Amines

<p>Applications 2,6-Diaminopimelic Acid is useful in biological studies involving amino acids and amino sugars as molecular indicators of the origins of organic matter in buried tephra soils.<br>References Hobara, S., et al.: Geoderma, 373, 114449 (2020)<br></p>

<p>Applications Tryptamine hydrochloride (cas# 343-94-2) is a useful research chemical.<br></p>

<p>Applications N-Alkyl(C12-16)-N-benzyl-N,N-dimethylammonium chloride, tech. (cas# 68424-85-1) is a useful research chemical.<br></p>

<p>Applications N,N-Dimethylbenzhydrylamine is a useful research chemical for organic synthesis and other chemical processes.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Protiva, M., et al.: Chemicke Listy pro Vedu a Prumysl, 47, 1621 (1953), Blicke, F. F., et al.: J. Am. Chem. Soc., 76, 3161 (1954), Estiu, G. L., et al.: Farmaco, 45, 889 (1990)<br></p>

<p>Applications N-Lauryldiethanolamine (cas# 1541-67-9) is a useful research chemical.<br></p>

<p>Stability Hygroscopic<br>Applications N-​(3-​Aminopropyl)​-​n-​dodecylpropane-​1,​3-​diamine is a reactant used in the synthesis of gluconamide derivatives as cationic surfactants with antimicrobial properties.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Prieto-Blanco, M. et al.: J. Chrom., 1431, 176 (2016); Zhi, L. et al.: J. Surf. Deter., 19, 337 (2016);<br></p>

<p>Applications 2-(2-Aminoethoxy)anisole is used as an additive to vinylphosphonic acid esters and acrylonitrile forming compounds displaying hypotensive activity. An impurity from the process of Carvedilol (C184625)<br>References Reznik, V. et al.: Russ. Chem. Bull., 48, 979, (1999); Hirohashi, M., et al.: Arzneim.-Forsch., 40, 735 (1990), Packer, M., et al.: N. Engl. J. Med., 334, 1349 (1996),<br></p>

<p>Applications Phenyl(9H-purin-6-yl)amine (cas# 1210-66-8) is a compound useful in organic synthesis.<br></p>

<p>Applications 3,4-Diaminoanisole (cas# 102-51-2) is a compound useful in organic synthesis.<br></p>

<p>Applications 6-(6-(6-Aminohexanamido)hexanamido)hexanoic Acid is used in the making of a preconjugate which serves as immunoreactive conjugate useful as a developer antigen in a competitive inhibition immunoassay for the polymorphic analyte. Also used in the efficient synthesis of a heterobifunctional coupling agent.<br>References Oh, C. S., et al.: PCT Int. Appl. (1994), WO 9416330 A1 19940721; Reddy, R. E., et al.: Bioconjug. Chem., 16, 1323 (2005)<br></p>

<p>Stability Hygroscopic<br>Applications 6-Amino-2-hydroxymethyl Hexan-1-ol (cas# 125162-81-4) is a compound useful in organic synthesis.<br>References Rubina, A., et al.: Anal. Biochem., 325, 92 (2004),<br></p>

<p>Applications Dibenzylamine, a chemical contaminant in L-(+)-β-hydroxybutyrate, exhibits direct anticonvulsant actions in vivo.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Rho, J.M., et al.: Epilepsia, 43, 358 (2002)<br></p>

<p>Applications 4-(3-Aminophenyl)-3-morpholinone is an intermediate during the preparation of imidazothiazoles as protein kinase inhibitors for treating cancers.<br>References Bamaung, N., et al.: PCT Int. Appl. (2009), WO 2009070516 A1 20090604.<br></p>

<p>Applications Ethylamine Solution is used as a reagent in the synthesis of a series of hexadentate ligands as potential antibacterial agents. Also used as a reagent in the synthesis of tetrahydrothiazolopyridine derivatives as potent smoothened antagonists.<br>References Zhang, M., et al.: Chem. Biol. Drug Des., 84, 659 (2014); Ma, H., et al.: Eur. J. Med. Chem., 89, 721 (2015)<br></p>

