Amines

<p>Please enquire for more information about 1,3-Thiazol-5-ylmethylamineHydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-tert-Butylcyclohexanamine is an unsymmetrical compound that is a potent antagonist of the dopamine D2 receptor. It is one of the stereoisomers of 4-tert-butylcyclohexaneamine. This drug has been synthesized by reacting naphthalene with amines and primary alcohols. The compound has optical properties, which may be due to its chiral nature and the presence of two rings in its structure. 4-tert-Butylcyclohexanamine crystallizes from water as needles or plates, depending on the concentration.</p>

<p>7-Aminoflunitrazepam is an active metabolite of flunitrazepam and a benzodiazepine. It can be detected in urine samples using an on-line LC-MS/MS method. The detection time of 7-aminoflunitrazepam is between 3 to 4 hours, which is longer than that of its parent drug, flunitrazepam. The use of monoclonal antibodies specific for fluoroquinolones allows the detection of 7-aminoflunitrazepam with high sensitivity and specificity. This method can be used to detect the presence of flunitrazepam in human serum samples, as well as in femoral vein blood samples, urine samples, and blood sputum samples. Solid phase microextraction (SPME) was used as the sample preparation technique for this study. SPME also allows for the extraction and analysis of lysine residues from protein matrices such as human serum.</p>

<p>Please enquire for more information about 3-Amino-5-bromobenzonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ammonium titanyl oxalate monohydrate is a compound that can be used as an antioxidant in a composition, including an electrophotographic composition. It has been shown to prevent photoreduction and nucleophilic attack on the surface of the photoconductor, as well as to reduce the magnitude of carboxylation reactions with transfer mechanism. Ammonium titanyl oxalate monohydrate may also be used for rechargeable batteries, which are devices that use electric current to generate chemical reactions. The addition of ammonium titanyl oxalate monohydrate to these batteries increases their capacity by reducing the number of cycles required before recharging. This compound also exhibits photocatalytic activity on metal surfaces in the presence of UV irradiation.</p>

<p>3-Aminobiphenyl is a biphenyl compound that is used in the production of dyes and pesticides. It has been detected in human urine samples using an analytical method based on chemical ionization. 3-Aminobiphenyl can be detoxified by conjugation with glutathione, but the conjugation process can be inhibited by the presence of amines such as caffeine, which competitively bind to glutathione. 3-Aminobiphenyl may also cause cancer, but there is no evidence for this theory at present.</p>

<p>Please enquire for more information about 3-Amino-6-bromo-2-methylquinazolin-4(3H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-6-chloropyrazine (2ACP) is an inhibitor that binds to the active site on human protein kinase C (PKC). It has been shown to inhibit PKC by hydrogen bonding with the hydroxide ion, which blocks its catalytic activity. 2ACP has been studied for its potential use in treating cancer and for inhibiting amine oxidases, which are enzymes associated with inflammation and chronic obstructive pulmonary disease. The inhibition of these enzymes may help to reduce stenosis in the lungs or other organs. 2ACP also has been shown to have antimycobacterial activity against Mycobacterium tuberculosis, M. avium complex, and M. leprae by inhibiting DNA synthesis and RNA synthesis. 2ACP inhibits the kinase receptor on the cell membrane that phosphorylates a water molecule into a chlorine atom, which then reacts with hydrogen peroxide to form free radicals that can kill bacteria</p>

<p>Please enquire for more information about 21-Amino-17-hydroxypregna-1,4-diene-3,11,20-trioneHydrochloride 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 (2S,6S)-2-Amino-2-(2-chlorophenyl)-6-hydroxycyclohexan-1-one HCl 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 Quaternary ammonium compounds, bis(hydroxyethyl) methyltallow alkyl, chlorides, salts with bentonite 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 3-(cyclopropylamino)azetidine-1-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(R)-(-)-2-Aminoheptane is a lipase inhibitor that can be used as an immobilized or soluble protein. This compound has been shown to inhibit monoamine oxidase, which is an enzyme that breaks down neurotransmitters in the brain, and helps maintain their levels. (R)-(-)-2-Aminoheptane also inhibits electron ionization, and can be used to study the chemical properties of amines.</p>

