthesized. It has been shown to form coordination complexes with metal ions, such as copper and zinc. The molecular structure of 2,6-Di(1H-pyrazol-1-yl)pyridine consists of a pyrazole ring, two amide groups and three nitrogen atoms. This molecule also possesses functional groups that can be found in chlorophyll A. 2,6-Di(1H-pyrazol-1-yl)pyridine is soluble in organic solvents such as alcohols and acetone. It is an orange solid at room temperature with a melting point of about 170°C. The UV absorption spectrum for 2,6-Di(1H-pyrazol-1-yl)pyridine shows strong absorption at 260 nm with an extinction coefficient of 12200 M</p>