<p>Applications Dimethyldimyristylammonium bromide is a cationic surfactant used in the study of lipid raft domains in membranes.<br>References Uyama, M.; et al.: J. Oleo Sci., 67, 67 (2018).<br></p>

<p>Impurity Niltazoxanide USP Related Compound A 2-Amino-5-nitrothiazole<br>Applications Niltazoxanide USP Related Compound A 2-Amino-5-nitrothiazole.<br>References Kariduraganavar, M. et al.; J. Mol. Struct. 987, 158 (2011). Tambe, S. J. et al.; Appl Polymer Sci. 114, 2291 (2009)<br></p>

<p>2-[3-[N-(4-tert-Butylbenzyl)-N-(pyridin-3-ylsulfonyl)aminomethyl]phenoxy]acetic acid is a synthetic chemical compound, which is derived from organic synthesis processes involving aromatic compounds. It functions primarily through the modulation of specific biochemical pathways, likely involving interactions with enzymatic or receptor targets due to its structural characteristics. This compound is particularly noteworthy for its potential applications in biomedical research, where it may serve as a lead or active molecule in the development of new pharmaceutical agents. Its unique structure, featuring both aromatic and sulfonyl groups, allows for versatile interactions with biological targets, opening possibilities for its use in therapeutic development. Further research into its exact mechanisms and potential therapeutic uses could yield significant advancements in the treatment of various ailments.</p>

<p>Purmorphamine is a cell factor that belongs to the group of morphogens. It is structurally related to dopamine and has been shown to be effective in the treatment of Parkinson's disease. Purmorphamine is involved in the regulation of neuronal survival, differentiation, proliferation, and axon guidance. Purmorphamine binds to a receptor on neurons called the cholinergic receptor, which stimulates a G-protein linked signal transduction pathway. This leads to an increase in intracellular calcium levels and activation of protein kinase C. Purmorphamine also has anti-inflammatory effects and can inhibit leukemia inhibitory factor (LIF). It has been shown to be effective against LPS-induced inflammatory responses by inhibiting protein synthesis. Purmorphamine also inhibits cancer cells through its ability to stimulate growth factor-β1 (GF-β1) gene expression.</p>

<p>1,2-Phenylenediamine is an aromatic amine that can be used as a precursor for the synthesis of various heterocyclic compounds. It has been shown to have an acidic character, which is due to its coordination geometry with three of its nitrogen atoms in the form of pyramidal nitrogen atoms. 1,2-Phenylenediamine is also a ligand for toll-like receptor (TLR) 4 and TLR9. It has been shown to activate these receptors by binding and activating downstream signaling pathways such as NF-κB and MAPK. This compound also has the ability to induce apoptosis in HL60 cells through inhibition of protein synthesis and activation of caspases.</p>

<p>1-(Methylbenzyl)amine sulphate is a high quality chemical that is an intermediate to the production of many useful compounds. It can be used in research as a building block for new compounds, or as a versatile building block for reactions. 1-(Methylbenzyl)amine sulphate has many uses, including being a reagent for the synthesis of complex compounds with high purity and usefulness as a speciality chemical in fine chemicals and research chemicals. CAS No.: 1026-97-3</p>

<p>2-Amino-3,4-diethoxybenzoic acid is a high quality chemical with a CAS No. 61948-72-9. It is an organic compound that belongs to the class of aromatic carboxylic acids and has a molecular weight of 174.2 g/mol. 2DHB is a useful intermediate in the synthesis of fine chemicals, research chemicals, and speciality chemicals like pharmaceuticals, pesticides, and dyes. It can also be used as a building block in the synthesis of many other compounds. The versatility of 2DHB makes it an important component in reactions involving nucleophilic substitution or addition reactions.</p>

