Hétérocycles azotés (N)

<p>Please enquire for more information about Methyl4-aminomethyl-1-boc-piperidine-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 4-(Piperazinomethyl)benzonitrile, 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 (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>2,6-Diamino-5-hydroxy-3-(phenylazo)pyridine is a versatile chemical substance that has various applications in different industries. It can be used as a dianhydride to create high-performance polymers or as an electrode material for batteries and fuel cells. This compound is also used in the production of lacosamide, a medication used to treat epilepsy. In addition to its industrial uses, 2,6-Diamino-5-hydroxy-3-(phenylazo)pyridine is also utilized in research laboratories as a reagent or marker. It is commonly used in aerosol compositions for testing purposes and in the analysis of toxicological samples. Researchers also rely on this compound for dispersive solid-phase extraction techniques and for studying photodegradation processes. Furthermore, 2,6-Diamino-5-hydroxy-3-(phenylazo)pyridine has shown potential in the development of polymeric compositions with</p>

<p>Piperidine-2,5-dione is a synthetic compound that is used for the synthesis of benzyl esters, stereospecific chiral compounds, and amides. It can be used as a building block in the synthesis of natural products. Piperidine-2,5-dione has been shown to inhibit the activity of enzymes such as lactamases and amidases. The mechanism by which piperidine-2,5-dione inhibits these enzymes is not yet known. This compound also can react with potassium hydride to form radical species or alkylate boronic acids to form stereochemically pure products.</p>

<p>Please enquire for more information about 1-(Cyclobutylcarbonyl)piperidin-4-one 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>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>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 7-[(3R)-3-[(N-Acetyl)amino]-1-oxo-4-(2,4,5-trifluorophenyl)butyl]-5,6,7,8-tetrahydro-3-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyrazi ne including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<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-(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>

<p>2,4-Dichloro-5-trifluoromethylpyrimidine is a synthetic compound that can be used as an additive in plastics and cellulose. It is also used to produce 2,4-dichloro-5-(trifluoromethyl)pyrimidine, which has been shown to inhibit the growth of cancer cells. The methylating properties of 2,4-dichloro-5-(trifluoromethyl)pyrimidine have been shown to be useful for the production of amines. This chemical can also be used as a solvent due to its low boiling point.</p>

<p>3-Ethynylpyridine is an amide that has been used to prepare palladium complexes. It has been shown that 3-ethynylpyridine can be used as a ligand for palladium-catalyzed coupling reactions. This compound has also been studied in the context of electrochemical data, where it was found to bind to a proton and form a hydrogen bond with trimethylphosphate. 3-Ethynylpyridine has also been investigated for its use in x-ray crystal structures and vibrational spectroscopy studies. Pharmacokinetic properties have also been studied, including binding constants and metabolism.</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>2-Amino-4,6-dichloropyrimidine is a chemical compound that has been used as a building block in the synthesis of other compounds. It has been shown to be useful for the preparation of 2-aminopyridine derivatives, which are used as an intermediate for research chemicals and pharmaceuticals. The compound has high purity and is available in bulk quantities.</p>

<p>2-Bromo-6-methoxypyridin-3-amine is a perovskite that has been shown to have a high photoluminescence quantum yield and can be used in solar cells. This compound interacts with both the ligands and the acceptors, boosting the efficiency of these compounds. The 2-bromo-6 methoxypyridin-3 amine is a semiconductor with an electron affinity of 1.9 eV and a band gap of 1.6 eV. It has been shown to be efficient as a photoluminescent material in nanocrystals.</p>

<p>Please enquire for more information about tert-butyl (2S)-2-Methyl-4-oxopiperidine-1-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<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>1-Pyridin-2-ylmethyl-piperazine is a fluorescent probe that has been shown to be useful in metal ion detection. The fluorescence of this compound is proportional to the concentration of metal ions, which can be detected with a spectrophotometer. 1-Pyridin-2-ylmethyl-piperazine has been used as a probe for determining the permeability of cells and their ability to transport metal ions. It is also used as a tool for studying the functional theory and theories of molecular interactions. This probe has been found to have low detection limits and high efficiency, making it an advance in fluorescence probes for metal ion detection.</p>

