Amines

<p>Please enquire for more information about N-(1H-Indol-4-ylmethyl)-N-[2-(4-methoxyphenyl)ethyl]amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(Benzyloxy)-1-ethanamine is a radionuclide that has been shown to have potent antitumor activity. It is an imidazopyridine that binds to the 5-HT2C receptor and blocks serotonin from binding to it. This leads to an increase in dopamine levels, which is associated with the therapeutic effects of this drug. The 2-(Benzyloxy)-1-ethanamine molecule has two isomers, with different pharmacological properties: 2-(benzyloxy)ethylamine and 2-(benzyloxy)propylamine. Both molecules are ligands that bind to metal ions and can be used as pharmaceutical formulations. They are also used as modifiers in drug molecules.</p>

<p>Please enquire for more information about (1S,2R)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenyl-1-propanol 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-(Dimethylaminocarbonyl)ethylboronic acid, pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Dodecyl-N,N-dimethyl-N-ethylammonium bromide is a cationic surfactant that can be used to treat microbial infections. It has been shown to be effective against influenza virus, tuberculosis, and other bacterial infections. Dodecyl-N,N-dimethyl-N-ethylammonium bromide is a reaction product of dodecanol and dimethyldodecylamine with silver ions. This surfactant has a benzyl group which provides biocompatibility. The surfactant also has a high affinity for water vapor, which means it will not react with the water in the human body. Dodecyl-N,N-dimethyl-N-ethylammonium bromide is used in titration calorimetry experiments to determine activation energies for reactions involving enzymes and catalysts.</p>

<p>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>

<p>(4-Aminophenyl)boronic acid pinacol ester is a semiconducting material that can be used in thin film devices. It has been shown to be a good candidate for transistor and device applications due to its high yield, low cost, and high stability. This compound can also be used to modify the structure of other compounds through substitution reactions. (4-Aminophenyl)boronic acid pinacol ester has been synthesized from inexpensive starting materials, such as triphenylamine and amines.</p>

<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.</p>

<p>Please enquire for more information about Fmoc-(S)-3-amino-3-(2-naphthyl)propionic 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 [(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>(2R)-2-Amino-3-phenylpropionyl amide is a synthetic cannabinoid that has been shown to bind to the CB2 receptor. It has been found to be an effective analgesic in rat models of inflammatory and neuropathic pain. This drug is also a serine protease inhibitor, with activity against ochrobactrum, an antibiotic-resistant bacteria. (2R)-2-Amino-3-phenylpropionyl amide is also used as a substrate for d-alanine synthesis and has been sequenced. It can form hydrogen bonds with water molecules and chloride ions. (2R)-2-Amino-3-phenylpropionyl amide has been synthesized by Clostridium coli K12 cells and is expected to have similar effects on human cells.</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>

<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>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>

<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>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>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>

<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>2-Amino-4,6-dimethylpyrimidine is a molecule that contains a hydroxyl group, copper chloride, nitrogen atoms, sodium carbonate, and hydroxybenzoic acid. The antimicrobial properties of 2-amino-4,6-dimethylpyrimidine are due to the presence of the hydroxyl group and copper chloride in its structure. This compound has been shown to have bactericidal activity against Pseudomonas aeruginosa and other gram-negative bacteria. It also inhibits the growth of these bacteria by interfering with their ability to synthesize proteins. 2-Amino-4,6-dimethylpyrimidine is a molecule that has an octahedral coordination geometry and forms hydrogen bonds with water molecules. It binds to the surface of minerals such as calcite or quartz and can be used for gravimetric analysis.</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>6-Amino-5,6,7,8-tetrahydronaphthalene-2,3-diol is a potent dopamine D2 receptor antagonist. It has been shown to inhibit the light emission of dopamine in vitro. This compound also has a high affinity for 5-HT receptors and has been shown to be a potent agonist at these sites. 6-Amino-5,6,7,8-tetrahydronaphthalene-2,3-diol has been found to induce pluripotent stem cells from human fibroblasts. These cells can differentiate into virtually any cell type in the body and may be used to study diseases such as Parkinson's disease and cancer.</p>

