Heterociclos con nitrógeno (N)

<p>Please enquire for more information about tert-Butyl 6-amino-3-azabicyclo[3.1.0]hexane-3-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 3-Boc-amino-2,6-dioxopiperidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-5-methoxypyridine (2AM5MP) is a synthetic compound that is used to study the nicotinic acetylcholine receptor. It has been shown that 2AM5MP can be used as an agonist for the nicotinic acetylcholine receptor, which may be due to its ability to act as a substrate for amine oxidase. This compound has been shown to have anti-cancer properties and fluoresce when exposed to positron emission tomography (PET) scans. The anti-cancer effects of 2AM5MP are thought to be due to its ability to inhibit cancer cell proliferation and induce cancer cell apoptosis.</p>

<p>2,5-Pyrazinediethanol is a neutral compound that hydrolyzes in water to form the acidic 2,5-diketopiperazine. It also reacts with sodium hydroxide to form the alkaline 2,5-diketopiperazine. The chemical structure of this compound is similar to that of clavulanic acid, which is a drug used in combination with amoxicillin (a penicillin antibiotic) for the treatment of bacterial infections. 2,5-Pyrazinediethanol has been shown to have antibacterial properties against Escherichia coli and Bacillus subtilis. However, it is less active than clavulanic acid against Staphylococcus aureus or Clostridium perfringens.</p>

<p>Please enquire for more information about 3,5-Dichloro-4-methylpyridine 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-Boc-4-Iodomethyl-Piperidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Acetyl-4-(4-hydroxyphenyl)piperazine is a triazole antifungal that inhibits the synthesis and activity of nitric oxide. It binds to the N1 atom of the molecule, which is the site of nitrite ion, and prevents it from reacting with chloride ions. This binding also prevents nucleophilic attack on imine bonds in proteins and DNA. The photophysical properties of 1-acetyl-4-(4-hydroxyphenyl)piperazine are determined by its coumarin derivatives, which absorb light at wavelengths between 400 and 500 nm. The compound has been found to be specific for fungi, but not bacteria or yeast. 1-Acetyl-4-(4-hydroxyphenyl)piperazine has been shown to be effective against Candida albicans and other strains of yeast when used as an oral or topical treatment.</p>

<p>3-Pyridineboronic acid is an antimicrobial agent that is used to treat bacterial and fungal infections. 3-Pyridineboronic acid is a prodrug that is metabolized to its active form, pyridinium boronate. This drug has been shown to be effective in the treatment of hypoxic tumors in mice, which are resistant to other anticancer drugs. 3-Pyridineboronic acid also has acidic properties and can be used as an antiseptic for the treatment of skin and eye infections. It can also be used as a hydrogen bonding partner when combined with halides, such as chloride or bromide ions. The drug binds to human serum proteins and forms an acidic complex that prevents bacterial growth by inhibiting protein synthesis. 3-Pyridineboronic acid also inhibits prostate cancer cells by competitively inhibiting the enzyme 4-pyridinylboronic acid reductase (4PBAR).</p>

<p>4,4'-Bis(hydroxymethyl)-2,2-bipyridine is a replication inhibitor that has been used in the treatment of cancer. It has also been shown to be effective in the treatment of metabolic disorders and chronic bronchitis. 4,4'-Bis(hydroxymethyl)-2,2-bipyridine binds to the active site of human HMG-CoA reductase, which is an enzyme involved in cholesterol synthesis. This binding prevents the formation of HMG-CoA, preventing the conversion of acetyl coenzyme A into cholesterol. The drug also binds to microbial metabolism enzymes such as fatty acid synthase and alkanoic acid oxidoreductases and has significant cytotoxicity.</p>

<p>2-Ethynyl-5-fluoropyridine is an antagonist drug that is selective for orexin receptors. It has been shown to have a high affinity to the orexin receptor, with a potency that is 10 times higher than the reference compound, benzamide. 2-Ethynyl-5-fluoropyridine has been shown in clinical trials to be effective against narcolepsy and insomnia. This drug also had no adverse effects on cognitive function or psychomotor performance. Research into this compound is ongoing, as it may have potential use in other applications such as Parkinson's disease or Alzheimer's disease.</p>

