Heterocycles with Nitrogen (N)

<p>5-[3-Methoxy-4-(4-methoxy-benzyloxy)-benzyl]-pyrimidine-2,4-diamine is a monoclonal antibody that blocks the signal of CTLA-4, a receptor on T cells. It has been shown to be effective in inhibiting skin cancer and primary breast cancers. This drug also has immunomodulatory effects and can be used to treat autoimmune diseases. 5-[3-Methoxy-4-(4-methoxy-benzyloxy)-benzyl]-pyrimidine-2,4-diamine binds to ctla-4 with high affinity and specificity, preventing the interaction of ctla-4 with its ligands such as CD80 (B7.1) and CD86 (B7.2). This prevents the activation of T cells by antigen presenting cells and suppresses the immune response.</p>

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

<p>2-Bromo-6-fluoropyridine is a versatile building block that can be used to create a range of compounds. It is a useful intermediate and can be applied in the synthesis of high quality reagents, speciality chemicals, and complex compounds. It has been used as a reaction component in the synthesis of 2-(2-bromoethoxy)pyridine and 2-bromopyridine. This compound has CAS No. 144100-07-2, which makes it an important research chemical.</p>

<p>4-Mercaptopyridine is a molecule that has been shown to have an unusual hydrogen bonding interaction. It is a chemical compound that can be hydrolyzed by enzymes. The reaction of 4-mercaptopyridine with enzymes is dependent on the pH of the solution and temperature. The rate of hydrolysis is also affected by the presence of disulfide bonds in the molecule. This active form has been shown to have an enhancement effect on detection sensitivity, which makes it useful for detecting trace amounts of chemicals or metals in water samples. Hydrogen bonding interactions between 4-mercaptopyridine and other molecules are involved in various chemical reactions, such as oxidation, reduction, and elimination reactions.</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>Racemic cis-1-benzyl-2-methyl-4-(N-propananilido)piperidine (SBP) is a synthetic opioid analgesic that has been shown to bind to the μ-opioid receptor. It is the racemic form of the more potent S(+)-isomer. SBP is metabolized in vivo by cytochrome P450 2C19 and cytochrome P450 3A5, and its metabolites can be detected in human liver. The metabolism of SBP also produces propanamide as an intermediate. Recreational use of SBP has been reported with adverse effects including nausea, vomiting, headache, and dizziness.</p>

<p>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>2,4,5-Trichloropyrimidine is a chemical compound that has reactive properties. It can be used in the Suzuki coupling reaction to form new molecules. 2,4,5-Trichloropyrimidine can also be used as a potent inhibitor of epidermal growth factor receptors (EGFRs). It has been shown to inhibit the growth of cancer cells and other autoimmune diseases. 2,4,5-Trichloropyrimidine has shown significant inhibitory activity against kinases. It is selective for EGFRs and does not have any effect on other kinases. This suggests that it may be an effective therapeutic agent for the treatment of certain cancers and autoimmune diseases.</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 (4-Benzylpiperazin-1-yl)piperidin-4-yl-methanone dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>3,5-Dimethylpyridin-2-yl)methanol is a compound used in the synthesis of esomeprazole. It is not considered an impurity or a target compound and does not need to be analyzed. 3,5-Dimethylpyridin-2-yl)methanol is synthesized by reacting 3,5-dimethylpyridine with methanol.</p>

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<p>2-Iodo-1H-imidazole is an asymmetric molecule that is synthesized by a Suzuki coupling reaction between malonic acid and tautomers of 2-iodo-1H-imidazole. This molecule inhibits the activity of inhibitor molecules, such as nitrogen atoms, which are used in pesticide production. It also has pesticidal activity and can be used to treat cancer or autoimmune diseases. 2-Iodo-1H-imidazole is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid.</p>

<p>Please enquire for more information about 2-Bromo-5,6-dihydro-8h-imidazo[1,2-a]pyrazine-7-carboxylic acid tert-butyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-(Methylnitrosoamino)-1-(3-pyridinyl)-1-butanone (NNK) is a carcinogenic chemical that has been identified in tobacco smoke. It induces squamous cell carcinomas in the respiratory tract of rodents and induces lung cancer in the offspring of pregnant rats exposed to NNK. This compound binds to double-stranded DNA, with high affinity for the minor groove, and inhibits DNA synthesis by binding to enzymes such as polymerase chain. In addition, it has been shown to cause transformation of epithelial cells into mesenchymal cells in vitro. 4-(Methylnitrosoamino)-1-(3-pyridinyl)-1-butanone binds to α7 nicotinic acetylcholine receptors and increases the response element activity.</p>

