Hétérocycles azotés (N)

<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>

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<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-(2-Chlorobenzyl)piperazine is a drug that binds to the adenosine receptor with high affinity. It has been shown to produce a bell-shaped dose-response curve, meaning that at low doses it increases the activity of adenosine receptors and at high doses it decreases the activity of these receptors. 1-(2-Chlorobenzyl)piperazine is an atypical agonist for this receptor because it does not have the typical skeleton structure of other drugs that bind to this receptor. It is also used as a research tool in assays to study the effects of drugs on adenosine receptors.</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>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>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>2,4-Bis(octylthio)-6-(4-hydroxy-3,5-di-tert-butylanilino)-1,3,5-triazine is a triazine that has been synthesized by the reaction of glycol esters with hydrogenated hydrochloric acid. This compound is used as a polymerization initiator and is a liquid crystal composition stabiliser. It can be used in sample preparation to provide protection against water vapor and light emission. 2,4-Bis(octylthio)-6-(4-hydroxy-3,5-di-tert-butylanilino)-1,3,5-triazine has antioxidant properties and can be used for determining functional groups in organic compounds.</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>Please enquire for more information about 6-Chloro-4-(trifluoromethyl)-2-pyridinamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Benzyl-3-carbethoxy-4-piperidone hydrochloride is a carboxylic acid that is used as a waterproofing agent in cyclohexane. It is absorbed by the skin and other tissues, which may lead to adverse effects on the body. Exposure to this compound has been shown to result in irritation of the skin, eyes, and respiratory tract, as well as changes in heart rate and blood pressure.</p>

<p>Pyridine-3-carboxaldehyde is a heterocyclic compound that is structurally related to nicotinic acid and picolinic acid. It has been shown to have anti-tumor activity, with hl-60 cells as the model system. Pyridine-3-carboxaldehyde has also been shown to be toxic to bacteria in biological studies. The chemical stability of this compound was studied by Langmuir adsorption isotherm and electrochemical impedance spectroscopy. It was found that pyridine-3-carboxaldehyde is stable at a pH range of 7 to 8 and at temperatures up to 60 degrees Celsius.</p>

<p>1-Piperonylpiperazine is a drug that is used to treat symptoms of diabetic neuropathy. It is an inhibitor of mitochondrial ATPases and blocks the synthesis of nucleotides in the liver. It also inhibits uptake processes in the brain and spinal cord, which are related to locomotor activity. The uptake assays showed that 1-piperonylpiperazine has a high affinity for receptors in the human liver, which could be useful for future research on drugs targeting this organ. 1-Piperonylpiperazine has been shown to have strong effects on mitochondrial membrane potential and ATP levels in primary cells, as well as increasing uptake into human liver cells. This drug may be useful for treating symptoms of diabetic neuropathy.</p>

<p>6-Methoxypyridine-2-boronic acid is a boronate ligand that can be used to form coordination complexes with metals. It has been shown to interact with silver ions, which are the most effective ligands for enhancing the fluorescence of organic dyes. 6-Methoxypyridine-2-boronic acid is able to rigidify organic molecules by binding to their steric and electronic properties, making them more resistant to photodegradation. This property makes it an excellent candidate for the use in the development of fluorescent labels in analytical chemistry.</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>2-Amino-4-chloro-3-nitropyridine is a potent inhibitory molecule that inhibits the activity of the enzyme acetylcholinesterase. It has been used in the treatment of chronic pain, and has been shown to be effective for inhibiting malonate esters and amino acid esters. This drug is an ethyl ester that can be synthesized from chlorobenzene and malonic acid by chlorinating it with chlorine gas. 2-Amino-4-chloro-3-nitropyridine has also been shown to have a high affinity for malonic acid diethyl esters.</p>

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

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<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>Pyrazine is a model system that has been used to investigate the reaction mechanism of pyrazinoic acid, an antimicrobial agent. Pyrazine reacts with water to give pyrazinoic acid and hydrogen gas. Pyrazine is also used as an analytical method for determining the concentration of odorant binding compounds in air and as a model system to study the electrochemical properties of odorant binding. The compound is characterized by intermolecular hydrogen bonding and synchronous fluorescence. Pyrazine has been shown to have an adsorption peak at 1780 cm-1 and a Langmuir adsorption isotherm at 10-4 M.</p>