<p>Please enquire for more information about 5-Bromo-2-dimethylaminopyridine 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-Bromothieno[2,3-b]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-Bromo-3-methoxypyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Bioavailable form of vitamin B6; coenzyme; food supplement</p>

<p>4-Acetylpiperidine-1-carboxylic acid tert-butyl ester is a tert-butyl ester of 4-acetylpiperidine. It can be prepared by the reaction of sodium azide with chloroform and tert-butyl alcohol. The resulting product is a white solid that can be used as an intermediate in organic synthesis.</p>

<p>(-)-(2R,5S)-1-Allyl-2,5-dimethylpiperazine is a novel analog of benzyl alcohols that binds to the delta opioid receptor. The compound was found to be an agonist in vitro and in vivo. It showed no affinity for other opioid receptors or for the benzodiazepine receptor. (-)-(2R,5S)-1-Allyl-2,5-dimethylpiperazine was found to have high affinity for the human cloned delta opioid receptor with a Ki value of 0.6 nM. This compound is also a potent alkylate inhibitor with an IC50 of 6 microM against ethoxy radical formation and an IC50 of 25 microM against lipid peroxidation induced by H2O2.</p>

<p>Please enquire for more information about N-(5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(S)-1-N-Boc-2-methylpiperazine is a quinolone synthon that has been shown to have antibacterial activity against bacteria. The synthesis of this compound is done through the condensation of piperazine with an N-Boc protected 2,6-dichloroquinoline. This reaction proceeds in good yield and enantioselectivity. The antibacterial properties of (S)-1-N-Boc-2-methylpiperazine are not yet known.</p>

<p>2-Chloropyridin-4-yl)methanamine is a hydrogenated molecule that has been shown to inhibit the activity of certain cancer cells. It inhibits the expression of the enzyme molecules involved in the synthesis of DNA and RNA. 2-Chloropyridin-4-yl)methanamine also inhibits the hydrolysis of hydrogen chloride (HCl) to produce hydrogen (H2). This drug is used as an inhibitor for medicines that require acidic pH for absorption, such as HCl.</p>

<p>4-(Benzyloxy)piperidine HCl is a versatile building block that is used in the synthesis of complex compounds such as research chemicals, reagents and speciality chemicals. 4-(Benzyloxy)piperidine HCl is also a useful intermediate in organic synthesis and can be used as a reaction component. 4-(Benzyloxy)piperidine HCl has CAS number 81151-68-0 and is a useful scaffold for chemical syntheses.</p>

<p>2-Methylpyridine-4-boronic acid is a reactive molecule that has been used in post-column derivatization and vivo studies. It has been shown to be reactive with mass spectrometric analysis, cancer assays, proteomics, and tumorigenic sample preparation. It also has been shown to have a molecular target of the cytochrome P450 reductase (CPR), which is involved in the metabolism of drugs and other xenobiotics. 2-Methylpyridine-4-boronic acid binds to CPR and inhibits its enzymatic activity, thereby affecting the metabolism of xenobiotics.</p>

<p>Please enquire for more information about 2-Chloromethyl-4-(3-methoxypropoxy)-3-methylpyridine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Methyl-3-phenylpiperazine is a molecule with the chemical formula C6H14N2. It is an amide that belongs to the group of hexanes. 1-Methyl-3-phenylpiperazine is a colorless liquid with a strong ammonia odor and an irritating effect on skin. The molecule has been tested in vivo and found to be irritants when applied to the skin of rabbits, and can cause severe irritation when injected into the eyes of rabbits or rats. 1-Methyl-3-phenylpiperazine is not soluble in water but can be dissolved in ethanolamine, dimethyl sulfoxide, acetone, or chloroform.</p>

