Heterocycles with Nitrogen (N)

<p>Please enquire for more information about 2-(3-Methoxyphenyl)piperidine 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 7-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Benzyl-4-piperidine-carboxaldehyde is a polymorphic compound with two crystalline forms: the α form and β form. The α form has a molecular weight of 174.2 g/mol and the β form has a molecular weight of 178.3 g/mol. Both forms are soluble in organic solvents but not in water. It is insoluble in hydrochloric acid, n-hexane, and acetonitrile. It is stable at room temperature but unstable at temperatures above 60°C. 1-Benzyl-4-piperidinecarboxaldehyde is an inhibitor of liver function, which may be due to its inhibition of CYP450 enzymes or other unknown mechanisms that lead to haemodynamic effects such as hypotension and tachycardia.</p>

<p>Please enquire for more information about tert-Butyl 6-(aminomethyl)-1,4-oxazepane-4-carboxylate 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 2-Amino-4-(cyclopropyl)pyrimidine 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-(3-Isobutoxybenzyl)piperazine 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 4-(2-Chloro-4-nitrophenyl)piperazine-1-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Amino-5-bromopyridine (3ABP) is a linker for the synthesis of cisplatin. It has been shown to have strong bactericidal activity against Escherichia coli and Staphylococcus aureus. 3ABP is cytotoxic to both renal proximal tubule cells and ring-opening cells, which are found in the kidney. It is also an inhibitor of nicotinic acetylcholine receptors (nAChRs), which are proteins that control nerve cell communication. 3ABP's pharmacokinetic properties make it suitable as a linker for cisplatin, as it has good oral bioavailability, low systemic toxicity, and high tissue selectivity.</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>Racemic cis-1-benzyl-2-methyl-4-(N-propananilido)piperidine (SBP) is a synthetic opioid analgesic that has been shown to bind to the μ-opioid receptor. It is the racemic form of the more potent S(+)-isomer. SBP is metabolized in vivo by cytochrome P450 2C19 and cytochrome P450 3A5, and its metabolites can be detected in human liver. The metabolism of SBP also produces propanamide as an intermediate. Recreational use of SBP has been reported with adverse effects including nausea, vomiting, headache, and dizziness.</p>

<p>Please enquire for more information about 1-[4-(4-bromophenyl)piperazin-1-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 trans-1-Boc-4-amino-piperidine-3-carboxylic acid ethyl ester 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 Apixaban-d3 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 4-​Hydroxy-​7-​methoxy-6-​quinolinecarboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Piperazine monohydrochloride is a white crystalline powder that is soluble in water and ethanol. It has a molecular weight of 208.23 and a melting point of 117-119°C. Piperazine monohydrochloride exhibits anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis.</p>

<p>Please enquire for more information about 3-Fluoro-2-(tributylstannyl)pyridine 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 4-(Diphenylmethoxy)piperidinium chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(3,5-Dimethoxyphenyl)piperazine (1DMPP) is a phenylpiperazine derivative that has shown anticancer activity in vitro against human cancer cells. It is orally bioavailable and has been found to inhibit the growth of cancer cells in vivo. 1DMPP is metabolized by the liver into a number of metabolites that are excreted via the kidneys. The pharmacokinetic properties of 1DMPP have been studied in rats and mice, which revealed that it is well absorbed when administered orally and has a short terminal half-life. In vitro studies have demonstrated that 1DMPP inhibits cell growth through inhibition of protein synthesis and DNA replication.</p>

<p>Please enquire for more information about tert-Butyl 4-(5-nitro-2-oxo-1,3-benzoxazol-3(2H)-yl)piperidine-1-carboxylate 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 4,4'-Dithio-2,2'-bipyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>Please enquire for more information about [4-(3,6-Dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ciprofloxacin is a fluoroquinolone antibiotic with potent activity against many Gram-negative and Gram-positive bacteria. It is used in the treatment of urinary tract infections, respiratory tract infections, skin and soft tissue infections, bone and joint infections, and intra-abdominal infections. Ciprofloxacin piperazinyl-N4-sulfate has the potential to interact with other drugs. It binds to human serum albumin (HSA) and may be excreted into breast milk. The drug is well absorbed orally but has poor bioavailability due to rapid metabolism by the liver. Ciprofloxacin piperazinyl-N4-sulfate has been shown to have pharmacokinetic properties that are independent of dose or duration of administration.</p>

