Amines

<p>3-Fluoro-Dopamine is a fluorinated catecholamine that is used in research as a radioligand and in animal models. It has been shown to be an agonist of β-adrenergic receptors and to have a safety profile similar to that of dopamine. 3-Fluoro-Dopamine has been shown to increase the uptake of dopamine in rat striatal membranes, which may be due to its affinity for β-adrenergic receptors.</p>

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<p>3-Amino-4-anisic acid is a conjugate of an aromatic carboxylic acid and an amino group. The vapor pressure of 3-amino-4-anisic acid is higher than that of the free 3-amino-4-anisic acid. Immunocompetent cells are the most sensitive to this compound, with metastasis and tumor growth being inhibited. This compound is also used in the treatment of cancer, although it has not been proven to be effective for all cancers. Sorafenib and other compounds that have similar structures may be used as substitutes for 3-amino-4-anisic acid in some cases. There are two isomers of 3-amino-4-anisic acid: cis and trans form. The cis form has better binding properties than the trans form, which can lead to decreased efficacy when a mixture of both forms is used. Hyaluronic acid and link</p>

<p>3-Amino-2-bromo-4,6-dimethylpyridine is a fine chemical that can be used as a versatile building block in the synthesis of other compounds. It is also an intermediate for the production of organic compounds and research chemicals. 3-Amino-2-bromo-4,6-dimethylpyridine is listed on the Chemical Abstracts Service (CAS) registry with the number 104829-98-3. This compound has a complex structure and is high quality and stable.</p>

6-Aminonicotinic acid is an inhibitor of bacterial DNA gyrase and topoisomerase IV. It has been shown to inhibit the growth of a number of bacteria, including E. coli K-12, with potent inhibitory activity against these enzymes. 6-Aminonicotinic acid binds to the active sites on these enzymes and prevents them from working. The detection time for 6-aminonicotinic acid is about 3 hours after exposure. 6-Aminonicotinic acid has been shown to be more potent than other inhibitors of bacterial DNA gyrase and topoisomerase IV such as 2,4-diaminopyrimidine (2,4DAP).

<p>N1,N4-Di(buta-2,3-dienyl)butane-1,4-diamine is a natural compound that inhibits polyamine oxidase (PAO), an enzyme that catalyzes the oxidation of polyamines. PAO is involved in the development of cancer and neuronal death. N1,N4-Di(buta-2,3-dienyl)butane-1,4-diamine has been shown to inhibit PAO activity in human carcinoma cell lines and to be neuroprotective in a rat model of Parkinson's disease. This agent also induces apoptosis by depolarizing mitochondrial membrane potential. It has been shown to be more potent than protocatechuic acid and irreversible inhibition can occur when cells are exposed for long periods of time.</p>

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This is a speciality chemical and is not intended for use in food, drug, or cosmetic applications. This fine chemical is a useful building block, which can be used to synthesize complex compounds. It has been shown to have high reactivity with a variety of reagents, making it an excellent research component.

<p>2-Amino-5-[1-hydroxy-2-(isopropylamino)ethyl]benzonitrile is a hydrophilic compound that is used as a probe in enzyme activity assays. It can be used to measure the activities of many enzymes, such as those involved in protein synthesis and degradation. 2-Amino-5-[1-hydroxy-2-(isopropylamino)ethyl]benzonitrile is also an excellent substrate for the nitrite reductase enzyme, which catalyzes the reduction of nitrite to ammonia and water. This reaction occurs in two steps: first, the 2-amino group on the molecule is reduced to an amino radical; second, this amino radical reacts with another molecule of nitrite to form ammonia and water. The product of this reaction (ammonia) can be quantified by measuring absorbance at 340 nm. 2-Amino-5-[1-hydroxy--2</p>

Dodecylamine HCl is a chemical inhibitor of energy metabolism that inhibits the synthesis of fatty acids. It is used in the treatment of infectious diseases, such as malaria and tuberculosis. Dodecylamine HCl is a molecule consisting of 12 carbon atoms with an ethylene chain. This inhibitor binds to the enzyme acyl-CoA synthase, which catalyzes the production of fatty acids from acetyl-CoA and malonyl-CoA. The optimum pH for dodecylamine HCl is around 7.0, but it can be solubilized in water at higher pH levels due to its intramolecular hydrogen bonds. Dodecylamine HCl has been shown to have a particle size distribution between 10-200 nm in size and can be used as a nanoparticulate composition for drug delivery systems with thermodynamic data.!--END-->

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<p>(E)-N-(3-Methylaminopropyl)-2-thiopheneacrylamide is a high quality chemical that can be used as an intermediate in the synthesis of complex compounds. It is also a useful scaffold and building block for the synthesis of speciality chemicals with versatile reactions.</p>