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

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

<p>3-(Diethylamino)-1,5-dihydro-2,4,3-benzodioxaphosphepin is a reagent used in the hydrogenolysis of alcohols. It is insoluble in water but soluble in organic solvents. 3-(Diethylamino)-1,5-dihydro-2,4,3-benzodioxaphosphepin has been used to prepare a number of alcohols including pyridinium and polyhydroxy alcohols. The compound has also been shown to be a messenger molecule that can induce transduction when it binds to the receptor protein.</p>

<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</p>

<p>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</p>

<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>

<p>Please enquire for more information about Fmoc-S-trityl-D-penicillamine 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-(Dimethylamino)-1-(1-methyl-1H-indol-2-yl)prop-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,N'-bis-Fmoc-diaminoacetic 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 1,4-Piperidinedicarboxylic acid, 4-aMino-, 1-(1,1-diMethylethyl) 4-ethyl 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 (2E)-3-(Dimethylamino)-1-(3-nitrophenyl)prop-2-en-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-(2-Aminoethyl)-3-aminopropylmethyldimethoxysilane is an antibacterial agent that inhibits the growth of bacteria by binding to the cell wall, thereby preventing the synthesis of proteins. It is used in dentistry and medicine as a coating for metal surfaces. This compound has been shown to be effective against Escherichia coli and Enterococcus faecalis. The optimum concentration for this compound is 1 mg/mL.</p>

<p>1-(4-(Aminomethyl)phenyl)pyridin-1-ium chloride is a chemical compound that belongs to the class of pyridines and has pinpoint as its molecular weight. It is an ionic liquid that can be used in analytical methods, such as liquid chromatography and ionization techniques, for the identification of unsaturated fatty acids. This compound can be analyzed by gas chromatography with either electron capture detection or chemical ionization. The GC separation column used for this analysis would have to be a phase column with an unsaturated fatty acid stationary phase. GC-EID and GC-CI are two common ionization techniques that could be used in conjunction with this analytical method. The lower limit of detection for this technique is about 0.1 ppm, which makes it a sensitive analytical tool for use in food production and quality control laboratories. The yield of 1-(4-(Aminomethyl)phenyl)pyridin-1-</p>

<p>2,6-Diamino-5-hydroxy-3-(phenylazo)pyridine is a versatile chemical substance that has various applications in different industries. It can be used as a dianhydride to create high-performance polymers or as an electrode material for batteries and fuel cells. This compound is also used in the production of lacosamide, a medication used to treat epilepsy. In addition to its industrial uses, 2,6-Diamino-5-hydroxy-3-(phenylazo)pyridine is also utilized in research laboratories as a reagent or marker. It is commonly used in aerosol compositions for testing purposes and in the analysis of toxicological samples. Researchers also rely on this compound for dispersive solid-phase extraction techniques and for studying photodegradation processes. Furthermore, 2,6-Diamino-5-hydroxy-3-(phenylazo)pyridine has shown potential in the development of polymeric compositions 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 Dimethylammonium dichlorotri(mu-chloro)bis[(R)-(+)-5,5'-bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole]diruthenate(II) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Amino-1H-pyrazole is a synthetic compound that inhibits the coagulation pathway by inhibiting the synthesis of prothrombin and factor VII. This compound has been shown to be effective in treating autoimmune diseases and cancer. 4-Amino-1H-pyrazole binds to a unique site on the coagulation enzyme, which is not present in other thrombin inhibitors, such as hirudin and heparin. The binding site overlaps with the kinase domain, which inhibits protein synthesis by preventing phosphorylation of key enzymes. In addition, it inhibits wild type strains of bacteria and has been shown to inhibit the growth of cancer cells.</p>

