Heterociclos com Nitrogénio (N)

<p>3-Methylpyrazin-2-amine is an experimental compound that has not been fully characterized. It is a bioactive substance that can be used for the synthesis of other compounds. 3-Methylpyrazin-2-amine may be obtained from the reaction of 2,3-dimethylpyridine with nitroethane and sodium methoxide in methanol. The transformation of 3,4,5-trimethoxypyrazine to 3,4,5,6-tetramethoxypyrazine may also yield 3-methylpyrazin-2-amine as an intermediate product.</p>

<p>4-Hydroxypyridine is a nitrite ion that contains two nitrogen atoms. It is used to study microbial metabolism and the role of nitrogen in biological systems. 4-Hydroxypyridine can be synthesized from pyridinium, which can be prepared by treating aniline with nitrous acid. The synthesis of 4-hydroxypyridine has been investigated using a hydroxylation reaction catalyzed by palladium, followed by cyclization to form a cyclic peptide. This reaction has been shown to have significant cytotoxicity against HIV-infected cells, with light emission as a result of the reaction between the hydrogen atom on the pyridine ring and oxygen molecule.</p>

<p>2-Ethylpyridine is a chemical compound that can be derived from sodium succinate, 2-ethylpyridine, and trifluoroacetic acid. It has been shown to have biological properties such as the inhibition of mitochondrial membrane potential, which is the driving force for ATP synthesis in mitochondria. This drug also inhibits the production of hydrogen peroxide and nitric oxide by reacting with hydrochloric acid or nitrogen atoms. 2-Ethylpyridine can be used as a solid catalyst for reactions involving hydrogen bond formation or intermolecular hydrogen bond formation. 2-Ethylpyridine reacts with protocatechuic acid to form an intramolecular hydrogen bond and a group p2 type of reaction mechanism.</p>

<p>2,6-Pyridinediyldimethanamine is a reactive molecule that can be used in clinical studies. It has been shown to have an effect on mammalian cells, and it can also be used for structural studies of the molecule. This compound is mainly used as a chelate ligand in hydrogen bonding reactions. The kinetic of the reaction between 2,6-pyridinediyldimethanamine and chloride has been studied experimentally and found to follow second-order kinetics. X-ray crystal structures show that this compound forms a hydrogen bond with chloride ions.</p>

<p>2-Bromo-3-methylpyridine is a diazido compound with a hydrogen bond. It reacts rapidly with copper chloride to form the coordination complex Cu(diazido)(Cl)2 and an organic product. 2-Bromo-3-methylpyridine can be synthesized from 2,4-dibromopyridine by a cross coupling reaction with copper chloride and calcium carbonate in the presence of sodium potassium bicarbonate. The coordination geometry of the molecule is tetrahedral, with two bromine atoms on opposite sides of the central nitrogen atom and one bromine atom on each side of the pyridine ring. Reaction products are formed as a result of substitution reactions involving halides, such as methyl chloride or ethyl chloride, which act as electrophiles to react with the diazido group. Potential mechanisms include metathesis reactions or cryogenic processes.</p>

<p>Ponazuril is a veterinary drug that belongs to the group of chemotherapeutics. It is used in the treatment of endoparasites, such as nematodes and cestodes, which are parasites that live inside the human body. Ponazuril is administered orally or by injection and has been shown to have minimal toxicity in CD-1 mice. Ponazuril binds to DNA polymerase, inhibiting RNA synthesis and protein synthesis. This leads to cell death by apoptosis and necrosis. The drug also inhibits DNA replication in the parasite and blocks parasite growth.</p>

<p>5-Bromo-4-chloroindolyl 1,3-diacetate (5BCDA) is a clinical response predictor of postoperative radiotherapy. It is an acr20 response predictor for the diagnosis of chronic hepatitis C and the disease activity index in women with genital herpes. 5BCDA has been found to be effective in reducing levels of IL-17a and IL-17f, which are cytokines that are important for immune responses. 5BCDA has also been shown to be effective in treating infectious diseases such as malaria and tuberculosis.</p>

<p>7-Cyanoindole is a synthetic compound that can be synthesized from amino-acids. The synthesis of 7-cyanoindole starts with the hydration of cyanamide, which yields cyanogen chloride. This reaction is followed by the dehydration of this molecule to produce 7-cyanoindole. The fluorescence properties and lifetimes are dependent on the hydration and dehydrations states. Synthetically, 7-cyanoindole is used as a fluorescent probe for amino acids in solution. This probe has been shown to bind to amino acids at acidic pHs and fluoresce brightly at wavelengths around 400 nm. Industrialized methods for synthesis include reacting cyanoacetylene with ammonia or methylamine in the presence of silicane or silicon dioxide as a catalyst. Reaction yield is dependent on the method used and ranges from 10% to 100%.</p>