<p>1-Aminohydantoin hydrochloride is an intermediate in the synthesis of the aminohydantoins, a class of drugs used to treat epilepsy. It is also used as a reagent for preparing monoclonal antibodies. 1-Aminohydantoin hydrochloride is prepared by reacting hydrochloric acid with hydrazine and sodium citrate, followed by purification using distillation and recrystallization. 1-Aminohydantoin hydrochloride can be used to determine the presence of chloride ions in animal tissues by measuring its chemical shift on a mass spectrometer. This drug has been shown to inhibit oxidative DNA damage in rat kidneys, which may be due to its ability to suppress reactive oxygen species production.</p>

<p>(+)-Biotin-(PEO)3-amine is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. (+)-Biotin-(PEO)3-amine is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>

<p>2-(4-Chlorophenoxy)ethyl]amine hydrochloride is a chemical that can be used as a building block for the synthesis of pharmaceuticals. It is an intermediate in the production of fine chemicals and other reagents. 2-[2-(4-Chlorophenoxy)ethoxy]ethylamine hydrochloride has CAS number 28769-06-4 and can be used for research purposes.</p>

<p>[(3-Methylphenyl)(phenyl)methyl]amine hydrochloride is a useful building block in the synthesis of many organic compounds. It has been used extensively as a research chemical, and is often used as an intermediate to synthesize other chemicals. [(3-Methylphenyl)(phenyl)methyl]amine hydrochloride is also a versatile scaffold for drug design, and has shown anti-inflammatory properties.</p>

(S)-trans-2-Amino-4-(2-aminoethoxy)-3-butenoic acid hydrochloride is a chemical pesticide that inhibits the production of ethylene in plants. It is used to control growth and enhance the fruit quality of horticultural crops. It is also used as an inhibitor of serine proteases, which are enzymes that catalyze the hydrolysis of proteins. This product has been shown to act as a growth regulator by inhibiting the activity of serine proteases and blocking the biosynthesis of ethylene. (S)-trans-2-Amino-4-(2-aminoethoxy)-3-butenoic acid hydrochloride also blocks the biosynthesis of human chorionic gonadotropin, a hormone involved in reproduction and development.

N1-(2-Aminoethyl)-N1-methylethane-1,2-diamine is a chromatographic cross-linking agent that is used in the preparation of monoclonal antibodies. It contains two amino groups and two ethyleneamine groups. N1-(2-Aminoethyl)-N1-methylethane-1,2-diamine binds to calcium carbonate and forms a chelate ring with the metal ion. The compound has been shown to have diagnostic properties, as it can be detected by nmr spectra and by the use of monoclonal antibody.

<p>7-Amino-2-bromo-9-fluorenone is a dye that can be used to label or visualize β-amyloid plaques in the brain. It has high binding affinity for β-amyloid, and can be used to identify the presence of this protein in the brain. 7-Amino-2-bromo-9-fluorenone is also useful for monitoring β-amyloid plaques in transgenic mice. This dye was injected into the brains of transgenic mice, and then stained with a fluorescent dye. Autoradiography was then used to identify where 7-Amino-2-bromo-9-fluorenone binds to β amyloid plaques.<br>7 - Amino - 2 - bromo - 9 - fluorenone</p>

4-Dimethylamino-4'-methylchalcone is a versatile building block that can be used in synthesis of fine chemicals, research chemicals, and reagents. It can also be used as a speciality chemical or useful intermediate for the preparation of other compounds. 4-Dimethylamino-4'-methylchalcone has been shown to react with many different functional groups and is useful as a scaffold for the synthesis of complex molecules. It has been shown to have high quality, making it an excellent choice for use in reactions.

<p>The compound (2R,3S)-3-(tert-Butoxycarbonyl)amino-1,2-epoxy-4-phenylbutane is an epoxide with a thionyl chloride mediated reaction. This compound has been shown to react with amines and nucleophiles to form epoxides. The time required for this reaction was found to be dependent on the concentration of the amine. The reaction was also found to be chiral as it produced a mixture of diastereomers. When irradiated, this compound undergoes a stereoselective reaction that leads to a new epoxide product.</p>

<p>2-Amino-8-hydroxyquinoline is a molecule that has been shown to have optical properties. 2-Amino-8-hydroxyquinoline has also been shown to be reactive in vitro and inhibit the growth of cancer cells. It is thought that this inhibition may be due to its ability to bind to the active site of DNA polymerase, preventing DNA replication. 2-Amino-8-hydroxyquinoline has also been shown in vitro studies and vivo studies to have potent inhibition activity against human serum albumin (HSA). The molecules that are used as linkers to attach 2-amino 8 hydroxyquinoline to other molecules are thermodynamically stable. The isomers of 2 amino 8 hydroxyquinoline have also been studied by X-ray crystallography and nuclear magnetic resonance spectroscopy, which provides information about the structure of the molecule. Finally, 2 amino 8 hydroxyquinoline has been found to be an odorant</p>

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3-Amino-4-methoxybenzanilide is a white, crystalline solid that is soluble in organic solvents. It reacts with hydrochloric acid to form hydrogen chloride and 3-amino-4-methoxybenzoic acid. 3-Amino-4-methoxybenzanilide is used as an analytical reagent for determining the chloride content of various materials. The heat energy needed for the reaction to occur optimally is between 55 and 75 degrees Celsius. The optimal reaction system includes hydrochloric acid, an organic solvent, and diazonium salt activated by hydrogen chloride gas. The reaction time is 2 hours at room temperature and the analytical method used is titrimetric analysis using triticum aestivum as the particle.