<p>Please enquire for more information about 1-Benzyl-4-phenylamino-4-(methoxymethyl)piperidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(Dimethylamino)ethyl methacrylate is a monomer that belongs to the class of water-soluble acrylic monomers. It is used as a polymerization initiator and in the preparation of hydrogels, which are materials with high water content. 2-(Dimethylamino)ethyl methacrylate copolymers have shown inhibitory properties against bacterial growth, including Staphylococcus aureus and Pseudomonas aeruginosa. The antimicrobial activity of these copolymers may be due to their acidic nature or their ability to form acid complexes with metal ions. Other biological properties include cytotoxicity and significant inhibition of cell proliferation. 2-(Dimethylamino)ethyl methacrylate polymerizes readily at low temperatures, making it useful for sample preparation techniques such as thin layer chromatography (TLC).</p>

<p>4-Aminoquinoline-2-one is a nonsteroidal anti-inflammatory drug that has tuberculostatic activity. It binds to the nitrogen atoms of the enzyme dihydropteroate synthase, which is involved in the synthesis of folic acid and DNA. This leads to an increase in reactive oxygen species and inflammation, which causes disease activity. 4-Aminoquinoline-2-one has been shown to be synergistic with monoclonal antibodies when used as a treatment for inflammatory diseases. In order for 4-aminoquinoline-2-one to be taken up by cells, it must bind to cellular uptake proteins through hydrogen bonds or disulfide bonds.</p>

<p>Diethylaminosulfur trifluoride (DAST) is a reactive chemical that can be used as a methylating agent. It reacts with the hydroxyl group of carotenoids, including β-carotene, to produce x-ray crystal structures with the alcohol methanol solvent. DAST also reacts with 6alkyl and methyl glycosides, such as sucrose, producing a hydroxy derivative. DAST has been shown to have carcinogenic properties in tumor cell lines and is able to induce apoptosis in these cells by damaging their DNA. The use of DAST for cancer treatment can be done through laser ablation or injection into tumors.</p>

<p>N,N'-Bis(salicylidene)ethylenediamine is a catalyst that belongs to the group of transition metal complexes. It is used in hydrogenation reactions in the presence of a palladium-based catalyst. The coordination geometry is octahedral with two bridging ethylene diamine ligands and one terminal ethylene diamine ligand. The complex has been shown to catalyze the reaction between aryl chlorides and alkynes as well as between alkenes and sulfur dioxide to produce corresponding nitriles. N,N'-Bis(salicylidene)ethylenediamine has also been shown to be active in polymerization reactions and can be used as an effective chiral catalyst for polymer compositions.</p>

<p>Tetramethylrhodamine isothiocyanate - mixed isomers (TMR-MI) is a fluorescent probe that can be used to study the interactions between cells and particles. TMR-MI binds to DNA and RNA molecules and has been used as a model system for studying enzyme inhibition. TMR-MI has also been shown to inhibit bowel disease in animal models, but it is not specific to any one cell type. This compound has been used extensively in biomedical research, including studies of autoimmune diseases, cancer, and tissue culture. It has also been used as a marker for detecting reactive oxygen species in laser ablation experiments in mitochondria. TMR-MI can be used to enhance the detection sensitivity of analytical chemistry measurements.</p>

<p>S-[2-(Dimethylamino)ethyl]isothiourea Dihydrochloride is an inhibitor of tyrosinase, an enzyme that catalyzes the oxidation of tyrosine to dopa and dopaquinone. It binds to the active site of the enzyme and blocks its activity. S-[2-(Dimethylamino)ethyl]isothiourea Dihydrochloride has been shown to inhibit tyrosinase in animal experiments and in vitro studies, with a concentration-response curve that can be described by a Michaelis-Menten kinetic model. The inhibition of tyrosinase activity may be due to steric hindrance by the thiourea group or a covalent binding to amino acid residues on the protein surface. S-[2-(Dimethylamino)ethyl]isothiourea Dihydrochloride is also known as monomethyl auristatin E (MMAE</p>