<p>2-[[(Heptadecafluorooctyl)Sulphonyl]Methylamino]Ethyl Methacrylate is a substance that belongs to the group of substances. It is a chemical substance with a molecular formula of CH2=C(COOCH2CF3SO2)-N(CH3)2. 2-[[(Heptadecafluorooctyl)Sulphonyl]Methylamino]Ethyl Methacrylate is used as an additive in paints, adhesives and sealants to improve their resistance to water, oil and acid. This substance also has a sulfonate group, which makes it soluble in organic solvents.</p>

<p>2-Iodobenzylamine HCl is an imine that is used in the synthesis of carboxamides. It can be produced by carbonylation of alkylamines with formaldehyde and hydrogen peroxide. In the presence of palladium, 2-iodobenzylamine HCl undergoes deprotection to give the desired carboxamide.<br>2-Iodobenzylamine HCl has been shown to react intramolecularly with amines to produce imines, which are useful intermediates in organic synthesis.</p>

<p>1,4-Diamino-2,3-dihydroanthraquinone is an impurity found in the manufacture of the drug dermatan sulfate. It can be used as a chromatographic method for the detection of skin tumor cells. This compound has been shown to have neurodevelopmental and environmental effects. The liquid chromatography methods for this compound are based on its fluorescence properties, but it can also be detected by optical absorbance or by nmr spectroscopy. 1,4-Diamino-2,3-dihydroanthraquinone has been shown to cause cytotoxicity and morphological changes in liver cells in vitro.</p>

<p>3-Nitro-5-(trifluoromethyl)benzene-1,2-diamine is a chemical compound that can be used as a reaction component or reagent in research. It is a useful scaffold and building block for complex compounds. 3-Nitro-5-(trifluoromethyl)benzene-1,2-diamine has CAS No. 2078-01-5 and is classified as a speciality chemical. This chemical is versatile because it has many uses in both organic chemistry and biology, including use as an intermediate or building block for more complex compounds.</p>

<p>3-Iodobenzylamine HCl is a weak anion that has a moderate affinity for the adenosine A3 receptor. 3-Iodobenzylamine HCl is used in the analysis of adenosine, d-xylose and other compounds. The binding of 3-iodobenzylamine to the A3 receptor causes an increase in cyclic AMP levels and an increase in intracellular Ca2+ levels, leading to cell signaling. 3-Iodobenzylamine HCl also acts as a competitive antagonist at the A3 receptor. This drug can also act as an agonist at the A3 receptor, with binding affinities for this site comparable to those of adenosine. This drug is able to inhibit cyanamide catalysis due to its ability to bind with fluorine atoms on the acceptor site of this enzyme.</p>

<p>a-[2-(Diisopropylamino)ethyl]-a-phenyl-2-pyridineacetamide is a hydrogen bond donor. It has been shown to have cytotoxicity in vitro, with parameters that can be used for accurate prediction of descriptors. These descriptors are informative and insightful, which can be used for regression analyses and linear regression methods. The pharmacokinetic properties of a-[2-(Diisopropylamino)ethyl]-a-phenyl-2-pyridineacetamide have been studied in humans and have shown linearity between dose and plasma concentration.</p>

<p>2-Amino-4-methyl benzoic acid (AMBA) is a methyltransferase inhibitor. It has been shown to inhibit the enzyme in the methyl group transfer process, which is important for the synthesis of anthranilic acid, an intermediate of choline. AMBA inhibits acetylcholine production by blocking the enzyme that converts choline to acetylcholine. In addition, this compound has been shown to be a potent anticancer agent and a chemical biology tool that can be used to study protein function.</p>

<p>Dimethyldistearylammonium chloride is a chemical compound that is used as an antimicrobial agent. It is a cationic quaternary ammonium salt that functions by forming a covalent bond with the sulfhydryl group of cysteine residues in proteins, which disrupts the disulfide bonds in the protein's tertiary or quaternary structure. Dimethyldistearylammonium chloride has been shown to have high antimicrobial activity against gram-positive bacteria and fungi but low activity against gram-negative bacteria. The optimum concentration for this compound is 0.2%. Dimethyldistearylammonium chloride has been used as a model system to study the effect of molecular weight on transfer reactions and polymer compositions, and it has also been used to study the biological properties of human immunoglobulin G (IgG).</p>