<p>3-Bromo-4-pyridinecarboxylic acid is a naphthyridine derivative that is used in drug development. It is a crystalline solid that can be dissolved in organic solvents. 3-Bromo-4-pyridinecarboxylic acid has been shown to have antiinflammatory properties and can be used as an oxidant. 3-Bromo-4-pyridinecarboxylic acid is being investigated as a receptor subtype for inflammatory diseases, and it has also been used to study the mechanism of chronic inflammatory diseases.</p>

<p>1-[4-(Methylthio)benzyl]piperazine is an organic compound that is used as a corrosion inhibitor in the treatment of industrial wastewater. The reaction solution is typically a mixture of copper chloride, ethylene diamine, and potassium dichromate. This compound is also known as a bound form of methylthiobenzoic acid. 1-[4-(Methylthio)benzyl]piperazine binds to copper ions, preventing the formation of copper oxide and hydroxide. It also reacts with chromium ions to form a soluble product that can be easily removed from the water by filtration or sedimentation. The profile for this compound shows that it has low energy and does not react with sodium hydroxide or hydrochloric acid.</p>

<p>3-Hydroxyisoquinoline is a non-nucleoside inhibitor of cyclic nucleotide phosphodiesterase (cNMP) that is used in the treatment of nervous system diseases. 3-Hydroxyisoquinoline has been shown to have an inhibitory effect on cyclic nucleotide phosphodiesterase and can be used for the treatment of neurological disorders such as Parkinson’s disease, Alzheimer’s disease, and epilepsy. It also has anti-inflammatory properties and can be used to treat pain. 3-Hydroxyisoquinoline has a photoelectron spectrum that peaks at 5.6 eV, with a strong absorption band at 2.1 eV due to hydrogen bonding. This compound is also able to absorb radiation in the form of light emission with an emission peak at 4.8 eV, with a maximum intensity around 830 nm and a half-life of 0.2 s. 3-Hydroxyisoquinoline is able to</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 1,4-Piperidinedicarboxylic acid, 4-aMino-, 1-(1,1-diMethylethyl) 4-ethyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>8-Bromo-imidazo[1,2-a]pyridine is a neutralizing agent that can be used in the synthesis of succinimide. It reacts with chloroacetaldehyde to yield the imidate ester. This reaction is catalyzed by alkali and requires filtration to remove the bromine and any other impurities. The reaction generates heat, so it must be performed in a well-ventilated area.</p>

<p>Please enquire for more information about 1-Boc-2,6-Dimethyl-4-oxopiperidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>Please enquire for more information about 7-[(4Methoxyphenyl)methyl]-5-methyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(4-Nitro-3-piperidin-1-ylphenyl)piperazine is a synthetic molecule that is used as a polymerization initiator. It can be used to prepare polymers with functional groups that contain nitro and piperidine groups. 1-(4-Nitro-3-piperidin-1-ylphenyl)piperazine reacts with monomers such as thiourea, which are then polymerized by the addition of other reagents such as solvents or catalysts. The most common use of 1-(4-Nitro-3-piperidin-1-ylphenyl)piperazine is in the synthesis of nalidixic acid, an antibiotic drug that inhibits bacterial growth by preventing DNA replication. This compound has been shown to be nonhazardous to humans and animals in bioassays, although it may cause toxic effects on the skin, eyes, and respiratory system when exposed</p>

<p>Imatinib (piperidine)-N-oxide is a by-product of the synthesis process for Imatinib, which is an inhibitor of tyrosine kinases. Imatinib (piperidine)-N-oxide has been shown to have antineoplastic activity in vitro and in vivo. It is structurally related to CGP 71422, a known tyrosine kinase inhibitor.</p>

<p>Please enquire for more information about N-(5-bromo-pyridin-2-yl)-2,2-dimethyl-propionamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<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>Pyridazine 3-carbaldehyde is a potential antiviral agent that has shown to be effective against herpes simplex virus type 1. It is a methylene compound that binds to the active site of the enzyme ribonucleotide reductase, which is required for DNA synthesis. This compound also exhibits synergistic effects with other antiviral agents and has cytotoxic properties. Pyridazine 3-carbaldehyde can be synthesized from pyridine-3-carboxaldehyde via a two-step process involving thermal decarboxylation followed by an oxidation reaction.</p>