<p>2-(Methyl-2-pyridylamino)ethanol (2MPE) is a small molecule that has been studied for its potential use as an inhibitor of the enzyme protein kinase C-alpha. The reaction mechanism of 2MPE with rosiglitazone, a drug used to treat type II diabetes mellitus, has been shown to be nucleophilic and proceeds through an addition-elimination mechanism. The kinetic parameters for this reaction have been determined by studying the effect of temperature on the reaction rate. Density measurements indicate that 2MPE is a low-molecular weight compound with a density of 1.08 g/mL at 25°C and 1 atm pressure. This study also found that microreactors are capable of producing high reaction yields in shorter amounts of time than larger reactors, making them well suited to the synthesis of small molecules such as 2MPE.</p>

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

<p>Imidazo[1,2-a]pyridin-8-ylamine dihydrochloride is an arylation agent that reacts with nucleophiles to form an amide linkage. Imidazo[1,2-a]pyridin-8-ylamine dihydrochloride is used in the synthesis of carboxylic acid derivatives and other biomolecules. It can be used for selective functionalization of unsymmetrical carboxylic acids.</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>Please enquire for more information about 1-[4-(4-Methylpiperidin-1-yl)phenyl]methanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Fluorophenethylamine is a molecule that can switch between two forms, one hydrophobic and one hydrophilic. When it is in the hydrophobic form, 2-fluorophenethylamine can bind to water molecules to form potential use products. When 2-fluorophenethylamine is in the hydrophilic form, it can desorb from the surface of water. 2-Fluorophenethylamine has been shown to be a neurotransmitter and may have potential use as an anti-depressant or anti-anxiety medication. It has also been suggested that 2-fluorophenethylamine may be used for the treatment of Parkinson's disease, because of its ability to inhibit dopamine degradation. An experiment conducted with spectra found that 2-fluorophenethylamine reacts with hydrogen bonds and other weak interactions to form dimers and monomers. The vibrational spectrum of this molecule shows that there are no strong</p>

<p>Please enquire for more information about N-(2-Aminoethyl)-4-(1,1-dimethylethyl)-2,6-dimethylbenzeneacetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methylamine thiocyanate is a chemical compound that is used in the production of silicone rubber. It can be synthesized by the reaction of methylamine and nitrous acid with a base such as sodium hydroxide or potassium hydroxide. Methylamine thiocyanate has been shown to have synergistic effects with a number of other chemicals, including hydrocarbons, silicates, and perovskites. This compound has also been shown to have a morphology that is dependent on the type of solvent it is mixed in, which can alter its commercialization potential. Methylamine thiocyanate has also been shown to interact with organic solvents and hydrogen bonds.BR&gt;BR&gt;Methylamine thiocyanate undergoes hydrolysis when exposed to water or acids such as hydrochloric acid or sodium hydroxide solution.</p>

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

<p>2-Amino-3-(4-hydroxy-3-methoxyphenyl)propanoic acid is a metabolite of levodopa in the body. It is formed by oxidation of levodopa via the enzyme catechol-O-methyltransferase (COMT). This compound is used as an analytical reagent to measure levels of levodopa and its metabolites in biological samples. 2-Amino-3-(4-hydroxy-3-methoxyphenyl)propanoic acid can also be used to diagnose Parkinson’s disease, since it is produced in excess when dopamine production decreases due to the degeneration of dopaminergic neurons. The concentration–time curve for this compound can be used to calculate the clearance rate of levodopa from the blood plasma.</p>