<p>4-Methylpyridine is an antimicrobial agent that is used to inactivate viruses, bacteria, and fungi. It binds to the DNA of these microorganisms by intercalation and disrupts their replication process. 4-Methylpyridine has been shown to inhibit the growth of microorganisms by binding to the nitrogen atoms in their dna and preventing the synthesis of proteins required for cell division. This drug also inhibits the activity of polymerase chain reaction (PCR) enzymes such as Taq DNA polymerase and Klenow fragment. The molecular weight of this compound is 92.14 g/mol and its molar mass is 152.2 g/mol.</p>

<p>2-Mercapto-4,6-dimethoxypyrimidine is a chemical reagent that belongs to the group of dibenzalacetone. This compound has been shown to selectively methylate benzene, dihydric alcohols, and aromatic ethers. It can be used in the chemical industry as a reagent for the production of zirconium metal oxide. 2-Mercapto-4,6-dimethoxypyrimidine has also been found to be an effective catalyst for the synthesis of dodecylbenzene from dimethylbenzene and sodium dodecylbenzenesulfonate.</p>

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<p>1-(3-Chlorobenzyl)piperazine (1CBPZ) is a selective and reversible inhibitor of ns3 protease, which plays an important role in plant resistance. 1CBPZ was found to be effective in controlling the growth of certain bacteria. It also has been shown to be useful for the prevention of liver lesions caused by casein in rats. 1CBPZ has optical properties that are sensitive to boron nitride and can be used as a control analysis for experiments involving this material. This chemical has been shown to inhibit the reaction mechanism of ns3 protease and is being used as an experimental model for studying this enzyme. The detection time for 1CBPZ is 3 hours, which makes it more energy efficient than other compounds.</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-(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>

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<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>4-Chloropyrimidine HCl is a covalent molecule that contains 4-chloropyridine and hydrogen chloride. It exists as two tautomers, the enol form and the keto form. The protonation of the proton on nitrogen will determine which tautomer it will exist in. When there is no proton present, the molecule will exist in its enol form. Resonance is also an important factor with this molecule because it can have a variety of resonance forms. Resonance spectrometry has been used to identify 4-chloropyrimidine HCl because it produces a specific resonance pattern when exposed to magnetic fields. 4-Chloropyridinium trifluoroacetate is another name for this compound that is formed when the chlorine atom bonds with trifluoroacetic acid. This chemical does not have any interactions with azide but can react with tetrazole to produce a stable compound, which can be easily</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>3,6-Dichloropyridazine is a chemical compound that belongs to the group of heterocycles. It is used as an intermediate for the production of other chemicals such as pharmaceuticals and pesticides. 3,6-Dichloropyridazine can be used in the treatment of inflammatory diseases by inhibiting cyclic nucleotide phosphodiesterase and preventing the accumulation of cyclic nucleotides. 3,6-Dichloropyridazine has been shown to inhibit cancer cells by binding to α7 nicotinic acetylcholine receptors in the cell membrane. The chlorine atom at position 3 on the pyridine ring is responsible for this effect. In addition, 3,6-dichloropyridazine has been shown to react with both nucleophilic and electrophilic groups. This chemical also displays a wide range of chemical diversity due to its three chlorine atoms.</p>

<p>1-(3-Bromophenyl)-piperazine is a furan compound with a piperazine base. It is used as an anti-cancer drug in the treatment of cancer and impurities are removed from this compound using chromatography. This compound has been shown to be homocoupled, which means that it can be used to synthesize other compounds. 1-(3-Bromophenyl)-piperazine is approved by the FDA and European Medicines Agency for the treatment of cancer, and has been shown to have immunological properties.</p>

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

<p>4-Ethyl-5-fluoropyrimidine is a white solid with a melting point of 258°C. It is soluble in organic solvents such as acetonitrile and methanol. The compound has been shown to have reversed phase chromatographic properties and can be used as a potential impurity in the synthesis of other compounds. 4-Ethyl-5-fluoropyrimidine is not susceptible to photolytic decomposition but can be oxidized by air, which may result in the formation of impurities. 4-Ethyl-5-fluoropyrimidine can be purified using chromatography methods with high sensitivity and low detection limits. The compound has also been shown to have good chemical stability under ambient conditions, making it suitable for storage or shipping.</p>

