Eterocicli con azoto (N)

<p>1-(3-Aminopropyl)pyridin-2(1H)-one HCl is a fine chemical that belongs to the group of heterocyclic compounds. It is a versatile building block that can be used as an intermediate or a scaffold in chemical synthesis. 1-(3-Aminopropyl)pyridin-2(1H)-one HCl is soluble in water and has been shown to react with a variety of other compounds, including amines, alcohols, thiols, and phenols. This compound also has high quality and can be used for research purposes.</p>

<p>5-Aminopyrimidine is a synthetic compound that has been shown to have inhibitory effects on the nervous system. The structural formula of 5-aminopyrimidine is C6H4N3O2. It is a structural analogue of pyrimidine and can be used as an anticancer drug. 5-Aminopyrimidine can also be used in the treatment of diseases such as diabetes and Parkinson’s disease. The reaction mechanism of 5-aminopyrimidine begins with the formation of an unstable diazonium salt, which then reacts with a chloride ion to form an alloxan intermediate. This intermediate then reacts with phosphate group to form a product that is soluble in water.</p>

<p>2,5-Dibromopyrazine is a heterocyclic compound that can be synthesized by the Suzuki coupling reaction of 2-bromo-1,3-dibromopropane with an acceptor. It has been shown to have glycemic parameters and a high rate enhancement for the water molecule photophysical isomerization reaction. Structural isomers of 2,5-dibromopyrazine exist as well and are thought to have different rates of photocatalytic activity. The rate enhancement may be due to the increase in electron density on the heteroatoms in the ring.</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>5-Fluoro-2-(trifluoromethyl)pyridin-4-amine is a fine chemical that is used to create other organic compounds. This compound is an intermediate in the production of pharmaceuticals, pesticides, and herbicides. It can also be used as a reagent or a speciality chemical in research. 5-Fluoro-2-(trifluoromethyl)pyridin-4-amine can be used as a reaction component to synthesize other compounds and has been shown to have versatile functions as a building block for complex molecules. This compound is not classified by the Chemical Abstract Service (CAS) and does not have any reported toxic effects on humans.</p>

<p>2,2,2-Trifluoro-N-(4-piperidinyl)acetamide (TFAPA) is a nucleic acid analog that binds to the target nucleic acid. TFAPA is a morpholino compound with an amide linkage between the morpholine ring and the acetic acid group. TFAPA is a sequence-specific DNA analog that inhibits protein synthesis by binding to the target nucleic acid. TFAPA can also be used as a probe for the detection of abnormal sequences in RNA.</p>

<p>Extensive research has been conducted on the antimicrobial activity of 6-fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-(1,3)thiazeto(3,2a)quinoline-3-carboxylic acid (FPMT). FPMT is a levorotatory compound that is rapidly metabolized by esterases to 6FMT, which is also active against bacteria. FPMT inhibits bacterial growth, but does not inhibit mammalian cell growth. The main mechanism of action for FPMT is probably through its ability to inhibit the synthesis of bacterial DNA and RNA. This drug has been shown to be effective against sinusitis caused by bacterial rhinosinusitis and urinary tract infections caused by Escherichia coli and Pseudomonas aeruginosa. FPMT can be used as an alternative to prulifloxacin for the treatment of these types of infections</p>

<p>2-Hydroxy-4-bromopyridine (2HBP) is a product with genotoxic activity that can be used for research. 2HBP has been shown to inhibit the synthesis of DNA by inhibiting the enzymatic reaction or binding to DNA. 2HBP is also an inhibitor of virus replication and causes monolayer cell death through radiation or chemical structures. It can be used as an anti-tumor agent and has been shown to have inhibitory properties on dna replication.</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>4,4'-Bis(bromomethyl)-2,2'-bipyridine is a cyclic molecule that can be synthesized by the reaction of 4-bromo-2,2'-bipyridine with a brominating agent. It is used as a precursor to ruthenium catalysts in organic synthesis, and as an additive in dendrimers. The compound has been shown to have light absorption properties and can be used in photovoltaics and electropolymerization.</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>Amine and sulfhydryl reactive crosslinker</p>

<p>Diacylglycerol kinase inhibitor II is a transcriptional regulator that inhibits diacylglycerol kinase. This inhibitor blocks the signaling pathways for growth factor-β1 by inhibiting the enzyme phosphatidic acid phosphatase, which plays an important role in cellular proliferation and migration. Diacylglycerol Kinase Inhibitor II has also been shown to inhibit cation channels and calcium release from intracellular stores. Diacylglycerol Kinase Inhibitor II binds to both cytosolic and nuclear proteins. It has been shown to inhibit cell proliferation and induce apoptosis in breast cancer cells.</p>