<p>2-[(2,6-Dichlorophenyl)amino]-N,N-dimethylbenzeneacetamide is a reagent, complex compound and useful intermediate with a CAS number of 21789-06-0. It is a fine chemical that can be used as a building block in the synthesis of other compounds. It has been shown to be useful in the production of speciality chemicals and research chemicals. The versatility of this compound makes it an excellent scaffold for the synthesis of other compounds. This product is not intended for human or animal use.</p>

3-Amino-2,4,6-tribromotoluene is a reactive organic compound that is a highly flammable additive. It has been used as an oxidizing agent in the production of polymeric materials and as a catalyst in the vulcanization of rubber. 3-Amino-2,4,6-tribromotoluene can react with hydrogen peroxide to form bromophenols and hydrochloric acid. When heated or exposed to light, 3-amino-2,4,6-tribromotoluene can produce toxic fumes such as hydrogen bromide and phosphorus pentoxide. This substance has been shown to be toxic to animals and humans if ingested or inhaled.

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<p>2-Amino-4,8-naphthalenedisulfonic acid is a structural analog of the natural amino acid phenylalanine. It is an inhibitor of the enzyme tyrosinase, which participates in the oxidation of dopamine to DOPA and subsequent conversion to melanin. 2-Amino-4,8-naphthalenedisulfonic acid has been shown to inhibit the growth of probiotic bacteria and can be used as a food additive. The compound also inhibits the oxidation catalyst that is required for some analytical chemistry tests. 2-Amino-4,8-naphthalenedisulfonic acid has been shown to have toxicological properties in animal studies and this toxicity is exacerbated by its ability to bind with pyridine nucleotides found in cells. The toxicological effects are thought to be related to the inhibition of protein synthesis that leads to cell death.</p>

<p>3-(Methylamino)-5,6-dihydro-2H-1,4-thiazin-2-ylidene]hydroxylamine HCl is a fine chemical that can be used as a versatile building block. It has been shown to be a useful intermediate in the synthesis of various compounds and for the preparation of research chemicals. 3-(Methylamino)-5,6-dihydro-2H-1,4-thiazin-2-ylidene]hydroxylamine HCl is a complex compound and can be used as a reagent or reaction component. 3-(Methylamino)-5,6-dihydro-2H-1,4-thiazin-2-ylidene]hydroxylamine HCl is also an excellent quality chemical.</p>

<p>4-Amino-3,5-dinitrobenzoic acid (4ADBA) is a reactive chemical compound with acidic properties. It reacts with nucleophiles to form diazo compounds, which are used in analytical methods for the detection of amines and phenols. 4ADBA can be used to measure the concentration of aspirin in pharmaceutical formulations. The reaction is linear over a wide range of concentrations and has an optimal reaction time of 10 minutes at pH 2.0–2.5. The half-life values for 4ADBA are approximately 3 hours at pH 3 and 7 hours at pH 5.</p>

<p>3-Aminophenylboronic acid hydrochloride is a chemical compound that is used for analytical chemistry, bioconjugate chemistry, and clinical diagnostics. The compound binds to model proteins with high affinity and specificity. 3-Aminophenylboronic acid hydrochloride has been shown to have low binding constants with polyols, which make it ideal for use in cell culture. 3-Aminophenylboronic acid hydrochloride has a pK of 2.7 at pH 7.4, making it acidic at this pH. The compound also has a pK of 9.3 at pH 4.5, making it neutral at this pH. 3-Aminophenylboronic acid hydrochloride is an electrochemically active molecule and can be used as an electrode material in electrochemical impedance spectroscopy experiments.</p>

<p>Biotinyl-6-aminoquinoline is a synthetic chemical that has been shown to inhibit the growth of cancer cells in laboratory mice. It was synthesized to be a substrate for the enzyme quinolinate synthase, which is involved in the synthesis of nicotinic acid. Biotinyl-6-aminoquinoline is an analytical method that has been used in urinary samples from patients with bladder cancer as well as healthy individuals. The sequences of each individual were determined and analyzed using an algorithm that performs logistic regression, which can predict whether or not the patient has bladder cancer.</p>