<p>Please enquire for more information about 5-[4-(3-Chlorophenyl)piperazin-1-yl]-5-oxopentanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Furo[3,4-b]pyrazine-5,7-dione is a chemical compound that belongs to the group of pyrazinoic acid derivatives. It has anti-inflammatory properties and is used as an ingredient in herbal products. Furo[3,4-b]pyrazine-5,7-dione shows a strong inhibitory effect on protease activity in vitro. This compound also inhibits tumor growth by modulating the expression of inflammatory cytokines such as IL1β, IL6, and TNFα. The molecular structure of Furo[3,4-b]pyrazine-5,7-dione can be accurately predicted using molecular modeling studies. In addition to its anti-inflammatory properties, furo[3,4-b]pyrazine-5,7-dione has been shown to be chemically stable at high temperatures and during chromatography.</p>

<p>Please enquire for more information about 4-(4-Bromophenyl)piperazine-1-carboxylic acid tert-butyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<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>

<p>Please enquire for more information about Methyl 1H-pyrrolo[2,3-b]pyridine-2-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 1-(2-Phenylethyl)piperidin-4-amine dihydrochloride 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 Haloperidol nonanoate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 3-Ethyl haloperidol decanoate 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-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 1-Piperidin-1-ylcyclopentanecarbonitrile 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-[(2,5-Dimethoxyphenyl)methyl]piperazine HCl 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>Please enquire for more information about 3-[4-(3,4-Dichlorophenyl)piperazin-1-yl]-3-oxopropanenitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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>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>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>Iloperidone is a white to off-white crystalline powder that is soluble in water and alcohol. It is used as an antipsychotic drug and belongs to the class of benzamides. Iloperidone has been shown to be effective for schizophrenia, bipolar disorder, and major depressive disorder. The chemical name for iloperidone hydrochloride is 4-(2,4-Difluorobenzoyl)piperidine hydrochloride. This drug also has a high affinity for serotonin 5-HT2A receptors in the brain, which may contribute to its therapeutic effects.</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>1-(4-Fluorobenzyl)piperazine is a potent tyrosinase inhibitor and has been shown to inhibit the proliferation of human cancer cells. It has been found to have inhibitory activity against the amine oxidase enzyme, which is involved in the biosynthesis of pro-inflammatory cytokines. The biochemical properties of 1-(4-fluorobenzyl)piperazine have been studied by liquid chromatography and mass spectrometry and it has been found to be synthesized from piperazine and an amine. There are no other studies available on this drug at this time.</p>

<p>Please enquire for more information about 2-Chloro-5-(trifluoromethyl)pyridin-4-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-4,6-dimethylpyrimidine is a molecule that contains a hydroxyl group, copper chloride, nitrogen atoms, sodium carbonate, and hydroxybenzoic acid. The antimicrobial properties of 2-amino-4,6-dimethylpyrimidine are due to the presence of the hydroxyl group and copper chloride in its structure. This compound has been shown to have bactericidal activity against Pseudomonas aeruginosa and other gram-negative bacteria. It also inhibits the growth of these bacteria by interfering with their ability to synthesize proteins. 2-Amino-4,6-dimethylpyrimidine is a molecule that has an octahedral coordination geometry and forms hydrogen bonds with water molecules. It binds to the surface of minerals such as calcite or quartz and can be used for gravimetric analysis.</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>4-Pyridazinecarboxylic acid is a salt that contains sodium. It is a white crystalline solid that is soluble in water, ethanol, and acetone. It has been shown to be effective against Leishmania species and Cryptococcus neoformans. 4-Pyridazinecarboxylic acid inhibits the growth of these fungi by binding to their cell membrane and inhibiting protein synthesis. 4-Pyridazinecarboxylic acid forms coordination complexes with metal ions that are involved in electron transfer reactions during the oxidative phosphorylation process. This leads to a decrease in ATP production and an increase in reactive oxygen species (ROS), which disrupts the function of macrophages and other phagocytic cells, leading to immunosuppression.</p>

