Eterocicli con azoto (N)

<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>

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<p>3-Chloro-4-nitropyridine 1-oxide is the condensation product of 2-chloro-3-nitropyridine and nitric acid. 3-Chloro-4-nitropyridine 1-oxide has an isomeric nature and can be purified by recrystallization from water. The compound has a molecular weight of 286.1 g/mol and a monoclinic crystal structure. It has two n-oxides, which are isomers of each other, with nmr spectra that differ by the shift in the chemical shifts of the protons on the aromatic ring. 3-Chloro-4-nitropyridine 1-oxide condenses with lanthanides to form lanthanide complexes, such as Eu(III)(3,5'-ClO 4 ) 2 . This compound is also used in the synthesis of phenoxathiine derivatives that have antihypertensive activity.</p>

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

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<p>4-Pyridazinecarboxylic acid is a salt that contains sodium. It is a white crystalline solid that is soluble in water, ethanol, and acetone. It has been shown to be effective against Leishmania species and Cryptococcus neoformans. 4-Pyridazinecarboxylic acid inhibits the growth of these fungi by binding to their cell membrane and inhibiting protein synthesis. 4-Pyridazinecarboxylic acid forms coordination complexes with metal ions that are involved in electron transfer reactions during the oxidative phosphorylation process. This leads to a decrease in ATP production and an increase in reactive oxygen species (ROS), which disrupts the function of macrophages and other phagocytic cells, leading to immunosuppression.</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>Please enquire for more information about 3,5-Dimethylpyrazine-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>

1-(3-Bromophenyl)-piperazine is a furan compound with a piperazine base. It is used as an anti-cancer drug in the treatment of cancer and impurities are removed from this compound using chromatography. This compound has been shown to be homocoupled, which means that it can be used to synthesize other compounds. 1-(3-Bromophenyl)-piperazine is approved by the FDA and European Medicines Agency for the treatment of cancer, and has been shown to have immunological properties.

<p>Please enquire for more information about N,N-Dimethyl-2-(1-(1-(pyridin-2-yl)ethyl)-1H-inden-2-yl)ethan-1-amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Fluoro-3-nitropyridine is a reactive chemical that can react with alcohols, amines, and amino acids. It has been shown to have absorption spectra in the ultraviolet region of the light spectrum. 4-Fluoro-3-nitropyridine is also a pyridine derivative.</p>

<p>Please enquire for more information about 2-Methyl-5-(tributylstannyl)pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Imidazole is a highly polar aromatic compound with two annular nitrogen atoms. Imidazole is widely used in the affinity purification of proteins with polyhistidine tags (His-Tag). In the protein purification process, imidazole is used for the elution of His-Tag-fused recombinant proteins from a metal-immobilised resins. In the elution buffers, imidazole is typically used in the 50 – 500 mM concentration range (Bornhorst and Falke, 2000).</p>

<p>1-(2-Methylbenzyl)piperazine is a piperazine derivative that is used as a medicine. It has been shown to have an inhibitory effect on the reuptake of dopamine and noradrenaline, which are neurotransmitters that play an important role in the regulation of mood and behaviour. 1-(2-Methylbenzyl)piperazine has been shown to be effective in animal experiments. It was found to be toxic at high doses, but had low toxicity at low doses. It also showed no adverse effects on mating behaviour or fertility.</p>

<p>3,6-Dichloropyridazine is a chemical compound that belongs to the group of heterocycles. It is used as an intermediate for the production of other chemicals such as pharmaceuticals and pesticides. 3,6-Dichloropyridazine can be used in the treatment of inflammatory diseases by inhibiting cyclic nucleotide phosphodiesterase and preventing the accumulation of cyclic nucleotides. 3,6-Dichloropyridazine has been shown to inhibit cancer cells by binding to α7 nicotinic acetylcholine receptors in the cell membrane. The chlorine atom at position 3 on the pyridine ring is responsible for this effect. In addition, 3,6-dichloropyridazine has been shown to react with both nucleophilic and electrophilic groups. This chemical also displays a wide range of chemical diversity due to its three chlorine atoms.</p>