<p>Diisopropylamine is a tertiary amine and a component of trifluoroacetic acid. It is an amide with physiological effects that are not well understood. The diisopropylamine molecule has been shown to undergo transfer reactions, which may be due to steric interactions between the intramolecular hydrogen and nitrogen atoms. Trifluoroacetic acid can be found in reaction solution, such as in the formation of diazo compounds or as an intermediate in the reaction of ethyl acetate and sodium hypochlorite. Diisopropylamine is metabolized through dehydrogenative reactions, which involve the conversion of a group from one part of a molecule to another by removal of hydrogen atoms. This process generates reactive oxygen species and free radicals that may lead to oxidative stress in cells.</p>

<p>6-Amino-5-nitroso-2-thiouracil is a water molecule that has been synthesized and characterized by the kinetic method. It has an intense absorption line at 514 nm and can be used as a marker for technetium. 6-Amino-5-nitroso-2-thiouracil is also a ligand, which is a chemical that binds to metal ions in order to form coordination complexes. 6-Amino-5-nitroso-2-thiouracil is formed by the reaction of chloramine with ammonia, as well as other reactions involving chlorine atoms. 6Amino - 5 nitroso - 2 thiouracil can be used as a chelate ring, which is a type of ligand that contains both nitrogen and sulfur atoms. Bleomycin, a five membered ring molecule, reacts with 6 amino - 5 nitroso - 2 thiouracil to</p>

<p>Please enquire for more information about 2-Amino-5-bromo-N-cyclohexyl-N-methylbenzylamine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Endogenous ligand for histamine receptors; neurotransmitterA toxic biogenic amine produced in spoiled and fermented food</p>

<p>Diclofenac epolamine is a nonsteroidal anti-inflammatory drug that belongs to the class of diclofenac. It has been shown in clinical studies, with statistically significant results, to be effective against allergic reactions. Diclofenac epolamine is a film-forming polymer that can be used as a matrix for microcapsules containing diclofenac or other NSAIDs. This drug was designed to target tissue and provide effective analgesia at low doses. Diclofenac epolamine has an experimental model that uses monoclonal antibody-mediated delivery of diclofenac into the target tissue through microcapsules, which are then degraded by proteases present in the target tissue.</p>

<p>Trans-4-aminocyclohexanol is a cell signaling molecule that belongs to the class of heterocyclic compounds. It has been shown to have an anti-inflammatory effect and inhibit the production of pro-inflammatory cytokines in vitro. Trans-4-aminocyclohexanol also inhibits cyclooxygenase (COX) activity, which is responsible for the conversion of arachidonic acid into prostaglandins. This inhibition leads to decreased inflammation and pain. Trans-4-aminocyclohexanol is orally bioavailable and can be detected in the blood plasma within one hour after administration. The compound has been shown to bind to the enzyme protein kinase C, which is involved in cell signaling pathways, and inhibit its activity.</p>

<p>5-Aminoorotic acid is an antimicrobial agent that has been shown to have anticancer activity. It has a nitrogen atom and two oxygen atoms in the molecule. The chemical structure of 5-aminoorotic acid can be determined using NMR spectroscopy and its biological properties are dependent on hydrogen bonding interactions with other molecules. 5-Aminoorotic acid is a chelate ring, which means it can bind to metal ions such as lanthanum (La3+). 5-Aminoorotic acid has been shown to inhibit the glycol oxidation reaction and may also be able to inhibit other enzymatic reactions. This drug is stable for use in model systems and may also be used for cancer treatment.</p>