<p>6-Methoxyindole-2-carboxylic acid methyl ester is a pyrroloquinoline alkaloid with cytotoxic and antiproliferative activities. It inhibits the growth of cancer cells in culture by inducing apoptosis and cell cycle arrest. 6-Methoxyindole-2-carboxylic acid methyl ester has been shown to be effective against breast cancer cell lines in vitro and to inhibit the proliferation of breast cancer cells in vivo. This compound also inhibits the growth of a number of other cancer cell lines such as prostate, colon, lung, liver, stomach, and leukemia. The mechanism of action for this compound is thought to be due to its ability to act as an intramolecular quencher of reactive oxygen species (ROS) or as an inhibitor of DNA synthesis through inhibition of ribonucleotide reductase activity.</p>

<p>3-Amino-2-bromo-4,6-dimethylpyridine is a fine chemical that can be used as a versatile building block in the synthesis of other compounds. It is also an intermediate for the production of organic compounds and research chemicals. 3-Amino-2-bromo-4,6-dimethylpyridine is listed on the Chemical Abstracts Service (CAS) registry with the number 104829-98-3. This compound has a complex structure and is high quality and stable.</p>

<p>3-(4-Morpholinyl)-1-(4-nitrophenyl)-5,6-dihydro-2(1H)-pyridinone is a synthetic coagulation factor that has been shown to be cost-effective and to have a high yield. It is an inhibitor of blood coagulation, which is detectable by x-ray powder diffraction. 3-(4-Morpholinyl)-1-(4-nitrophenyl)-5,6-dihydro-2(1H)-pyridinone has been synthetically prepared from 3,5,6,7,8,9,10,-hexahydro-[2]benzo[e][1]pyridinone and 4-morpholinecarboxylic acid.</p>

<p>5-Amino-1-phenylpyrazole-4-carboxamide (APC) is a synthetic compound that has been shown to have potential as an antitumor agent. This compound has been shown to inhibit the growth of cancer cells in vitro, with cytometric analysis showing that it inhibits DNA synthesis and cell proliferation. It also has antibacterial activity, which may be due to its ability to inhibit bacterial DNA gyrase and topoisomerase IV. APC has been found in wastewater at concentrations of 2.6 μg/L, indicating that it is currently being produced and used for industrial purposes. APC can be synthesized by reacting 1-(3-aminopropyl)piperazine with 3-(2H)-furanone and triethylamine to form 5-amino-1-[(2H)-pyridin-2-yl]pyrazole-4-- carboxylic acid chloride, which can then</p>

<p>7-Hydroxyindole is a biochemical that is produced by wild-type strains of Escherichia coli. It has been shown to inhibit the action of an efflux pump, which is a protein that pumps drugs and other foreign substances out of the cell. The alkoxy radical reacts with 7-hydroxyindole to form a hydroperoxide intermediate. This intermediate then reacts with molecular oxygen to form hydrogen peroxide, which may be responsible for the antimicrobial activity of 7-hydoxyindole. Studies have shown that this compound can also inhibit multidrug efflux pumps in Pseudomonas aeruginosa cells, which may lead to an increase in antibiotic uptake.</p>

<p>Pitolisant is an inverse agonist and antagonist of the histamine (H3) receptor. It acts as an allosteric modulator of the H3 receptor to increase the activity of histamine at the M1 receptor. Pitolisant has been used in the treatment of narcolepsy, schizophrenia and Alzheimer's disease. Its mechanism of action involves binding to the amide group on histamine, which increases its affinity for the H3 receptor and enhances its activity at this site. Pitolisant has been shown to improve cognitive ability and reduce fatigue in patients with Alzheimer's disease.</p>

<p>2-Fluoroadenine is an inhibitor of DNA synthesis, which is used to study the effect of carcinogens on the cell cycle. It is a potent inducer of G2/M arrest in HL-60 cells, and has been shown to be cytotoxic to a number of different carcinoma cell lines. 2-Fluoroadenine disrupts collagen gel networks by binding to nitrogens in the protein matrix. This inhibits the glycosylation process that stabilizes collagen networks. The use of 2-fluoroadenine as a chemotherapeutic agent has been studied in animal models and clinical trials. 2-Fluoroadenine has been shown to inhibit mitochondrial membrane potential, leading to apoptosis caused by oxidative stress.</p>

<p>7-Bromoindole is a synthetic compound that has been used as an analog for indole. It has been shown to have some biological activity in vivo, but it is not known if this activity is due to the drug itself or its breakdown products. 7-Bromoindole can be decarboxylated under acid conditions and saponified with sodium hydroxide. The isolated yield of this reaction is about 2 grams per mole of reactant. 7-Bromoindole shows hemolytic activity against human pathogens such as Staphylococcus aureus and Escherichia coli, but not against Bacillus subtilis or Pseudomonas aeruginosa.</p>

