Aminas

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

<p>S-(+)-1-Aminotetrahydronaphthalene is an amido derivative that is the enantiomer of S-(-)-1-amino-N,N'-diphenylformamide. It has been shown to have anti-obesity effects in mice by increasing energy expenditure and reducing food intake. S-(+)-1-Aminotetrahydronaphthalene also inhibits the release of fatty acids from adipose tissue, which may be due to its ability to suppress lipolysis. The molecular mechanism for these effects is not yet known, but it is thought that the amide group on this compound interacts with certain protein surfaces and steric interactions are involved in its activity.</p>

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

Ammonium bicarbonate is a substance that has been used as a buffer to maintain pH in wastewater treatment. Ammonium bicarbonate has also been shown to be effective in the treatment of metabolic disorders, such as glycogen storage diseases and urea cycle disorders. Ammonium bicarbonate is synthesized by reacting aqueous solutions of ammonium chloride and sodium or potassium carbonate. It can also be produced through the reaction of ammonia with carbon dioxide in water vapor. The analytical method for ammonium bicarbonate is based on the reaction with trifluoroacetic acid (TFA) and the formation of ammonium trifluoroacetate. This compound can react with water to produce carbon dioxide and ammonia, which may function as a nutrient solution for microorganisms. Cyclic nucleotide phosphodiesterases are enzymes that break down cyclic nucleotides, which are important for many physiological functions, including muscle contraction and regulation of blood pressure

2-Chloro-3,4-dimethoxyphenethylamine is an intermediate in the synthesis of zepines. It can be synthesized by reduction of borohydride with 2-chloro-1,2,3,4-tetrahydrobenzaldehyde.

<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>

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6-Bromo-1H-indazol-3-yl-amine is an indazole derivative that has shown anti-cancer effects in vitro and in vivo. 6-Bromo-1H-indazol-3-yl-amine inhibits the proliferation of cancer cells, which may be due to its inhibition of cell cycle progression at the G2/M phase. It also inhibits the growth of tumor cells by inducing apoptosis. The drug's mechanism of action is not yet fully understood, but it has been shown to inhibit the activity of axitinib, a tyrosine kinase inhibitor. This drug has also shown anti-proliferative activities with acid catalysts and supramolecular systems. In addition, 6-bromo 1H indazol 3 yl amine contains functional groups such as nitro and pyrrole groups.

<p>N,N'-Diisopropylethylenediamine is a light-resistant, microprocessor-grade ligand that binds to imatinib. It is used in the synthesis of acrylonitrile and potassium clavulanate. N,N'-Diisopropylethylenediamine has been shown to bind to copper ions and bortezomib, which are drugs used for the treatment of cancer. This chemical may be an organic solvent that can cross-link proteins and prevent them from unfolding.</p>

<p>Please enquire for more information about Boc-trans-1,2-aminocyclohex-4-ene 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 Fmoc-(4-aminomethyl) benzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>

4-Aminoisoxazole is a triazole that has been found to be active against tumor cell lines. It is synthesized by reacting zinc powder with an acid solution containing 4-nitrobenzaldehyde, which results in the formation of 4-aminobenzonitrile, which subsequently undergoes nitration and reduction to form 4-aminoisoxazole. The synthesis of this compound can also be achieved by reacting ammonium nitrate with nitric acid in the presence of hydrochloric acid.

Dihydroergotamine mesylate is a medication that is used in the treatment of migraines. It belongs to the group of drugs called ergot alkaloids and has been shown to have high values in cerebral metabolism. Dihydroergotamine mesylate has also been shown to have an effect on dopamine levels in human serum, which may be due to its ability to inhibit neuronal death. Dihydroergotamine mesylate is administered intravenously, orally or intramuscularly for the treatment of acute migraine attacks. The drug can also be given rectally for the prevention of chronic migraine episodes. This drug may cause side effects such as nausea, vomiting and dizziness.

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Ammonium carbonate is an inorganic salt that consists of ammonium ion and carbonate ion. It is a white crystalline solid with a molecular weight of about 166.4 g/mol. Ammonium carbonate is soluble in water, alcohol, acetone, and other organic solvents. It has been used as a buffer solution for pH adjustment and as a source of ammonium ions in analytical chemistry. Ammonium carbonate can be formed by the reaction of sodium carbonate with ammonia gas or liquid ammonia, or the reaction of sodium bicarbonate with ammonia gas or liquid ammonia. The thermal expansion coefficient of ammonium carbonate is higher than those of sodium salts such as sodium chloride and potassium chloride. Electrochemical impedance spectroscopy (EIS) measurements have shown that the reactivity between ammonium carbonate and plasma mass spectrometry is high due to its high values on the electric spectrum graph at low frequencies (1 kHz).

