Heterocycles with Nitrogen (N)

<p>1-[[2-(4-Chlorophenyl)-4,4-dimethylcyclohex-1-enyl]methyl]piperazine is a high quality compound that can be used as a reagent or intermediate. It is a complex compound with the CAS No. 1228780-72-0 that is useful in the production of fine chemicals, research chemicals and speciality chemicals. 1-[2-(4-Chlorophenyl)-4,4-dimethylcyclohex-1-enyl]methyl]piperazine is a versatile building block that can be used in reactions to produce specialized products such as pharmaceuticals, agrochemicals, dyes and fragrances.</p>

<p>5-Methoxy-3-(1,2,5,6-tetrahydro-4-pyridinyl)-1H-indole hemisuccinate is a serotonin receptor agonist that has been shown to stimulate the 5HT1A receptor. It stimulates insulin secretion and glucose uptake in rats and inhibits feeding behavior in mice. It has also been shown to have antihypertensive effects on rats by blocking the 5HT2 receptors. In addition, it stimulates regeneration of injured nerve cells. This drug has potential uses as a treatment for neurological diseases such as Parkinson's disease and depression.</p>

<p>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.</p>

<p>2,3,3-Trimethyl-3H-benzo[e]indole is a reactive molecule that has been shown to be an effective treatment for cervical cancer. It can be used in conjunction with monoclonal antibodies that have been designed to target the acidic protonation sites on the surface of cervical cancer cells. This active form binds to the site and emits fluorescence when illuminated with a laser, which can then be detected by a confocal microscope. This technique can also be used for the diagnosis of other cancers. 2,3,3-Trimethyl-3H-benzo[e]indole is not toxic to human serum as it does not react with this type of tissue.</p>

<p>2-Mercapto-1H-imidazole is an irreversible inhibitor of xanthine oxidase. It binds to the nitrogen atoms of the enzyme's active site and forms a strong hydrogen bond with the oxygen atom of the xanthine substrate. The steric interactions between 2-mercapto-1H-imidazole and the substrate prevent binding and catalysis. The crystal structures of 2-mercapto-1H-imidazole in complex with xanthine oxidase have been determined using X-ray crystallography. FTIR spectroscopy has shown that 2-mercapto-1H-imidazole coordinates in a geometry similar to that of the reactant, hydrochloric acid. Electrochemical impedance spectroscopy (EIS) has revealed that proton transfer takes place when 2-mercapto-1H imidazole binds to xanthine oxidase, which is consistent with reaction mechanism involving elect</p>

<p>2-(2,6-Dioxo-piperidin-3-yl)-4-fluoroisoindoline-1,3-dione (2,6DPI) is a synthetic chemical compound that has been shown to inhibit NF-κB activation in vitro. 2,6DPI is a competitive inhibitor of the p65 subunit of NF-κB and functions by binding to the cysteine residue on the p65 subunit. It has been shown to be effective against inflammatory diseases such as pulmonary disease and inflammation. This drug also inhibits deacetylases, which are enzymes involved in regulating gene expression. 2,6DPI may have therapeutic potential for the treatment of inflammatory diseases and cancer.</p>

<p>1-Allylpiperazine is a synthetic molecule that has affinity values for the binding sites of 4-hydroxy-3-nitrophenylacetic acid and zearalenone. It has been shown to have anticancer activity in vitro, as well as antiadrenergic effects by acting as a competitive antagonist at adrenergic receptors. This compound also has potential use as a template molecule for the design of novel drugs with anticancer and antiadrenergic activity. 1-Allylpiperazine is synthesized from the monomers trimethylolpropane and piperazine in two steps. It is also known to be an inhibitor of cellular protein synthesis.</p>

<p>6-Ethylmercaptopurine is a purine analogue that inhibits the synthesis of DNA. It is used as an inhibitor of protein synthesis and in the treatment of inflammatory bowel disease. 6-Ethylmercaptopurine has been shown to inhibit the activity of ATPase, which may be responsible for its ability to suppress the proliferation of cells. This drug can also act as an analog to adenosine, which can be used to determine ATP levels in a cell or tissue sample by measuring the amount of p-nitrophenyl phosphate produced. 6-Ethylmercaptopurine has been shown to block phosphatase activity, which may lead to inflammation in some cases.<br>6-Ethylmercaptopurine has a molecular weight of 194.2 g/mol and an optimum pH of 4.5</p>

<p>2-Bromo-1H-imidazole is an environmental pollutant that has been detected in the atmosphere, water, and soil. It is used as a pesticide and has been found to be an impurity in biphenyl. 2-Bromo-1H-imidazole can be used as a substrate for the Suzuki coupling reaction or as a starting material for the synthesis of imidazole derivatives. The compound spontaneously fragments under acidic conditions to form nitric acid and hydrogen bromide. 2-Bromo-1H-imidazole has been shown to inhibit hepatitis C virus (HCV) replication and induce cancer cell apoptosis in vitro.<br>2-Bromo-1H-imidazole is also known to cause DNA fragmentation in cells through oxidation by reactive oxygen species or through spontaneous decomposition of the molecule into acid, bromine radicals, and ammonia.</p>