<p>Didecyl dimethyl ammonium chloride is a quaternary ammonium compound that has been shown to have a broad-spectrum antimicrobial activity. It has been used in disinfectants and as an active ingredient in pharmaceuticals, cosmetics, and foods. The compound is not toxic to humans or animals at concentrations up to 50%. Didecyl dimethyl ammonium chloride has been shown to be effective against infectious diseases caused by bacteria, viruses, fungi, and protozoa. This compound also has an effect on the epithelial-mesenchymal transition (EMT) process. Didecyl dimethyl ammonium chloride can be prepared by titration calorimetry or analytical method. The preparation of didecyl dimethyl ammonium chloride can be done using chloroform and benzalkonium chloride or glycol ether.</p>

<p>N-Phenylhydroxylamine is a chemical compound that is used in wastewater treatment. It is a hydrophobic compound that has been shown to irreversibly inhibit the nitrite reductase enzyme, which is responsible for converting nitrite ions into nitrate ions. This reaction mechanism was studied using in vitro assays with picolinic acid and nitrobenzene. N-Phenylhydroxylamine binds to the active site of the enzyme and blocks access by the substrate, preventing it from being converted into its product. The reaction can be reversed by adding hydrogen fluoride, which displaces the N-phenylhydroxylamine molecule from its binding site. N-Phenylhydroxylamine also binds to nitrogen atoms and participates in transfer reactions with other molecules, making it reactive and capable of reacting with other compounds. The sample preparation process should include separating N-phenylhydroxylamine from water samples after extraction because it will react with</p>

<p>Please enquire for more information about (2-{2-[2-(2-Aminoethyl)-4,5-dimethoxybenzyl]-4,5-dimethoxyphenyl}ethyl)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 4-Methyl-5-nitrothiazol-2-amine 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-(4-Ethoxyphenyl)-1H-pyrazol-3-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Methoxybenzylamine is an organic amine that has a redox potential of -0.14 V (vs. SHE) and a pK a of 10.5. It is used in the synthesis of trifluoroacetic acid esters, which are used as pharmaceutical intermediates. 4-Methoxybenzylamine has been shown to be effective in alleviating pain in animal models, and its mechanism of action may be due to inhibition of the enzyme cyclooxygenase. The kinetic data for this reaction were obtained by studying the deuterium isotope effect, which is characterized by a low energy barrier and rapid reaction rate. The hydrolysis step is also important for the reaction mechanism, with protocatechuic acid being an intermediate product. Hydrochloric acid is needed for dehydration of the reactants, while an aryl halide can be used instead in some cases. In these reactions, there are many possible reaction</p>

<p>Please enquire for more information about 4-Benzyloxy-3-methoxy-N-methylphenethylamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<p>(2H-Tetrazol-5-yl)methylamine is a sweetener that has been used as an analog of saccharin. It is not approved for use in the United States. The sweetness of (2H-tetrazol-5-yl)methylamine is due to its interaction with sodium ions, which make it a sodium salt. This compound is not sweet by itself but it does have optical properties that can be used to measure the concentration of sodium ions in solution. The chemical structure of (2H-tetrazol-5-yl)methylamine consists of a tetrazole group, an amine group and two methyl groups.</p>

<p>O-Chloramine T is a chemical compound that is used in the treatment of cancer. It is an endoreduplication agent and has been shown to cause endothelial cell growth and apoptosis in cancer cells. O-Chloramine T binds to the membrane of cancer cells, which leads to a decrease in autocrine activity and cell binding. O-Chloramine T also inhibits endothelial cell growth by inhibiting protein synthesis and blocking the synthesis of DNA and RNA. This drug has been shown to have anti-cancer properties in animal models and hyperosmolarity properties, which may be due to its ability to cause vessels to collapse.</p>

<p>Alanine,n,N'-[[5-[2-amino-5-(2,2-dimethyl-1-oxopropyl)-4-thiazolyl]-2-furanyl]phosphinylidene]bis[2-methyl-,1,1'-diethylester] is a metabolic inhibitor that is used in the treatment of type 2 diabetes. It inhibits gluconeogenesis by inhibiting the enzyme phosphoenolpyruvate carboxykinase (PEPCK), which catalyzes the conversion of oxaloacetate to phosphoenolpyruvate. This compound has been shown to reduce fasting blood glucose levels in diabetic animals and humans.</p>