<p>2-[Ethyl-[2-(3-hydroxy-2,6-dimethyl-anilino)-2-oxo-ethyl]amino]-N-(3-hydroxy-2,6-dimethylphenyl)acetamide is a reaction component that is used in the synthesis of complex compounds. It is a versatile building block and useful intermediate for the synthesis of fine chemicals. This chemical has been shown to be an effective reagent for the preparation of high quality research chemicals. CAS No. 2200280-96-0</p>

<p>6-Aminopyrimidin-4-ol is an intermediate in the synthesis of orotic acid. It is also a precursor to 6-chloropurine, which is used in the manufacture of orotic acid and 6-aminopurine. 6-Aminopyrimidin-4-ol can be prepared by benzannulation of phosphorus oxychloride with orotic acid or by hydrolysis of 6-chloropurine with thiourea. The latter method is preferred because it results in less waste.<br>6-Aminopyrimidin-4-ol is labile and must be stored under an inert gas at low temperature to prevent decomposition. It undergoes inactivating reactions with strong oxidizing agents, such as chlorine dioxide, peracetic acid, hydrogen peroxide, and potassium permanganate. <br>It also reacts with nucleophiles such as ammonia or amines to form stable taut</p>

Methyl 4-amino-3-bromobenzoate is a benzodiazepine derivative that is used as an anxiolytic, sedative, and muscle relaxant. It has also been shown to have anti-convulsant properties. Methyl 4-amino-3-bromobenzoate can be synthesized from the corresponding amino acid. The structure of this compound is similar to that of diazepam, but it does not bind to the benzodiazepine receptor. Methyl 4-amino-3-bromobenzoate has been shown to inhibit protein–protein interactions between cellular proteins by dimerizing them, which may be related to its ability to induce cancer cell death. Methyl 4-amino-3-bromobenzoate has been shown to inhibit protein–protein interactions between cellular proteins by dimerizing them, which may be related to its ability to induce cancer cell death.

The Michaelis-Menten kinetics of N-(Aminoethyl)-5-naphthylamine-1-sulfonic acid (NENSA) have been determined by studying the reaction of NENSA with a variety of acceptors. Basic fibroblasts were found to be a good substrate for this compound and it was shown that proteolytic activity is required for the hydrolysis of NENSA. The toxin is also reactive with the enzyme polymerase chain, which inhibits bacterial growth. In the presence of epidermal growth factor, NENSA has been shown to inhibit proliferation in fetal bovine retinal cells and human epidermal keratinocytes.

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Dihexadecyl dimethyl ammonium chloride is a cationic surfactant that has been used as a phase transfer agent for the isolation of picolinic acid from plant material. It has also been used as a reagent in analytical chemistry to measure the concentration of potassium dichromate. Dihexadecyl dimethyl ammonium chloride is soluble in water and it exhibits a phase transition temperature at about -2 °C. The compound's frequency shift can be observed with an nmr spectroscopy.

<p>DL-Phenylethanolamine is a hydroxy amine that is used in the synthesis of other chemicals. It is obtained by reacting phenylacetic acid with hydroxylamine. DL-Phenylethanolamine is an intermediate in the synthesis of the anti-inflammatory drug Indomethacin. This molecule contains a asymmetric carbon atom, which can be distinguished using infrared spectroscopy. The uptake of DL-phenylethanolamine into cells can be measured by detecting the release of amines from lysosomes and mitochondria. In addition, this molecule has conformational properties that can be detected by NMR spectroscopy, making it useful for detection sensitivity and identification purposes.</p>

2,5-Dichlorobenzoic acid is a chemical compound that is used as an intermediate in the production of herbicides and other agricultural chemicals. It is also used for the synthesis of pharmaceuticals and dyes. 2,5-Dichlorobenzoic acid has been shown to have significant physiological effects at high doses. The use of 2,5-dichlorobenzoic acid may cause death in humans through kidney failure, although it has not been shown to be toxic to humans at low doses. The mechanism by which this effect occurs is not known. 2,5-Dichlorobenzoic acid has been found to be moderately toxic in animal studies with acute oral LD50 values ranging from 1,000 mg/kg body weight (mg/kg BW) to 10,000 mg/kg BW depending on the animal species tested.

<p>2-Aminobenzhydrazide is a hydrogen bond donor that binds to the 5-HT2 receptor. It has been shown to be effective in treating infectious diseases such as malaria and dengue fever. 2-Aminobenzhydrazide inhibits the production of the inflammatory hormone prostaglandin E2 by inhibiting cyclooxygenase, which is responsible for converting arachidonic acid into prostaglandins. This drug also has anti-inflammatory properties because it blocks the action of amide and hydrazide receptors, which are associated with pain transmission. 2-Aminobenzhydrazide has been shown to inhibit the growth of bacteria and fungi in culture, with inhibition constants of 4.4 x 10 M for Escherichia coli and 8 x 10 M for Candida albicans.</p>

