Aminas

(2S,3S)-5-[2-(Dimethylamino)ethyl]-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4-one hydrochloride is a racemic mixture of two enantiomers. It is a prodrug that is hydrolyzed to its active form, diltiazem. The drug has been shown to be effective in the treatment of hypertension and angina pectoris. (2S,3S)-5-[2-(Dimethylamino)ethyl]-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4-one hydrochloride has been shown to inhibit the activity of the enzyme phosphodiesterase which breaks down cyclic AMP. This inhibition results in an increase in levels of

<p>5-Oxo Rosuvastatin is a drug product that has been synthesized from natural ingredients. It is an analytical standard for the impurity, 5-oxo-rosuvastatin, which is a potential impurity in the API, rosuvastatin. This drug product has been custom synthesized in order to provide an Impurity Standard for HPLC. This drug product is also used as a Synthetic Reference Standard for Drug Development and Research and Development.</p>

(1,3-Benzodioxol-5-ylmethyl)methylamine hydrochloride (BZMA) is a drug that has been used in research to study the role of serotonin in psychological effects and as a marker for fingerprinting. BZMA is a synthetic compound that is structurally similar to drugs like amphetamine and MDMA. It is not known to have any recreational use. BZMA can be detected using matrix-assisted laser desorption/ionization mass spectrometry. This technique requires a sample containing less than 1% impurities, which are usually silicon compounds or other ions.

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9-(Benzylamino)-1,2,3,4-tetrahydroacridin-1-ol maleate is a cholinergic drug that is used for the treatment of inflammatory diseases. It inhibits phosphodiesterase activity and has been shown to be effective in clinical studies against a number of inflammatory diseases. This drug also has anti-inflammatory properties and can be used to treat acute inflammation. 9-(Benzylamino)-1,2,3,4-tetrahydroacridin-1-ol maleate is also conjugated with fatty acids and this formation helps to increase its bioavailability.

Methyl 2-(methylamino)benzoate is a compound that belongs to the group of antimicrobial agents. It is used in the preparation of pharmaceuticals and other chemical substances. Methyl 2-(methylamino)benzoate has been shown to be toxic to the liver and may cause liver lesions. In addition, this compound has photochemical properties, which make it a potential environmental pollutant. Methyl 2-(methylamino)benzoate can react with uv light and form compounds such as benzene, phenols, and fatty acids. These products can lead to toxicity in humans and animals.

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

1-Methylhexylamine is a chemical compound that has been shown to be an effective treatment for inflammatory bowel disease. It works by activating the H1 receptor, which blocks the production of proinflammatory cytokines and reduces inflammation. 1-Methylhexylamine also has anti-inflammatory effects and can inhibit the growth of bacteria in vitro. This compound can be used as an analog for histamine in sample preparation, where it is used to reduce hydrochloric acid from acidic samples. The uptake of 1-methylhexylamine into cells is pH dependent and can be enhanced by adding sodium citrate or redox potential. 1-Methylhexylamine has been shown to cause symptoms such as headache, nausea, vomiting, dizziness, and depression when it is injected or ingested at high doses. Toxicity studies have shown that this drug may cause liver damage and kidney failure at high doses.

(±)-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>(aR)-a-[[[2-(4-Nitrophenyl)ethyl]amino]methyl]benzenemethanol is a chiral, carbonyl compound that has been used in the synthesis of mirabegron. It is synthesized by reacting an amide with a hydrochloric acid salt. The product yield of (aR)-a-[[[2-(4-Nitrophenyl)ethyl]amino]methyl]benzenemethanol is high and it does not react with aluminium or amide impurities. This compound can be used for the industrial synthesis of mirabegron, which is a drug for the treatment of urinary incontinence. The reduction reaction and hydrolysis reactions are both important to this process.</p>

<p>1-(4-Aminophenyl)-1H-pyridin-2-one is a synthetic chemical that is used in the manufacturing of 8-hydroxyquinoline. It is an industrial chemical that is used to produce potassium carbonate by a reflux reaction with potassium and carbonate. 1-(4-Aminophenyl)-1H-pyridin-2-one is a gas at room temperature and pressure and has been shown to be stable under these conditions.</p>

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<p>2-Amino-4-picoline is a protonated nitrogenous base that has a chemical structure of 2-amino-4-picoline. It is used in the titration calorimetry of copper complexes. This compound has been shown to have antiinflammatory activity and can be used for the treatment of inflammatory diseases such as malonic acid and alkanoic acid induced inflammation. 2-Amino-4-picoline is also used in cisplatin induced nephrotoxicity, where it was shown to prevent high values in urine protein excretion and creatinine clearance by preventing oxidative stress and inhibiting the production of reactive oxygen species (ROS). This compound also reacts with hydrochloric acid to form an aminopyridine salt and hydrogen bond with a hydroxyl group.</p>

<p>Diphenhydramine is a drug that belongs to the class of antihistamines, and is used to treat allergic symptoms such as hay fever, urticaria, and other allergic reactions. It has been shown to inhibit the production of hydrogen fluoride in analytical methods for measuring this compound. Diphenhydramine is also known to have potential interactions with other drugs, including α1-adrenergic antagonists (i.e., h1-antagonists), cyclic peptides, and surfactants. In addition, it has been shown to bind to the α1 subunit of G protein receptors within the gastrointestinal tract in a reaction mechanism that is not yet fully understood. This binding inhibits the response of these receptors to certain stimuli from neurotransmitters and hormones, which can lead to bowel disease.</p>

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3,4-Diaminobenzotrifluoride is a photophysical agent that emits light of a specific wavelength when irradiated with ultraviolet light. It has been shown to inhibit the growth of human cervical carcinoma cells in vitro and to cause apoptosis in these cells. 3,4-Diaminobenzotrifluoride also inhibits the proliferation of human liver and lung cancer cells in vitro. The mechanism by which this agent causes cell death is unknown. 3,4-Diaminobenzotrifluoride is an acid catalyst and stabilizes the chloride ion. This agent may inhibit DNA synthesis or affect proteins that are involved in signal transduction pathways for cell proliferation.

<p>Please enquire for more information about [2-(1-Isobutyl-1H-benzimidazol-2-yl)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 (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>