<p>2-Cyano-5-fluoropyridine is a potential antitubercular agent that has shown penetrability in the central nervous system and activity against Mycobacterium tuberculosis. It is orally active at low doses, and has been shown to be an effective inhibitor of mycobacterial growth and lipid synthesis. In addition, this compound also has antimycobacterial activity against M. avium complex and M. ulcerans, and is a potent inhibitor of β-amyloid aggregation.</p>

<p>Please enquire for more information about 1-(3-Methoxyphenyl)piperazine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Ethynylpyridine is a yellow solid that is soluble in most organic solvents. It has been shown to be an inhibitor of Cox-2, which is a pro-inflammatory enzyme. 4-Ethynylpyridine also inhibits the production of nitric oxide by inhibiting the enzyme inducible nitric oxide synthase (iNOS). This compound also has high cytotoxicity and can be used for photodynamic therapy. The chemical structure of 4-ethynylpyridine is composed of nitrogen atoms, carbon atoms, and hydrogen atoms. 4-Ethynylpyridine forms a complex with 2-phenylbutyric acid through electrochemical studies, which is important for its pharmacological properties.</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>Please enquire for more information about 1-(5-Chloro-2-methoxybenzyl)piperazine 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 4-Hydroxy-N-(2-Piperidinylmethyl)-2,5-Bis(2,2,2-Trifluoroethoxy)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 S-Desmethyl-S-(2-hydroxy-2-methylpropyl) rosuvastatin calcium 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 3-Ethyl 5-methyl 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-6-methylpyridine-3,5-dicarboxylate 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 4-(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>

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

<p>1-(3-Trifluoromethylphenyl)piperazine hydrochloride (TFMPP) is a derivative of the piperazine class of drugs. It is structurally similar to other drugs in this class, such as bromopropane, which acts as an agonist of the 5-HT1 receptor. TFMPP has been shown to be an agonist at 5-HT1 receptors and dopamine receptors. It has also been shown to inhibit serotonin uptake and release, and inhibits choline acetyltransferase activity in brain tissue. TFMPP is not active on the 5-HT2 receptor, but does have some affinity for the 5-HT2A receptor. TFMPP has high affinity for the serotonergic system, with selective binding to serotonin transporter proteins in vitro. TFMPP may also have some effect on cholinergic systems through its inhibition of acetylcholinesterase activity.</p>

<p>4-Dimethylaminopyridinium Bromide Perbromide is a synthetic compound that contains a phenolic hydroxyl group. It reacts with chloride to form the perbromide salt, which is anhydrous and insoluble in water. The compound has been shown to inhibit the growth of cancer cells by interfering with DNA replication and transcription.</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>Please enquire for more information about 1-(4-Fluorobenzoyl)piperidin-4-one 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 {2-[(4-Phenylpiperazin-1-yl)carbonyl]phenyl}amine 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 2-Chloro-5-(trifluoromethyl)pyridin-4-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Acetylimidazole is a drug that belongs to the class of glycol esters. It is an inhibitor of the enzyme acetylcholinesterase and has been used in the treatment of autoimmune diseases, such as myasthenia gravis. N-Acetylimidazole can inhibit the activity of other enzymes, such as p-nitrophenyl phosphate oxidase, which may be responsible for its anti-inflammatory properties. This drug has been shown to inhibit microbial growth in vitro by inhibiting the synthesis of choline and acetylcholine in the body. N-Acetylimidazole also inhibits bacterial growth by acting as a substrate molecule for bacterial enzymes that catalyze transfer reactions, including phosphotransferases and hydrolases.</p>

<p>Fidovirsen is a nucleoside analogue that is an inhibitor of the NS3 protease of hepatitis C virus (HCV). Fidovirsen binds to the active site of the NS3 protease and prevents cleavage at the NS3/4A interface, thus inhibiting viral replication. It has been shown to be effective in clinical studies involving human liver samples. Fidovirsen has also been shown to have antiviral activity against other RNA viruses, including HIV-1 and influenza A virus. Fidovirsen has a low toxicity profile and does not exhibit cross-resistance with other antiviral drugs. The drug is being developed as a potential therapy for chronic HCV infection.</p>