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

<p>4-Anilino-1-benzylpiperidine is a synthetic opioid analgesic that is a prodrug of the active metabolite pethidine. It is an agonist at µ-opioid receptors and is used as an analgesic medication. 4-Anilino-1-benzylpiperidine has been shown to have a high affinity for the δ subtype of opioid receptor and also inhibits the reuptake of naloxone, which may be related to its antinociceptive effects. 4-Anilino-1-benzylpiperidine has been shown to be effective in humans when given in doses around 100mg. The drug binds to functional groups on proteins, such as serine hydroxyls and cysteine sulfhydryl groups, which may account for its efficacy 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>

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<p>2-(Tributylstannyl)pyridine is a protonation-sensitive, unsymmetrical trifluoroacetic acid derivative with a photophysical and skeleton that can react with halides. It has been used in the synthesis of Pd(II) complexes, which have been shown to have pharmacokinetic properties and are active against tuberculosis. 2-(Tributylstannyl)pyridine has also been shown to be effective against cancer cells, but not against healthy cells.</p>

<p>7-Chlorothieno[3,2-B]pyridine is a nucleophilic compound that is used as an inhibitor of the tyrosine kinase enzyme. It binds to the ATP binding site and blocks the enzymatic activity of the enzyme, preventing cell proliferation. 7-Chlorothieno[3,2-B]pyridine has been shown to inhibit growth in tumour cell lines and has been shown to be effective against tyrosine kinase receptor positive cancer cells. This drug also shows a cytotoxic activity against tumour cells in vivo, which may be due to its ability to inhibit factor receptor and receptor tyrosine.</p>

<p>Please enquire for more information about 1-[(1-Methyl-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>2,5-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>1,3,5-Triacryloylhexahydro-1,3,5-triazine (TTH) is a particle that absorbs UV light. It is a reactive chemical with a high thermal stability and low reactivity to air. TTH has been used as a cross-linker in polymer films and as a microsphere filler. The absorption of UV light by TTH may be due to the presence of hydroxyl groups or nitrogen atoms. The nmr spectra show that TTH contains trimethylolpropane groups.</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>

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<p>5-Chloro-1H-imidazo[4,5-b]pyridin-2(3H)-one is a chemical compound that is used in analytical chemistry as an insecticide. It has been shown to cause genotoxic activity in weevils exposed to light. The compound has also been shown to have long term efficacy in plants and toxicity studies on animals. 5-Chloro-1H-imidazo[4,5-b]pyridin-2(3H)-one is metabolized by detoxification enzymes and excreted through the urine.</p>

<p>4-Chloropyridine HCL is a regulatory chemical that can be used to inhibit the population growth of microbes. It functions as a biotransforming agent and is typically used in the production of other substances, such as pharmaceuticals and plastics. 4-Chloropyridine HCL is not readily biodegradable and has been shown to be toxic to ciliates, but it may still have some use in the treatment of certain bacterial infections. The compound's molecular descriptors include a constant value of -0.8, an isomer count of 1, and a molecular weight range between 112 and 142.</p>

<p>Please enquire for more information about 7-Bromo-1-methyl-1H-imidazo[4,5-c]pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<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>1-(3-Phenylpropyl)piperazine (1PP) is a piperazine derivative that can be synthesized by the condensation of 3-phenylpropylamine and formaldehyde. 1PP has been shown to have neuroprotective effects in animal models of amyotrophic lateral sclerosis (ALS), brain injury, spinal cord injury, and traumatic brain injury. It has also been shown to act as a ligand for various receptors with therapeutic potential for cancer therapy. 1PP may be able to protect neurons from oxidative damage by scavenging reactive oxygen species. This drug has also been observed to inhibit the growth of cancer cells in vitro and in vivo.</p>