<p>(S)-tert-Butyl 3-(methylamino)pyrrolidine-1-carboxylate is a research chemical that can be used as a versatile building block for the synthesis of complex compounds. It is also a reaction component in the synthesis of speciality chemicals and useful scaffolds. It has been shown to have high quality, reagent grade and purity.</p>

<p>1-Amino-9-fluorenone is a hydrogen bond acceptor molecule that has been shown to have anticancer activity and rate enhancement. The 1-Amino-9-fluorenone binds to the DNA of cancer cells, inhibiting cell growth and proliferation. This molecule also interacts with the cellular membrane by reversible binding, which leads to an increase in the concentration of intracellular nitric oxide (NO). This increase in NO levels inhibits the growth of cancer cells by blocking their ability to produce ATP. 1-Amino-9-fluorenone has been shown to inhibit hCT116 human colon cancer cells.</p>

<p>Please enquire for more information about [2-(5-Fluoro-1-methyl-1H-indol-3-yl)ethyl]amine 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 [1-Methyl-2-(7-methyl-1H-indol-3-yl)ethyl]amine 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 Z-3-(Tributylstannyl)-2-propen-1-amine 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 Benzyl 4-aminopiperidine-1-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1H-1,2,3-Benzotriazol-4-amine is a hydroxylated compound that belongs to the group of benzotriazole derivatives. It has been shown to inhibit the growth of cells in culture by binding to the nitrogen atoms in glutamate and inhibiting the production of nitric oxide synthase. 1H-1,2,3-Benzotriazol-4-amine also has binding constants for certain growth regulators that are 10 times higher than for other benzotriazoles. In vitro assays have shown that 1H-1,2,3-benzotriazol-4-amine is a potent corrosion inhibitor with an optical purity greater than 98%. The molecule was modeled using molecular modeling software and found to be stable when exposed to light. The molecule has also been tested on Sprague Dawley rats and found not to cause skin reactions.</p>

<p>Please enquire for more information about (3-IMidazol-1-yl-propyl)-[4-(4,4,5,5-tetraMethyl-[1,3,2]dioxaborolan-2-yl)-benzyl]aMine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(2-Aminothiazol-4-yl)acetic acid HCl is a white to off-white crystalline solid that is soluble in organic solvents. It is an intermediate used in the synthesis of thiourea derivatives, which are used as pharmaceuticals and agrochemicals. 2-(2-Aminothiazol-4-yl)acetic acid HCl is synthesized by the reaction of 2-aminothiazole with acetic anhydride. The purity can be determined using GC or NMR spectroscopy. Impurities may be removed by recrystallization with a solvent such as chloroform or dichloromethane. The melting point of 2-(2-aminothiazol-4-yl)acetic acid HCl is 147°C (298K). 2-(2-Aminothiazol-4-yl)acetic acid HCl can be purified by distillation at</p>

<p>Please enquire for more information about 1-(Boc-amino)-4,9-dioxa-12-dodecanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Nitroso-di-n-butylamine is a nitrosamine that is a product of wastewater treatment. It has been shown to inhibit mitochondrial function and induce liver lesions in rats at high doses. N-Nitroso-di-n-butylamine is structurally similar to the natural substrate ribose, which leads to inhibition of xanthine oxidase, an enzyme involved in purine metabolism. The structural analysis revealed the presence of reactive sites that are susceptible to attack by nucleophiles, such as hydroxyl radicals or hydrogen peroxide. This indicates that N-Nitroso-di-n-butylamine may be a precursor for other carcinogenic compounds. NADH is reduced by NADH dehydrogenase (complex I) in mitochondria to produce NAD+, which subsequently donates electrons to the electron transport chain and generates ATP. The ability of NNDB to inhibit complex I activity was assessed using hl60</p>