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

<p>Methiopropamine is a synthetic psychoactive substance that has been associated with long-term health effects. It is used recreationally for its stimulant properties, such as increased alertness and wakefulness. Methiopropamine may cause paranoia and delusions, as well as other long-term effects. The drug can be detected in the urine for up to five days after ingestion. Methiopropamine is an amphetamine analogue of cathinone, which is a naturally occurring substance found in the khat plant. It is classified by the DEA as a Schedule I controlled substance in the United States.</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>4-Nitro-1,2,5-oxadiazol-3-amine is a molecule that has been shown to be an inhibitor of the epidermal growth factor receptor (EGFR). The optimal reaction conditions for this molecule were determined by crystallography. These results were confirmed by prognosis assays and the determination of tautomers. This molecule may be used in diagnosis and as a potential treatment for cancer. 4-Nitro-1,2,5-oxadiazol-3-amine binds to the EGFR at a site different from that of erlotinib, an inhibitor currently used in the clinic. This binding leads to inhibition of protein synthesis and cell division by preventing the activation of downstream signal transduction pathways. The molecule also inhibits tumor cell proliferation and induces apoptosis by preventing the production of nitric oxide (NO) and reactive oxygen species (ROS).</p>

<p>Please enquire for more information about 8-[(2-Hydroxyethyl)(methyl)amino]-1,3,9-trimethyl-3,9-dihydro-1H-purine-2,6-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</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 (S)-N-Boc-3-amino-1-butyne including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Aminopicolinic acid is a carboxylate that can be found in the cytosol, mitochondria, and nucleus of cells. It is an efficient method for the synthesis of picolinic acid from 3-aminopyridine-2-carboxylic acid. The synthesis of picolinic acid has been shown to have structural analogs to molecules involved in nucleotide metabolism such as single-stranded DNA, mitochondrial DNA, and mitochondrial RNA. 3-Aminopicolinic acid has been shown to increase renal blood flow by stabilizing complexes with chloride and phosphoenolpyruvate. This compound also enhances the renal excretion of picolinic acid. 3-Desacetylcefotaxime potassium Tilmicosin Gatifloxacin 3-Aminopicolinic acid</p>

<p>3-(1-Piperidin-1-ylcyclohexyl)phenyl]amine hydrochloride is a ligand that binds to the acetylcholine receptor. 3-(1-Piperidin-1-ylcyclohexyl)phenyl]amine hydrochloride is an active analogue and has a high binding affinity for the cholinergic receptor. It has been shown to have a kinetic effect on the excitatory system, enhancing excitatory effects of acetylcholine without affecting inhibitory effects. 3-(1-Piperidin-1-ylcyclohexyl)phenyl]amine hydrochloride also has an antagonistic effect on modifiers of acetylcholine activity such as amantadine, but enhances the effects of other drugs, such as clonidine.</p>

<p>Rac-8-hydroxy-2-dipropylaminotetralin hydrobromide is a potent 5-HT agonist that has been shown to inhibit the release of prolactin in the serum of rats. Rac-8-hydroxy-2-dipropylaminotetralin hydrobromide was found to be an antagonist of 5HT receptors, with a potency comparable to that of 8-OHDPAT and WAY 100635. Rac rac8-hydroxy-2-dipropylaminotetralin hydrobromide also inhibits locomotor activity induced by the 5HT1A agonist 8OHDPAT. Experiments in vivo have shown that rac rac8-hydroxy-2-dipropylaminotetralin hydrobromide binds to benzodiazepine binding sites and has a low affinity for dopamine receptors. It also blocks cholinergic transmission in the brain, which may explain its</p>

<p>2-Aminomethylpyrazine (2-AP) is a molecule that has been studied for its potential as an anti-cancer agent. It has been shown to bind to the DNA of tumor cells and prevent them from dividing, leading to cell death. 2-AP also prevents the production of survivin, which is a protein that promotes cancer cell growth and survival. 2-AP can be used in positron emission tomography (PET) scans to detect tumors, and has shown promise in treating acute myeloid leukemia.</p>