<p>1-(1-Naphthyl)piperazine hydrochloride is a 5-HT3 receptor antagonist that has been shown to act as a potent serotonergic agent in the central nervous system of mammals. It is believed to inhibit the presynaptic serotonin uptake, resulting in an increase of serotonin concentration at the postsynaptic 5-HT1A receptor cells. 1-(1-Naphthyl)piperazine hydrochloride has also been shown to be a potent 5-HT1A receptor agonist and has antinociceptive effects following administration. This drug has been found to be more selective for the peripheral nervous system than other drugs of this type. It does not cross the blood-brain barrier and therefore does not interfere with mental function or behavior.</p>

<p>[(3S,4R)-4-(4-Fluorophenyl)-3-piperidinyl]methanol is a chemical with the molecular formula C10H17FN2O. It is a versatile building block that can be used as an intermediate in organic synthesis, or in the synthesis of complex compounds such as pharmaceuticals. This product has been shown to have high quality and is a useful reagent in research.</p>

<p>6-Bromo-2-(4-bromophenyl)-indole is a fine chemical with CAS No. 28718-96-9 that can be used as a versatile building block for the synthesis of complex compounds, useful scaffold for research chemicals, and reaction component for speciality chemicals. This compound has high quality and is a reagent in the synthesis of other compounds.</p>

<p>Please enquire for more information about 5,6,7,7a-Tetrahydrothieno[3,2-c]pyridine-2(4H)-onepara-toluenesulfonic acidsalt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methylimidazole is a crystalline solid that has been used in the preparation of coordination compounds. The compound is prepared by reacting 2-methylimidazole with an appropriate metal cyanide, such as copper cyanide or nickel cyanide. The crystal structure of 2-methylimidazole shows strong hydrogen bonding interaction between the nitrogen atoms and the carboxylate groups. This compound has been used in clinical pathology to detect increased levels of ammonia, uric acid, and lactic acid in the blood. 2-Methylimidazole is not toxic to humans but has shown some toxicity to mice when injected intravenously at high concentrations. It can be used as an analytical method for determining trace amounts of chlorine in chemical compounds by way of electrochemical impedance spectroscopy (EIS).</p>

<p>3-Cyano-2-hydroxypyridine is an inhibitor of the noradrenaline transporter, which is a type of l-type calcium channel. 3-Cyano-2-hydroxypyridine has been shown to be a potent inhibitor of the noradrenaline transporter. It inhibits the binding of neurotransmitters to their receptors by blocking active methylene sites on the transporter molecule. This drug also has a cavity that can accommodate bulky inhibitor molecules, making it more difficult for these inhibitors to bind to the active site and compete with neurotransmitters for uptake. 3Cyano-2-hydroxypyridine also inhibits nitric oxide synthase, which may provide anti-tumor activity as well as inhibit tumor cell growth. The inhibitory effect of this drug is due to structural studies that have revealed hydrogen bonding interactions with the drug's nitrogen and oxygen atoms.</p>

<p>Methyl 3-cyano-1H-indole-7-carboxylate is a fine chemical that belongs to the class of useful scaffolds, versatile building blocks, and useful intermediates. It is used as a research chemical and a reaction component. Methyl 3-cyano-1H-indole-7-carboxylate is also a speciality chemical with high quality and can be used as a reagent in the production of other compounds.</p>

<p>6-Amino-2-pyrazinecarboxylic acid is a high quality reagent that is used as an intermediate for the synthesis of complex compounds. It is also a useful scaffold for the production of valuable speciality chemicals. This chemical is also used as a reaction component in research and development to produce versatile building blocks. 6-Amino-2-pyrazinecarboxylic acid has been shown to be useful for producing fine chemicals and speciality chemicals, which are often used in many industries.</p>

<p>2-[(4-Chlorophenyl)-2-pyridinylmethoxy]-N,N-dimethylethanamine maleate salt (DCLM) is a controlled-release preparation of an antihistamine that is used for the relief of allergic symptoms. It is a prodrug that is hydrolyzed to 2-[(4-chlorophenyl)-2-pyridinylmethoxy]ethanol (DCPEM) in vivo. DCLM has been shown to be effective against viruses and has been found to have receptor activity in human serum. The drug can be administered either orally or by injection. DCLM has also been shown to suppress allergic symptoms in vitro with LC-MS/MS analysis.</p>

<p>4-Amino-pyridine-2-carboxylic acid methyl ester is a compound that is used as a reactant, reagent, and building block in organic synthesis. It is also useful for the preparation of complex compounds. 4-Amino-pyridine-2-carboxylic acid methyl ester is soluble in water and has a melting point of 183°C. The CAS number for this chemical is 71469-93-7.</p>

<p>5-Chloro-8-iodoimidazo[1,2-a]pyridine HBr is a fine chemical that can be used as a versatile building block in the synthesis of complex compounds. This chemical is also useful as a reagent or speciality chemical for research purposes. This product has been shown to have high quality and is an efficient reaction component for organic synthesis. 5-Chloro-8-iodoimidazo[1,2-a]pyridine HBr has CAS No. 1031289-77-6 and is a useful scaffold for the preparation of other compounds.</p>