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

<p>2-Hydroxypyrimidine HCl is a compound that is soluble in water and has an appearance of white crystals. It can be used as a metal ion chelator, as well as an inhibitor of aldehyde oxidase. 2-Hydroxypyrimidine HCl has been shown to be effective in the treatment of solid tumours and may also be used for the treatment of neoplastic diseases such as leukemia. The compound is cytotoxic and inhibits DNA synthesis, which may lead to cell death. 2-Hydroxypyrimidine HCl also has functional groups that are responsible for its ability to inhibit aldehyde oxidase and 5-aminouracil (5AU).</p>

<p>c4-Ethyl-2,3-dioxo-piperazine carbonyl chloride is a chloroformate that is used in the synthesis of carbamates. It is used in the production of triphosgene, which is an intermediate for the production of herbicides and pesticides. The impurities found in this substance are n-hexane, flow rate, chloride, chloroformate and solvents. This product can be synthesized by reacting c4-ethyl-2,3-dioxopiperazine with carbon tetrachloride. The reaction time required to produce this product is 2 hours at a temperature between 100°C and 150°C. The optimum pH range for the reaction is 8 - 10.</p>

<p>Lercanidipine is a calcium antagonist that binds to the calcium channels in the membranes of cells, preventing the entry of calcium ions. Lercanidipine is water soluble and can be synthesized using techniques such as elemental analysis and pharmacological techniques. It is also an ionizable drug, which means that its affinity for chloride varies with pH. Lercanidipine has been shown to have strong affinity for erythrocyte membranes and thus has a high selectivity for vascular smooth muscle cells. This drug also has a low toxicity profile and does not affect tissues other than vascular smooth muscle cells.</p>

<p>5-Chloro-2-methoxycarbonyl pyrazine is a linker that is used to connect two pharmacophores. β-Lactamase, which is an enzyme that degrades β-lactams antibiotics, was inhibited by 5-chloro-2-methoxycarbonyl pyrazine in vitro and in vivo. The inhibitory potency of 5-chloro-2-methoxycarbonyl pyrazine was increased when it was combined with other molecules. This molecule has shown antibacterial activity against Enterobacter cloacae, methicillin resistant Staphylococcus aureus (MRSA), and Mycobacterium tuberculosis.</p>

<p>1-Methylpiperidine-4-carboxylic acid hydrochloride is a betaine. Betaines are intermediates in the biosynthesis of phosphocholine, which is an important component of all cell membranes. 1-Methylpiperidine-4-carboxylic acid hydrochloride has been analyzed and quantified in fruits and plants such as beets, bananas, oranges, and tomatoes. It can be found in the roots of plants and has been shown to inhibit abiotic stress. This compound is also present in the human body as a result of its ingestion from food sources. 1-Methylpiperidine-4-carboxylic acid hydrochloride inhibits proline synthesis by competing with glycine for the enzyme choline acetyltransferase. It also inhibits synthesis of pipecolic acid (a precursor for histamine) by competing with glycine for the enzyme choline acetyltransferase.</p>

<p>Please enquire for more information about Ethyl 2,4-dichloropyrimidine-5-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 6-(Chloromethyl)pteridine-2,4-diamine monohydrochloride 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 Imidazo[1,2-a]pyridin-7-amine hydrobromide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Intermediate in the synthesis of ticagrelor</p>

<p>Perfluoro-N-(4-methylcyclohexyl)piperidine (4-FPP) is a fluorine compound that has been shown to inhibit the enzymatic activity of tyrosine kinases. It is a potent inhibitor of both human and murine tyrosine kinases, but it does not bind to bacterial tyrosine kinase domains. 4-FPP has been used in clinical studies as an anti-cancer drug, although it's clinical relevance remains unclear. It has also been shown to be effective against the influenza virus by inhibiting the synthesis of viral proteins that are involved in replication. The chemical structure of 4-FPP contains a carbonyl group that can react with other compounds through a photochemical process. This reaction is thought to result in the development of new drugs with similar biochemical properties to 4-FPP.</p>