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

<p>Dinonylamine is an industrial chemical that is used as a solvent for waxes and resins. It has been used as a substrate film for the production of polycarbonate plastics and in the manufacture of amines, nitroaromatic compounds, and fluoropolymers. Dinonylamine has been shown to have an inhibitory effect on the growth of microorganisms by reacting with their aromatic hydrocarbons. This chemical reacts with carbonyl groups to form hydroxyl groups, which are toxic to bacteria. It also reacts with radiation to form a patterned surface that can be used to immobilize enzymes or other proteins.br&gt;br&gt; br&gt;br&gt; Dinonylamine is used in industrial processes as a precursor for amines and hydroxy groups, which are important components in many organic molecules including pharmaceuticals. These reactions take place in solvent vapor phase reaction vessels at high temperatures.br&gt;br&gt; br&gt;br&gt; Din</p>

<p>4,6-Diaminobenzene-1,3-dicarboxylic acid is an inorganic copper compound that is used as a copper salt. It has been shown to be effective as a chelating agent for the treatment of copper toxicity. 4,6-Diaminobenzene-1,3-dicarboxylic acid binds to metal ions and forms a complex with them. This complex can then be excreted from the body through urine or bile.</p>

<p>Please enquire for more information about [2-(1,2-Dimethyl-1H-indol-3-yl)ethyl]amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<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>

<p>3-Aminobenzotrifluoride is a chemical substance that can be used as an intermediate in the synthesis of pharmaceuticals. It is an aryl halide and has been shown to react with hydrogen fluoride, hydrochloric acid, nitrous acid, and trifluoroacetic acid to produce 3-aminobenzotrifluoride derivatives. This product is not readily bioavailable due to its low solubility in water and high lipophilicity. The preparation of 3-aminobenzotrifluoride requires a sample preparation step such as diazonium salt or diphenyl ether. Magnetic resonance spectroscopy has been used to identify the chemical structures of 3-aminobenzotrifluoride derivatives.</p>

<p>Please enquire for more information about 2-Phenylpropan-1-amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Aminopiperidine is a hydrochloric acid derivative that is used to treat tuberculosis. It inhibits the enzyme catalysis of phospholipase A2 (PLA2) and blocks the release of arachidonic acid from cell membranes. 1-Aminopiperidine has been shown to have tuberculostatic activity in vivo by inhibiting PLA2 and blocking the release of arachidonic acid. This agent also exhibits antitumor properties, which may be due to its ability to inhibit the production of prostaglandin E2 (PGE2), an inflammatory mediator that can stimulate tumor growth. 1-Aminopiperidine binds to cannabinoid receptors, but does not bind to opioid or benzodiazepine receptors. This drug also exhibits antagonist activity against rimonabant, a type of receptor blocker for cannabinoid receptors.</p>

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

<p>3,5-Diamino-2,4,6-trimethylbenzenesulfonic acid (DTMS) is an aromatic hydrocarbon that has been found in the environment. DTMS is used as a chlorine scavenger in water treatment plants and wastewater treatment facilities to remove chlorinated organics from the water. It has been shown to be a ligand for uranium. DTMS reacts with cyanuric acid to form 3,5-dichloro-2,4,6-trimethylbenzenesulfonyl chloride (CAS No. 52834-57-1). DTMS also exhibits affinity for metal ions such as copper and nickel.</p>

<p>Please enquire for more information about N,N-Bis[3-(methylamino)propyl]methylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Hydroxylamine HCl is a chemical compound that has been shown to exhibit anti-inflammatory properties. It is a nitrosobenzene derivative with the molecular formula NH2OH, and it is also known as hydroxylamine salt or hydroxylamine sulfate. Hydroxylamine HCl has been used in pharmaceutical preparations for the treatment of inflammatory bowel diseases such as ulcerative colitis and Crohn's disease. This drug inhibits the production of inflammatory cytokines by binding to the receptor sites on cells in the body. Hydroxylamine HCl binds to the herpes simplex virus (HSV) and inhibits viral replication, which may be due to its ability to inhibit protein synthesis at an early stage of HSV infection. This drug also binds to CD-1 mouse liver cells and blocks cellular respiration, leading to cell death.</p>