<p>6-Amino-4-hydroxy-2-mercaptopyrimidine monohydrate (6AP) is a chemical compound that has been shown to have potent antibacterial activity against Gram-positive bacteria. It is also effective at inhibiting the growth of S. aureus, both in vitro and in vivo. 6AP can be used as an alternative treatment for cancer, where it inhibits the growth of tumor cells by blocking ferrocene, which plays an important role in cancer cell proliferation and survival. The efficacy of 6AP against bacterial infections has been demonstrated in vitro with a variety of Gram-positive pathogens, including S. aureus, Streptococcus pneumoniae, Enterococcus faecalis, and Bacillus anthracis.</p>

<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>Columbamine chloride is an alkaloid compound, which is a synthetic derivative known for its relevance in biochemical and pharmacological research. This compound is derived from plant sources, primarily found in specific species within the Berberidaceae family. It functions by interacting with cellular pathways, influencing various cellular processes through its effects on signaling pathways and enzyme activity.</p>

<p>3-(Methylamino)propiophenone hydrochloride is a synthetic compound that can be used as an alternative to fluoxetine in microwave irradiation. It has similar effects to the drug, including advances in neurodegenerative diseases. 3-(Methylamino)propiophenone hydrochloride has been shown to improve the effects of radiation therapy on cancer cells, by inhibiting the production of reactive oxygen species and improving cell survival.</p>

<p>7-Amino-4-methyl-3-coumarinacetic acid N-succinimidyl ester is a synthetic amino acid with a reactive carboxylic acid group. It is used as a crosslinker in biochemistry and has been shown to have biological properties in plants. 7-Amino-4-methyl-3-coumarinacetic acid N-succinimidyl ester reacts with the acidic groups of proteins, DNA, or RNA, and is an important component of some second order rate constants. This chemical is also used for the neutralization of histological stains such as haematoxylin.</p>

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

<p>p-Aminophenyldichloroarsine hydrochloride (APD) is a reversible alkylating agent that binds to sulphydryls and reversibly inhibits the activity of nicotinic acetylcholine receptors. It is also an arsenical that has been shown to react with other proteins, such as acetylcholine receptor subunits. When it reacts with the acetylcholine receptor, it forms stable complexes and irreversible bonds. This prevents the receptor from functioning normally and leads to paralysis of muscles. The APD also binds to the reactive sites on DNA and blocks rRNA synthesis, leading to cell death.<br>APD is active against many bacteria, including Mycobacterium tuberculosis, but not against Gram-positive bacteria such as staphylococci or streptococci. It is also active against some fungi and protozoa but not against viruses.</p>

<p>1-[2,(3)-Methylanilino]-4-(methylamino)anthraquinone is a diazo dye that emits light when irradiated with UV-A or UV-B radiation. It is used as a fluorescent stain in electron microscopy to detect and identify the presence of metals and metal oxides in films. The compound is also used in polyvinyl chloride (PVC) films to increase thermal expansion and viscosity. 1-[2,(3)-Methylanilino]-4-(methylamino)anthraquinone may be used as a substrate film for the production of polyurethane foam for furniture cushions and automotive components. The compound can be acylated with fatty acids such as p-hydroxybenzoic acid to give it desirable properties such as lower viscosity, better adhesion, or improved light emission. This reaction can be catalyzed by heat or radiation.</p>

<p>2,3-Dimethyl-1H-indol-7-amine is an organic compound that belongs to the group of ethyl acetoacetate esters. It is a colorless liquid with a sweet odor and can be used as a solvent and in the manufacture of other compounds such as dibenzoylmethane. 2,3-Dimethyl-1H-indol-7-amine reacts with acetylacetone to form acetoacetic acid, which is then catalyzed by alcohol dehydrogenase to form oxaloacetate. This reaction also produces acetoacetate, which is oxidized by the enzyme dibenzoylmethane to form benzaldehyde.</p>