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<p>3-Tributylstannylpyridine (3-TBS) is a synthetic compound that is used in cross-coupling reactions to form carbon-carbon bonds. It reacts with unsaturated compounds and halides, providing nitrogen atoms in the final product. 3-TBS can be used for the synthesis of quinoxalines, which are chemical compounds that have been shown to have anti-inflammatory properties. The reaction of 3-TBS with chlorobenzene and chloride yields a phosphine and a tetrahydropyridine, which can be oxidized to form an N-(2,4,6-trichlorophenyl)pyridinium salt. This salt has been shown to have anti-inflammatory effects by inhibiting prostaglandin synthesis.</p>

<p>1-Benzyl-4-piperidinol is a n-hexane soluble synthetic compound. It has been shown to inhibit the cholesterol acyltransferase enzyme in rat liver microsomes, which is involved in the synthesis of cholesterol. 1-Benzyl-4-piperidinol can also be used for the treatment of cancers, such as prostate adenocarcinoma, due to its potent antagonistic activity against prostate cancer cells. This compound has also been shown to induce apoptosis in cancer cells and inhibit growth. The mechanism of action may be due to bond cleavage and inhibition of protein synthesis.</p>

<p>Please enquire for more information about 4-[4-(3-Chlorophenyl)piperazin-1-yl]-4-oxobutanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>7-Chlorothieno[3,2-B]pyridine is a nucleophilic compound that is used as an inhibitor of the tyrosine kinase enzyme. It binds to the ATP binding site and blocks the enzymatic activity of the enzyme, preventing cell proliferation. 7-Chlorothieno[3,2-B]pyridine has been shown to inhibit growth in tumour cell lines and has been shown to be effective against tyrosine kinase receptor positive cancer cells. This drug also shows a cytotoxic activity against tumour cells in vivo, which may be due to its ability to inhibit factor receptor and receptor tyrosine.</p>

Segetalin A trifluoroacetic acid is a protein-based product, which is a derivative of a natural compound isolated from the seeds of the plant Vaccaria segetalis. This plant is traditionally recognized for its medicinal properties, and segetalin A represents one of the active proteins responsible for these biological effects.

<p>Please enquire for more information about tert-Butyl 4-chloro-5,6-dihydropyrido[3,4-d]pyrimidine-7(8H)-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Anilino-1-benzylpiperidine is a synthetic opioid analgesic that is a prodrug of the active metabolite pethidine. It is an agonist at µ-opioid receptors and is used as an analgesic medication. 4-Anilino-1-benzylpiperidine has been shown to have a high affinity for the δ subtype of opioid receptor and also inhibits the reuptake of naloxone, which may be related to its antinociceptive effects. 4-Anilino-1-benzylpiperidine has been shown to be effective in humans when given in doses around 100mg. The drug binds to functional groups on proteins, such as serine hydroxyls and cysteine sulfhydryl groups, which may account for its efficacy in humans.</p>

<p>4-Methylpyridine is an antimicrobial agent that is used to inactivate viruses, bacteria, and fungi. It binds to the DNA of these microorganisms by intercalation and disrupts their replication process. 4-Methylpyridine has been shown to inhibit the growth of microorganisms by binding to the nitrogen atoms in their dna and preventing the synthesis of proteins required for cell division. This drug also inhibits the activity of polymerase chain reaction (PCR) enzymes such as Taq DNA polymerase and Klenow fragment. The molecular weight of this compound is 92.14 g/mol and its molar mass is 152.2 g/mol.</p>

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<p>2-Hydroxy-4-methylpyrimidine is a heterocyclic compound that is used in the synthesis of other heterocycles. It is prepared by the reaction of methylbenzene and nitrous acid, followed by hydrolysis to form an imine. This compound has been synthesized with various substituents at different positions on the ring and also as a series of homologues. The 2-hydroxy-4-methylpyrimidine molecule has four nitroso groups, which are substituted with methyl groups. X-ray crystallography studies have shown that the molecule can exist in two different forms: one with the methyl groups pointing "homotopically" towards each other and the other with them directed "heterotopically."</p>

<p>1-(4-Fluorobenzyl)piperazine is a potent tyrosinase inhibitor and has been shown to inhibit the proliferation of human cancer cells. It has been found to have inhibitory activity against the amine oxidase enzyme, which is involved in the biosynthesis of pro-inflammatory cytokines. The biochemical properties of 1-(4-fluorobenzyl)piperazine have been studied by liquid chromatography and mass spectrometry and it has been found to be synthesized from piperazine and an amine. There are no other studies available on this drug at this time.</p>