<p>Ai Product Descriptions 50 Creative</p>

<p>Piperic acid is a metal chelate that has synergistic effects with other antimicrobial agents. It can be used to treat infectious diseases and carcinoma. Piperic acid is a natural compound found in plants, fruits, and vegetables, which has been shown to inhibit drug transporter proteins P-glycoprotein (P-gp) in the mitochondrial membrane potential. This inhibits the transport of drugs from outside the cell into the mitochondrial membrane, which also prevents the production of reactive oxygen species.</p>

<p>Please enquire for more information about Benzenesulfonic acid, 4-methyl-2-(3-pyridinylmethylene)hydrazide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4,5-Diamino-6-hydroxy-2-mercaptopyrimidine is a primary amino that binds to the sulfur in a molecule. It has potent antibacterial activity and can be used for desulfurization of petroleum products. 4,5-Diamino-6-hydroxy-2-mercaptopyrimidine has been shown to react with some cancer cells in vitro and may be used as an anticancer agent. It can also be used as a catalyst for the oxidation of organic compounds in wastewater treatment or hydrochloric acid production. 4,5-Diamino-6-hydroxy-2-mercaptopyrimidine can be synthesized by reacting 3 mercapto propionic acid with 5 aminopyrimidines. The synthesis was optimized using a kinetic method and coordination chemistry. It has also been shown to inhibit cell growth when used on human erythrocytes using patch clamp experiments and assays.br&gt;br</p>

<p>1-Benzylpiperazine is an analytical method for measuring the levels of monoamine neurotransmitters, such as dopamine and serotonin, in wastewater. It is used for the treatment of wastewater because it has been shown to be effective at removing nitrogen from wastewater. 1-Benzylpiperazine is also a metabolite of benzylpiperazine, which has been shown to have physiological effects on locomotor activity and the production of lc-ms/ms. The physiological effects are probably due to its ability to increase dopamine levels in the brain by inhibiting its reuptake by monoamine transporters. 1-Benzylpiperazine can also form a glucuronide conjugate with dopamine, hydroxyl group.</p>

<p>3-Amino-2-piperidinone is a metabolite of ornithine, which is a nonessential amino acid. It is produced by the metabolism of arginine and lysine, both of which are essential amino acids. 3-Amino-2-piperidinone has been found in urine samples from patients with bladder cancer and hyperornithinemia. It has also been detected in saccharomyces cerevisiae strain during energy metabolism experiments. This metabolite can be identified using chromatographic techniques such as gas chromatography and mass spectrometry.<br>3-Amino-2-piperidinone can be used to identify the presence of cancer or metabolic disorders such as hyperornithinemia by measuring its concentration in urine samples or reaction solutions.</p>

<p>The compound 4-Chloro-3-methoxy-2-methylpyridine N-oxide is an organic compound with a neutral chemical nature. It is a byproduct of the production of methylpyridine, which is achieved through the reaction between phosphorus oxychloride and toluene. The toxicological properties of this substance are unknown.</p>

<p>4-Chloropyridine-3-carboxaldehyde (4CPCA) is a potent inhibitor of the enzyme, formylation. 4CPCA is synthesized in an experimental method involving reaction of 4-chloropyridine and 3-bromoformaldehyde with a base, followed by hydrolysis to produce the desired product. This compound has been shown to inhibit formylation in vitro with inhibition potentials as high as 5000 μM. The IC 50 value for 4CPCA was found to be 0.6 mM. Formylation activity was inhibited in cell free systems and in cells from rat liver and human erythrocytes. The pharmacokinetic profile of 4CPCA is dose dependent and it is metabolized into inactive compounds by oxidation or conjugation with glucuronic acid.</p>

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

<p>4,6-Dimethyl-N-phenylpyrimidin-2-amine is a fungicide that is effective against the production of nitrite ion in the liver. It has been shown to be a potent inhibitor of hepatic steatosis. 4,6-Dimethyl-N-phenylpyrimidin-2-amine was also shown to have an inhibitory effect on the growth of fungal strains in vitro. This compound has been demonstrated to be active against a number of plant pathogens and may be useful in postharvest applications. 4,6-Dimethyl-N-phenylpyrimidin-2-amine interacts with the hippocampus formation and may play a role in preventing neurodegenerative diseases such as Alzheimer's disease or Parkinson's disease.</p>