<p>Please enquire for more information about 4-Piperazinylphenylboronic acid, pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,3,3-Trimethyl-4,5-benzo-3H-indole is a fine chemical that is used as a versatile building block for research chemicals and speciality chemicals. It can be used to synthesize drugs. 2,3,3-Trimethyl-4,5-benzo-3H-indole is also a reaction component in the synthesis of complex compounds with high quality.</p>

<p>2-Aminopyrimidine-5-boronic acid pinacol ester is a boronic acid derivative that has been shown to inhibit the activity of protein kinase C. This compound is also an effective linker for cross-coupling reactions and has a low reactivity with nucleophiles, which makes it safer than other boronic acids. 2-Aminopyrimidine-5-boronic acid pinacol ester has been shown to be potent against cancer cells in vitro and in vivo and synthetic cells. 2-Aminopyrimidine-5-boronic acid pinacol ester inhibits the growth of cancer cells by binding to the ATP site on protein kinase C, thereby inhibiting its function.</p>

<p>2-Methyl-1H-imidazole-5-carboxylic acid is a molecule that belongs to the class of antibiotics. It has been shown to be an effective inhibitor of lipases and other enzymes, which is due to its carboxylate group. The immobilization of this molecule has been studied by X-ray crystallography. The oxygen atoms in the molecule are covalently immobilized on a silica surface via a linker chain, which prevents the loss of these atoms. Dichroism spectroscopy was used to study the effects of different solvents on this molecule's ability to rotate light. 2-Methyl-1H-imidazole-5-carboxylic acid was also successfully immobilized using an enzyme called lipase, with residue carboxylate groups positioned at the bottom of the binding cavity.</p>

<p>tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate is an organic compound that can be synthesized by the reduction of 5-bromo-2-nitro pyridine with a palladium catalyst. It has been shown to inhibit the growth of cancer cells in vitro and in vivo, and is being investigated as a potential treatment for breast cancer.</p>

<p>Please enquire for more information about Methyl 4-piperazin-1-ylmethylbenzoate 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 Bis(ethylamino)-1,3,5-triazin-2-ol 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 5-Chloropyridine-2-boronicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Acefylline piperazine is a hydrogen-bonded molecule with the chemical formula C8H14N4O. It is an occlusive profile that inhibits human serum lipoprotein lipase and cardiac lipases. Acefylline piperazine has been shown to inhibit fatty acid and eosinophil cationic protein production in vitro. This drug also possesses anti-inflammatory properties, which may be due to its ability to inhibit the enzyme activity of lipoprotein lipase, thereby reducing the levels of fatty acids present in tissues. Acefylline piperazine has a molecular weight of 168.2 daltons, which is consistent with most drugs that are administered intravenously as pharmaceutical dosages.</p>

<p>Please enquire for more information about 5-Bromo-1-methyl-1H-1,2,3-triazole 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-(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-Dihydro-1-(2-methylpropyl)-4H-imidazo[4,5-c]quinolin-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-Chloro-7H-pyrrolo[2,3-d]pyrimidin-4-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Pyridine-sulfur trioxide complex is a sodium salt of sulfuric acid and pyridine. It is an intramolecular hydrogen acceptor, which means that it can act as a hydrogen donor to other molecules. Pyridine-sulfur trioxide complex has been shown to be effective against HIV infection in vitro. The biological properties of this drug are due to its ability to inhibit the proliferation of cells. Pyridine-sulfur trioxide complex also has antiproliferation activity against a variety of cancers, including prostate, breast, lung, ovarian, and pancreatic cancers. Pyridine-sulfur trioxide complex inhibits fatty acid synthase enzymes and is used as an analytical method for measuring cholesterol levels in the blood.</p>