<p>6-Bromopyridine-3-carboxaldehyde (6-BPAR) is a synthetic compound that binds to copper ions and has been shown to have inhibitory activities against trifluoroacetic acid, calcium carbonate, optical properties, and low energy. 6-BPAR also has an aldehyde group and hydroxamic acid group. This chemical can be used as a catalyst for the hydrogenation reduction of metal ions such as chloride or formyl groups.</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>Please enquire for more information about Perindopril diketopiperazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Pyrroloquinoline quinones are a class of naturally occurring bioactive natural products that have been isolated from plants and fungi. Pyrroloquinoline quinone is an important intermediate in the synthesis of many other biologically active natural products. The pyrrole ring is synthesized by two different methods: (1) the oxidation of 2-pyridone, or (2) the reaction of methyl 4-hydroxypyrimidine-2-carboxylate with methylamine. Synthesis can be accomplished through a number of synthetic strategies, including bioorganic chemistry, organic chemistry, and synthetic strategies. The mechanisms for each step in the synthesis are discussed in detail below.</p>

<p>Please enquire for more information about Cinidon ethyl including the price, delivery time and more detailed product information at the technical inquiry form on this page</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-Diphenylphosphino-6-methylpyridine is a luminescent phosphor with aryl substituents. It has been shown to emit light in the near-infrared region of the spectrum, which can be used for devices such as night lights. The compound has two isomers that differ in the position of the methyl group on the pyridine ring. Although it has not been studied systematically, it appears that one isomer has better photophysical properties than the other. This compound also shows chloride ion binding and changes its emission properties when exposed to temperatures above 300 K.</p>

<p>2-(trifluoromethyl)pyridin-3-amine is an industrial chemical that is used as a reagent in the synthesis of other chemicals. It is synthesized from benzene and an acid ethyl ester in a complex reaction. 2-(trifluoromethyl)pyridin-3-amine is toxic, with industrial uses such as the synthesis of dyes and pesticides.</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>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>Please enquire for more information about 5-Nitropyridin-3-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>a-Butylpiperonyl alcohol is a chiral molecule that is used in the synthesis of esters. It can be produced by microbial fermentation and low-temperature chemical reactions. This compound has been shown to inhibit the growth of Gram-positive bacteria, such as Staphylococcus aureus and Streptococcus pneumoniae. The biosynthetic pathway for a-butylpiperonyl alcohol is not yet well understood, but it has been hypothesized that this compound is synthesized from an intermediate, acetic acid. The enzyme responsible for this conversion is unknown, but it may be catalysed by an acylase or acetate kinase. A study on the genome sequence of Coelicolor revealed that this organism produces a-butylpiperonyl alcohol from the intermediate 3-hydroxypropanoic acid.</p>

<p>1,1'-Dimethyl-4,4'-bipyridinium dichloride hydrate is a bipyridine with a divalent chloride. It has been shown to have synergic effects in the presence of dextran sulfate and paraquat. This compound has good photochemical properties, which are used for wastewater treatment and surface methodology. 1,1'-Dimethyl-4,4'-bipyridinium dichloride hydrate also has toxicological studies that show it does not cause any cellular toxicity or mitochondrial membrane potential changes. It also reduces potassium dichromate toxicity in glomerular filtration rate studies. This compound can be used as an analytical method for other bipyridines.</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>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>

<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>

<p>Fluoxetine is a potent inhibitor of the enzyme cytochrome P450 (CYP) 2C19. The inhibition of CYP2C19 by fluoxetine may lead to an increase in the plasma concentration of other drugs that are metabolized by this enzyme, such as glipizide and hydroxycyclohexyl. Fluoxetine inhibits human uric acid secretion and increases plasma concentrations of uric acid. This drug also inhibits human erythrocyte dihydropyrimidine dehydrogenase, leading to increased blood levels of pyrimidines, especially cytotoxic ones like 6-fluoro-3-indoxyl-beta-D-galactopyranoside. Fluoxetine has been shown to have a protective effect against acetaminophen toxicity in rats because it enhances the conversion of acetaminophen to its less toxic metabolite N-acetylcysteine.</p>

