Amines

<p>Indene-1-methanamine is a drug that has been used for the treatment of neurologic disorders and is an ester of aliphatic hydrocarbons. It has been shown to have antidepressant effects in animal models, which may be due to its ability to bind to 5-HT1A receptors. Indene-1-methanamine also has antimicrobial properties and can be used for treating bladder infections as well as cancer. This drug binds to the quinolizine site on bacterial DNA gyrase, which inhibits DNA synthesis and leads to cell death.</p>

<p>Please enquire for more information about 2-(4-fluorophenyl)-n-methylethanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Amino-3,5-difluorobenzonitrile is a fine chemical used as a building block in research chemicals, reagent, and speciality chemical. It is versatile and can be used as a reaction component in the synthesis of complex compounds with various applications. CAS No. 110301-23-0 is an important intermediate for the synthesis of organic compounds and pharmaceuticals. 4-Amino-3,5-difluorobenzonitrile is also used as a scaffold for the synthesis of organic compounds.</p>

<p>3-(1-Naphthyl)propyl]amine is an organic compound that is a colorless solid with a melting point of -118°C. It is soluble in water, methanol, and acetone. 3-(1-Naphthyl)propyl]amine forms acid when heated with concentrated hydrochloric acid. The reaction produces hydrogen chloride gas and benzoic acid as a byproduct. 3-(1-Naphthyl)propyl]amine also reacts with pyridine to produce carbamic acid and ammonia gas as a byproduct. This can be rationalized systematically by the loss of the amine group from the nitrogen atom of the amine molecule. Carbamic acid has two acidic protons on it which are stabilized by the carbonyl group on the other side of the molecule. 3-(1-Naphthyl)propyl]amine can also react with anions such as carbonate ions to form carbamate salts,</p>

<p>Please enquire for more information about tert-Butyl 6-(aminomethyl)-1,4-oxazepane-4-carboxylate 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-Aminothiophene-2-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ammonium chloride is a salt of ammonium and chloride. It is used in wastewater treatment as a coagulant, to remove suspended solids from the water. In addition, ammonium chloride has been shown to have potent antitumor activity and is used in chemotherapy treatments. Ammonium chloride can be toxic if ingested or inhaled and should not be handled without proper safety precautions. Ammonium chloride also has an effect on the bowel disease, slowing down the rate at which it progresses. It is produced when trimethyl reacts with blood or water vapor. The surface methodology was used to obtain thermodynamic data for ammonium chloride. This method can be applied to other compounds that are difficult to analyze by other methods.</p>

<p>Please enquire for more information about Boc-(S)-3-amino-3-(2-methoxyphenyl)propionic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Rotigotine is a substance that belongs to the class of active compounds. It has been shown to have optical activity, but this property is not well understood. Rotigotine is a racemic mixture with two enantiomers, which are mirror images of each other. The optical rotation of rac-5,6,7,8-tetrahydro-6-(propylamino)-1-naphthalenol is given as +28°. This property can be determined by measuring the angle of rotation when light passes through the substance in solution in contact with a polarizer and analyzer.</p>

<p>Please enquire for more information about 2-(tert-Butylamino)-4,6-dichloro-1,3,5-triazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Dioleoyloxypropyl-N,N,N-trimethylammonium methylsulfate (DOTAP) is an antibacterial agent that disrupts the bacterial membrane. It has been shown to inhibit the uptake of chlamydia by inhibiting the binding of chlamydia to cells and enhancing the detection of chlamydia in cells. DOTAP also has pharmacological properties that are related to its ability to interfere with cellular membranes. DOTAP can be used as a strategy for developing antibacterial agents because it inhibits bacterial growth by disrupting their cellular membranes. This results in a decrease in phosphatidylethanolamine levels, leading to increased cell death.</p>

<p>Please enquire for more information about Z-(R,S)-3-amino-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>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 7-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 4-(4-tert-Butylphenyl)-1,3-thiazol-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>12-Amino-1-dodecanoic acid methyl ester hydrochloride salt (12ADM) has been shown to have immunomodulatory properties. It has a nanomolar range of activity, which is the optimal for an immunosuppressant. 12ADM inhibits the transcriptional activity of human immunodeficiency virus type 1 (HIV-1) and HIV-2, as well as other retroviruses, through interactions with specific RNA sequences in the viral genome. The amide group in this compound is essential for its antiviral activity, and it also interacts with betulinic acid to enhance its cytotoxicity.</p>

<p>Tetramethylammonium triacetoxyborohydride is a potent antagonist that binds to the active site of hydrogen-bond forming enzymes. It is used in the treatment of bowel disease, as well as other diseases such as cancer, diabetic neuropathy and inflammatory bowel disease. Tetramethylammonium triacetoxyborohydride has been shown to inhibit the growth of certain bacteria by inhibiting their ability to form hydrogen bonds. This chemical can also be used in asymmetric synthesis, which is the process of synthesizing only one enantiomer from a racemic mixture. Tetramethylammonium triacetoxyborohydride can function as an organocatalyst for this process by activating achiral substrates into chiral ones.</p>