<p>3-Pyridazinemethanamine is an amide that binds to the vasopressin V2 receptor. It is a selective agonist of the vasopressin V2 receptor and has a high affinity for this receptor. 3-Pyridazinemethanamine has been shown to be a functional antagonist at the vasopressin V1A receptors, which may be due to its chemical structure. 3-Pyridazinemethanamine is not metabolized by cytochrome P450 and does not inhibit other cytochrome P450 enzymes, making it an attractive drug candidate for use in humans.</p>

<p>Please enquire for more information about Ethyl 1-N-Boc-3-oxopiperidine-4-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>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>2-(Tributylstannyl)pyrimidine is a synthetic heterocycle that has antibacterial activity. It is a guanine analog that binds to the ribonucleic acid (RNA) of bacterial cells and inhibits protein synthesis by attacking the 4-chloropyrimidine moiety of nucleoside monophosphates. 2-(Tributylstannyl) pyrimidine also has antiviral properties and acts as an inhibitor of vitamin B1, which is required for the synthesis of DNA. This drug can be used in the treatment of sulfamethoxazole-resistant infections caused by bacteria such as Streptococcus pneumoniae, Staphylococcus aureus, and Pseudomonas aeruginosa.<br>2-(Tributylstannyl)pyrimidine is effective at inhibiting the growth of bacteria due to its ability to form an ion pair with chloride ions. This property makes it highly reactive for transmetall</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>Hindered amine light stabilizer in polymer synthesis; TEMPO and LTMP precusor</p>

<p>5-Methylindole is a chemical that has been used as a building block in the synthesis of many complex compounds. It has been found to be useful in research due to its versatility, and it can also be used as a reaction component in the synthesis of speciality chemicals. 5-Methylindole is an intermediate for other chemical compounds, and is an important solvent for some reactions. 5-Methylindole is also used as a reagent for the production of indole derivatives.</p>

<p>Please enquire for more information about 1-(2,5-Dichlorophenyl)piperazinedihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 4-(2-(2-amino-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-5-yl)ethyl)benzoate is a prodrug that is hydrolyzed to form the active drug pemetrexed disodium. The drug has been shown to be effective for the treatment of cancer and has been used in clinical trials for patients with lung cancer. The conversion of this prodrug to its active form occurs through a hydrolysis reaction at high temperature and by saponification with sodium hydroxide. Methyl 4-(2-(2-amino-4-oxo-4,7-dihydro-3H-pyrrolo[2,3 - d]pyrimidin -5 -yl)ethyl)benzoate can also be converted into its active form by enzymatic action using ester</p>

<p>3,3-dimethylpiperidine is a chemical compound that is used in wastewater treatment. It has been shown to inhibit the production of serotonin and other substances by binding to serotonin receptors. 3,3-dimethylpiperidine has been shown to be selective for the l-type of calcium channels, which are involved in blood vessel contraction and relaxation. This chemical has also been shown to increase the permeability of cell membranes, which may be due to its ability to bind with receptor sites on cell membranes. The binding of 3,3-dimethylpiperidine with these sites leads to an increase in the hydrophilicity of the membrane surface and an increase in receptor binding.</p>

<p>2-Methyl-6-(tributylstannyl)pyridine is a synthetic organometallic compound that can be thermolysed to form azide and monoxide. It has been shown to react with tert-butyl lithium, leading to the formation of a nucleophilic radical species in the presence of an azide. This process is analogous to the Suzuki reaction. 2-Methyl-6-(tributylstannyl)pyridine can also be synthesized from 2,6-dibromopyridine and tributyltin chloride.</p>

<p>Please enquire for more information about 1-Isobutyrylpiperidin-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 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>

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

<p>1-(4-(Aminomethyl)phenyl)pyridin-1-ium chloride is a chemical compound that belongs to the class of pyridines and has pinpoint as its molecular weight. It is an ionic liquid that can be used in analytical methods, such as liquid chromatography and ionization techniques, for the identification of unsaturated fatty acids. This compound can be analyzed by gas chromatography with either electron capture detection or chemical ionization. The GC separation column used for this analysis would have to be a phase column with an unsaturated fatty acid stationary phase. GC-EID and GC-CI are two common ionization techniques that could be used in conjunction with this analytical method. The lower limit of detection for this technique is about 0.1 ppm, which makes it a sensitive analytical tool for use in food production and quality control laboratories. The yield of 1-(4-(Aminomethyl)phenyl)pyridin-1-</p>