<p>3-(Methylamino)-3-oxopropanoic acid is a metabolite of nitroprusside. It is a potent inhibitor of the uptake of nitrates by cells, which causes cell lysis. 3-(Methylamino)-3-oxopropanoic acid has been shown to inhibit the uptake and transport chain of amino acids in the human metabolism. This results in an accumulation of metabolites that are toxic to cells and can lead to necrosis. 3-(Methylamino)-3-oxopropanoic acid is also a biocide with anti-inflammatory properties. It inhibits monoclonal antibody production by blocking protein synthesis and has been shown to be effective against tumor growth in animal models.</p>

<p>3-Aminophenylboronic acid hemisulphate is a cross-linking agent that has been shown to induce apoptosis in mammalian cells. It also has the ability to bind to glycan, a sugar molecule on the surface of cells. The binding of 3-aminophenylboronic acid hemisulphate induces morphogenetic protein (MP) secretion, which leads to cell death. This compound is used as an adjuvant in vaccines and also as a research reagent for studying protein sequences and antigen/antibody interactions.</p>

<p>3,4-Diaminofurazan is a chemical compound that is stable in an oral environment. It has an optimal reactivity with a pyrazole ring and methoxy groups. 3,4-Diaminofurazan is active against Staphylococcus aureus strains that are resistant to other antibiotics. The molecule has been shown to inhibit bacterial growth by inhibiting the synthesis of DNA and RNA. The kinetic of 3,4-diaminofurazan was studied using nitro as the substrate, and it had an activation energy of 11.8 kcal/mol at 298 K. The chemical structure of 3,4-diaminofurazan has been determined by x-ray crystallography and nuclear magnetic resonance spectroscopy (NMR). It can be synthesized using nitric acid or hydrochloric acid as solvents: 1) Nitric Acid Synthesis: 2) Hydrochlor</p>

<p>Please enquire for more information about [1-(Morpholin-4-ylcarbonyl)propyl]amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

1,1,2,2,3,3,4,4a,5-Octadecafluoronaphthalene is a fluorinated derivative of an organic compound that is used as an intestinal antiseptic and as a cardioplegic solution. Sodium salts of this drug are used to treat intestinal disorders such as colitis and Crohn's disease. It is also used to treat cardiac diseases such as myocardial infarction by reducing the size of the infarcted area. The drug has been shown to be effective in preventing muscle degeneration in patients with AIDS. 1,1,2,2,3,3-Heptafluoropropan-1-amine is a chemical that belongs to the group of adjuvant therapies. It is used as a pharmaceutical preparation for kinetic studies and particle characterization.

Bis(2-pyridylmethyl)amine is an anti-cancer compound that has been shown to have a number of biological properties. It has been observed to inhibit the growth of cancer cells in culture, as well as inducing apoptosis in human serum. Bis(2-pyridylmethyl)amine also exhibits redox potentials that are consistent with a group p2 element. The compound has been studied for its ability to act as a fluorescence probe, which can be used in synchronous fluorescence and structural analysis. The crystal structure of bis(2-pyridylmethyl)amine has been determined using X-ray crystallography, and it was found that this compound binds to hydrogen bonding interactions and transfer reactions.

<p>Ethyl 3-amino-4-(cyclohexylamino)benzoate is a potent inhibitor of cellular death. It induces ferroptosis, a caspase-independent cell death mechanism, in cells that are normally resistant to apoptosis. Ethyl 3-amino-4-(cyclohexylamino)benzoate has been shown to induce the release of iron from ferritin and inhibit iron uptake by macrophages. This drug has also been shown to protect against oxidative injury and radiation, as well as neuronal death. Ethyl 3-amino-4-(cyclohexylamino)benzoate may be beneficial for treating bowel disease by reducing inflammation and protecting against damage from radiation therapy.</p>

<p>Ethyl 4-aminophenylacetate is a synthetic compound that has been shown to have anticancer activity in vitro. It has been shown to inhibit the activation of mouse splenocytes by carbonyl group-containing compounds, which are induced by lipopolysaccharide (LPS). Ethyl 4-aminophenylacetate also inhibits the binding of primary amines to opioid receptors in vitro. This compound has not been tested in vivo for its anticancer activity.</p>

(S,S)-N-(p-Toluenesulfonyl)-1,2-diphenylethanediamine(chloro)(p-cymene)ruthenium(II) is an organic compound that belongs to the class of solvents. It is a reagent that is used in acidic conditions. The elimination of hydrocarbons from (S,S)-N-(p-toluenesulfonyl)-1,2-diphenylethanediamine(chloro)(p-cymene)ruthenium(II) is carried out by chloroform or hexane and potassium hydroxide. This compound can be purified by recrystallization from aqueous ethanol or preparative thin layer chromatography with chloroform as eluent. Recycling of this compound is possible.