<p>Please enquire for more information about [2-(2,5-Dimethyl-1H-indol-3-yl)ethyl]amine 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 (S)-N-Ethyl amphetamine 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 6-(Aminomethyl)pyridin-3-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Amino-2-(1,3-benzoxazol-2-yl)phenol (4APB) is a fluorescent compound that has been used to study the fungal cell wall. It has shown to cause morphological changes in the conidia of some fungi, including transfer and swelling of the contents. 4APB has also been used to study the transfer mechanism of conidia by fluorescence microscopy and epifluorescence microscopy. This chemical can be stained with tosylates, which are reagents used for staining proteins and other molecules that contain sulfur atoms.</p>

<p>4,4'-Bis(dimethylamino)diphenyl carbinol is a bathochromic compound that belongs to the group of amines. It has been synthesized from 4,4'-diaminodiphenylmethane and hydrochloric acid. This molecule has been shown to react with protonated nitrogen atoms in an oxidation-reduction reaction. The protonation process occurs via kinetic, thermodynamic, and photophysical mechanisms. 4,4'-Bis(dimethylamino)diphenyl carbinol was used to study the proton transfer reactions between chlorine and nitrogen atoms in molecular modeling studies. On the other hand, this molecule has been shown to have fluorescence properties due to its carbonyl group.</p>

<p>1,2,3,4-Tetrahydronaphthalen-2-amine hydrobromide (THNA) is an amine that inhibits the enzyme tyrosine hydroxylase. This inhibition leads to a decrease in the synthesis of dopamine and norepinephrine. THNA has been shown to have inhibitory properties on locomotor activity, acid complex formation, and aminotransferases. It also exhibits receptor binding and agonist binding site activity. One study found that THNA had no effect on rat striatal tissue. The drug has been shown to be effective in metabolic disorders such as obesity.</p>

<p>DL-1-phenylethylamine is a chiral compound that has been studied for its biological properties. It can exist in either of two forms, or stereoisomers. DL-1-phenylethylamine is an amide and a methyl ester of phenethylamine hydrochloride. This compound has shown to have a high affinity for copper chloride and copper sulfate, and the 1R form is more soluble in water than the 2S form. The biological properties of DL-1-phenylethylamine are not fully understood but it may play a role in autoimmune diseases because it acts as an immunosuppressant and has anti-inflammatory activities.</p>

<p>Please enquire for more information about 2-(2-Aminoethyl)-3',6'-bis(diethylaMino)spiro[isoindoline-1,9'-xanthen]-3-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(Methylamino)adamantane is a dopamine receptor ligand that has been shown to be neuroprotective in rodent models of ischemia-reperfusion injury. 1-(Methylamino)adamantane exhibits high affinity for the D2 subtype, with potency and efficacy that are comparable to those of dopamine. It also acts as an agonist at the D1 and D3 receptors, although it displays weaker binding affinity than dopamine. The neuroprotective effects of 1-(methylamino)adamantane have been demonstrated in wild-type mice following ischemia-reperfusion injury, but not in animals with a mutant form of the gene encoding dopamine receptors. These findings suggest that 1-(methylamino)adamantane may be able to provide protection against ischemia-reperfusion injury by acting on downstream pathways such as protein kinase C or nitric oxide synthase.</p>

<p>Please enquire for more information about 4-Amino-2-methylphenylboronic acid, pinacol 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 1-Benzyl-3-[3-(diethylamino)propoxy]-1H-indazole 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-{[(3,4-Dichlorophenyl)amino]carbonyl}bicyclo[2.2.1]hept-5-ene-2-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 [(4-Methyl-1H-imidazol-5-yl)methyl]amine 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-Methyl-1,3-thiazol-2-yl)methyl]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 (R,S)-Z-3-Amino-7-chloro-2-oxo-5-phenyl-1,4-benzodiazepine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N,N,N',N'-Tetramethyl-p-phenylenediamine is a chemical compound that has been found to have a high affinity for proteins and nucleic acids. It interacts with these molecules by steric interactions and can change the phase transition temperature of water. N,N,N',N'-Tetramethyl-p-phenylenediamine reacts with surfactant sodium dodecyl (SDA) to produce protonated SDA species. These protonated SDA species are able to react with nucleophiles such as p-hydroxybenzoic acid (PHBA), which leads to an exchange reaction. The redox potentials of PHBA and N,N,N',N'-tetramethyl-p-phenylenediamine vary from -0.85 V to -1.05 V at pH 7.4, depending on the number of nitrogen atoms in the molecule. The x-ray</p>