<p>Please enquire for more information about 4-(Piperidin-4-yl)benzonitrile 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 Noratropine 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 (R)-1-Boc-3-ethyl-piperazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-5-chloropyridine is an organic compound that is a metabolite of nicotinic acid. 2-Amino-5-chloropyridine has been detected in urine samples and can be extracted from urine with hydrochloric acid. It can also be prepared by the reaction of picolinic acid and malonic acid, which are both found in the human body. The compound has been shown to have pharmacokinetic properties, including a half life of approximately 1 hour and a volume of distribution of 0.3 L/kg. 2-Amino-5-chloropyridine has also been shown to have structural analysis and binding properties with hydrogen bonding interactions. The structure was determined by X-ray crystal structures, which revealed the presence of a reactive group p2 and the absence of any other reactive groups. 2-Amino-5-chloropyridine is used as an analytical method for fluorescence detection in combination</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>Piperidinium acetate is a photochemical agent that has been used in the photochemical oxidation of organic compounds. It is also used as a catalyst for the oxidative coupling of piperidinium salts with sodium salts to form piperidine. Piperidinium acetate can be used for the treatment of metabolic disorders, such as lactic acidosis and hyperglycemia, and autoimmune diseases such as rheumatoid arthritis and systemic lupus erythematosus. This compound is also known to cause allergic symptoms and anhydrous sodium may be generated in the process.</p>

<p>(R)-(-)-a-[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]benzeneacetic Acid is an inhibitor of the enzyme histamine N-methyltransferase (HNMT), which is responsible for the synthesis of histamine. The inhibition of HNMT leads to a decrease in histamine levels and therefore has been used as a treatment for chronic prostatitis, lacrimal gland, and energy efficiency. Histamine N-methyltransferase also participates in the regulation of apoptosis by methylating proapoptotic proteins like Bax, so inhibition can lead to an increase in apoptosis. This chemical is also able to bind with chloride ions and form diphenyl ethers through a reaction solution, which are known to have anticancer properties.</p>

<p>2-Chloro-6-cyanopyrazine is a compound that has been shown to have antimycobacterial activity against Mycobacterium avium. It may also have tuberculostatic activity and be useful for the treatment of tuberculosis. 2-Chloro-6-cyanopyrazine inhibits bacterial growth by binding to DNA, RNA, and protein synthesis in mycobacteria. The antibacterial effect is due to its ability to inhibit amidation and alkylation reactions, as well as its nucleophilic properties. 2-Chloro-6-cyanopyrazine is an acidic compound with a pKa of 3.2, which makes it more soluble in water than hydrophobic compounds such as alkanoic acids.</p>

<p>3H-Spiro[2-benzofuran-1,4'-piperidine] is a ligand with affinity for melanocortin receptors. It has been shown to bind with low affinity to the melanocortin receptor and act as an agonist. 3H-Spiro[2-benzofuran-1,4'-piperidine] has high affinity for benzene, which may be due to its ring system. This ligand also has a penetrable structure that allows it to bind to piperidine binding sites.</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>1-N-Boc-4-bromopiperidine is a Grignard reagent that is used for the preparation of amines. It can be prepared by reacting 1-bromo-4-methylpiperidine with magnesium metal in an ether solution. This compound has been shown to be efficient for the synthesis of biologically active molecules, such as dihydropyridones and isoquinolines. This product may cause skin irritation.</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>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>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>1-Pyridin-3-ylmethyl-piperazine (1PMP) is a synthetic psychoactive substance that can be used as an antidepressant. It has been shown to increase the affinity of chloride ions for diborane, and it has also been shown to be an effective neuroprotective agent. 1PMP is a piperazine derivative, which is chemically similar to piperidine and morpholine. It can be synthesized by reacting borane with 3-chloropyridine. Further reactions with amines or alcohols yield the desired product.<br>The synthesis of 1PMP can also be achieved by reacting 3-chloropyridine with 2,2-dimethylpropanoyl chloride in the presence of triethylamine and tetrahydrofuran (THF). This reaction may occur in two different ways, yielding either the cis or trans isomers of 1PMP. The cis isomer has been found to have</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 5-Chloro-2-(ethylsulfonyl)pyrimidine-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</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 Fmoc-N-(1-Boc-piperidin-4-yl)glycine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methylthio-4-hydroxypyrimidine is a protonated thione that inhibits the growth of bacteria, including Streptococcus faecalis. It has been shown to have an inhibitory effect on UV absorption and halide ions, such as mercury chloride. 2-Methylthio-4-hydroxypyrimidine is an analog of pyrimidine nucleosides and has a constant and regiospecific synthesis. The compound has also demonstrated antibacterial activity against bacteria, such as Staphylococcus aureus, Enterobacter aerogenes, Pseudomonas aeruginosa, Proteus vulgaris, Salmonella typhimurium, Escherichia coli, and Shigella flexneri.</p>