<p>p-Xylylenediamine is a chemical compound that has hydrogen bonding interactions with its environment and is a substrate for film deposition. It also has the ability to form hydrogen bonds with other molecules such as DNA duplexes and sodium salts. p-Xylylenediamine is soluble in water and can be used to coat the surface of objects, which can result in reduced transport properties. This molecule has been found to be present in urine samples and may be used as a biomarker for prostate cancer diagnosis.</p>

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<p>5-Aminovaleric acid is a cyclic peptide that is an antagonist of the enzyme 5-aminovaleric acid hydrolase that catalyzes the conversion of 5-aminovaleric acid to succinic semialdehyde. The physiological function of 5-aminovaleric acid hydrolase is not known, but it has been implicated in a number of neurological disorders, such as Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis. The reaction solution contains 5-aminovaleric acid (5AVA), hydrogen fluoride (HF), and l-lysine (Lys). Upon addition of HF to the solution, it reacts with Lys to form a dinucleotide phosphate intermediate. This intermediate then reacts with 5AVA to form an intramolecular hydrogen bond with the amino group of Lys and release hydrogen gas. The detection sensitivity for this reaction can be increased by using a cyclic peptide inhibitor.</p>

<p>Chemically a chlorinated salicylanilide, niclosamide is clinically used as an anthelmintic agent. The action of niclosamide has been proven to proceed by inhibiting the STAT3 signaling pathway. Recently, niclosamide, has been considered as an antiproliferative agent in cancer treatment, e.g. melanoma and colorectal cancer. In 2021, niclosamide has been tested for the treatment of COVID-19 patients.</p>

<p>2-Amino-4-chloropyrimidine is an amido compound that is used to treat infectious diseases. It is a potent inhibitor of the enzyme topoisomerase II, which is involved in DNA replication and transcription. This drug has shown cytotoxic activity against du145 cells, an immortalized prostate cancer cell line. 2-Amino-4-chloropyrimidine has also been shown to be effective against MDA-MB-231 cells and thp1 cells, which are human breast cancer cell lines. 2-Amino-4-chloropyrimidine binds to the active site of topoisomerase II, preventing the enzyme from binding with the two ends of DNA and causing DNA breakage. The drug has also been shown to inhibit the growth of cervical cancer cells by binding with amine groups on proteins found on these cells.</p>

<p>4-Amino-2,5-diethoxyphenyl)benzamide is a small molecule that inhibits the enzyme activity of polymerase chain reaction (PCR), DNA topoisomerase I, and DNA gyrase. It has been shown to inhibit the growth of human leukemia cells in culture. 4-Amino-2,5-diethoxyphenyl)benzamide also inhibits rat liver microsomes and can be used for the treatment of neurodegenerative diseases.</p>

<p>[1-(3-Methoxyphenyl)-1-methylethyl]amine hydrochloride is an organic compound that can be used as a reagent and a building block. It has been shown to be a useful intermediate in the synthesis of various other compounds, such as pharmaceuticals. This chemical is also used in research, as it is versatile and can react with other compounds easily. [1-(3-Methoxyphenyl)-1-methylethyl]amine hydrochloride can be purchased at our store if you are interested in purchasing this product.</p>

4-Amino-2-methylbenzoic acid ethyl ester is a versatile building block that can be used in the synthesis of complex compounds. It has been shown to have a number of useful applications, such as in the synthesis of pharmaceuticals, research chemicals, and speciality chemicals. 4-Amino-2-methylbenzoic acid ethyl ester is also an important reagent for the production of high quality pharmaceuticals and intermediates. This chemical is also a useful scaffold for organic reactions.

<p>2-Amino-3-nitrobenzoic acid (2ABN) is a peroxide that is used as an antiviral. 2ABN has been shown to inhibit the formation of reactive oxygen species in cancer cells, leading to apoptosis. It also inhibits the growth of carcinoma cell lines and tissues. 2ABN reacts with chloral hydrate to form a particle that can be encapsulated for delivery and release in vivo. This drug has been expressed in Escherichia coli, which may lead to improved stability and ease of production. 2ABN is thought to have anti-inflammatory properties due to its ability to inhibit the production of prostaglandins. The reactivity of 2ABN with surfactants such as sodium laureth sulfate (SLES) has been shown, which leads to it being used as an emulsifying agent for topical application.</p>

<p>Useful chiral building block</p>

<p>2-Hydroxy imipramine is a metabolite of imipramine, which is an antidepressant drug that belongs to the tricyclic antidepressant class. It is formed through enzyme hydrolysis by liver microsomes and monoclonal antibodies. 2-Hydroxy imipramine has been shown to have an affinity for the norepinephrine transporter in rat heart cells and human liver cells. The metabolism of 2-hydroxy imipramine can be inhibited by drugs such as chlorpromazine and fluoxetine, which induce hepatic enzymes responsible for the metabolic transformation of this drug. 2-Hydroxy imipramine may also have anti-inflammatory effects on cardiac tissue due to its ability to inhibit the activity of cytochrome P450, which are enzymes that metabolize many drugs in humans.</p>