<p>2-Methyl-5-nitropyridin-3-amine is a heterocyclic compound that is synthesized by the cyclization of 2-methylpyridine with sodium nitrite. The reaction product is hydrolyzed to yield the desired compound, 5-nitropyridine. The synthesis of this compound can be used as a target for organic synthesis.</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>1-(4-Methoxybenzyl)piperazine is a chemical compound that has been shown to have inhibitory activities against cancer cells. It also shows potential for the treatment of type 2 diabetes and Alzheimer's disease. The mechanism of action is not well understood, but it may be due to its ability to induce mitochondrial biogenesis and insulin sensitivity. 1-(4-Methoxybenzyl)piperazine has also been shown to improve memory in rats with spontaneous dementia, similar to the effects of donepezil (a drug used for Alzheimer's disease). 1-(4-Methoxybenzyl)piperazine can be taken orally or administered via injection.</p>

<p>1-(3,4-Dichlorobenzyl)piperazine is an amine that is used as a reagent in organic synthesis. It is a buffered, acidic compound that emits fluorescence under UV light. It has been shown to be an electron donor and electron acceptor. 1-(3,4-Dichlorobenzyl)piperazine reacts with phenylpiperazines in the presence of acid to form a mixture of phenylpiperazines with different aliphatic chains. The reaction is characterized by emission of fluorescence that can be measured using spectroscopy techniques.</p>

<p>1-[(2-Pyridyl)methyl]piperazine is a fluorescent organic solvent. It is a piperazine derivative with low detection limit, which can be used for the detection of metal ions. 1-[(2-Pyridyl)methyl]piperazine has also been shown to be a hyperpolarizing agent in organic solvents and has been used as an optical sensor for 4-chloro-7-nitrobenzofurazan, which is a compound that exhibits fluorescence properties. 1-[(2-Pyridyl)methyl]piperazine can be used as a linker in microscopy techniques to immobilize biomolecules on the surface of glass slides.</p>

<p>Tris(2-phenylpyridine)iridium (IrCl) is a coordination compound that is used as a catalyst to initiate cationic polymerization of biphenyl. It is also used as an analytical reagent for determining the content of fatty acids in oils and fats. The steric interactions between the phenyl groups and the electron-rich iridium atoms lead to a high degree of conversion of ethylene oxide to ethylene glycol, which can be observed by UV absorption. The synthesis of IrCl occurs in two steps: first, the reaction of chloroacetone with phenylmagnesium bromide followed by addition of hydrated iridium chloride. The product crystallizes in red needles, which are analyzed using x-ray crystal structures. Analysis using nmr spectroscopy reveals that IrCl contains four nitrogen atoms and three oxygen atoms. Its redox potentials are -0.9 volts for oxidation and +1.3 volts for reduction, making</p>

<p>Please enquire for more information about N-Boc-amino-(4-N-fmoc-piperidinyl)carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,5-Dichloropyrazine is a ligand that binds to the bromodomain of a protein and causes it to deform. The bromodomain contains a metal ion at its core and is an important component of many proteins that regulate gene expression. 2,5-Dichloropyrazine has been shown to bind to the metal ion in the bromodomain of some proteins and cause them to deform. This deformation results in changes in the shape of the protein's DNA-binding site, which can alter the way it regulates gene expression. 2,5-Dichloropyrazine also interacts with hexamethylenetetramine (HMT) to form anions and chlorinating agents. These interactions may be responsible for 2,5-dichloropyrazine's high yield.</p>

<p>Please enquire for more information about 5-Fluoropyridine-2-boronic 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 tert-Butyl 4-azidopiperidine-1-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 5-Oxo-1-(pyridin-3-ylmethyl)pyrrolidine-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>

<p>Pyridin-4-ylmethanamine is a chemical compound that contains a pyridine ring and an amine (-NH2) group. It is usually used as a building block for the synthesis of other compounds. Pyridin-4-ylmethanamine can be synthesized from picolinic acid, which is obtained through a reaction with sodium hydrochloride in an alkaline solution. This reaction proceeds via two steps: first, the formation of a pyridinecarboxylic acid ester and then the addition of ammonia to form pyridin-4-ylmethanamine. The transfer reactions that occur during this process are highly dependent on temperature and pH. The frequency shift effect can be observed when pyridin-4-ylmethanamine interacts with amines, which changes its absorption spectrum.</p>