<p>Bis(pyridine)iodonium tetrafluoroborate is a reagent that can be used to iodinate organic compounds. It is prepared by the reaction of pyridine with iodine and bromine in tetrafluoroboric acid. Bis(pyridine)iodonium tetrafluoroborate is an active compound that can be used for amino acid analysis, optical properties, and functional groups. This compound also can be used for magnetic resonance analysis, palladium-catalyzed coupling, and synthetic reactions. Bis(pyridine)iodonium tetrafluoroborate has been found to have radiation transport properties and a strong reactivity towards acids.</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>N-Benzyl-4-carboethoxypiperidine (NBP) is a potential drug for the treatment of Alzheimer's disease. It is an acetylcholinesterase inhibitor that blocks the breakdown of acetylcholine, leading to increased levels of this neurotransmitter in the brain. NBP has been shown to inhibit butyrylcholinesterase, an enzyme responsible for breaking down acetylcholine. This inhibition leads to increased levels of acetylcholine in the brain and prevents the development of Alzheimer's disease. NBP has also been shown to have a low level of toxicity in mice and rats and does not inhibit other enzymes such as carboxypeptidases or aminopeptidases.</p>

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

<p>3-(1-Piperidin-1-ylcyclohexyl)phenyl]amine hydrochloride is a ligand that binds to the acetylcholine receptor. 3-(1-Piperidin-1-ylcyclohexyl)phenyl]amine hydrochloride is an active analogue and has a high binding affinity for the cholinergic receptor. It has been shown to have a kinetic effect on the excitatory system, enhancing excitatory effects of acetylcholine without affecting inhibitory effects. 3-(1-Piperidin-1-ylcyclohexyl)phenyl]amine hydrochloride also has an antagonistic effect on modifiers of acetylcholine activity such as amantadine, but enhances the effects of other drugs, such as clonidine.</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>2-Fluoropyrazine is a heterocyclic compound that has been shown to be an efficient catalyst for the palladium-catalyzed cross-coupling reaction. It reacts with nucleophiles such as hydroxy group, chlorine atom, and hydroxyl group. The 2-fluoropyrazine catalyzes the formation of a carbon-nitrogen bond in a nucleophilic attack on an oxadiazole ring. 2-Fluoropyrazine has been found to inhibit the growth of cancer cells and infectious diseases by inhibiting the synthesis of RNA and protein. It also inhibits the replication of viruses by binding to their RNA polymerase.</p>

<p>Pyridine-3-sulfonic acid is a reactive molecule that can exist in two forms. It reacts with iron oxides to form pyridine-3-sulfonic acid amide and reacts with picolinic acid to form pyridine-3-sulfonic acid phosphoric acid complex. Pyridine 3 sulfonic acid is an intermediate in the synthesis of picolinic acid and is involved in the genetic mechanisms of bacteria. It has been shown to be effective at concentrations of 10 mM or higher when used in tissue culture experiments. The optimum concentration for the reaction varies depending on the reactant and its environment, which is why experimentation should be conducted before using it as a reagent.</p>