<p>3,4-Difluorobenzyl amine (3,4-DFBA) is a synthetic compound that has been shown to have anti-cancer properties. It has been used in the synthesis of perovskites as an alternative strategy for solar cell applications. 3,4-DFBA has also been used to investigate the effect of hydrophobic and deformation on the biological activity of amines. This compound inhibits aldehyde oxidase and catalase from glyoxal and hydrogen peroxide respectively, which may be due to its ability to form microcapsules with a diameter of less than 50 nm.</p>

<p>4-Amino-5-methoxy-2-methyl-N-methylbenzenesulfonamide is a surfactant that is used in the chemical industry to dissolve diazotized aromatic amines. It is also used in the preparation of coupling agents, such as naphthol, and hydrochloric acid. 4-Amino-5-methoxy-2-methylbenzenesulfonamide can be prepared by the diazotization of aniline followed by coupling with hydrochloric acid and sodium phosphate. The product can then be purified by recrystallization from a salt solution containing sodium acetate.</p>

<p>Please enquire for more information about (R)-1-Boc-3-(aminomethyl)pyrrolidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Aminoethyl isopropylether (2-AP) has been shown to have inhibitory effects on the growth of Staphylococcus aureus, Bacillus subtilis and Escherichia coli. It also showed in vitro antifungal activity against Trichophyton mentagrophytes and Candida albicans. 2-AP inhibits the synthesis of unsaturated fatty acids by inhibiting the enzyme enoyl coenzyme A reductase, which is involved in the degradation of fatty acids. 2-AP is metabolized by two pathways: one is through hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid; the other pathway involves cyclobutanol formation. The cytotoxic effect of 2-AP has been shown to be due to inhibition of protein synthesis and cell division</p>

<p>2-Aminoindan is a compound that has inhibitory properties against the human liver enzyme dopamine β-hydroxylase. It binds to the active site of the enzyme and inhibits its activity, which decreases the production of dopamine and other monoamines in the body. 2-Aminoindan has been shown to be effective in animal models of Parkinson's disease by reducing oxidative stress and restoring dopamine levels. The drug also has a chemical diversity, with many different possible structures for medicinal use. 2-Aminoindan has been shown to inhibit the formation of carbonic acid, which is used by mammalian tissue as a buffer for pH regulation. This property may account for its inhibitory effect on carbonic anhydrase II (CAII), an enzyme involved in tissue respiration and acid-base balance. 2-Aminoindan has also been shown to have inhibitory effects on two bacterial enzymes: ddpP and ddpD, which are involved</p>

<p>Tetraethylenepentamine is a cell-signaling agent that binds to the MCL-1 protein and inhibits its function as a cell factor. This inhibition prevents the induction of apoptosis, which is important for the development of bowel disease. Tetraethylenepentamine can be used in wastewater treatment to remove glycol ethers from industrial effluent. It also has been shown to adsorb at acidic pH levels, making it an ideal candidate for use in solid phase microextraction (SPME) experiments. Tetraethylenepentamine interacts with fluorescence probes such as hydroxycoumarin, which makes it useful for surface methodology studies.</p>

<p>12-Aminododecanoic acid is a fatty acid that is used in the manufacture of magnetic particles. It is synthesized by cationic polymerization of 4-tert-butylbenzoic acid and dodecanedioic acid. The process involves the use of water vapor to remove hydrochloric acid from the solution and form a salt, which then reacts with dodecanedioic acid to produce 12-aminododecanoic acid. This compound has been shown to have transport properties for nitrogen atoms and can be used in exfoliated materials such as nanometals. 12-Aminododecanoic acid has also been shown to exhibit redox activity due to its ability to react with hydrogen peroxide.</p>