<p>2,3-Pyrazinedicarboxylic acid is a molecule that can be found in bacteria and is the product of an intramolecular hydrogen reaction. It has been shown to have antibacterial activity against a strain of Bacillus subtilis. 2,3-Pyrazinedicarboxylic acid has been shown to react with hydrochloric acid to form an acid complex. The intramolecular hydrogen bond of 2,3-pyrazinedicarboxylic acid makes it hydrophilic and therefore it is soluble in water. This molecule also has the ability to form hydrogen bonding interactions with other molecules.<br>2,3-Pyrazinedicarboxylic acid has been shown to have anti-inflammatory properties because it inhibits prostaglandin synthesis by inhibiting cyclooxygenase and lipoxygenase enzymes.</p>

<p>4-Mercaptomethyl dipicolinic acid is a polymerized, bifunctional molecule that can be used as a luminescent probe to study the structure and dynamics of proteins. It has been shown to bind to lanthanide ions and has fluorescence properties. 4-Mercaptomethyl dipicolinic acid can be synthesized by a method involving the reaction of mercaptoethanol with sodium dithiocarbamate and copper(II) sulfate in an aqueous solution. This reaction produces two molecules of 4-mercaptomethyl dipicolinic acid for every one molecule of mercaptoethanol used, which then reacts with two molecules of 2,4-dinitrophenol in an aqueous solution. The resulting product is then purified by recrystallization from hot water. The conformational properties of 4-mercaptomethyl dipicolinic acid are dependent on temperature, pH,</p>

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

<p>6-Cyanoindole is a reactive intermediate in organic synthesis. It is used as a building block for the synthesis of other chemical compounds.</p>

<p>6-Methylpurine is a product of the nucleotide metabolism in E. coli, which is a model organism for protein synthesis. 6-Methylpurine inhibits protein synthesis and exerts significant cytotoxicity. It has been shown to inhibit the enzyme activities of DNA polymerase alpha, DNA ligase, and RNA polymerase, as well as other enzymes involved in nitrogen metabolism. 6-Methylpurine has been shown to be an analog of adenine and has a similar reaction mechanism. The uptake of 6-methyl purine by cells is mediated by hydrogen bonds with amino acid residues on the cell membrane surface. This molecule also forms glycosidic bonds with ribose sugar groups on cellular surfaces. 6-Methylpurine plays an important role in energy metabolism through its incorporation into glucose and glycogen molecules.</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>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>1-Acetyl-4-(2-hydroxyethyl)piperazine is a fine chemical that can be used as a reagent in research. It is a versatile building block and reaction component that is also useful for the synthesis of complex compounds. The CAS number for 1-acetyl-4-(2-hydroxyethyl)piperazine is 83502-55-0.</p>

<p>4,4'-Dichloro-2,2'-bipyridine (4,4'-DDBP) is a polydentate ligand that has been shown to be highly cytotoxic against cancer cells. 4,4'-DDBP binds to amines in the cancer cell and uses its nucleophilic character to activate the amine by displacement of chloride ions. This leads to the production of an excited state that can be used for photodynamic therapy or as a fluorescence probe. This compound has also been shown to have operational kinetic properties in the inhibition of bilirubin oxidase.</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>Please enquire for more information about (4-(2-Fluorophenyl)piperazinyl)-N-propylformamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>2-Pyridine selenyl bromide is a co-precursor for the synthesis of 2-selenides. It can be prepared by reacting 2-pyridinesulfonyl chloride with sodium periodate in acetonitrile. This compound can then be converted to a 2-selenide by treatment with methanol and periodic acid. The analytical and preparative methods are shown below:<br>Analytical: Dissolve the sample in dichloromethane, add triethylamine, and extract into diethyl ether. Add a small amount of potassium bromide to the organic layer and evaporate to dryness under vacuum. Recrystallize from acetonitrile.<br>Methanolysis: Dissolve the sample in methanol, add a catalytic amount of hydrochloric acid, and heat at reflux for 12 hours. Cool the solution, filter off any insoluble material, evaporate to dryness</p>

<p>4,6-Diamino-2-thiopyrimidine is a glycosidic bond that has been shown to inhibit the growth of bacteria in cell culture. It has also been shown to have an anticoagulant effect on human serum. The molecular weight of heparin is typically between 5000 and 15000 Da. In this study 4,6-Diamino-2-thiopyrimidine was found to be the most potent inhibitor of heparinase I activity with an IC50 of 1.5 mM. This compound is a trifluoroacetate salt that has a neutral pH and low solubility in water. It can be detected by electrochemical impedance spectroscopy (EIS). Hydrolysis by hydrochloric acid yields 4,6-diamino-2-thiopyrimidine trifluoroacetic acid as the only product. The chemical name for this substance is 4,6 diamino 2 thiop</p>