<p>N-[1-(4-Fluorophenyl)propan-2-Yl]-N-methylprop-2-Yn-1-amine is a synthetic molecule that has been shown to be an inhibitor of the enzyme nitroethane reductase. This drug is also capable of inhibiting the activity of other enzymes and is being investigated for its potential use in the treatment of various types of cancer. N-[1-(4-Fluorophenyl)propan-2-Yl]-N-methylprop-2-Yn-1-amine inhibits nitroethane reductase by binding reversibly to the active site and competitively inhibiting the substrate. The potency of this drug against nitroethane reductase has been shown to be increased by alkylation.br&gt;<br>The inhibition of nitroethane reductase by N-[1-(4-fluorophenyl)propan-2-Yl]-</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>5-(2-Aminopropyl)-2-methoxybenzenesulphonamide is a trimethyl derivative of the aminopropyl group. It is used as a reagent to introduce hydroxymethyl groups into organic compounds. 5-(2-Aminopropyl)-2-methoxybenzenesulphonamide reacts with hydrochloric acid and an organic solvent in the preparation process. In the Friedel-Crafts reaction, 5-(2-Aminopropyl)-2-methoxybenzenesulphonamide reacts with d-alanine to form an optical isomer, which can be converted to its racemic form by ammonolysis. This compound is also used as a prostatic agent and an amide in the synthesis of benzene and phenoxymethyl alcohols.</p>

<p>6-Hydroxytryptamine creatinine sulfate (HTPS) is a metabolite of serotonin and dopamine that can be found in human urine. HTPS is not active on its own, but it has been shown to increase blood pressure in rats when administered together with other substances such as 5-hydroxytryptamine. HTPS also interacts with noradrenaline and hydroxylates serotonin to produce 6-hydroxyserotonin. The biosynthesis of HTPS starts with the hydroxylation of tryptophan by tryptophan 4-hydroxylase (TPH), followed by the conversion of 5-hydroxytryptophan to 5-hydroxyindoleacetic acid (5HIAA). This enzyme is inhibited by drugs such as clozapine, which is used for treatment of schizophrenia. 6-Hydroxytryptamine creatinine sulfate can be found in many tissues, including the brain and kidney</p>

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

<p>3-Amino-1-diphenylmethylazetidine (3ADM) is a dopaminergic antagonist that binds to the D4 receptor. This compound has been shown to have affinity for the D4 receptor and can inhibit the binding of dopamine to its receptors, thereby blocking its effects. 3ADM is a potent antagonist of the dopaminergic system and has been shown to be effective in animal models.</p>

<p>Please enquire for more information about Bis(tert-butoxycarbonyl) Lisdexamphetamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N,N-Diethylaminoethyl 2,2-diphenylvalerate hydrochloride is a depressant drug that inhibits the growth of bacteria by inhibiting fatty acid synthesis. It has been shown to inhibit group P2 enzymes that are involved in the production of fatty acids. In this way, it inhibits the formation and release of ATP, which is essential for bacterial growth. N,N-Diethylaminoethyl 2,2-diphenylvalerate hydrochloride also has inhibitory properties against bacteria that cause infectious diseases. This drug is effective against Hl-60 cells and can be used as a diagnostic tool for detection sensitivity and detection time.</p>

<p>L-2-Aminobutanamide is a compound that is used as an industrial preparation and as a reagent in kinetic studies. It has been shown to be effective in the analytical method for the determination of hydrochloric acid in titration, with a detection limit of 0.1%. L-2-Aminobutanamide can also be used to produce asymmetric synthesis by adding it with sodium hydroxide solution or hydroxide solution and using chromatographic science. This compound has been shown to have antibacterial effects on Brucella, which can be attributed to its ability to inhibit protein synthesis and disrupt cell membrane integrity. L-2-Aminobutanamide is a chiral compound that can exist in two different forms, L -(+)-2-aminobutanamide or D -(-)-2-aminobutanamide.</p>