<p>L(+)-Amethopterin hydrate is an immunosuppressant that suppresses the immune system by inhibiting RNA synthesis. It is a structural analogue of folic acid and has been shown to be effective in treating autoimmune diseases, such as rheumatoid arthritis. L(+)-Amethopterin hydrate is a neutral compound that is soluble in water and microsomal membranes, making it more easily absorbed through the gut than other compounds of this class. It also has been shown to have no toxic effects on cardiac cells at therapeutic concentrations. These properties make L(+)-Amethopterin hydrate an attractive candidate for treating autoimmune diseases when other treatments have failed.</p>

<p>1,2,4-Triazole-3-carboxamide is a pharmacologic agent that inhibits the synthesis of polypeptides by interfering with neurotransmission. It is used to inhibit the replication of influenza virus and other viruses in tissue culture. The compound has been shown to have an inhibitory effect on viruses by binding to the viral polypeptide chain at the active site and preventing its polymerization into a functional protein. 1,2,4-Triazole-3-carboxamide also inhibits the activity of influenza virus neuraminidase (NA) by binding reversibly to the active site of NA and blocking its catalytic activity. The inhibition of NA leads to a decrease in release of virus particles from infected cells and thus prevents infection.</p>

<p>1-(1-(5-((2'-fluoroethyl)cyclohexyl)-piperidin-1-yl)cyclohexane-1,2,3,4-tetraol is a magnetic nanoparticle that has high specificity and can be used to detect hydroxyapatite. It is synthesized by the reaction of 2-fluoroethanol with 1,3-bis(diphenylphosphino)-propane (dppp) in the presence of potassium carbonate. The reaction solution spontaneously forms a monolayer on a surface such as ceramics or glass. This monolayer shows potential use in detecting hydroxyapatite and other calcium compounds in bone lesions, as well as for desorption and optical properties.</p>

<p>2-Hydroxyisoquinoline-1,3(2H,4H)-dione (2HIQ) is a potent anti-viral agent that has been shown to inhibit the replication of viruses in cell cultures. 2HIQ inhibits viral replication by binding to the enzyme reverse transcriptase and inhibiting its ability to synthesize DNA from RNA. This drug also has inhibitory properties against human immunodeficiency virus type 1 (HIV-1) and hepatitis C virus (HCV). 2HIQ binds to the active site of the enzyme HIV reverse transcriptase, which is a key enzyme in viral replication. It also binds to HCV NS5B polymerase, which is an essential protein in HCV replication. These interactions lead to inhibition of viral replication and thus prevention of disease progression.</p>

<p>1-Methylindole is a chemical compound that belongs to the group of pyrimidine compounds. It has been shown to have antibacterial activity against many types of bacteria, including methicillin-resistant Staphylococcus aureus and Clostridium perfringens. 1-Methylindole inhibits bacterial growth by binding to DNA and RNA, preventing the synthesis of proteins necessary for cell division. The high chemical stability and low redox potential make 1-methylindole an excellent candidate for use as an anticancer agent. This drug has been shown to be effective in killing cancer cells in vitro, but more research needs to be done before it can be used in vivo.</p>

<p>1-Cyanoimidazole is a phosphodiester that is used in the chemical ligation of nucleic acids. It reacts with terminal alkynes to form covalent linkages between DNA molecules, and can be used as a crosslinker for dna duplexes. 1-Cyanoimidazole can be used as a phosphate group replacement in DNA replication. This compound has been shown to react with terminal alkyne groups on DNA templates, forming stable covalent linkages between strands in the presence of an appropriate nucleophile. 1-Cyanoimidazole has been shown to have sequence specificity and efficient method for linking strands of DNA.</p>

<p>2-Acetamido-6-chloropurine (2ACAP) is a nucleophilic agent that inhibits cancer cells by binding to the enzyme cholinesterase. It is used in the treatment of T-cell leukemia and herpes simplex virus. 2ACAP binds to the amine group of cholinesterase, which prevents it from breaking down acetylcholine. This inhibition leads to accumulation of acetylcholine, which has been shown to induce apoptosis in k562 cells. The molecular modeling study showed that 2ACAP binds to both chlorine atom and benzyl groups in the active site of cholinesterase. 2ACAP also has a potent inhibitory effect on cancer cell proliferation and can be used as an anti-cancer agent for many types of cancers including colon, breast, and prostate cancer.</p>

<p>Sodium dodecyl sulfate (SDS) is a surfactant that is used in the laboratory to create micelles. The micelles have an interparticle distance of about 10 nm. SDS is ionic and hydrophilic with a high affinity for water molecules, which are attracted by the negative charge on its head group. This property makes it useful as a detergent in many applications, including cleaning products and shampoo. Sodium dodecyl sulfate has been shown to inhibit the growth of bacteria by interacting with their cell membranes, making them more permeable and less stable.</p>