<p>2,5-Diamino-4,6-dichloropyrimidine is a biomolecule that is made of carbon, hydrogen, nitrogen, and chloride. It has been shown to inhibit cell growth in culture by reacting with malonic acid to form an oxidation product. This product can then react with trifluoroacetic acid to form a chlorinating agent which reacts reversibly with amine groups on the nucleobases in DNA. The reaction mechanism may be due to the ability of 2,5-Diamino-4,6-dichloropyrimidine to react with amino function and amide groups on nucleobases in DNA. 2,5-Diamino-4,6-dichloropyrimidine has also been shown to have anti-cancer activity against leukemia cells.</p>

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

<p>5-Amino-2-mercaptobenzimidazole is a molecule that has been shown to have antibacterial activity. It binds to the active site of bacterial ribosomes, which prevents the synthesis of proteins. This binding also inhibits the growth of bacteria such as Staphylococcus aureus and Escherichia coli. 5-Amino-2-mercaptobenzimidazole has been studied using vibrational spectroscopy, molecular modeling and surface-enhanced Raman spectroscopy. The binding constants have been determined by measuring the dissociation constant using sodium carbonate as an electrolyte. The optimum concentration for this molecule is when it is in anhydrous sodium at a constant concentration of 0.1 M.</p>

<p>2,4-Dimethyl-5-hydroxypyridine (DMHP) is a useful intermediate that can be used to synthesize other compounds. DMHP has been shown to be a useful scaffold in the synthesis of various complex compounds, such as pharmaceuticals and fine chemicals. DMHP is also a versatile building block that can be used to produce many different types of chemical compounds. It can also be used as a research chemical or as a speciality chemical for use in laboratories.</p>

<p>(2R)-1-(Phenylmethyl)-N-[3-(spiro[isobenzofuran-1(3H),4'-piperidin]-1-yl)propyl-2-pyrrolidinecarboxamide HCl is an endogenous opioid that has been shown to have antidepressant-like effects. It can bind to γ-aminobutyric acid (GABA) receptors, catecholamine receptors, and nociceptin receptors. This drug also has anti-cancer properties and may be used for the treatment of autoimmune diseases. The interaction of this drug with other drugs is not well understood, but it has been shown to modulate the effects of opioids and increase the aversive nature of some substances.</p>

<p>5-Bromo-2-cyano-3-nitropyridine is a medication that has been shown to be an effective inhibitor of the RET tyrosine kinase. It has been used in clinical studies to treat chronic kidney disease and has been shown to inhibit the growth of cancer cells. The molecular electrostatic potential (MEP) simulations have shown that 5-bromo-2-cyano-3-nitropyridine interacts with the reactive site of RET, inhibiting its function by binding to the nucleophilic substitutions. 5-Bromo-2-cyano-3-nitropyridine is synthesized from 2,5 dibromopyridine and 3 nitrobenzene at high yield. The molecule is chromatographically separated from impurities such as 4 bromo pyridine.</p>

<p>2-Chloro-5-aminomethylpyridine is an active substance that is used in medicine. It is a chlorinated compound, which has been shown to be effective against resistant mutants of bacteria. The mechanism of action is not yet clear, but it may be due to the formation of hydrogen chloride, which inhibits the growth of bacteria by binding to DNA and RNA. 2-Chloro-5-aminomethylpyridine has also been shown to act as an inhibitor for enzymes such as succinic dehydrogenase and glucose 6 phosphate dehydrogenase. This drug can also be detected in urine samples with a high sensitivity analytical method.</p>

<p>5-Hydroxy-3-methylindole (5HMI) is a metabolite of the drug tamoxifen, which is used for the treatment of breast cancer. It is also found in urine samples and has been shown to be reactive with cytochrome P450 2E1 (CYP2E1). 5HMI has been shown to inhibit the activity of CYP2E1 in humans, rats, and mice. 5HMI has also been shown to have anti-epileptic properties in epileptics. This active form is metabolized by adipose tissue or liver cells through oxidation and conjugation with glucuronic acid. The human liver cells show constitutive androstane receptor (CAR) activation, which may be due to its ability to act as an agonist or partial agonist.</p>

<p>2-Aminoacridone is a fluorescent dye.  The applications of 2-Aminoacridone are extensive in biochemical and analytical research. It is commonly employed in glycoprotein and glycoconjugate studies, leveraging its high sensitivity and specificity in detecting saccharide structures. Researchers utilize this dye in various assays, including high-performance liquid chromatography (HPLC) and electrophoresis, to analyze carbohydrate content and structure. Its role is critical in advancing our understanding of carbohydrate-related biological processes, such as cell signaling and disease pathogenesis, facilitating developments in both diagnostics and therapeutic strategies.</p>