<p>Phentolamine is a cyclase inhibitor and a drug that is used to treat high blood pressure. It is also used in the diagnosis of primary pulmonary hypertension. Phentolamine blocks the conversion of l-phenylalanine to tyrosine, which prevents the production of catecholamines such as dopamine, epinephrine, and norepinephrine. This drug has been shown to improve brain functions when administered to rats with Parkinson's disease. Phentolamine is prepared by reacting phenylmethylsulfonyl fluoride with phentolamine mesylate. The reaction produces phentolamine mesylate sodium salt.</p>

<p>N-Nitrosodiisopropylamine is an alkylating agent that binds to DNA and inhibits the synthesis of proteins, leading to cell death. It has been shown to be carcinogenic in animal studies, where it caused bladder cancer in Sprague-Dawley rats. N-Nitrosodiisopropylamine is also a reactive chemical compound that reacts with other chemicals in the body. It is often found as a contaminant in urine samples of smokers who are exposed to nitrites and other nitrogen oxides and can be detected using gas chromatography mass spectrometry (GC-MS/MS) methods. The most common method for sample preparation is liquid–liquid extraction followed by hydrolysis with hydroxide solution.</p>

<p>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>

<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>

<p>N-(2-Aminoethyl)aminomethyl polystyrene resin, cross-linked with 1% DVB, 50-100mesh, loading 3.1-3.5mmol/g is a fine chemical that can be used to synthesize complex compounds. This resin is a versatile building block that can be used as a reagent or reaction component in chemical synthesis. It is also useful as a scaffold for drug discovery and as a building block for the synthesis of complex molecules. N-(2-Aminoethyl)aminomethyl polystyrene resin, cross-linked with 1% DVB, 50-100mesh, loading 3.1-3.5mmol/g is available in high quality and is supplied with CAS No., which makes it an ideal research chemical for use in laboratories.</p>

<p>5-Carbomethoxytryptamine hydrochloride is a chemical building block that can be used as a reaction component for organic synthesis. It is a versatile intermediate and can be used in the production of fine chemicals, such as pharmaceuticals, dyestuffs, and pesticides. 5-Carbomethoxytryptamine hydrochloride is also an important reagent in both organic synthesis and analytical chemistry. The compound belongs to the group of indole alkaloids, which are found in plants of the Apocynaceae family. CAS No.: 74884-81-4.</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>3-Aminopyrazole is a redox potential small molecule drug that has been shown to have tuberculostatic activity. It binds to the 5-HT2 receptor on the surface of tumor cells, which causes an increase in intracellular calcium levels and cell death. 3-Aminopyrazole also inhibits growth factor production, and this may be a part of its mechanism of action. 3-Aminopyrazole has been shown to be active against gram positive bacteria such as staphylococcus aureus and streptococcus pneumoniae. It also shows antimicrobial activity against gram negative bacteria such as pseudomonas aeruginosa, e.g., in vitro assays.</p>

<p>Ethyl 6-aminoveratrate (EAOV) is a urea derivative that has been shown to have analgesic effects in vitro and in vivo. EAOV was found to be more potent than morphine, but with less side effects. EAOV's antinociceptive effects are due to its ability to inhibit the activity of protein kinase C and phosphorylate the extracellular signal-regulated kinases ERK1/2. EAOV also showed metabolic stability and chemical stability, which may be due to its lack of reactive functional groups. The low potency of EAOV makes it an attractive candidate for research into the development of a new generation of painkillers.</p>

<p>2-Bromo-5-fluorobenzylamine hydrochloride is a high quality, reagent, complex compound that is useful as an intermediate for the synthesis of fine chemicals, speciality chemicals and research chemicals. This chemical can be used as a versatile building block in the synthesis of various compounds with different functional groups. 2-Bromo-5-fluorobenzylamine hydrochloride is also a useful scaffold for the synthesis of new organic compounds. It has been shown to react with other chemical compounds to produce a wide range of products that are useful in industry and research.</p>