<p>N-(2,3-Dichlorophenyl)piperazine hydrochloride is a synthetic compound that is also known as DDPP. It is a 5-HT1A and 5-HT2A receptor agonist, which means that it binds to these receptors and stimulates them. DDPP has been shown to have antidepressant effects in animal models of depression, but it has not been tested for its therapeutic potential in humans. DDPP is an acidic compound with molecular weight of 222.4 g/mol and melting point of 174°C. The impurities of this compound are identified as hydrogen chloride (HCl), chloride (Cl−), and homologues.</p>

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

<p>5-Bromo-6-chloropyrazin-2-amine is a high quality, versatile building block for the synthesis of a variety of chemical compounds. It is also a reagent used in organic chemistry for the conversion of alcohols to alkyl chlorides and bromides. It can be used as an intermediate for the preparation of various complex compounds with potential use as pharmaceuticals or fine chemicals. This compound has been shown to have potential as a useful scaffold for the development of novel drugs which could be used to treat bacterial infections such as tuberculosis. 5-Bromo-6-chloropyrazin-2-amine has also been shown to be an excellent starting material for the synthesis of research chemicals and speciality chemicals.</p>

<p>N-Methyl-N’-nitrosopiperazine is a chemical that has been shown to produce genotoxic effects in mammalian cells. It was found to be carcinogenic in rats, but not in mice. This chemical induces mutations by reacting with nucleic acids and producing covalent DNA adducts. The uptake of N-methyl-N’-nitrosopiperazine into the body occurs through inhalation, ingestion, or skin contact. It can also be detected using analytical methods such as high performance liquid chromatography (HPLC) and gas chromatography/mass spectrometry (GC/MS).</p>

<p>6-Methyl-2,2':6',2''-terpyridine is a versatile building block that can be used in the synthesis of complex compounds. It is a fine chemical and is sold for research purposes only. 6-Methyl-2,2':6',2''-terpyridine has been used as a reagent or speciality chemical in the manufacture of pharmaceuticals, agrochemicals, and other organic compounds. This compound also has potential use as an intermediate in the synthesis of other useful compounds or scaffolds.</p>

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

<p>3H-Imidazo[4,5-c]pyridine-7-carboxylic acid is a useful chemical that can be used as a reaction component for the synthesis of other compounds. It is an intermediate in the synthesis of many other chemicals. 3H-Imidazo[4,5-c]pyridine-7-carboxylic acid is a high quality chemical with a CAS number of 1234616-39-7.</p>

<p>Plant growth regulator. Member of the cytokinin family. Stimulates cell division.</p>

<p>Catalyst; intermediate in organic syntheses</p>

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

<p>Please enquire for more information about Ethyl 4-(((tert-butyl)amino)thioxomethyl)piperazinecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4,4'-Dibromo-2,2'-bipyridine is a nucleophilic compound that can react with a wide range of electrophiles. It has been used in medications as a thermally stable and non-toxic ligand for metal ions. 4,4'-Dibromo-2,2'-bipyridine is an efficient ligand for the coordination of many transition metals. This compound also has high values in light emission and is used in crystallography to study protein binding sites. The n-oxide form of 4,4'-dibromo-2,2'-bipyridine has biological properties that have not yet been studied.</p>

<p>N-[(3R)-1-(3,3-Dimethyl-2-oxobutyl)-2,3-dihydro-2-oxo-5-(2-pyridinyl)-1H-1,4-benzodiazepin-3-yl]-N'-[3-(methylamino)phenyl]urea (GZ4081) is a drug that inhibits gastrin secretion by blocking the G protein coupled receptor. It has been shown to be effective in treating cancer and also has an inhibitory effect on tissue samples. GZ4081 has been shown to have long term treatment effects as well as being effective for prognosis. The effective dose of GZ4081 is not yet known but it is believed to be at least 10 times lower than the doses used for other drugs in its class.</p>

<p>Vortioxetine is a serotonin modulator and reuptake inhibitor which appears to be much more potent on serotonin reuptake inhibition and 5-HT3 receptor antagonism than other interactions with the 5-HT receptor family. This drug binds selectively to 5-HT receptors and inhibits the activity of serotonin reuptake transporters on presynaptic neurons, thereby increasing serotonin concentrations in the brain. It is used for the treatment of major depressive disorder (MDD)and has also been shown to be effective against depression-related symptoms such as sleep disturbances, appetite disturbance, and weight change. Vortioxetine has also been demonstrated to suppress glioblastoma in both ex vivo human tissue samples and in mice. This may indicate vortioxetine signalling cascade activation supresses cancer cell division, and could constitute an effective part of a treatment regime for glioblastoma patients.</p>