<p>Ethyl 4-butoxy-5-fluoro-2,6-dioxohexahydropyrimidine-5-carboxylate is a drug that has been used in clinical studies for the treatment of primary brain tumors. It has shown clinical response rates of up to 87%, with the most favourable response observed in patients with low tumor grade and well differentiated histology. The drug is administered orally and penetrates tissues, including the central nervous system. Ethyl 4-butoxy-5-fluoro-2,6-dioxohexahydropyrimidine-5 carboxylate has been found to be toxic to ameloblasts and cancer cells in vitro. Tumor regression was observed in animals treated with ethyl 4 butoxy 5 fluoro 2 6 dioxohexahydropyrimidine 5 carboxylate, which led to decreased symptoms such as weight loss and cachexia.</p>

<p>3-Benzoylpyridine is a c1-c4 haloalkyl that absorbs UV light. It is a weak base and can be prepared by the reaction of 3-nitrobenzoyl chloride with benzene, amines, or ammonia. 3-Benzoylpyridine reacts with hydroxide to form the hydroxy derivative. The molecule has nitrogen atoms on the ring and a hydrogen bond between the two benzene rings. The hydroxy group is attached to an oxygen atom. Preparative high performance liquid chromatography (HPLC) can be used to separate 3-benzoylpyridine from other compounds in a mixture. The structural analysis of 3-benzoylpyridine was done using photoreduction followed by mass spectrometry. This compound is used in pharmaceuticals and as a solvent for dyes and oils.</p>

<p>Pyrazine-2-carbaldehyde is a synthetic compound that has been shown to have reactive properties. It is used as a model system in x-ray crystallography and structural studies of heart disease. Pyrazine-2-carbaldehyde can be prepared from an ethylbenzimidazole derivative substituted with substituents such as C1-6 alkyl, N, or NH groups. The nitrogen atoms in this molecule form hydrogen bonds with the carbonyl group and the C=O bond in its structure. This compound also has metabolic disorders including neurosis and benzimidazole derivatives. It reacts with alkynyl groups with the loss of HCl to form dihydropyridine derivatives.</p>

<p>Guanine is a purine base that is found in the DNA and RNA of all living cells. It plays an important role as a component of the nucleic acid molecule, where it is paired with cytosine. Guanine is involved in many chemical reactions and biological processes, including protein synthesis and cell division. The lack of guanine can lead to deficiency symptoms such as hemolytic anemia or erythrocyte cytoplasmic inclusion bodies. Guanine has been shown to have chemiluminescent properties, which can be used to detect its presence in samples containing DNA or RNA. This reaction occurs when guanine reacts with hydrogen peroxide (H2O2) to form guanidine (HN=C(NH2)NH2). The reaction produces excited states that emit light at a wavelength of 395 nm when they return to their ground state. Guanidine also has electrochemical impedance spectroscopy properties, which can be used for analytical purposes</p>

<p>2-Chloro-3-hydroxypyridine is a reactive chemical that can be synthesized from hydrochloric acid and ammonia. It has a high melting point, which is an indication of its strength. 2-Chloro-3-hydroxypyridine has been used in the kinetic and population growth studies for bacteria. The reaction of 2-chloro-3-hydroxypyridine with sodium hydrogen is exothermic and has a red shift, which indicates that the activation energy for this reaction is low. Activation energies are important because they indicate the stability of molecules.</p>

<p>Building block</p>

<p>5-Bromo-2-fluoro-3-methylpyridine is a fine chemical that is used as a scaffold for building more complex compounds. This chemical can be used in the synthesis of sulfonamides, thiocarbamates, and other organic compounds. 5-Bromo-2-fluoro-3-methylpyridine is also a versatile intermediate that can be used in the production of research chemicals and speciality chemicals. The purity of this compound is high and it has been shown to be a useful reagent in various reactions.</p>

<p>2-Amino-3,5-dichloropyridine is a molecule that is synthesized by the reaction of hydrochloric acid with copper chloride. The synthesis of 2-amino-3,5-dichloropyridine is a two step process. In the first step 2-chloroethanol reacts with an excess of hydrochloric acid to produce chloroethane and hydrogen chloride gas. In the second step, chloroethane reacts with an excess of copper chloride to produce 2-amino-3,5-dichloropyridine. 2-Amino-3,5-dichloropyridine can be used in organic synthesis for a number of reactions including as a substrate molecule for enzymes that require chloride ions as cofactors. 2-Amino-3,5-dichloropyridine has been shown to inhibit cancer cells by inhibiting DNA and protein synthesis.</p>

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

<p>a-[2-(Diisopropylamino)ethyl]-a-phenyl-2-pyridineacetamide is a hydrogen bond donor. It has been shown to have cytotoxicity in vitro, with parameters that can be used for accurate prediction of descriptors. These descriptors are informative and insightful, which can be used for regression analyses and linear regression methods. The pharmacokinetic properties of a-[2-(Diisopropylamino)ethyl]-a-phenyl-2-pyridineacetamide have been studied in humans and have shown linearity between dose and plasma concentration.</p>