<p>Please enquire for more information about 4-chloro-5-fluoropyrimidin-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 4-(2-(2-amino-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-5-yl)ethyl)benzoate is a prodrug that is hydrolyzed to form the active drug pemetrexed disodium. The drug has been shown to be effective for the treatment of cancer and has been used in clinical trials for patients with lung cancer. The conversion of this prodrug to its active form occurs through a hydrolysis reaction at high temperature and by saponification with sodium hydroxide. Methyl 4-(2-(2-amino-4-oxo-4,7-dihydro-3H-pyrrolo[2,3 - d]pyrimidin -5 -yl)ethyl)benzoate can also be converted into its active form by enzymatic action using ester</p>

3-Pyridazinemethanamine is an amide that binds to the vasopressin V2 receptor. It is a selective agonist of the vasopressin V2 receptor and has a high affinity for this receptor. 3-Pyridazinemethanamine has been shown to be a functional antagonist at the vasopressin V1A receptors, which may be due to its chemical structure. 3-Pyridazinemethanamine is not metabolized by cytochrome P450 and does not inhibit other cytochrome P450 enzymes, making it an attractive drug candidate for use in humans.

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N-Methyl-N-hydroxyethyl-4-aminobenzaldehyde (NHABA) is a bathochromic molecule that absorbs light at wavelengths of 400 to 500 nm. It is reactive and reacts with metal cations to form chromophores. NHABA has been shown to be a fluorescent probe for the detection of tyrosinase and autophagy in human serum. It also has inhibitory properties against tyrosinase, which may be due to its ability to inhibit the formation of melanin. NHABA is used as an analytical chemistry reagent for the determination of ammonia, nitrite, and nitrate ions in water samples. This molecule can also be used as a chemosensor for the detection of phenolic compounds in water samples.

<p>2-(4-Aminophenoxy)acetamide is a chemical compound that belongs to the class of acetamides. It is used in the production of polyester fibers and dyes. 2-(4-Aminophenoxy)acetamide is a colorless, crystalline solid that has not been identified in nature.</p>

<p>2-(Methylmercapto)-ethylamine is a chemical that is used in the synthesis of the ruthenium complex, which is used to detect and destroy cancer stem cells. 2-(Methylmercapto)-ethylamine has been shown to be toxicologically safe in animal studies. 2-(Methylmercapto)-ethylamine can react with aziridine and pyrite to form nanogels, which are structures that have potential applications in drug delivery. The optical properties of 2-(methylmercapto) ethylamine are sensitive to its environment, especially pH. 2- (Methylmercapto) Ethylamine can bind to the pleuromutilin derivatives, which are active against infectious diseases such as tuberculosis.</p>

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

<p>3-Amino-4-methoxypyridine is a molecule that has been shown to have anesthetic activity. It has been shown to inhibit the uptake of glycogen by glioblastoma cells and decrease the rate of glycogen synthesis in these cells. 3-Amino-4-methoxypyridine also inhibits the production of ATP in cardiac muscle cells, which may be due to its ability to inhibit glycogen synthase kinase-3 (GSK3) and glycogen synthase. This drug also inhibits cancer cell growth by inhibiting protein synthesis, as well as inflammatory disease progression by inhibiting NFκB activation and cytokine production. 3-Amino-4-methoxypyridine can be synthesized from aminopyridines such as isonicotinic acid or nicotinic acid, which are oxidized with hydrogen peroxide and sodium nitrite in the presence of a base catalyst.</p>

(±)-N-Methyl-p-methoxyamphetamine (MEM) is a synthetic cannabinoid that is used as an ingredient in the manufacture of designer drugs. MEM can be detected by gas chromatography and mass spectrometry, although it is not possible to distinguish MEM from other synthetic cannabinoids by these methods. MEM produces no significant adverse effects on human liver, but may have serious adverse effects on the heart and blood vessels. The drug can be found in urine samples with a chemical ionization detector or electrochemical detector. The analytical method for MEM detection is based on liquid chromatography-tandem mass spectrometry (LC/MS/MS). The LC/MS/MS technique separates and identifies compounds by creating ions through the use of an electric field. This method has been shown to accurately detect MEM, while also eliminating false positives due to its specificity.