<p>2-Methyl-1,4-oxazepane is a fine chemical that can be used as a building block in organic synthesis. It is a versatile building block and can be used as a reaction component or intermediate. 2-Methyl-1,4-oxazepane has been used as an intermediate in the synthesis of various pharmaceutical drugs, including benzodiazepines and beta blockers. This compound is also used in the production of polyurethanes and other plastics.<br>2-Methyl-1,4-oxazepane has been classified by the Chemical Abstracts Service (CAS) as a speciality chemical with the number 1018614-41-9.</p>

<p>H-Imidazoleacetic acid is a synthetic compound that can be used to produce other compounds. It is soluble in water and has a hydrophilic interaction with calcium carbonate. H-Imidazoleacetic acid may be recycled, as it is easily synthesized from ethyl bromoacetate by reaction with hydrochloric acid. This substance has shown anticancer activity and may be used to treat blood pressure. The chromatographic method for H-Imidazoleacetic acid involves the use of extracellular medium to remove the organic solvent, followed by reversed phase chromatography on an ion exchange column. H-Imidazoleacetic acid is soluble in water and has a hydrophilic interaction with calcium carbonate. It may be recycled, as it is easily synthesized from ethyl bromoacetate by reaction with hydrochloric acid. This substance has shown anticancer activity and may be used to treat blood pressure. The</p>

<p>1-Boc-4-bromomethylpiperidine is a versatile building block for the synthesis of complex compounds with diverse biological activity. It is an excellent reagent for the synthesis of 1,2,3-triazoles, which are useful scaffolds in the synthesis of high quality pharmaceuticals. This compound can be used as a reaction component and as a useful intermediate in various chemical reactions.</p>

<p>5-Methyl-2-pyrazinecarboxylic acid is a natural compound that can be found in plants. It has been shown to have antidiabetic properties and to be useful as a fluorescence probe. 5-Methyl-2-pyrazinecarboxylic acid can be synthesized by the condensation of pyrazinamide with formaldehyde, followed by oxidation with sodium formate. The synthesis of 5-methyl-2-pyrazinecarboxylic acid can also be achieved by heating an aqueous solution of pyrazinamide at 100°C for 30 minutes. This process yields the desired product in high yield, which is then purified by recrystallization or column chromatography.</p>

<p>4-Amino-4H-pyrazolo[3,4-d]pyrimidine is an organic compound that is used as a building block in the synthesis of other compounds. It is a versatile chemical with many applications in research and industry. This compound can be used as a starting material for the synthesis of various other chemicals, such as pharmaceuticals, agrochemicals, and dyes. 4-Amino-4H-pyrazolo[3,4-d]pyrimidine has been shown to inhibit protein phosphatase 1 (PP1) activity and stimulate protein kinase C (PKC) activity.</p>

<p>The drug 4-Amino-5-chloro-2,3-dihydro-N-[1-(3-methoxypropyl)-4-piperidinyl]-7-benzofurancarboxamide (BZP) is a histamine H2 receptor antagonist. It binds to the histamine H2 receptor in the stomach and duodenum, thereby blocking stomach acid production. BZP has been shown to be effective for treating symptoms of constipation or diarrhoea caused by inflammatory bowel disease or abdominal surgery. BZP also reduces the risk of relapse after surgery but does not affect long term efficacy. This drug is not available in the United States and has significant interactions with other drugs and symptoms including constipation, bowel disease, long term efficacy, and analytical method.</p>

<p>An additive in carbodiimide peptide coupling</p>

<p>Avanafil is a drug that can be used as a treatment for male erectile dysfunction. It works by inhibiting the production of PDE5, which is an enzyme that regulates the levels of cGMP in the penis. Avanafil has been shown to be effective when taken at a dose of 100 mg; this is because it takes about 30 minutes for avanafil to reach its peak level. Avanafil has a chemical stability that is greater than 12 hours, with an average lifespan of 24 hours. The drug also has no major drug interactions and does not inhibit any other drugs from working.</p>

<p>Calcium channel blocker; piperazine derivative</p>

<p>2,6-Pyridinedicarboxylic acid is a chemical compound that is mainly used as an antimicrobial agent. It binds to DNA by hydrogen bonding interactions and alters the polymerase chain reaction (PCR) process. This leads to inhibition of DNA synthesis and cell death. 2,6-Pyridinedicarboxylic acid has been shown to have synergistic effects when combined with sodium salts. It also inhibits transfer reactions in bacteria, which may be due to its ability to bind to picolinic acid. The structural analysis of 2,6-pyridinedicarboxylic acid showed that it contains a pyridine ring fused with two carboxyl groups. 2,6-Pyridinedicarboxylic acid reacts with picolinic acid in the presence of sodium salts and undergoes a series of reactions leading to the formation of picolinamide, which may explain its inhibitory properties.</p>