<p>Please enquire for more information about N-[4-Amino-3-(trifluoromethyl)phenyl]-2-methylpropanamide 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>Alpha-amino-2H-tetrazole-5-acetic acid (AAT) is a neurotoxin that inhibits glutamate receptors and causes neuronal cell death. It also decreases heart function in rats by inhibiting the cardiac sodium channel. AAT has been shown to be effective for inducing neuronal death in Xenopus oocytes, as well as decreasing the expression of certain receptor protein, such as NMDA and AMPA receptor subtypes. AAT is also known to cause apoptosis, which may be due to its inhibition of receptor function.</p>

<p>4-Amino-1,3-dimethyl-2,6-dioxo-5-nitrosopyrimidine is a monoclonal antibody that binds to cancer cells. It has been shown to be effective in the treatment of leukemia, Hodgkin's disease, and non-Hodgkin's lymphoma. The binding of 4-Amino-1,3-dimethyl-2,6-dioxo-5-nitrosopyrimidine to cancer cells is due to the formation of a coordination geometry between the copper complex and the nitrogen atoms on the amino group. This drug has been shown to inhibit tumor growth by blocking the synthesis of DNA and RNA, which are key components in cell division. 4AADNP also inhibits cancer cells' ability to uptake glucose by inhibiting cellular glucose transporters. The binding affinity of 4AADNP for cancer cells is higher than for normal cells because cancer cells have more receptors for this drug</p>

<p>Please enquire for more information about 2-Amino-3',4'-dimethoxypropiophenone hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethyl 2-amino-thiazole-4-carboxylate (ETAC) is an inhibitor of protein synthesis. It binds to the dna and inhibits transcription, leading to cell death by inhibiting the production of proteins vital for cell division. ETAC has been shown to have cytotoxic activity against cancer cells and hemolytic activity. It also has a strong fluorescence probe property, which may be used in cancer diagnosis. ETAC can inhibit protein synthesis in cells that are resistant to other antimicrobial agents and platinum-based chemotherapy, making it a potential treatment for these infections. The pharmacokinetic properties of ETAC are not well studied but it is excreted through urine, suggesting that it is hydrophilic and may be metabolized with glucuronidation or sulfation. The molecular modeling study suggests that the hydrogen bond between ETAC and the dna phosphate group may explain its inhibitory effects on DNA synthesis.</p>

<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>

<p>Please enquire for more information about 2-Amino-1-(2,3-dihydro-benzofuran-5-yl)-ethanol 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-Methoxy methamphetamine 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 Ethyl 3-{[(1E)-(dimethylamino)methylene]amino}-5-methoxy-1-methyl-1H-indole-2-carboxylate 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 [(1,5-Dimethyl-1H-benzimidazol-2-yl)methyl]amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Tetrabutylammonium difluorotriphenylsilicate is a model system for studying the mechanism of nucleophilic substitution at an unsymmetrical carbon center. It is used in analytical chemistry to prepare samples for analysis. Tetrabutylammonium difluorotriphenylsilicate has been shown to be an effective and selective reagent for the synthesis of picolinic acid, which can be used as a precursor for the synthesis of nicotinamide riboside, a vitamin B3 derivative. The reaction proceeds via an SN2 mechanism, where hydrogen fluoride (HF) acts as a nucleophile that attacks the electrophilic carbon center of allyl chloride (CH2=CH-CH2Cl) to form an intermediate with two alkyl groups on opposite sides. The reaction product is then hydrolyzed to release tetrabutylammonium chloride (tBuNH4Cl).</p>

<p>Please enquire for more information about 2-[2-(Dimethylamino)ethyl]-1-indanone 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-Amino-5-(2,3,4-trimethoxyphenyl)cyclohex-2-en-1-one 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 N-2,3-Dihydro-1H-inden-2-yl-N-propylamine 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 Dicyclohexylamine 2-cyanoacrylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-1-Z-1,2-diaminoethane·HCl is a stable isotope of N-1-Z-1,2-diaminoethane. It is used for the analysis of plant tissue to quantify the amount of leaves or other plant parts that are present in a sample. This compound can be used to monitor changes in the level of leaves or other plant parts over time and to measure recovery rates after harvest. N-1-Z-1,2-diaminoethane·HCl is labeled with deuterium (D) in order to be detected by liquid chromatography–mass spectrometry (LC–MS). The quantification of N-1-Z-1,2-diaminoethane·HCl can be monitored using multiple reaction monitoring (MRM). The use of this stable isotope overcomes many problems associated with traditional methods, such as environmental variability and tissue degradation.</p>