<p>(1R,2R)-1-Amino-2-benzyloxycyclopentane is achiral. It is a synthetic chemical that has been used as an initiator for polymerization of amines and hexafluoroisopropanol. The synthesis of this compound can be achieved through a chiral technique known as interfacial polymerization. (1R,2R)-1-Amino-2-benzyloxycyclopentane is an initiator for the production of polymers with alternating helical chains. This process relies on the presence of achiral molecules to initiate the polymerization process.</p>

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<p>Rac benzphetamine hydrochloride is a repurposed drug that has been shown to have the ability to modulate the activity of various receptors, including the dopamine receptor. Rac benzphetamine hydrochloride is a layered molecule with two stereogenic centers and three chiral centers. It has been shown to have hydroxylase activity, which is catalyzed by the enzyme aryl hydrocarbon hydroxylase. Rac benzphetamine hydrochloride also has potential as an anti-inflammatory agent because it inhibits myelination in mice. Rac benzphetamine hydrochloride was found to be carcinogenic in animal studies, but not in human trials. The drug can be given intravenously or intraperitoneally, depending on the desired effect.</p>

<p>2-(2-Aminoethoxy)ethanol (2-AE) is a natural compound that has been synthesized from ethanol and 2-aminoethanol. It has been shown to react with sodium carbonate to form stable complexes that are resistant to hydrolysis by amines. The stability of the complex is attributed to the formation of an intermolecular hydrogen bond between the hydroxyl group on the 2-AE molecule and the carboxylate group on the sodium carbonate molecule. 2-AE reacts with benzalkonium chloride, a quaternary ammonium salt, in water vapor to produce an alcohol and a fatty acid, which is then hydrolyzed by glycol ethers into glycolates. This mechanism is similar to that of other reactions involving quaternary ammonium salts, such as those in fatty acids or glycol ethers.</p>

<p>2-Amino-1,3,5-triazine is a hydrogen bond donor that has been shown to have growth inhibiting effects. It reduces the viscosity of aqueous solutions and is used as an enantiopure for amines. 2-Amino-1,3,5-triazine can be used in reactions with metal surfaces to produce surface coatings or used as a bifunctional crosslinking agent for polymer materials. 2-Amino-1,3,5-triazine has been shown to have degenerative disease inhibitory activity and inflammatory disease inhibitory activity. It also inhibits the production of inflammatory cytokines such as tumor necrosis factor alpha (TNFα) and interleukin 6 (IL6).</p>

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(S)-(-)-1-Boc-3-aminopyrrolidine is an inhibitor that inhibits the activity of phosphoinositide 3-kinase (PI3K) by binding to the ATP binding site and inhibiting PI3K. It has been shown to inhibit the activation of PI3Kδ, which plays a key role in tumorigenesis and metastasis. The drug also has metabolic stability and selectivity for PI3Kδ over other kinases, as well as high affinity for this enzyme. The drug was found to have low toxicity in vitro, but its effects on humans are unknown.

<p>4-Aminobiphenyl is a chemical compound that belongs to the group of aromatic amines. It is a human carcinogen and has been shown to cause cancer in animals. 4-Aminobiphenyl has been detected in the environment as an environmental pollutant and can be found in small quantities at low levels in food, air, and water. 4-Aminobiphenyl can be hydrolyzed by acid or alkaline hydrolysis to form its hydrolysate, which contains nitroarenes that are not present in the original compound. The DNA modification caused by 4-aminophenol may be due to its ability to modify DNA bases through reactive metabolites such as nitroarenes.</p>

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<p>Please enquire for more information about {[5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl]methyl}amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Cis-1,3-cyclohexanediamine is a reactive molecule that has been shown to have an inhibitory effect on cancer cells. It is thought to act by binding to the amines in the cell membrane, leading to steric interactions with the protein and disruption of the cancer cell's function. Cis-1,3-cyclohexanediamine also has an anti-inflammatory effect as it can chelate metal ions such as iron and copper. This molecule has been shown to have a high affinity for acidic environments, with a pK a of 4.5.</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>