<p>Please enquire for more information about 3-(2-((3-Bromophenyl)amino)ethyl)oxazolidin-2-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-N-[2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide hydrochloride is a magnetic compound that has been shown to be an effective cancer antigen. It is a derivative of the amino acid sequence of α,β-unsaturated fatty acids and can be used as a dietary supplement. 2-Amino-N-[2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide hydrochloride has been shown to bind to fatty acid receptors on the surface of antigen presenting cells (APCs). It also activates the immune system by activating APCs, which leads to the production of cytokines and chemokines. This compound has also been shown to stimulate T cells in culture, leading to activation and proliferation of tumor cells.</p>

<p>4-Aminobenzhydrazide is a reactive chemical that can be used to study the kinetics of reactions. It is used in vitro as an antimicrobial agent against human eosinophils, HL-60 cells, and K562 cells. 4-Aminobenzhydrazide has been shown to inhibit the production of eosinophil peroxidase by inhibiting mmp-9 activity. This drug also inhibits the growth of bacteria such as Staphylococcus aureus and Escherichia coli in vitro. 4-Aminobenzhydrazide is chemically stable and does not decompose at high temperatures or react with sodium ferulate (a common oxidant).</p>

<p>1-Phenylcyclohexanamine hydrochloride is a secondary amine that binds to the nicotinic acetylcholine receptor. It has been shown to inhibit the activity of rat liver microsomes and dopamine, with a primary amino group. The analogs of 1-phenylcyclohexanamine hydrochloride are active and have been shown to inhibit acetylcholinesterase in rat brain tissue. This inhibition leads to an increase in the neurotransmitter acetylcholine, which causes an excitatory effect on the central nervous system. 1-Phenylcyclohexanamine hydrochloride is also used as a molecular model for studying glutamate receptors because of its similar structure.</p>

<p>Chloroquine metabolite</p>

<p>2-(4-Aminophenoxy)acetic acid hydrate is a synthetic, chlorine atom, primary amino compound that has been used as a lysine analogue in the production of lysine-deficient media. It also has been shown to be an inhibitor of the uptake of L-lysine by rat liver cells. 2-(4-Aminophenoxy)acetic acid hydrate can also be used to synthesize conjugates with other compounds such as fluorescein and luciferin. This compound is acidic and can form hydrogen bonds with other molecules. 2-(4-Aminophenoxy)acetic acid hydrate has shown novartis in fluorescence techniques, which may be due to its ability to emit light when excited at specific wavelengths.</p>

<p>Please enquire for more information about 3-((4-(dimethylamino)phenyl)amino)-5,5-dimethylcyclohex-2-en-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Methyl 4-aminobutyrate HCl is an ester hydrochloride that is used as a chiral auxiliary in the synthesis of aminobutyric acid. It has been shown to have cognitive enhancing effects and to increase brain levels of l-glutamic acid. Methyl 4-aminobutyrate HCl also inhibits the uptake of chloride ions into synaptic vesicles, which may be due to its ability to bind with plasma proteins. This drug has been shown to have pharmacological effects on rats when administered at a dose of 1mg/kg.

<p>5-Amino-2-fluorobenzoic acid (5AFBA) is a synthetic aniline that is used as a fluoroquinolone antibiotic. 5AFBA inhibits the synthesis of trehalose, which is vital for bacterial growth. This drug also has been shown to be active against Mycobacterium tuberculosis and Mycobacterium avium complex. 5AFBA has also been shown to have antifungal properties, inhibiting the synthesis of ergosterol in the fungal cell membrane. 5AFBA can be modified by alkylation with geranyl groups or N-methylation at the amino group. These modifications have been shown to increase its antibacterial activity against Pseudomonas aeruginosa.</p>

<p>5-Aminogramine is a fine chemical that is used as a versatile building block for the synthesis of complex compounds. 5-Aminoguanidine is an aminoguanidine compound that has been reported to be useful in the synthesis of reagents and speciality chemicals, such as heterocycles, polymers, and pharmaceuticals. 5-Aminoguanidine has been used as a reactant in the preparation of high quality products with various applications. It is also known to be a useful intermediate for reactions involving nucleophiles or electrophiles. Furthermore, it can be used as a scaffold for the synthesis of other compounds.</p>

<p>Please enquire for more information about 2-amino-1-(1-aza-2-(4-(dimethylamino)phenyl)vinyl)ethene-1,2-dicarbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Please enquire for more information about N-[(1-Methyl-1H-indol-3-yl)methyl]cyclohexanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>5-Carboxymethoxytryptamine hydrochloride (5CMT) is a chemical compound that belongs to the group of useful building blocks. It is a versatile intermediate that can be used in the synthesis of many important compounds. 5CMT reacts with amines and alcohols to form amides and esters. It also reacts with carboxylic acids to form acid halides and anhydrides. 5CMT has been shown to be a useful scaffold in organic synthesis, as it can be converted into various derivatives. 5CMT is soluble in water, methanol, ethanol, acetone, and dichloromethane.</p>