<p>1-Benzyl-3-piperidinol is a synthetic chemical that has been used as a long-acting calcium antagonist. It is synthesized by the reaction of 1,2-dibromoethane with piperidine and benzaldehyde in the presence of an acid catalyst. The reaction yield is high, and impurities are low. This drug substance is soluble in organic solvents, such as chloroform, ethyl acetate, and ether. The synthesis process uses chiral catalysts to produce the desired enantiomeric form of the drug substance. The use of immobilized catalysts improves the conversion rate, kinetic parameters, and reaction yield of this process.</p>

<p>3-Ethylpyridine is a type of compound that has been found in bacteria. It has been shown to be a mitochondrial membrane potential inhibitor and matrix molecules inducer. 3-Ethylpyridine also inhibits the mitochondrial pathway of 2-ethylpyridine, which is a major metabolite of nicotine in mammals. This inhibition leads to lung cancer. 3-Ethylpyridine can be used as an alternative to chemotherapeutic agents for lung cancer treatment.</p>

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<p>1-(3-Fluorobenzyl)piperazine is a potent inhibitor of annexin A1. It has been shown to inhibit the proliferation of pancreatic cancer cells and induce apoptosis in these cells by inhibiting cholinesterase activity. 1-(3-Fluorobenzyl)piperazine also inhibits tumor growth in vivo and induces apoptosis, which may be due to its ability to inhibit the mitochondrial membrane potential. The compound has also been shown to have antitumor effects in other types of cancer cells. This drug is an amine that emits acidic compounds as a result of hydrolysis.</p>

<p>2-(2-Dimethylamino)Ethyl) Pyridine is a chemical compound that contains oxygen atoms, hydroxo, and nitrogen atoms. It has a tetranuclear hexahydrate form and the molecular formula C5H7N3O2. 2-(2-Dimethylamino)Ethyl) Pyridine has been shown to have desilylation properties. 2-(2-Dimethylamino)Ethyl) Pyridine binds to group P2 of RNA and represses translation by preventing ribosomal binding to the mRNA strand. This drug is also an x-ray data collection agent in which it is used as a ligand in magnetic resonance imaging (MRI).</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>

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<p>5-Cyanopyridine-2-carboxylic acid is a small molecule that has been found to have significant biological activity in a number of different areas, including neurotherapeutics. It is the result of a scalable synthesis and is soluble in water. The molecule has two chiral centers and can exist as four different stereoisomers (enantiomers). In vitro studies show that 5-cyanopyridine-2-carboxylic acid inhibits fatty acid uptake by blocking the proton pump, which transports lipids into cells. This compound also binds to the cytosolic protein pyrazine 2-carboxylic acid receptor 1 (PYZR1), which may provide an explanation for its effects on fatty acid uptake.</p>

<p>WAY 316606 is a potent, orally administered small molecule that inhibits the Wnt signaling pathway by blocking the action of β-catenin. It has been shown to have potential for treating eye disorders, including age-related macular degeneration. This drug also has potential for treatment of cell and nervous system diseases such as Alzheimer's disease and Huntington's disease. WAY 316606 inhibits the transcriptional activity of the β-catenin/Tcf4 complex by binding to it and preventing its translocation into the nucleus. In addition, WAY 316606 prevents downstream activation of genes regulated by β-catenin signaling, including c-myc and cyclin D1. This drug also blocks growth factor receptor tyrosine kinases and monoclonal antibodies that activate these receptors.</p>

<p>Apixaban is a novel, orally active, and selective factor Xa inhibitor. It is the first oral anticoagulant that has been developed to inhibit both free and clot-bound thrombin. Apixaban binds reversibly to the active site of factor Xa and inhibits factor Xa-mediated conversion of prothrombin to thrombin, resulting in an increased concentration of prothrombin in blood. Apixaban also inhibits the activity of thrombin-activated protein C (APC) that degrades fibrin clots by proteolytic cleavage of fibrinogen. This drug has a crystalline form with a particle size between 10 and 100 μm.</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>

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