Heterocycles with Nitrogen (N)

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6-Bromo-2-oxindole is a crystalline compound with a molecular formula of C10H6BrO. It has been shown to have a high efficiency in the production of butyric acid and other organic acids. 6-Bromo-2-oxindole is also used in electron microscopy studies as an electron acceptor, and can be used for producing polymers with crystalline structures and dihedral angles. The compound has been shown to inhibit the growth of breast cancer cells by preventing the synthesis of mda-mb-231 breast cancer cells. It also has been shown to inhibit the production of isoindigo and morphology.

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3-Benzylpiperidine Hydrochloride is a competitive inhibitor of protein targets. It binds to the active site of the target protein, making it unable to bind with other proteins or molecules. 3-Benzylpiperidine Hydrochloride has been shown to inhibit the synthesis of DNA and RNA, and has also been shown to be effective in reducing tumour size in mice. 3-Benzylpiperidine Hydrochloride may have potential as a cancer treatment because it inhibits the growth of cancer cells by interfering with their metabolism. This molecule can be added as a supplement for strategies for cancer prevention and treatment. The hydrophobic nature of this molecule enables it to cross cell membranes, which makes it an ideal candidate for targeted drug delivery into cells. 3-Benzylpiperidine Hydrochloride interacts with human genome by binding to specific regions on the DNA strand, which indicates that this molecule may have therapeutic applications in humans.

4,4'-Dinitro-2,2'-bipyridine is a dihedral molecule that is used in biosensors to detect nitro compounds. It is synthesized by the reaction of osmium tetroxide with pyridine. The transfer of electrons from the pyridine ring to the osmium atom results in an oriented molecule with a positive charge on one end and a negative charge on the other end. This orientation can be reversed by oxidation. 4,4'-Dinitro-2,2'-bipyridine has been shown to react with monoalcohols and nucleophiles such as water to form covalent bonds. It also reacts with radiation, which may account for its use in dosimeters for measuring radiation exposure.

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6-Bromopyridin-2-ol is an isomeric organic compound that belongs to the group of triphenylphosphanes. It has a crystal x-ray diffraction pattern with a space group of P21/c and unit cell dimensions of a = 20.7, b = 23.1, c = 25.8 Å, β = 98.4°. 6-Bromopyridin-2-ol has been shown to react with 3-bromo-5-hydroxypyridine in the presence of light and heat to form 2-(3,5-dibromopyridin)-6-(hydroxymethyl)pyridine and 2-(3,5-dibromopyridin)-6-(methyloxymethyl)pyridine. These reactions are catalyzed by copper (II) acetate in acetic acid solution at room temperature or by naphthyl chloride

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Applications 2-Amino-4-chloro-5-nitropyridine (cas# 24484-96-6) is a compound useful in organic synthesis.

(1-Methylpiperidin-2-yl)methanol is a gaseous organic acid that belongs to the piperazine class of compounds. It is used as an intermediate in the synthesis of various pharmaceuticals, including antipsychotics and antidepressants. (1-Methylpiperidin-2-yl)methanol has been shown to be an agonist of ganglion cells and can be used for the treatment of glaucoma. This compound also has shown to have anti-inflammatory properties, which may be due to its ability to inhibit nitric oxide production. Furthermore, (1-methylpiperidin-2-yl)methanol has been shown to inhibit 13c nuclear magnetic resonance spectroscopy with epoxides and hydroxyl groups. The reaction product is a crystalline solid with a molecular formula of C6H14O3N2, which corresponds to the molecular formula of 2-(dimethylam

Applications 4-Iodopyrazole is used in the synthesis of (pyrazolyl)oxobenzocycloheptapyridinyl acetamides that act as inhibitors of c-Met. References Northrup, A. et al.: J. Med. Chem., 56, 2294 (2013);

7-[4-[4-(4-Fluorobenzoyl)Piperidin-1-Yl]Butyl]-1,3-Dimethylpurine-2,6-Dione is a drug that belongs to the group of adenosine receptor antagonists. It has been shown to inhibit phosphodiesterase activity and is used as a pharmaceutical dosage. 7-[4-[4-(4-Fluorobenzoyl)Piperidin-1-Yl]Butyl]-1,3-Dimethylpurine-2,6-Dione has been shown to bind to the 5HT2C receptor in vitro. This drug may have therapeutic potential for obesity and type 2 diabetes mellitus treatment.