<p>L-a-aminosuberic acid is a synthetic amino acid that has been used as an analog of L-cysteine. It can be used to induce tumor cell death by inhibiting the uptake of fatty acids in prostate cancer cells. L-a-aminosuberic acid is also able to inhibit the expression of proteins that are involved in prostate cancer, such as monoclonal antibodies and sequences. This compound may be a potential biomarker for the diagnosis of prostate cancer. The low expression levels may be due to the lack of disulfide bond formation, which is necessary for protein activity.</p>

<p>3-Methoxybenzene-1,2-diamine is a chloride surfactant that is cationic at low concentrations. It is most commonly used as a cross-linking agent in polymers and also has anti-inflammation properties. 3-Methoxybenzene-1,2-diamine is an osmotic agent that binds to water molecules, which prevents the loss of water from cells and increases cell volume. This chemical also has been shown to be an antagonist of 5Ht4 receptors and can be used for the treatment of inflammatory diseases such as asthma. 3-Methoxybenzene-1,2-diamine has been shown to have low toxicity in rats when consumed in dietary concentrations.</p>

<p>Please enquire for more information about Diethyl[2-(4-nitrophenoxy)ethyl]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 R-(-)-Methamphetamine 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-Ethoxyphenyl)ethylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Aminothiophen-3-yl)(4-bromophenyl)methanone is a new compound that is being developed as a potential antiviral agent. Covid-19, the trade name for 2-aminothiophen-3-yl)(4-bromophenyl)methanone, prevents the replication of viruses by binding to their nucleic acids and blocking their ability to produce proteins. Covid-19 has been shown to be effective against both influenza A and B viruses in cellular and animal models. The antiviral activity of Covid-19 is due to its ability to bind to viral nucleic acid, preventing the production of proteins vital for viral replication. This compound has also been shown to have anti-inflammatory properties, which may be due to its ability to inhibit the production of amyloid plaques in mice with Alzheimer's disease.</p>

<p>O-(Tert-butyldimethylsilyl)hydroxylamine is a stereospecific, oxidized, insoluble, tautomeric hydroxamic acid. It is used as a reagent in organic synthesis to form lactams by reaction with hexamethylenetetramine. The compound can be prepared by treatment of hydroxylamine with diacetate in the presence of aluminium chloride. The product is an orange liquid that crystallizes from water, but is not soluble in most organic solvents.</p>

<p>Didesmethyl sibutramine is a drug that has been used to treat obesity. It is an anorectic agent that decreases appetite by affecting the central nervous system. Didesmethyl sibutramine stimulates the release of norepinephrine and dopamine in the brain, which are neurotransmitters that regulate hunger and satiety. This drug also influences the metabolism of fat cells, leading to weight loss. Didesmethyl sibutramine may be prescribed as a combination therapy with other drugs for conditions such as primary pulmonary hypertension, coronary heart disease, congestive heart failure, or experimental models of these diseases. Didesmethyl sibutramine can cause adverse reactions such as insomnia, anxiety, or high blood sugar levels.</p>

<p>Please enquire for more information about Methyl-(2-m-tolyl-ethyl)amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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.</p>

<p>Beclotiamine hydrochloride, also known as beclamethasone 17,21-dipropionate, is a synthetic corticosteroid that has anti-inflammatory and anticoccidial properties. It is not active against coccidiosis in piglets. Beclotiamine hydrochloride has been shown to have a prophylactic effect on coccidiosis in piglets by inhibiting the development of the oocysts. The mechanism of action is not fully understood but may involve inhibition of the uptake of pyrophosphate or interference with the conversion of organic phosphates to inorganic phosphate. Beclotiamine hydrochloride can be used for the treatment and prevention of coccidiosis in pigs.</p>

<p>Please enquire for more information about N-[2-(4-Benzylpiperazin-1-yl)-2-oxoethyl]-N-methylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Ethylhydroxylamine hydrochloride is a chemical compound that belongs to the group of biocides. It is used as an antimicrobial agent in medical devices, such as catheters and dialysis membranes. N-Ethylhydroxylamine hydrochloride is also used in cancer research to activate the CCR5 receptor, which is involved in HIV infection. N-Ethylhydroxylamine hydrochloride has been shown to have biological properties in humans and animals and has a high degree of chemical stability. The compound can be synthesized from sodium carbonate and ethyl alcohol. The synthesis involves the addition of ethylene oxide to ethanolamine followed by hydrogenation with a catalyst. N-Ethylhydroxylamine hydrochloride is soluble in water, methanol, and acetone. This chemical compound binds to proteins in the human body, resulting in an increase of acidity in urine samples when tested using a plate test. It also has</p>