<p>4-Chloro-2,3-dimethylpyridine N-oxide is a chemical compound that belongs to the class of medicines. It is used in the manufacture of hydrogen peroxide, which is an oxidizing agent and a bleaching agent. 4-Chloro-2,3-dimethylpyridine N-oxide has been used as a reagent for organic synthesis and as a catalyst in organic reactions. This compound also has the ability to inhibit proton pumps, which are membrane proteins that pump protons across biological membranes. The presence of sodium impurities can lead to scaling problems because it affects the solubility of 4-chloro-2,3-dimethylpyridine N-oxide. The exothermic reaction with chlorine leads to the formation of chloride, sulfoxide, and chloride ions. These products are more soluble than 4-chloro-2,3-dimethylpyridine N-oxide itself.</p>

<p>tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate is a chemical compound that is used as a reagent in organic synthesis. It is also used as a building block for the preparation of other compounds. This compound can be used in the synthesis of complex molecules such as heterocycles and natural products.</p>

<p>3,5-Dibromopyrazin-2-amine is a triethyl orthoformate derivative that reacts with formamide to form 3,5-dibromopyrazine. The reaction time is typically less than 10 minutes and the yield is high. The product can be stored in a dry, inert atmosphere for up to 3 months without degradation. The compound has been shown to inhibit cyclic nucleotide phosphodiesterase (PDE) enzymes and cancer cells in vitro.</p>

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

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<p>Hindered amine light stabilizer in polymer synthesis; TEMPO and LTMP precusor</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>4,4'-Dinitro-2,2'-bipyridine-N,N'-dioxide is a high quality reagent that can be used for a variety of purposes including as a building block for the synthesis of complex compounds or as an intermediate in fine chemicals. The CAS number is 51595-55-2 and it has a molecular weight of 138.10 g/mol. This reagent can be used to synthesize useful scaffolds, useful building blocks, speciality chemicals and research chemicals. It also has versatile applications that allow it to react with other compounds to form different products.</p>

<p>Please enquire for more information about N-Isopropyl carvedilol 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>3-Aminopyridine is a compound with the chemical formula C6H5N3. It is used in biological studies as a model for the hydrogen bond, and has been shown to be effective against some bacteria and fungi. 3-Aminopyridine may also have antimicrobial activity. The mechanism of action of 3-aminopyridine is not well understood, but it is thought that this compound might bind to the active site of an enzyme or receptor and deactivate it. 3-Aminopyridine has been found to inhibit dinucleotide phosphate (DNP) reductase, which may play a role in carcinogenesis. There are two nitrogen atoms in 3-aminopyridine, one in the amine group and one in the pyridine ring. The hydroxyl group on the molecule can form hydrogen bonds with other molecules such as hydrochloric acid or hydrogen tartrate, which may be why it reacts with these substances so easily.</p>

<p>2-Aminomethylpyrazine (2-AP) is a molecule that has been studied for its potential as an anti-cancer agent. It has been shown to bind to the DNA of tumor cells and prevent them from dividing, leading to cell death. 2-AP also prevents the production of survivin, which is a protein that promotes cancer cell growth and survival. 2-AP can be used in positron emission tomography (PET) scans to detect tumors, and has shown promise in treating acute myeloid leukemia.</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 α-Hydroxymethylatropine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>3-Chloro-2-nitropyridine is a chemical compound that has been shown to have anticancer activity. It is a structural analog of the nucleophilic piperazine, which can react with hydrogen fluoride in an electrophilic substitution reaction to form 3-chloro-2-nitropyridine oxide. The anticancer activity of this compound may be due to its ability to inhibit the growth of tumor cells by binding to the d4 receptor, inhibiting the production of inflammatory cytokines and growth factors. 3-Chloro-2-nitropyridine has also been shown to have antiinflammatory activities, which may be due to its inhibition of nitric oxide synthesis and 5'-lipoxygenase.</p>

<p>Piperazine is a pharmacological agent that has been used as an antihelminthic drug and for the treatment of metabolic disorders. It is a basic heterocyclic amine, with a piperazine ring fused to an imidazole ring. Piperazine can be synthesized from benzaldehyde, nitroethane, and ammonia. The piperazine ring is the central part of the molecule and consists of two nitrogen atoms (N) connected by three carbon atoms (C). Piperazine has a hydrogen bonding interaction with metal hydroxides such as LiOH and NaOH. This compound also acts as an enzyme inhibitor by binding to receptor activity sites on enzymes and blocking their function. Piperazine forms hydrogen bonding interactions due to its structural analysis, which includes a nitrogen atom in each of the two rings that are bonded together. These nitrogen atoms form hydrogen bonds with other nitrogen atoms in other molecules such as malonic acid or other water molecules in solution.</p>