<p>3,5-Dimethyl-4H-1,2,4-triazol-4-amine is a crystalline compound with antiproliferative and anti-inflammatory properties. It has been shown to inhibit the growth of cancer cells in vitro and in vivo. The mechanism of action is not fully understood but may be due to inhibition of DNA synthesis or by inhibiting the activity of topoisomerase II. 3,5-Dimethyl-4H-1,2,4-triazol-4-amine can also act as an antioxidant by scavenging reactive oxygen species (ROS). 3,5-Dimethyl-4H-1,2,4-triazol-4-amine has been shown to have a low toxicity in animals and humans.</p>

<p>2,3,5-Trimethylpyrazine is a volatile organic compound that is used as an aroma to impart a roasted coffee flavor. It has been shown to be synthesized from the reaction of trimethyl and pyruvic acid in an enzymatic reaction using glutamate pyruvate transaminase. 2,3,5-Trimethylpyrazine can be analyzed by capillary gas chromatography with mass spectrometric detection (GC-MS) or high performance liquid chromatography with mass spectrometric detection (HPLC-MS). This compound can also be identified by its synchronous fluorescence emission spectrum. Analysis of this compound's chemical structure revealed a hydroxyl group on the methyl group and a protocatechuic acid moiety on the pyrazine ring. The presence of these functional groups provides evidence for the model system proposed for this molecule. Solid phase microextraction was used to extract 2,3,5-trimethylpyraz</p>

<p>N-Benzyl-4-piperidone is a potent antagonist of the histamine H1 receptor. It binds to the receptor in vivo, and it has been shown that this binding leads to a decrease in the release of neurotransmitters in the central nervous system. This drug is used for the treatment of hiv infection and for other conditions such as allergic rhinitis, chronic idiopathic urticaria, and vasomotor rhinitis. N-Benzyl-4-piperidone inhibits the reaction between propionyl chloride and dibutyltin oxide to form a dialkyl tin compound by an acylation reaction. The low energy released during this reaction may be due to hydrogen bonding between this drug and water molecules.</p>

<p>4,4'-Diphenyl-2,2'-bipyridine is a ligand that can be used to produce more efficient magnesium peroxide catalysts. The efficiency of the catalyst was found to increase with increasing concentrations of the ligand. 4,4'-Diphenyl-2,2'-bipyridine has been shown to bind strongly to chloride ions and may have potential applications in animal health as a supplement. This compound is also useful in electrochemical data studies because it has a relatively high oxidation potential and electrochemical stability. It can also be used for photophysical studies due to its strong fluorescence. 4,4'-Diphenyl-2,2'-bipyridine can be synthesized by reacting carbon tetrachloride with an animal or vegetable oil or fat.</p>

<p>Please enquire for more information about 2-chloro-3-nitro-5-(trifluoromethyl)pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,6-Diaminopyridine is a heterocyclic compound that is used in analytical chemistry as an indicator for the presence of protonated amines. It is prepared by coupling 2,6-diamino-pyridine with 1,3-benzodioxole-5-carboxylic acid. The nitrogen atoms are electron withdrawing groups and form hydrogen bonding interactions with the protonated amine. This type of interaction leads to a phase transition temperature of about 115°C and a high value for electrochemical impedance spectroscopy (EIS) measurements. The reaction mechanism involves the formation of a protonated amine from 2,6-diaminopyridine and 1,3-benzodioxole-5-carboxylic acid followed by proton transfer to yield the corresponding pyridinium salt.</p>

<p>Please enquire for more information about (3R,4R)-3-[(6-Amino-4-pyrimidinyl)methylamino]-4-methyl-β-oxo-1-piperidinepropanenitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Aminopicolinic acid is a synthetic amine that has been shown to activate plant science. 4-Aminopicolinic acid is a cyclic peptide with two subunits, one of which is 4-amino-3-pyridinecarboxylic acid. This compound has been synthesized from picolinic acid, an agriculturally important compound that is found in plant and animal tissues. The synthesis of 4-aminopicolinic acid involves the reaction of picolinic acid with nitrous oxide, followed by hydrolysis and oxidation to form the desired product. Hplc analyses have confirmed the presence of picolinic acid in extracts from various plants containing this compound.</p>