<p>Please enquire for more information about 1-Acetyl-5-(2-aminopropyl)-2,3-dihydro-1H-indole-7-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(4-methoxyphenyl)ethyl]methylamine is a pharmacological agent that inhibits protein synthesis. It has been shown to have an optimum concentration of 1 μM, with maximal inhibition at 10 μM. 2-(4-methoxyphenyl)ethyl]methylamine binds to the basic amino acid residues of proteins and inhibits the activity of eosinophil cationic protein, which is responsible for histamine release. 2-(4-Methoxyphenyl)ethyl]methylamine has also been shown to reduce the activity of epidermal growth factor, which is responsible for cell proliferation and differentiation. The drug has been demonstrated to be an effective inhibitor of activated eosinophils, but not normal cells. 2-(4-Methoxyphenyl)ethyl]methylamine may be used as a treatment for chronic asthma patients who suffer from eosinophilic inflammation in their</p>

<p>3-Amino-2-methylquinazolin-4(3H)-one is a bidentate ligand that has been shown to have antibacterial and anticancer activity. The functional theory of the compound is based on its ability to form an imine nitrogen with metal ions such as Fe(II) or Cu(II). 3-Amino-2-methylquinazolin-4(3H)-one is not active against Staphylococcus aureus, but inhibits the growth of other bacteria by binding to their ribosomes and inhibiting protein synthesis. 3-Amino-2-methylquinazolin-4(3H)-one also has in vitro anticancer activity, which may be due to its ability to inhibit DNA synthesis and cell division.</p>

<p>Please enquire for more information about cis-Dichloro(N,N,N',N'-tetramethylethylenediamine)palladium(II) 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-[(Dimethylamino)methylene]-5-(2,3,4-trimethoxyphenyl)cyclohexane-1,3-dione 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-Bromophenylethylamine HCl 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>2-Amino-4-chloro-3-nitropyridine is a potent inhibitory molecule that inhibits the activity of the enzyme acetylcholinesterase. It has been used in the treatment of chronic pain, and has been shown to be effective for inhibiting malonate esters and amino acid esters. This drug is an ethyl ester that can be synthesized from chlorobenzene and malonic acid by chlorinating it with chlorine gas. 2-Amino-4-chloro-3-nitropyridine has also been shown to have a high affinity for malonic acid diethyl esters.</p>

<p>2-Aminomethyl-4-(4-fluorobenzyl)morpholine (2AMFM) is a prokinetic agent that has been shown to be effective as a treatment for gastrointestinal motility disorders. This drug binds to the 5HT4 receptors, which are found on the enteric nervous system and in the gut. 2AMFM has been shown to increase the frequency of contractions in rat ileum and small intestine preparations. It also increases gastric emptying time and decreases postprandial acidity in dogs. 2AMFM is an enantiomeric mixture of two chiral molecules that are mirror images of each other. The racemic mixture is synthesized by reacting 2-aminomethyl-4-(4-fluorobenzyl)morpholine with chloroacetic acid ethyl ester.</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>Please enquire for more information about 4-(N-Methylamino)phenylboronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(Diphenylphosphino)ethylamine is a palladium complex that is used as a catalyst for the oxidation of alcohols to aldehydes and ketones. However, this compound can also be used in the synthesis of molybdenum complexes. 2-(Diphenylphosphino)ethylamine has been shown to catalyze the oxidation of aliphatic alcohols to corresponding aldehydes and ketones in homogeneous solution. This reaction proceeds by a transfer mechanism, with an irreversible oxidation at the metal center. The reaction products are not observed due to the high reactivity of hydrogen peroxide and its decomposition products. Control experiments showed that 2-(diphenylphosphino)ethylamine does not oxidize other substrates such as benzene or nitrobenzene, which are more stable than alcohols.</p>