<p>Indole is a heterocyclic aromatic organic compound. It is a colorless solid that has a strong, unpleasant odor. Indole is classified as a nitrogenous base and is found in many natural products such as the amino acid tryptophan and the alkaloid caffeine. Indole can also be used as a building block for complex molecules, such as pharmaceuticals, herbicides, and pesticides. Indole is soluble in water, but insoluble in most organic solvents. It can be used to synthesize other compounds through reactions with other chemicals or by heating it with different reagents.</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>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>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>Please enquire for more information about 2-Fluoro-5-hydrazinylpyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>1-Piperidinecarbonylchloride is a molecule that has been shown to have anti-inflammatory and anti-cancer properties. It is an aliphatic hydrocarbon with a prenyl group that has been shown to bind to the chloride channel, which leads to increased chloride secretion in the small intestine and decreased chloride secretion in the colon. This may contribute to its therapeutic effects on inflammatory bowel disease. 1-Piperidinecarbonylchloride also inhibits fatty acid synthesis, which may be responsible for its therapeutic effects on metabolic disorders such as diabetes and obesity.</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>3-Bromoquinoline is a brominated quinoline derivative that can be synthesized by cross-coupling reactions. The compound's chemical structure is similar to the 3-azidoquinoline, which was studied in quantum theory and molecular modeling. The 3-bromoquinoline molecule has been shown to exist in two different coordination geometries: octahedral and trigonal bipyramidal. In the octahedral geometry, the 3-bromoquinoline molecule is bound to three bromine atoms and one nitrogen atom, with an intramolecular hydrogen bond between the nitrogen atom and the quinoline ring system. The trigonal bipyramidal geometry also features an intramolecular hydrogen bond between the nitrogen atom and quinoline ring system, as well as a halogen bonding interaction with one of the three bromine atoms.</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>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>3-Aminopyridine-4-carboxaldehyde (3APCA) is an acridone that is a colorless, crystalline solid. It has a molecular formula of C8H6N2O2 and a molecular weight of 174.14 g/mol. 3APCA can be synthesized by heating 2-pyridinecarboxylic acid with chloroacetyl chloride in the presence of pyridine as a solvent. The compound can be detected by nmr spectra, which are efficient methods for characterization of this chemical. The spectrum shows peaks at δ 8.22 ppm (1H), 7.61 ppm (1H), 6.99 ppm (2H), 5.87 ppm (1H), 4.06 ppm (2H). 3APCA has been shown to react with alkyl bromides to form carboxylic acids, which are shown by the peaks at δ 8.22 ppm and</p>

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<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>

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<p>N-Benzoylpiperidone is a synthetic piperidine derivative that is used in the synthesis of other organic compounds. It can be synthesized by reacting phenylacetaldehyde with chloroacetonitrile and hydroxybenzene. It can also be synthesized by reacting bromoacetonitrile with hydroxybenzene in the presence of sodium hydroxide. The compound has two stereoisomers, which are determined by the configuration at the nitrogen atom. The N-benzoyl group on one stereoisomer binds to the intramolecular hydrogen molecule, which signifies its structural analysis. These two isomers are distinguished by their hydroxy group, amide and alkylation properties. They react differently with rat liver microsomes due to different substrate concentration.</p>

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<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>Pyrrolidine is a hypoglycemic agent that has been shown to have antibacterial efficacy against some gram-positive bacteria. It inhibits bacterial growth by binding to the enzyme ribonucleotide reductase, which is required for DNA synthesis. Pyrrolidine also has an antimicrobial effect on human cells and is a substrate for the enzyme IDO1, which may be responsible for many of its biological effects. Pyrrolidine binds to methanol solvent and has been shown to inhibit the activity of endometrial cells by reducing glucose uptake. The reaction with methanol solvent also causes pyrrolidine molecules to change conformation, making them more susceptible to inhibition by IDO1.</p>