<p>6-Azaindole is a drug that inhibits the activity of the enzyme aromatase, which is responsible for the conversion of testosterone to estrogen. 6-Azaindole has shown potent inhibitory activity against cancer cells in vitro and in vivo. It also has an inhibitory effect on pain relief mechanisms at low doses, but not at high doses. The mechanism of action is complex and multifactorial; it may involve inhibition of proton transfer, receptor activity, and/or inhibition of nitrogen atoms. The synthesis of 6-azaindoles can be carried out using a variety of methods and starting materials, including asymmetric synthesis or reduction of an n-oxide moiety.</p>

<p>1-(3-Chloropropyl)-4-methylpiperazine is an analog of chlorpromazine. It has been shown to be a transactivator, which causes the activation of genes in response to a variety of stimuli and plays a role in the pathogenesis of infections. 1-(3-Chloropropyl)-4-methylpiperazine also interacts with chloride ions, causing an increase in intracellular chloride concentrations. This increased concentration leads to an increase in transcription and replication rates. The structures of viral RNA were determined using 1-(3-chloropropyl)-4-methylpiperazine as a fluorescent probe.</p>

<p>4,5-Dichloro-3-hydroxypyridine is a reactive chemical that is a building block in organic synthesis. It is used as a reactant in the preparation of other compounds and as a reagent for various reactions, such as those involving amines, alcohols, and thiols. 4,5-Dichloro-3-hydroxypyridine has been found to be useful in the synthesis of heterocyclic compounds with an aromatic ring. It can also be used as an intermediate in the synthesis of pharmaceuticals. This chemical is classified by CAS number 1261269-63-9 and has an MW of 138.2 g/mol.</p>

<p>N-Cyanopiperidine is a cyclohexane ring with a trifluoroacetic acid group. It is used in the synthesis of pharmaceutical preparations and has been shown to be stable in low-energy environments, such as when mixed with glycol ethers or chlorides. N-Cyanopiperidine is also used as an intermediate for the preparation of other compounds, such as metal carbonyl complexes and derivatives. N-Cyanopiperidine can be synthesized by reacting anhydrous hydrogen cyanide with piperidinium chloride in the presence of metal hydroxides. This reaction mechanism is known to produce two products: 1) a stable complex with a metal ion, and 2) a reaction product that contains the desired product and hydrogen cyanide.</p>

<p>5-Aminoindole is a hydrogen bond acid. It has been shown to have an optimum concentration of 0.1 mM in the presence of 0.2 mM potassium chloride and 2 mM magnesium chloride, which is similar to the pH range for biological systems. 5-Aminoindole also acts as a competitive inhibitor of quinoline derivatives, such as chloroquine and hydroxychloroquine, which are used in the treatment of malaria and rheumatoid arthritis. The compound has been shown to be active against primary cells grown in culture, including mouse erythrocytes and human hepatocytes. When used with agarose gel electrophoresis or electrochemical impedance spectroscopy, 5-aminoindole shows excellent selectivity for kinases over other enzymes. 5-Aminoindole is not reactive under physiological conditions because it does not have any redox potentials that can be measured by Langmuir adsorption isother</p>

<p>Cyclo-Val-Pro-diketopiperazine is a drug that inhibits the growth of colon cancer cells by inducing apoptosis. It has been shown to have an inhibitory effect on the proliferation of p. aeruginosa and other bacteria, which may be due to its ability to interfere with DNA replication. Cyclo-Val-Pro-diketopiperazine also induces tumor cell apoptosis in vitro. The mechanism for this is not yet known, but it may involve interference with mitochondrial membrane potential or inhibition of acetate extraction from colonic cells. In addition, this drug has been shown to induce apoptosis in colorectal adenocarcinoma cells by causing an increase in reactive oxygen species and a decrease in mitochondrial membrane potential. Cyclo-Val-Pro-diketopiperazine can cause an increase in the levels of acetate extractable from caco2 cells as well as a decrease in mitochondrial membrane potential, which are both</p>

<p>1-(4-Methoxyphenyl)piperazine hydrochloride is a high-potency inhibitor of the K+ channels. It has been shown to inhibit the activity of these channels in lead compound screening and optimization. The modification of potassium channels by 1-(4-Methoxyphenyl)piperazine hydrochloride has been evaluated using a patch clamp technique on rat erythrocytes. This inhibitory activity was found to be concentration dependent and voltage sensitive. 1-(4-Methoxyphenyl)piperazine hydrochloride was also shown to have pharmacological effects, such as analgesia, sedation and muscle relaxation.</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>Boc-4-hydroxypiperidine-2-carboxylic acid is a high quality, reagent, and complex compound. It has CAS No. 917835-93-9 and can be used as an intermediate or building block in synthesis of other chemicals. In addition, Boc-4-hydroxypiperidine-2-carboxylic acid is a versatile building block that is used in the manufacture of speciality chemicals and research chemicals.</p>