<p>4-Methylcyclohexylamine is a compound that is used as an inhibitor of the enzyme ornithine decarboxylase. It also has been shown to have anti-inflammatory properties in cell culture and in animal models of inflammatory bowel disease. 4-Methylcyclohexylamine binds to the active site of the enzyme, preventing it from converting ornithine into putrescine. Ornithine decarboxylase inhibitors are a new class of drugs for the treatment of inflammatory bowel disease, which are effective against both ulcerative colitis and Crohn's disease.</p>

<p>Please enquire for more information about 2-(2-Methyl-1H-indol-3-yl)ethanamine oxalate 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 Methyl4-aminomethyl-1-boc-piperidine-4-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl aminomethanimidothioate hydroiodide (MAI) is a nitro-substituted methylated analogue of the natural amino acid methionine. It has been shown to inhibit creatine kinase, which is an enzyme that regulates the conversion of energy from ATP to creatinine. MAI also inhibits adenosine receptors and can be used as an anti-inflammatory agent. It has been shown to suppress inflammatory diseases, such as arthritis and cancer, by inhibiting the production of inflammatory cytokines. MAI has been shown to be effective against viruses such as HIV and herpes simplex virus type 1 (HSV-1).</p>

<p>Please enquire for more information about 3-Bromo-N,N-dimethylpropan-1-amine hydrobromide 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 Des[5-(2-dimethylamino)ethyl] diltiazem including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Amino-cyclopentane carbonitrile is a pharmacological agent that can be used to treat angiotensin II and other peptides. It has an amine group with a hydroxyl group, which allows it to interact with the active site of angiotensin converting enzyme (ACE). 1-Amino-cyclopentane carbonitrile's mechanism of action is based on its ability to react with the halide and phenyl groups in ACE. The hydrolysis of ACE leads to the production of angiotensin I, which is then converted into angiotensin II by angiotensin-converting enzyme 2 (ACE2). 1-Amino-cyclopentane carbonitrile also interacts with amines such as histamine and serotonin, inhibiting their synthesis.</p>

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

<p>S-Aminoethyl-L-cysteine hydrochloride is an amino acid that is used in the diagnosis of metabolic disorders. It has been found to have a high concentration in plasma and can be used to measure the activity of bowel disease. S-Aminoethyl-L-cysteine hydrochloride is also used as a diagnostic marker for inflammatory diseases. It is extensively metabolized by acidic hydrolysis, which results in the release of chloride ions and amines.</p>

<p>2-(2-Chlorophenyl)ethylamine is an amine that inhibits the production of proteins vital for cell division. It binds to bacterial 16S ribosomal RNA and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. 2-(2-Chlorophenyl)ethylamine has been shown to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Clostridium perfringens, although is not active against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex. 2-(2-Chlorophenyl)ethylamine has shown anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis.</p>

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

<p>N-Nitrosodiethylamine (NDEA) is a genotoxic carcinogen that is formed as an intermediate in the industrial production of nitric acid. It has been shown to be a potent inhibitor of DNA polymerase and topoisomerase II, which are involved in DNA replication and repair. NDEA has been detected in human blood samples and has been shown to induce squamous cell carcinoma in animal models. This chemical can also cause inflammation by binding to toll-like receptor 4, which activates the inflammatory response. The biocompatible polymer used for this product is not known to produce any genotoxic or mutagenic effects.</p>

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

<p>1H-Indol-7-amine is a molecule that belongs to the group of basic proteins. It has been shown to be an optimum concentration for biological activity and can be used in the treatment of diseases such as cancer and diabetes. 1H-Indol-7-amine binds to acidic molecules and exhibits redox potentials that are suitable for hydrogen bond formation with other molecules. The molecule is also involved in protein kinase selectivity, which may be due to its ability to bind with nitrogen atoms. 1H-Indol-7-amine has been shown to have beneficial effects on agarose gels through x-ray crystal structures and has a number of favorable electrochemical properties, including low charge transfer resistance, high electron mobility, and good chemical stability.</p>