<p>Solriamfetol is a drug that belongs to the class of psychostimulants. It is used as an adjunct in the treatment of major depressive disorder, and has been shown to be clinically relevant in patients with major depression. Solriamfetol has been shown to have long-term efficacy and stable doses, which may be due to its chemical stability. It also has dose-dependent effects on dopamine release in the striatum, which can lead to increased symptoms of depression. The drug has also been shown to increase cardiac rate, even at stable doses and does not affect renal function. This may be because solriamfetol does not undergo oxidative injury or cause decreased glomerular filtration rate (GFR).</p>

<p>N-(1-Naphthyl)ethylenediamine 2HCl is a diazonium salt that is used as an analytical reagent for the determination of nitrite ion in biological samples. It can be prepared by reacting 1-naphthylamine with ethylenediamine and hydrochloric acid. The optimum concentration of N-(1-naphthyl)ethylenediamine 2HCl is between 0.5 and 1.0 M, which should be determined before use. Sulphuric acid or sodium hydroxide can be added to adjust the pH of the solution to around 2.5, although this may change the color of the solution from orange to yellow. The reaction product is then extracted into chloroform and dried over anhydrous sodium sulphate or magnesium sulfate, followed by filtration and evaporation under reduced pressure at 40°C until dryness. The final product is stored in a dark place away from</p>

<p>2-Amino-4-bromocinnamic acid is a fine chemical with a CAS number of 914636-63-8. It is used in the synthesis of complex compounds and useful building blocks, as well as in research. This compound has been shown to be an intermediate for the preparation of derivatives with potential pharmaceutical applications, such as antihistamines, antipsychotics, and antibiotics. 2-Amino-4-bromocinnamic acid is also an important reagent for organic syntheses.</p>

<p>5-Aminoimidazole-4-carboxamide HCl (5-AICA) is a compound that is used for the treatment of bowel disease. It inhibits the synthesis of 5'-nucleotidase and phosphoribosyl transferase, which are enzymes responsible for the conversion of nucleotide monophosphates to nucleotide diphosphates. This inhibition leads to a decrease in the amount of adenosine triphosphate (ATP) produced by cells, which may be due to its ability to inhibit ATP synthase activity. 5-AICA also has been shown to bind to DNA and inhibit transcriptional activities. The binding of 5-AICA may be due to its ability to form hydrogen bonds with guanine residues in DNA or its capability to form covalent bonds with thymidine residues in DNA. 5-AICA also has been shown to have cytotoxic effects on HL60 cells, as well as other</p>

N,N-Dimethylaminoethyl chloride HCl is a reactive compound that inhibits the amine binding site on chitosan. It is used for the preparation of chitosan quaternary ammonium salts and esters. N,N-Dimethylaminoethyl chloride HCl has an inhibitory effect on both chitosan and suzuki coupling reactions. This compound also has a safety profile similar to other halides such as chlorine and hydrogen chloride.

<p>6-Chlorotryptamine is an indole alkaloid that is found in plants such as "Inula helenium". It has vasoconstrictive properties, which is due to its ability to inhibit the enzyme tryptophan decarboxylase. This inhibition leads to a decrease in serotonin levels, which causes blood vessels to narrow and slows blood flow. 6-Chlorotryptamine also inhibits protein synthesis by preventing the cross-coupling of amino acids. The compound can be found in a number of natural sources, including aerocolonigenes and plant species such as "Inula helenium" and "Lysimachia nummularia".</p>

<p>Produces fluorescent benzimidazole derivatives; detects aromatic aldehydes</p>

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6-Aminonicotinamide is an experimental drug that has shown promising results in animal studies. This compound may be useful for the treatment of cancer, due to its ability to inhibit reactive oxygen species and maintain mitochondrial membrane potential. 6-Aminonicotinamide also has a protective effect against radiation-induced cell damage, as it prevents oxidative injury to DNA and protein. In addition, 6-aminonicotinamide can stimulate the proliferation of pluripotent cells, which are cells that have the ability to differentiate into any type of cell in the body. Finally, this compound was shown to have antitumor effects by inhibiting squamous carcinoma tumor growth in experimental models.

<p>Dantrolene sodium is a muscle relaxant that belongs to the group of pharmacological agents. It is used to treat muscle spasms and hyperactivity in patients with neuromuscular disorders. Dantrolene sodium inhibits calcium release by blocking the activity of the enzyme ryanodine receptor in skeletal muscle cells. This inhibition prevents uncontrolled contraction of muscles and reduces their energy consumption. The drug also has an effect on malignant hyperthermia, which is caused by an increase in the production of adenosine triphosphate (ATP) due to increased cellular metabolism. Dantrolene sodium can inhibit ATP synthesis, thus reducing energy production and stabilizing cell membranes, thereby preventing cell death in neurons and other tissues.</p>