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N-(3-Chloropropyl)piperidineHydrochloride is a hydrochloric acid solution, which is an alkali and a strong base. It is used as a catalyst in organic syntheses by converting hexahydropyridine to tetrahydrofuran. Its reaction system includes triethylamine and an organic solvent such as tetrahydrofuran. The efficiency of the reaction depends on the condition of the reaction system, such as pH and temperature.

4-Amino-6-bromoindole is a potent and selective antagonist of the 5-HT6 receptor, which is a subtype of serotonin receptor. It has been shown to bind with high affinity to this receptor in both rat and human brain tissue. 4-Amino-6-bromoindole has been synthesised by medicinal chemistry methods and has been shown to block the effects of scopolamine in animal models. 4-Amino-6-bromoindole has also shown promise as a potential treatment for schizophrenia, depression, anxiety disorders, and other psychiatric disorders.

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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.

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1-(4-Bromophenyl)piperazine is a chemical that is used in the synthesis of pharmaceuticals, such as antidepressants. It has been shown to inhibit monoamine neurotransmitter reuptake, including serotonin and dopamine. It also has an inhibitory effect on 5-hydroxytryptamine (5HT) release from nerve terminals and its binding to the 5HT7 receptor. 1-(4-Bromophenyl)piperazine can be used in chromatographic methods for validation of impurities, potential impurities, and other substances.

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7-Ethyl-10-(4-N-aminopentanoic acid)-1-piperidino)carbonyloxycamptothecin hydrochloride is a carbamate that has been shown to have hypnotic properties in animal models. It is metabolized by esterases to formic acid, which can cause hypersomnia, apnea, and acidosis. The solvated form of the drug has shown to be more potent than the nonsolvated form at inhibiting animal behavior. 7-Ethyl-10-(4-N-aminopentanoic acid)-1-piperidino)carbonyloxycamptothecin hydrochloride is also used as a prodrug for the synthesis of other drugs with anticancer activity.

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1-(3-Aminopropyl)pyridin-2(1H)-one HCl is a fine chemical that belongs to the group of heterocyclic compounds. It is a versatile building block that can be used as an intermediate or a scaffold in chemical synthesis. 1-(3-Aminopropyl)pyridin-2(1H)-one HCl is soluble in water and has been shown to react with a variety of other compounds, including amines, alcohols, thiols, and phenols. This compound also has high quality and can be used for research purposes.

2,6-Dibromopyrazine is a quinoxaline molecule with two nitrogen atoms. It is an electropolymerizable material that can be used to create patterned surfaces. 2,6-Dibromopyrazine has been used in the fabrication of devices such as fluorescent lamps and light emitting diodes (LEDs). The fluorescence of these devices depends on the alignment of molecules within the device. The number and position of nitrogen atoms in the molecule determine the wavelength emission. 2,6-Dibromopyrazine is a structural isomer of 1,8-dibromopyrazine. 2,6-Dibromopyrazine has homologues such as anilines and amines that have been used in organic synthesis for decades.

4-Pyridylhydrazine HCl is a bactericidal antibiotic that has been shown to be effective against a wide range of bacteria, including staphylococcus, escherichia, and candida. 4-Pyridylhydrazine HCl inhibits the synthesis of proteins in bacteria by blocking amino acid synthesis at the ribosome level. This antibiotic also has an antimicrobial effect on yeast and fungi. 4-Pyridylhydrazine HCl blocks cross-coupling reaction in bacterial cells by competing with benzyl for the cyano group in the reaction and preventing formation of the pyridinium salt intermediate. The drug is not active against Gram-negative bacteria such as E. coli or Pseudomonas aeruginosa due to its inability to penetrate these cells.

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5-Methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]thio]-1H-benzimidazole N-oxide is a sulfoxide that belongs to the family of medicines called proton pump inhibitors. It is a stereoselective proton pump inhibitor due to its cyclic nature and has been used as a pharmaceutical preparation for the treatment of gastroesophageal reflux disease. 5-Methoxy-2-[(4-methoxy-3,5-dimethylpyridinium) methylthio]-1H benzimidazole N oxide has been shown to be an enantiomerically pure salt form with magnesium chloride.

1-(Phenylacetyl)piperazine (1PAP) is a non-peptide ligand that activates the thrombin receptor. It binds to the peptide binding site on the receptor and increases the affinity of 1PAP for the thrombin receptor by 2 orders of magnitude. This leads to disruption of platelet function, which can lead to thrombus formation. 1PAP has been shown to have antiplatelet activity in vivo and in vitro, which could be due to its ability to activate the thrombin receptor.