<p>Please enquire for more information about 4-Bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Ethyl-2-pyridineethanol is an anti-diabetic drug that belongs to the class of thiazolidinediones. It is the active form of pioglitazone, which has been shown to bind to peroxisome proliferator-activated receptor gamma (PPARγ). This binding results in increased expression and activity of insulin receptors on cell membranes. 5-Ethyl-2-pyridineethanol also binds to PPARγ in a similar manner as pioglitazone, and it has been shown to be an agonist for PPARγ. This compound has a number of other biological effects such as inhibition of the production of acetone by the liver, which is due to its ability to inhibit diazotization.</p>

<p>Please enquire for more information about 2-Imidazo[1,2-a]pyridin-2-yl-ethylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 4-[(2,5-Dimethyl-1H-pyrrol-1-yl)methyl]piperidine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 4-(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 7-(Difluoromethyl)-5-methyl[1,2,4]triazolo[1,5-a]pyrimidine-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>5-Bromo-2-chloro-3-fluoropyridine is a catalytic reagent for the amination of anilines. It is extracted from coal tar, and is used in the manufacture of pesticides and pharmaceuticals. 5-Bromo-2-chloro-3-fluoropyridine has been shown to be an effective catalyst for the synthesis of functionalized adducts. This compound can also be used as a chemoselective agent in palladium catalysis, where it selectively adds hydrogen bromide to form aryl halides.</p>

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

<p>2-Ethynylpyridine is a structural analog of pyridine and is used in the synthesis of polymers. 2-Ethynylpyridine has been shown to have significant cytotoxicity, which may be due to its ability to bind to receptors. Using X-ray crystallography, it has been determined that 2-ethynylpyridine binds to a receptor by forming hydrogen bonds with the nitrogen atoms on the receptor. 2-Ethynylpyridine can also be activated by hydrochloric acid (HCl) and reacts with sodium hydroxide (NaOH) solution and x-rays to form an x-ray crystal structure. 2-Ethynylpyridine is synthesized by the reaction between ethyne and nitric acid in the presence of aluminum chloride (AlCl3). The product is reacted with hydrochloric acid (HCl) or sodium hydroxide (NaOH) solution, which causes a change in</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>

<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>

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

<p>Please enquire for more information about 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>Prasugrel is a pharmaceutical compound that belongs to the class of thienopyridines. It has been shown to inhibit platelet aggregation and is used for the prevention of blood clots in patients with coronary artery disease. Prasugrel binds to the P2Y12 receptor on the surface of platelets, which prevents ADP from binding, thereby inhibiting platelet aggregation. Prasugrel is a crystalline solid that is soluble in water.</p>

<p>5,6-Diphenyl-1,2,4-triazine-3(2H)-thione is a chemical compound that is used as an antiviral agent. It is structurally related to both the hydrazines and the triazines. 5,6-Diphenyl-1,2,4-triazine-3(2H)-thione has inhibitory concentrations of 2.5 mg/mL against influenza A virus and can be used in the treatment of viral infections. The structure of this compound consists of a spacer between two sulfur atoms with a disulfide bond. The 5 position is substituted with a phenyl group and the 6 position is substituted with an amine group. This compound also has nmr spectra that can be analyzed for structural information about the molecule.</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>3-Acetyl-6-methylpyridine is a chemical compound that has been found to have antibacterial properties. It can be used for the treatment of bacteria in wastewater and other biological treatments. 3-Acetyl-6-methylpyridine is insoluble at room temperature, but becomes soluble when heated to 100 degrees Celsius. This chemical compound has been shown to inhibit the growth of Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli. 3-Acetyl-6-methylpyridine also has anti-inflammatory properties and can be used in the treatment of Alzheimer's disease.</p>

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<p>1-(2-Bromophenyl)piperazine is a drug that inhibits the activity of dehydrogenase, an enzyme that catalyzes the oxidation of NADH to NAD. It has been shown to inhibit other enzymes as well, such as those involved in the synthesis of amino acids and nucleic acids. 1-(2-Bromophenyl)piperazine has shown potential as a therapeutic agent for Parkinson's disease. This drug is being tested in clinical trials for its efficacy in treating a variety of diseases, including metabolic and cardiovascular disorders, hepatobiliary diseases, and neurodegenerative diseases.</p>