N-(2-Aminoethyl)piperazine (NAPE) is a chemical compound that can be used as an environmentally friendly catalyst for the degradation of ethylene diamine and other amines. NAPE has been shown to be stable under alkaline conditions, and its fluorescence probe has been used to monitor the progress of the reaction. This compound is a coordination complex with nitrogen atoms at the corners of a square and two amines at opposite corners of the square. The amine groups are coordinated to metal ions in a geometry that is determined by the atomic number of the metal ion. Disulfide bonds form between two cysteine residues on adjacent chains. Glycol ethers can also form disulfide bonds with NAPE, forming glycol ether-NAPE complexes. Antibodies have been shown to bind to glycol ether-NAPE complexes, suggesting that these complexes may play a role in antibody response, although experimental solubility data have not yet confirmed this

Tetramethylammonium hydroxide is a strong base that is used in analytical chemistry for the quantitative determination of zirconium. It is an analytical reagent and has a pH of 14. Tetramethylammonium hydroxide forms complexes with metals such as zirconium and titanium, which are then analyzed by various methods such as atomic absorption spectroscopy, x-ray fluorescence spectroscopy, and inductively coupled plasma mass spectrometry. The optimum concentration of tetramethylammonium hydroxide for this application is approximately 25%. Tetramethylammonium hydroxide reacts with p-nitrophenyl phosphate to form a pink product, which can be detected by colorimetric analysis. This reaction also produces hydrogen fluoride gas, which must be removed before the solution can be used again. Tetramethylammonium hydroxide reacts with ammonium to form tetramethylammonium ion and water. It also reacts

Cyclohexanemethylamine is a nonsteroidal anti-inflammatory drug that belongs to the class of amines. This drug has been shown to inhibit the cyclooxygenase activity of the enzyme prostaglandin synthase, which is responsible for converting arachidonic acid into prostaglandins. Cyclohexanemethylamine also has antioxidant properties and has been shown to inhibit lipid peroxidation. Cyclohexanemethylamine has been shown to have both anticancer and antiviral effects in cell culture experiments and in animal studies. It inhibits cell proliferation in muscle cells and suppresses muscle cell proliferation induced by metal carbonyls or phorbol esters. Cyclohexanemethylamine also inhibits cancer-related protein synthesis, such as protein kinase C and DNA polymerases, while it enhances the synthesis of heat shock proteins (HSPs).

<p>3-Amino-2-oxazolidinone-d4 is a methanol solvent that can be used to analyze the muscle tissue. 3-Amino-2-oxazolidinone-d4 can be synthesized by reacting oxalyl chloride and 2 nitrobenzaldehyde in acetonitrile. It can also be prepared by dehydrating and analyzing the synthesis of 3 amino 2 oxazolidinones in chloroform and bromoacetic acid. 3 - Amino - 2 - oxazolidinone - d4 is deuterated, which means it has an extra neutron in its nucleus.</p>

Methscopolamine bromide is a leukotriene receptor antagonist that is used to treat various conditions including bowel diseases and autoimmune diseases. Methscopolamine bromide binds to muscarinic receptors and blocks the action of acetylcholine, which mediates inflammation. Methscopolamine bromide can also be used to treat congestive heart failure. This drug has significant interactions with other medications, including thermal expansion, fatty acid metabolism, or symptoms of bowel disease. The drug should not be taken by patients who have had a stroke or who have asthma. It is contraindicated in patients who are pregnant or breastfeeding.

Please enquire for more information about 1-(RS)-2-(Dibutylamino)-2-[2,7-dichloro-9-(4-chlorobenxylidene)]-9H-fluoren- 4-yl]ethanol - E/Z mixture including the price, delivery time and more detailed product information at the technical inquiry form on this page

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

<p>(4-Bromobenzyl)methylamine hydrochloride is a reagent that is used for the analysis of carboxylic acids. It has been used in a number of studies to analyze cellular metabolism and energy metabolism. This reagent has also been used to study the functional groups of organic acids, as well as their reactivity. (4-Bromobenzyl)methylamine hydrochloride can be used in liquid chromatography or electrospray ionization methods to analyze samples using mass spectrometry.</p>

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<p>Cis-4-Methylcyclohexylamine is a cyclic amine that is found in the form of its decarboxylated derivative, 4-methylcyclohexanamine, which is used as an inhibitor for various enzymes. The methyl group on the cyclohexane ring is responsible for the compound's activity. Magnetic resonance spectroscopy has shown that cis-4-Methylcyclohexylamine binds to the active site of carbonyl reductase and inhibits its enzymatic activity, thereby blocking a step in the citric acid cycle. Cis-4-Methylcyclohexylamine has also been shown to have anti-inflammatory effects by inhibiting protein kinase C (PKC) and NFkB activation.</p>