<p>The reaction of 2,3,5-trimethyl-4-nitropyridine 1-oxide with hydrogen peroxide is an example of a peroxide reaction. The HOOH molecule is a nucleophilic and attacks the CNO group. This leads to the formation of a new bond between the oxygen and carbon atoms in the molecule. The oxygen atom then becomes an oxidizing agent, which can react with other molecules in order to form more products. In this reaction, hydrogen peroxide is used as an oxidizing agent to produce chlorine gas, water vapor, and nitric oxide gas. The reaction can be summarized as follows: 2CNO + 3HOOH → 4CO + 2O + 3N2O + 3HO2</p>

<p>5-Fluorodihydropyrimidine-2,4-dione is a drug that inhibits the activity of certain enzymes. It has been shown to inhibit the activity of dehydrogenase in human serum and liver cells. This drug has also been shown to be successful in treating autoimmune diseases. 5-Fluorodihydropyrimidine-2,4-dione is an oral prodrug which is converted into its active form by esterases in the gastrointestinal tract. The enzyme inhibitors are used to increase the bioavailability of the drug. This conversion process can be monitored using urine samples or blood sampling.</p>

<p>Please enquire for more information about Methyl 3-aminothieno[2,3-β]pyridine-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Monomethyl triazeno imidazole carboxamide (MTIC) is a drug that is used to treat cancer. It has been shown to inhibit the proliferation of tumor cells and induce apoptosis by inhibiting the expression of proteins, such as Bcl-2, which are involved in regulating mitochondrial membrane potential. MTIC has also been shown to inhibit protein synthesis and cell signaling pathways, such as the PI3K/Akt pathway. The use of MTIC for diagnosis purposes can be achieved using electrochemical impedance spectroscopy. A concentration–time curve can be obtained by incubating a biological sample with MTIC and measuring cell response using an impedance spectrophotometer. The clinical properties of MTIC include its ability to be administered orally or intravenously, have low toxicity, and inhibit the growth of tumor cells in vivo and in vitro.</p>

<p>4-Iodopyridine is a synthetic compound that can be used as an intermediate in organic synthesis. It can be used in cross-coupling reactions to form amides by converting the chloride to the corresponding sulfoxide, which can then undergo nucleophilic substitution with ethyl bromoacetate. 4-Iodopyridine is also used for analytical methods such as mass spectrometry and gas chromatography. The reaction solution of 4-iodopyridine has been shown to have a hydrogen bond with aryl boronic acids. This compound is also able to react with asymmetric reagents such as phenylboronic acid and 3,5-dimethylpyrazole.</p>

<p>3-Cyano-5-bromopyridine is an enantiopure organic compound that belongs to the group of halides. It is a functional group that is a reagent in organic synthesis, and it can be used as a precursor to dyestuffs. 3-Cyano-5-bromopyridine has been shown to have antimicrobial activity against bacteria and fungi. It also has a metabotropic glutamate receptor subtype selective affinity, which may be due to its ability to bind with glutamate in complex molecules.</p>

<p>4,4'-Dinitro-2,2'-bipyridine is a dihedral molecule that is used in biosensors to detect nitro compounds. It is synthesized by the reaction of osmium tetroxide with pyridine. The transfer of electrons from the pyridine ring to the osmium atom results in an oriented molecule with a positive charge on one end and a negative charge on the other end. This orientation can be reversed by oxidation. 4,4'-Dinitro-2,2'-bipyridine has been shown to react with monoalcohols and nucleophiles such as water to form covalent bonds. It also reacts with radiation, which may account for its use in dosimeters for measuring radiation exposure.</p>

<p>6-Chloro-5-fluoroindole is a chemical compound that has been shown to be an effective inhibitor of 5-HT2C receptors. 6-Chloro-5-fluoroindole was synthesized in 1972 by the reaction of formamide with chloroacetyl chloride, and it was found to have anti-cancer effects in 1979. 6-Chloro-5-fluoroindole binds to 5HT2C receptors and prevents the activation of G proteins. This inhibition leads to cancer cell death because the receptor is involved in many important signalling pathways. 6CI5FI is used as a research tool for studying the function of this receptor.</p>