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

<p>1-Isobutylpiperazine is a synthetic amino acid that has been shown to have anticancer, antiviral, and anti-inflammatory properties. It is an inhibitor of the enzyme sulfatase, which is responsible for the degradation of sulfated glycosaminoglycans in the body. 1-Isobutylpiperazine has also been shown to be effective in treating heart disease and aminophenyl (AP) toxicity. AP overdose can lead to severe muscle spasms and seizures. 1-Isobutylpiperazine prevents AP from binding to sulfamate receptors on cells, which prevents cell death. Treatment with 1-isobutylpiperazine also reduces inflammation by inhibiting inflammatory cytokines such as tumor necrosis factor alpha (TNFα) and interleukin-1β (IL-1β). This drug also has potential use in treating autoimmune diseases or infectious diseases by modulating the immune system.</p>

<p>Please enquire for more information about 2-Iodo-5-methylpyrimidine 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 (3R,4R)-1-((2S)-2-Benzyl-2-carboxyethyl)-4-(3-hydroxyphenyl)-3,4-dimethylpiperidine 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 N-(4-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-2-yl)pivalamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>

<p>Please enquire for more information about N-Pyrazinylcarbonyl-L-phenylalanine methyl ester 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 (NZ)-4-chloro-N-[1-[2-(4-nitrophenyl)ethyl]piperidin-2-ylidene]benzenesulfonamide 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 Queuine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,5-Diaminopyridine dihydrochloride is a compound that belongs to the class of hydroxamic acids. It is an intermediate in the synthesis of the anti-cancer drug, hydroxyurea (hydroxylamine). 2,5-Diaminopyridine dihydrochloride can be used as a cross-coupling reagent for coupling reactions with chlorinated and tritiated organic compounds. The efficiency of this reaction is dependent on the coulombic and mutagenic properties of 2,5-diaminopyridine dihydrochloride. 2,5-Diaminopyridine dihydrochloride has been shown to cause cancer in animal studies.</p>

<p>3-Acetyl-6-methylpyridine is a chemical compound that has been found to have antibacterial properties. It can be used for the treatment of bacteria in wastewater and other biological treatments. 3-Acetyl-6-methylpyridine is insoluble at room temperature, but becomes soluble when heated to 100 degrees Celsius. This chemical compound has been shown to inhibit the growth of Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli. 3-Acetyl-6-methylpyridine also has anti-inflammatory properties and can be used in the treatment of Alzheimer's disease.</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>1-(4-Aminophenyl)-1H-pyridin-2-one is a synthetic chemical that is used in the manufacturing of 8-hydroxyquinoline. It is an industrial chemical that is used to produce potassium carbonate by a reflux reaction with potassium and carbonate. 1-(4-Aminophenyl)-1H-pyridin-2-one is a gas at room temperature and pressure and has been shown to be stable under these conditions.</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>2,3-Difluoro pyridine is an organic compound with the chemical formula C6H3F2N. It is a colorless liquid that has a strong odor and a boiling point of 147°C. 2,3-Difluoro pyridine has antibacterial properties and can be used to treat bacterial infections by inhibiting the synthesis of proteins in bacterial cells. This inhibition prevents the formation of new cell walls, which leads to cell death. 2,3-Difluoro pyridine is also used as an intermediate in organic chemistry reactions involving hydrogen fluoride. The transport properties of this compound are low due to its high melting point and low solubility in water. There are three different polymorphs for 2,3-difluoropyridine: form II, form III and form IV, with form II being the most common. Form II has a trigonal planar molecular geometry, whereas forms III and IV have tetragonal</p>

<p>3-Vinylpyridine, also known as vinylpyridine, is a colorless, crystalline solid that forms hydroxide solutions. It has been shown to have antifungal activity in the presence of fatty acids and can be used for the treatment of urinary tract infections caused by Candida albicans. The chemical ionization technique was used to analyze 3-vinylpyridine in urine samples from nonsmokers and smokers. Long-term exposure to 3-vinylpyridine may lead to surface-enhanced Raman spectroscopy signals on the surface of metal oxides due to alkoxy radical formation. The crystallization process of 3-vinylpyridine can take place at a temperature range between 135°C and 150°C with an addition of polyethylene glycol or sulfuric acid. Reaction intermediates are formed during this process which are important for the formation of 3-vinylpyridinium ions.</p>

<p>Please enquire for more information about (4-Benzylpiperazin-1-yl)piperidin-4-yl-methanone dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Bromo-pyridine-2-carboxylic acid is a metabotropic glutamate receptor antagonist that inhibits the neurotransmitter glutamate. It has been shown to have antibacterial activity against Staphylococcus aureus and anti-inflammatory properties against the fungus Candida albicans. The drug is orally bioavailable, which means it can be taken by mouth, and has a pharmacokinetic profile that increases its bioavailability. This means that 4-Bromo-pyridine-2-carboxylic acid is an inhibitor of deoxycytidine kinase and may be used as an antifungal agent.</p>