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Ethyl 4-amino-2-hydroxypyrimidine-5-carboxylate (EAHPC) is an enzyme hydrolysis product that is metabolically converted to ethyl pyrimidine carboxylate (EPC). EAHPC is a germ cell mutagen and may be a carcinogen. It has been shown to cause chromosome damage in spermatocytes and the subsequent production of germ cells with chromosomal aberrations. EAHPC has low activity as a mutagen, but it can have a maximal effect on the induction of mutations. The mechanism by which EAHPC causes these effects is not well understood.

2-Chloro-5-hydroxymethylpyridine is a metabolite of the active substance 2-chloro-5,6-dihydroxymethylpyridine (mk-0674), which has been shown to inhibit cytochrome P450 enzymes. It is found in urine samples from patients treated with mk-0674 and can be used to monitor the efficacy of treatment. The biochemical properties of 2-chloro-5,6-dihydroxymethylpyridine have been studied in yeast cells and it has been shown that this compound is glucuronidated and excreted as a conjugate with glycine. The yeast strain Saccharomyces cerevisiae was used for these studies.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

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2-Chloro-3-methyl-5-nitropyridine is a crystalline solid with an isomeric composition. It is a monomer that has optical properties. The potassium salt of 2-chloro-3-methyl-5-nitropyridine can be obtained by reacting the sodium salt with potassium hydroxide. 2CMP is used as an intermediate in the production of biphenyl, which is used to make optical films and lenses. The sodium salt of 2CMP can be obtained by reacting the potassium salt with sodium carbonate or sodium bicarbonate.

Ethyl-4-methylpyrimidine-5-carboxylate is a pyrimidine derivative that is used to synthesize other compounds. It has been shown to react with hydrochlorides in the presence of a base to form mixtures. The reaction mechanism is not known, but it may involve nucleophilic attack by the chloride ion on the carboxyl group. Ethyl-4-methylpyrimidine-5-carboxylate could also react with hydrochlorides in water to form mixtures. This reaction is reversible and results in the formation of ethyl 4,5-dimethylpyrimidine-2,6(3H,7H)-dicarboxylate. Ethyl 4,5-dimethylpyrimidine 2,6(3H,7H)-dicarboxylate can also be formed by reacting ethyl 4,5-dimethylpyrimidine 5-carboxylate with hydrochlor

2,4,6,8-Tetrachloropyrimido[5,4-d]pyrimidine is a pyrimidine compound that has been shown to inhibit amine oxidase. The pharmacokinetic properties of this drug have been studied in rats and dogs. It was found that the plasma levels of 2,4,6,8-tetrachloropyrimido[5,4-d]pyrimidine are proportional to the dose given. This drug is metabolized by hydrolysis in the liver to an inactive form that is excreted through urine. 2,4,6,8-Tetrachloropyrimido[5,4-d]pyrmido[1′,-2′:1″,-3″]pyrimidine also inhibits the enzyme α1 acid glycoprotein and has been shown to be effective against some strains of methicillin resistant Staphylococcus aureus (MR

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Applications 2,3-Dimethyl-5H,6H,7H,8H-imidazo[1,2-a]pyrazine is used in the preparation of a pluripotent stem cell inhibitor. References Furukawa, Yusuke. et al., Jichi Medical University(2019);

N-(2,6-Dimethylphenyl)-1-piperazineacetamide is a byproduct of solvents and stabilizers. It has been found to be a crystalline solid with a molecular weight of 233.3 g/mol. The crystal structure was determined and found to be composed of two molecules of acetamide that are connected through hydrogen bonds. N-(2,6-Dimethylphenyl)-1-piperazineacetamide is soluble in ethanol and ether, but insoluble in water. This compound interacts with other substances, such as recrystallizing or substituting acetamides.

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(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.

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2-Bromo-4-chloropyridine is a 4-chloropyridine derivative with the chemical structure of a heterocyclic amine. It has been synthesised as an analog of 2,4,6-trimethylaniline to explore its pharmacological effect. 2-Bromo-4-chloropyridine has been shown to have a bladder carcinogenic effect in animals. The compound was evaluated for its potential to cause bladder cancer in humans by determining the concentration of the compound in human urine following oral administration and by measuring the frequency of bladder tumors in rats. It has also been found that 2-bromo-4-chloropyridine inhibits serotonin receptors (5HT2C) and dopamine receptors (D2).