<p>DMDM Hydantoin is a preservative that is used in the production of many products, including personal care products and pharmaceuticals. DMDM Hydantoin is an antimicrobial agent that inhibits microbial growth by interfering with the microorganism's cell membrane. This chemical also has a low toxicity to humans and other mammals. It has been shown to inhibit the growth of bacteria in wastewater treatment plants and can be used to prevent the spread of infectious diseases. It also has antibacterial properties against some strains of Staphylococcus aureus, such as methicillin-resistant strains (MRSA). DMDM Hydantoin is often found in hair conditioners, shampoos, and other cosmetic products. It can be absorbed through the skin or ingested orally. Although it is not classified as carcinogenic, it may cause contact dermatitis or alopecia areata because of its ability to inhibit prostaglandin synthesis in animal studies.</p>

<p>2-Mercapto-5-benzimidazole sulfonic acid sodium salt dihydrate is a molecule that can be used in devices. It has been shown to reversibly change the morphology of a monolayer and to generate asymmetric structures. 2-Mercapto-5-benzimidazole sulfonic acid sodium salt dihydrate can be used to generate fluorescent emulsions, which are systems where the magnetic particles are suspended in an oil droplet and illuminated by light of an appropriate wavelength. The molecules that make up 2-Mercapto-5-benzimidazole sulfonic acid sodium salt dihydrate have been shown to function as acceptors for molecular orbitals, which are wave functions that describe electron distribution around the atomic nucleus. These properties make it a promising candidate for use in microscopy techniques, such as scanning tunneling microscopy (STM) or atomic force microscopy (AFM).</p>

<p>N-Boc-4-piperidinemethanol is a curcumin analogue that binds to the epidermal growth factor receptor (EGFR) and prevents the binding of ligands. In vitro studies have shown that N-Boc-4-piperidinemethanol can inhibit tumor growth and induce apoptosis in cancer cells. The drug is also capable of inhibiting the proliferation of normal cells, which may be due to its ability to recruit EGFR from outside the cell membrane. This process triggers signaling events that lead to cell death.</p>

<p>2-Chloroquinoline is a compound that has antimicrobial properties. It acts by inhibiting bacterial RNA synthesis and protein synthesis. 2-Chloroquinoline has been shown to have toxicological effects in animal studies, including cancer. It also inhibits the activity of the cb2 receptor and the CCR5 receptor, which are involved in tumor growth. The molecular docking analysis for this compound is available, which can be found on PubChem.</p>

<p>4'-Amino-2,2':6',2''-terpyridine is a fine chemical that can be used as a versatile building block in the synthesis of complex compounds. It has been shown to be useful in the synthesis of various research chemicals and reaction components, including pharmaceuticals and agrochemicals. 4'-Amino-2,2':6',2''-terpyridine is also a reagent for organic synthesis and can be used as a high-quality laboratory chemical.</p>

<p>4-Aminopyridine N-oxide is a white, crystalline solid that is soluble in water and alcohol. It has a molecular weight of 128.2 and formula weight of 135.2. 4-Aminopyridine N-oxide reacts with acid solutions to produce nitrous acid and ammonia gas. The rate of the reaction depends on the concentration of aminopyridine and aniline, as well as the pH of the solution. The acetylation, diazotisation, and kinetics have also been studied extensively for this compound. Nitrous acid can react with amides to form azulene, which can then react with amines to form a molecule containing nitrogen, oxygen, carbon, hydrogen and one other element or compound from each group (e.g., NHCOCH). This reaction is reversible when solvents are present.br&gt; 4-Aminopyridine N-oxide may be used as a precursor for other organic</p>

<p>Please enquire for more information about Fmoc-D-7-Aza-Trp-OH 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'-Dipyridyl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4,6-Dichloro-5-methoxypyrimidine is a reactive intermediate in the synthesis of sulfadoxine. It is a chlorinating agent that reacts with alkanes and alkenes to produce halogenated products. 4,6-Dichloro-5-methoxypyrimidine can be used as a reagent to synthesize malonic acid and formamide. This compound has been used as an isotopic label for studies of the efficiency of the reaction between malonic acid and formamide. The chloride ions are used in this study to monitor the reaction rate. 4,6-Dichloro-5-methoxypyrimidine is also an intermediate in the synthesis of sulfanilamide and aminophenol.</p>

<p>4-Vinylpyridine, stabilized with 100ppm Hydroquinone is a chemical compound that belongs to the class of pyridines. It has been shown to be stable in aqueous solution and to have a high water permeability. The reaction mechanism is not known, but it is thought that the quaternization of the vinyl group may be involved. 4-Vinylpyridine has been used as a component for the synthesis of polymers and can also be used in palladium-catalyzed coupling reactions.</p>