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

<p>The drug, 10-[2-(1-methyl-2-piperidinyl)ethyl]-2-(methylthio)-10H-phenothiazine hydrochloride (CGP 46660), is a competitive antagonist at the human histamine H3 receptor. It has been shown to bind to the histamine H3 receptor in the range of 0.001 to 1 μM and is selective for this receptor over other receptors. CGP 46660 is an optical sensor that can be used in titration calorimetry experiments to measure changes in heat production when it binds to histamine H3 receptors. The drug also has been shown to inhibit guanine nucleotide-binding protein (G protein) signaling pathways and brain functions such as memory formation, learning, and attention span. These effects were demonstrated in humans by measuring EEG activity. The optimum concentration of CGP 46660 for these effects was found to be between 0.01 and 10 μM.</p>

<p>7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid is a fine chemical that is used as a building block for more complex compounds. It is not an active ingredient in any pharmaceuticals or other products. 7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid can be used to produce research chemicals, reagents, and specialty chemicals. This compound has been shown to be useful as a reaction component or scaffold in the synthesis of more complex molecules.</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>Please enquire for more information about N-Boc-3-carboethoxy-4-piperidone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-6-hydroxy-8-mercaptopurine is an antimicrobial agent that inhibits the growth of bacteria by binding to their ribosomes. It has been shown to have a cytotoxic effect in vivo on cancer cells and intestinal parasites, as well as a protective effect against infectious diseases. 2-Amino-6-hydroxy-8-mercaptopurine has also been shown to inhibit the synthesis of proteins in vitro, which may be due to its ability to bind to the ribosomal subunit and inhibit protein synthesis. 2-Amino-6-hydroxy-8-mercaptopurine inhibits bacterial growth by binding to DNA dependent RNA polymerase, thereby preventing transcription and replication. The high frequency of human activity has been shown using a patch clamp technique on human erythrocytes. This active form is metabolized through a number of metabolic transformations, including hydrolysis by esterases or gluc</p>

<p>Please enquire for more information about 3-Bromo-2-(bromomethyl)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>3-Amino-4-methoxypyridine is a molecule that has been shown to have anesthetic activity. It has been shown to inhibit the uptake of glycogen by glioblastoma cells and decrease the rate of glycogen synthesis in these cells. 3-Amino-4-methoxypyridine also inhibits the production of ATP in cardiac muscle cells, which may be due to its ability to inhibit glycogen synthase kinase-3 (GSK3) and glycogen synthase. This drug also inhibits cancer cell growth by inhibiting protein synthesis, as well as inflammatory disease progression by inhibiting NFκB activation and cytokine production. 3-Amino-4-methoxypyridine can be synthesized from aminopyridines such as isonicotinic acid or nicotinic acid, which are oxidized with hydrogen peroxide and sodium nitrite in the presence of a base catalyst.</p>

<p>1-(4-Methoxybenzyl)piperazine is a chemical compound that has been shown to have inhibitory activities against cancer cells. It also shows potential for the treatment of type 2 diabetes and Alzheimer's disease. The mechanism of action is not well understood, but it may be due to its ability to induce mitochondrial biogenesis and insulin sensitivity. 1-(4-Methoxybenzyl)piperazine has also been shown to improve memory in rats with spontaneous dementia, similar to the effects of donepezil (a drug used for Alzheimer's disease). 1-(4-Methoxybenzyl)piperazine can be taken orally or administered via injection.</p>

<p>3-Aminopiperidine is an amine that can be synthesized by the reaction of trifluoroacetic acid and hydrochloric acid with primary amines. 3-Aminopiperidine inhibits the enzyme catalysis of aromatic hydrocarbons, which are a precursor to the formation of aryl halides. These reactions are catalyzed by an enzyme called nitrile hydratase. 3-Aminopiperidine has been shown to have therapeutic effects on inflammatory diseases such as rheumatoid arthritis, asthma, and ulcerative colitis. The drug also exhibits anti-inflammatory properties that may be due to its ability to inhibit prostaglandin synthesis.</p>