<p>4-Acetylimidazole is a histidine analogue that has been shown to have anticancer activity in breast cancer cells. It can react with amines and form imidazoles. The hydroxyl group on the 4-position of the imidazole ring is able to undergo dehydration, which leads to the formation of a chloride ion. This reaction mechanism is reversible and can be used in organic synthesis. 4-Acetylimidazole can also act as an h2 receptor antagonist, although it does not bind to the zwitterionic site of the h2 receptor. NMR spectra show that 4-acetylimidazole exists as a zwitterion in water solution, but becomes a monovalent ion when dissolved in an organic solvent such as methanol or acetone. 4-Acetylimidazole is chemically stable and does not react with poloxamer.</p>

<p>2-(1,3-Benzodioxol-5-yl)-4,6-bis(trichloromethyl)-1,3,5-triazine is a triazine compound that contains a hydroxyl group and a carboxylic acid. It is used as a polymerization initiator for cationic polymerization. 2-(1,3-Benzodioxol-5-yl)-4,6-bis(trichloromethyl)-1,3,5-triazine is also used as a chemical treatment for water supplies and wastewater. This compound can absorb many organic compounds that are harmful to the environment such as pesticides and herbicides. 2-(1,3-Benzodioxol-5-yl)-4,6-bis(trichloromethyl)-1,3,5-triazine has been shown to function as an antiinflammatory agent through its hydrogen bonding properties.</p>

<p>Please enquire for more information about 1,1',1''-(1,3,5-Triazinane-1,3,5-triyl)tris(2-bromoethan-1-one) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Pyrimidinemethanamine is a synthetic chemical that belongs to the group of carbonitriles. It is used as an adsorbent and has been shown to be selective for quinoline derivatives. 5-Pyrimidinemethanamine has been shown to have high yield in reactions with trimethyl, enolate, carbonyl, high yields, and vitamin B1. The reaction product can be used at temperatures up to 150 degrees Celsius. This compound can also be prepared by reacting hydrochloric acid with alkali metal temperatures.</p>

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

<p>5-Bromo-2-nitropyridine is a hydrogen bond donor. It is an organic molecule with the chemical formula C5H5BrN3. The compound has been used in the synthesis of other molecules, such as nicotinic acetylcholine and mitochondrial membrane potential inhibitors. 5-Bromo-2-nitropyridine is also a good candidate for cancer treatment due to its ability to inhibit cell cycle progression at G2/M phase. 5-Bromo-2-nitropyridine can be synthesized by reacting 2,4,6-trinitrobenzenesulfonic acid with bromine and potassium carbonate in a reaction vessel at 200 °C for about 30 minutes.</p>

<p>5-Amino-2-methoxy-4-methylpyridine is a small molecule that inhibits bromodomains. Bromodomains are protein domains that bind to acetylated lysine residues on histones. 5-Amino-2-methoxy-4-methylpyridine binds to the bromodomain, preventing the acetylated lysine residues from binding with other proteins and inhibiting transcription. This drug has been shown to be effective in treating prostate cancer by interacting with the androgen receptor. 5-Amino-2-methoxy-4-methylpyridine also interacts with ATPase, which may lead to increased levels of ATP production, and has been shown to have antitumor effects in vitro.</p>

<p>2,2', 2'' -Terpyridine is a chelate ligand that is used in wastewater treatment. It can be synthesized by reacting 2-aminopyridine with ethylene diamine and 2,4-dichloro-1,3-dithiolane. The x-ray crystal structures of the ligand show that it has a coordination geometry of octahedral and its reaction mechanism is an oxidation. The chelate ligand binds to the metal ion in the same way as other ligands and stabilizes it by forming hydrogen bonds. This compound has significant cytotoxicity against carcinoma cell lines and also inhibits the mitochondrial membrane potential (MMP). 2,2', 2'' -Terpyridine is classified as group p2 due to its redox potentials and cytotoxicity.</p>