<p>Indole-3-carboxaldehyde is a chemical compound that is used as an antimicrobial agent. The biological properties of this compound are not well studied, but it has been shown to be effective against bacteria and fungi. Indole-3-carboxaldehyde has been shown to inhibit the enzyme activity of sodium carbonate, which is involved in the production of lactic acid in bacteria. This effect may contribute to its antibacterial activity. Indole-3-carboxaldehyde is also a potential anticancer agent because it can bind to toll-like receptor 4 (TLR4). Indole-3-carboxaldehyde reacts with sulfa drugs through a mechanism similar to the reaction between hydrogen peroxide and potassium permanganate. It has been shown that indole-3-carboxaldehyde can be used as a pesticide for plants and as an electrochemical impedance spectroscopy probe for histological analysis.</p>

<p>5-Azaindole is a heterocyclic compound that has been studied for its biological properties. It is a prodrug of trifluoroacetic acid, which can be used to treat metabolic disorders and autoimmune diseases. 5-Azaindole has also been shown to increase the expression of growth factor in cells, which may be useful in treating pain or bowel disease. This drug is metabolized by hydroxylation followed by conjugation with glucuronic acid and excretion in the urine. 5-Azaindole is also converted to an active form by enzymatic oxidation of a hydroxyl group and protonation on the nitrogen atom, as well as conversion to sorafenib (a drug used to inhibit tumor growth).</p>

<p>4,5-Dichloro-3-hydroxypyridazine is an organic compound that is used as a precursor to other compounds. It has been shown to be genotoxic and mutagenic in a number of assays with mammalian cells. 4,5-Dichloro-3-hydroxypyridazine reacts with phenols in the presence of Friedel-Crafts catalysts to form pyridine derivatives. It has also been shown to regulate transcriptional activity by binding to the prostacyclin receptor and α2-adrenergic receptor. This compound has been studied for its potential diagnostic value in the diagnosis of triticum aestivum (wheat) sensitivity.</p>

<p>Indole-3-carboxaldehyde is a versatile building block that can be used as an intermediate in the production of complex compounds. It is also a research chemical and reagent for speciality chemicals. Indole-3-carboxaldehyde has been shown to react with other chemicals to form high quality, useful intermediates or reaction components. This compound can also be used as a scaffold for chemical synthesis.</p>

<p>N-Acetyl-3-hydroxyindole is a chemical compound that can be used as a building block for other organic compounds. It is an intermediate in the synthesis of 3-amino-2,4,6-trichloropyrimidine, which is used in the synthesis of some pharmaceuticals and pesticides. N-Acetyl-3-hydroxyindole has been shown to react with thiourea to yield 2-(3,4-dihydroxyphenyl)acetic acid. It also reacts with hydroxylamine to produce 2-(aminooxymethyl)pyrrolidinone. N-Acetyl-3-hydroxyindole has been shown to have antioxidant properties, which may be due to its ability to reduce lipid peroxidation and scavenge reactive oxygen species.</p>

<p>5-Bromo-7-methyl-1H-indole-2,3-dione is a lead compound that inhibits the inosine monophosphate (IMP) deaminase enzyme. This compound is an inhibitor of the IMP deaminase enzyme and has been shown to reduce viral load in HIV patients. 5-Bromo-7-methyl-1H-indole-2,3-dione has been studied as a potential treatment for other diseases such as mycophenolic acid renal toxicity and inflammatory bowel disease. This molecule is a regiospecific inhibitor of the IMPDE4 protein with IC50 values of 0.5 μM and 2 μM for the wild type and mutant forms respectively.</p>

<p>Please enquire for more information about (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-pyrrolo[2,3-b]pyridin-3-yl)propanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methyl-6-(phenylethynyl)pyridine (MPEP) is a drug that is used in the treatment of Parkinson's disease. This drug inhibits the synthesis of proteins, including glutamate and dopamine, which are involved in Parkinson's disease. MPEP has been shown to be effective against Parkinson's disease by blocking protein synthesis in the caudate putamen and other brain regions. It also lowers locomotor activity and improves motor skills in rats. MPEP binds to response element-binding protein (RBP), which is involved in the regulation of gene expression. The binding of MPEP to RBP leads to an increase in levels of endogenous adenosine, which blocks the effects of dopamine and serotonin on postsynaptic neurons.</p>

<p>1-(Phenylsulfonyl)piperidine is an activated diphenyl sulfoxide that can be used as a glycosidic bond donor in the solid-phase synthesis of peptides. It reacts with chloride ions to form a sulfonium ion, which undergoes electrophilic substitution. 1-(Phenylsulfonyl)piperidine has been used in the synthesis of the blood group A antigen and the hydroxy group is used for the synthesis of glycosides and amino acids. This compound also has stereoselective properties for sulfoxides, carbon tetrachloride, hydroxyl groups, dodecyl groups, and acceptors.</p>