<p>2-Methyl-5-nitroimidazole, also known as menidazole, is an impurity of metronidazole, which is used as an antibacterial and antiprotozoal medication in the treatment of infections, including rosacea. 2-Methyl-5-nitroimidazole is a derivative of nitroimidazole and has potential antimicrobial and antitrichomonal activities. Its synthesis can be achieved using various methods, including nucleophilic reaction, ester derivatives, reaction with metronidazole, and substitution reactions. Several derivatives of 2-Methyl-5-nitroimidazole have been synthesized and tested for their antibacterial, antifungal, and antitrichomonal activities. Both 2-Methyl-5-nitroimidazole and its derivatives have potential applications as antimicrobial and antitrichomonal agents.</p>

<p>Canagliflozin is a pharmaceutical drug that is used to treat type 2 diabetes. It is an oral medication that works by blocking the absorption of glucose in the intestine, which lowers blood sugar levels and improves insulin sensitivity. Canagliflozin has been shown to have a number of effects on metabolism, including increased bile acid production and decreased fat absorption. This drug also has a number of side effects, including diarrhea, nausea, and vomiting. Canagliflozin is used in combination with metformin or insulin for the treatment of type 2 diabetes. The drug's most common side effect is diarrhea, which can be managed by eating more fiber-rich foods and drinking plenty of fluids.</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>Please enquire for more information about 2-(((4,6-dimethylpyrimidin-2-yl)amino)ethylidene)indane-1,3-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>4-(2,6-Dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamide HCl (PD1693) is a small molecule that has been shown to selectively inhibit the transcriptional coactivator HIF-1α. PD1693 inhibits the hypoxic response in tumor cells by preventing the upregulation of HIF-1α. This leads to an increase in hypoxia-inducible genes, which are involved in the regulation of cell proliferation, angiogenesis and apoptosis. PD1693 also affects the expression of genes involved in metabolism and energy production. The subpopulation algorithm was used to identify differentially expressed transcripts in glioma cells following exposure to PD1693. The data from this algorithm were validated using qRT-PCR and Western blotting on human glioma cells.</p>

<p>6-Chloro-3-aminopyridine-2-carboxamide is a small molecule that inhibits tumor growth in human prostate cancer cells. It binds to a pharmacophore, which is a three dimensional arrangement of atoms that is responsible for the biological activity of the drug. This compound has been shown to inhibit tumor cell proliferation and induce apoptosis. 6-Chloro-3-aminopyridine-2-carboxamide also inhibits the oncogenic signaling pathways, including the PI3K/Akt and MAPK pathways, leading to antiproliferative activity in cancer cell lines. 6-Chloro-3-aminopyridine-2-carboxamide also inhibits phosphorylation of Akt and Erk1/2, which are downstream targets of PI3K/Akt pathway activation. The compound was found to have no significant effects on noncancerous cells or normal prostate tissue.</p>

<p>5-Methylpyrimidin-2-ol is a photophysical, hydroxy group, and hydroxyl group. It has been shown to have an inhibitory effect on DNA methylation by glycosidic bond with the sugar moiety of the nucleotide. 5-Methylpyrimidin-2-ol reacts with the base moiety of the nucleotide to form an analog that inhibits RNA synthesis and is competitive against pyrimidine nucleosides. 5-Methylpyrimidin-2-ol also has a hydrogen bonding property that can react with other molecules such as proteins or sugars to form hydrogen bonds. This reaction rate is increased by fluorescence resonance energy transfer (FRET).</p>

<p>tert-Butyl-4-(2-bromoethyl)piperidine-1-carboxylate is a white solid with a molecular weight of 215.07. It is soluble in organic solvents such as dichloromethane, ethanol, acetone and ether. The CAS number for this chemical is 169457-73-2. This product can be used as a reagent or complex compound to synthesize other fine chemicals, useful scaffolds and building blocks, speciality chemicals and research chemicals. It has many versatile uses due to its wide range of functional groups that are easily modified by various synthetic reactions.</p>

<p>5-Nitroindole is a nitro functionalized indole. It is a fine chemical that has a wide range of uses in research, industry and education. 5-Nitroindole can be used as a versatile building block for the synthesis of complex compounds and as an intermediate for the production of other chemicals. 5-Nitroindole is soluble in organic solvents and can be used to synthesize other compounds with high purity. This compound is also known as CAS No. 6146-52-7 and is considered to be of high quality.</p>