<p>1-(2-Phenylethyl)piperazine is a potential drug for the treatment of insulin resistance. It has been shown to increase insulin sensitivity in mice and humans, as measured by glucose uptake rates, pharmacokinetic properties, and insulin sensitivity. This compound may be used in combination with other drugs to treat cancer or skin conditions. 1-(2-Phenylethyl)piperazine has also been shown to bind to the aminophenyl receptor, which is a G protein-coupled receptor that is involved in cell proliferation and apoptosis. The aminophenyl receptor also binds to multidrugs such as HIV protease inhibitors (e.g., indinavir), which suggests that it may have antitumor effects.</p>

<p>3-Chloro-2-nitropyridine is a chemical compound that has been shown to have anticancer activity. It is a structural analog of the nucleophilic piperazine, which can react with hydrogen fluoride in an electrophilic substitution reaction to form 3-chloro-2-nitropyridine oxide. The anticancer activity of this compound may be due to its ability to inhibit the growth of tumor cells by binding to the d4 receptor, inhibiting the production of inflammatory cytokines and growth factors. 3-Chloro-2-nitropyridine has also been shown to have antiinflammatory activities, which may be due to its inhibition of nitric oxide synthesis and 5'-lipoxygenase.</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>

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<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>1-Butylpyridinium Chloride is an ionic liquid that is a colorless, water-soluble liquid. It has been reported to have detergent compositions and can be used as a solvent or cleaning agent. 1-Butylpyridinium chloride has been shown to have strong hydrogen bonding interactions with other molecules. It also exhibits electrochemical impedance spectroscopy, ft-ir spectroscopy, and thermal expansion properties.</p>

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<p>Please enquire for more information about 3-(4-Oxopiperidine-1-carbonyl)phenylboronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<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>

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<p>3-Hydroxyisoquinoline is a non-nucleoside inhibitor of cyclic nucleotide phosphodiesterase (cNMP) that is used in the treatment of nervous system diseases. 3-Hydroxyisoquinoline has been shown to have an inhibitory effect on cyclic nucleotide phosphodiesterase and can be used for the treatment of neurological disorders such as Parkinson’s disease, Alzheimer’s disease, and epilepsy. It also has anti-inflammatory properties and can be used to treat pain. 3-Hydroxyisoquinoline has a photoelectron spectrum that peaks at 5.6 eV, with a strong absorption band at 2.1 eV due to hydrogen bonding. This compound is also able to absorb radiation in the form of light emission with an emission peak at 4.8 eV, with a maximum intensity around 830 nm and a half-life of 0.2 s. 3-Hydroxyisoquinoline is able to</p>

<p>3-Hydroxy-1-methylpyridinium iodide is a solute that has a molecular weight of 183.12 and the chemical formula CHNO. It is synthesized by the reaction of hydrogen peroxide with pyridinium dichromate in the presence of vitamin B6. 3-Hydroxy-1-methylpyridinium iodide has been shown to be an effective probe for 13C NMR spectroscopy and can be used as a boronic ester with an electron withdrawing group. The synthesis of 3-hydroxy-1-methylpyridinium iodide may also include halides such as bromo or chloro compounds, which are added to increase the solubility of the product.</p>

<p>2-Benzylpiperidine is a reactive compound that has been shown to be active against pancreatic cancer cells. It binds to the pancreatic lipase receptor and inhibits its activity. 2-Benzylpiperidine is also able to inhibit the production of diacylglycerol, a molecule that is involved in inflammatory pain. This compound has an affinity for the receptor, which may be due to its similarity with saponins found in plants such as ginkgo biloba. The dry extract of this plant has been shown to have an inhibition potential on prostaglandin E2 levels, which are responsible for inflammation. 2-Benzylpiperidine can be used for palliative treatment of Alzheimer's disease by reducing amyloid beta plaque formation and preventing oxidative damage.</p>

4-Oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester is a white solid that is soluble in organic solvents and oils. It can be used as a source of lithium carbonate in alkaline solutions. 4-Oxo-3,4-dihydro-2H-pyridine-1 -carboxylic acid tert -butyl ester is typically used in the preparation of lithium carbonate from lithium hydroxide.

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