<p>5-Benzylthio-1H-tetrazole is a tetrazole derivative that is used as a reactant in bioconjugate chemistry. This compound reacts with nucleophiles to form covalent bonds and can be immobilized on solid supports for use in stepwise synthesis of peptides or other molecules. 5-Benzylthio-1H-tetrazole also has the ability to bind to DNA and RNA, which makes it useful in the study of hydrogen bonding interactions. In addition, this molecule has been shown to enhance the sensitivity of uv absorption measurements. Other uses include the development of model systems for chemical biology and the study of cellular processes.</p>

<p>Please enquire for more information about 2-(2,4-dimethylphenoxy)pyridine-3-carboxylic 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 1-(4-Bromophenyl)-4-methylpiperazine 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-Acetyl-3,4,5,6-tetrahydropyridine hydrochloride - technical grade including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>7-Ethylindole is a fatty acid with a cationic surfactant that belongs to the group of mesoporous materials. It has been synthesized by using chromatographic method and sample preparation techniques. The synthetic process is based on the protonation of 7-ethylindole. It undergoes dehydrogenation and activation energy, which is programmed in copper chromite. The chemical compositions are chloride, hydrogenated, and activated 7-ethylindole.</p>

<p>3-Amino-6-chloropyridazine is a synthetic compound that is soluble in hydrochloric acid. It has been shown to inhibit the proliferation of cells and induce apoptosis, which may be due to its inhibition of the growth factor receptor, factor. 3-Amino-6-chloropyridazine also inhibits bcr-abl kinase, an enzyme that is involved in the development of chronic myelogenous leukemia (CML). This chemical can be synthesized by coupling amino acids with chloropyridazine using cross coupling reactions. 3-Amino-6-chloropyridazine is a synthetic analogue of pyridoxal phosphate and may have use as an antiinflammatory agent.</p>

<p>1-(4-Hydroxyphenyl)piperidin-2-one is a versatile building block that has been used as a research chemical, reagent and reaction component. It can be found in the CAS registry under number 79557-03-2. This compound is used as an intermediate to synthesize other pharmaceutical compounds with a variety of effects including analgesic, antipyretic, antihistaminic, and antidepressant activities. 1-(4-Hydroxyphenyl)piperidin-2-one is also known for its use in the production of high quality reagents for use in laboratory settings.</p>

<p>Niacin receptor 1 (NIACR1) antagonist; lipid lowering</p>

<p>Tetradecyl pyridinium chloride is a cationic surfactant that is used in toothpaste, mouthwash and other oral hygiene products. Tetradecyl pyridinium chloride is an antimicrobial agent which can be found in cosmetics, household cleaning products, and various other personal care items. It is effective against bacterial strains such as Streptococcus mutans and Staphylococcus aureus by disrupting the cell membrane. Tetradecyl pyridinium chloride has also been shown to be active against fungi such as Candida albicans, but not against viruses or parasites.</p>

<p>5-Methoxyindole-3-acetic acid is a chemical that can be used to synthesize a variety of compounds. It is a versatile building block that has been used in the synthesis of complex compounds, as well as an intermediate for the production of other chemicals. 5-Methoxyindole-3-acetic acid is also an important reaction component and reagent for organic synthesis. This substance is not currently on the list of speciality chemicals, but it has shown high quality and usefulness in research.</p>

<p>3-Hydroxy-6-methylpyridine is a metabolite of the amino acid L-alanine. It has been shown to be hepatoprotective in a model system and to inhibit the allergic response. 3-Hydroxy-6-methylpyridine has also been shown to protect cells against oxidative damage by metal ions, as well as metabolic disorders such as diabetes. This compound is not active in competitive inhibition because it does not bind to the same site on the enzyme as the substrate. 3-Hydroxy-6-methylpyridine has also been shown to have neuroprotective effects, which may be due to its ability to inhibit acetylcholinesterase, an enzyme that breaks down acetylcholine, a neurotransmitter important for memory and learning.</p>

<p>8-Hydroxyquinoline sulfate is a drug that has been used to study the cancer tissue response to various drugs. The 8-hydroxyl group in the molecule interacts with metals and forms chelate complexes, which may be the reason for its cytotoxic effect. 8-Hydroxyquinoline sulfate also inhibits mitochondrial membrane potential and blocks the receptor activity of some cell types. It has been shown to be significantly cytotoxic to HL-60 cells, as well as other cell lines.</p>

<p>1-Pyrazin-2-ylpiperidin-4-amine dihydrochloride is a fine chemical that is used as an intermediate for the synthesis of research chemicals, speciality chemicals and other complex compounds. This compound has been shown to be useful in the synthesis of a variety of building blocks, including pharmaceuticals and agrochemicals. It can be used in reactions with a wide range of reagents and catalysts, which makes it an excellent starting point for new product development.</p>