<p>3-[(Aminocarbonyl)amino]-5-[4-(morpholin-4-ylmethyl)phenyl]thiophene-2-carboxamide is a chemical inhibitor that inhibits the activity of kinases. It has been shown to be cytotoxic against cancer cells and to induce apoptosis through a number of different mechanisms. 3-[(Aminocarbonyl)amino]-5-[4-(morpholin-4-ylmethyl)phenyl]thiophene-2-carboxamide binds to DNA and induces DNA repair, which can lead to cell death. This drug also has an anti-inflammatory effect, which may be due to its ability to inhibit pro-inflammatory cytokines such as TNFα and IL1β.</p>

<p>Rac octopamine hydrochloride is an alkyl alkyl amine. It is used as a diagnostic agent and has been shown to be a substrate for the enzyme dopamine β-hydroxylase in human blood serum. Rac octopamine hydrochloride is also metabolized by enzymes such as monoamine oxidase, which may lead to toxicological effects. The metabolic rate of rac octopamine hydrochloride has been shown to be increased in patients with cardiac disease or undergoing chemotherapeutic treatment.</p>

<p>Diethylstilbestrol (DES) is a synthetic, nonsteroidal estrogen that is used to treat breast cancer and other estrogen-dependent conditions. DES binds to the estrogen receptor and acts as an agonist. It has minimal liver toxicity and is not metabolized by the body because it is rapidly excreted in urine. DES can be synthesized from benzyl chloride and diethylstolbesterol. This process requires two steps: first, benzyl chloride reacts with diethylstilbesterol to form a triazene intermediate; second, treatment of the triazene intermediate with hydrogen chloride yields DES.</p>

<p>2-Amino-5-chlorobenzoic acid is a drug that inhibits the enzyme dopamine beta-hydroxylase. It has been used to treat Parkinson's disease, as well as schizophrenia and depression. This drug binds to the enzyme by forming a coordination complex with the 5th position of the substrate, which prevents it from binding to other substrates. 2-Amino-5-chlorobenzoic acid also inhibits prostaglandin E2 synthesis by inhibiting cyclooxygenase activity in rats. The inhibitory properties of this drug are enhanced when it is dissolved in hydroxide solution or in solutions containing sodium hydroxide. The synthesis of 2-amino-5-chlorobenzoic acid involves reacting 3,4-dihydroxybenzeneacetic acid with hydrochloric acid and sodium hydroxide solution. This reaction produces a carboxylate anion that reacts with hydrogen chloride gas to form</p>

<p>2-(Butylamino)ethylamine is a cationic dye that is used in optical regulation. It has been shown to regulate optical properties of organic solvents, such as pH and viscosity, by altering the dipole moment of the solvent. The reaction solution contains 2-(butylamino)ethylamine and an organic solvent with a high boiling point (e.g., tetrahydrofuran). This reaction can be carried out in a magnetic field to increase yields. The reaction time can be shortened by using magnesium chloride as the catalyst instead of sulfuric acid.</p>

<p>Tetraethylammonium acetate tetrahydrate (TEAT) is a trifluoroacetic acid salt that is used as a cyclase inhibitor. TEAT inhibits the activity of cyclases, which are enzymes that catalyze the formation of cyclic AMP (cAMP). This inhibition prevents the activation of protein kinases and subsequent phosphorylation of cytosolic proteins. TEAT has been shown to inhibit human serum albumin binding, transport properties, and fluorescence detector response in vitro. It also binds to DNA as a hydrogen-bond acceptor and can be used in enzymatic assays for DNA polymerase chain reaction.</p>

<p>N-Nitroso-N-phenylhydroxylamine aluminium (NNPA) is a nitrated organic compound that belongs to the thioxanthone family. It is a colorless, oily liquid that has a strong odor of hydrochloric acid. NNPA is used in the production of polyester resins and coatings, as well as in the manufacture of methacrylate polymers. The reaction system for this compound consists of aluminum chloride and calcium carbonate. This substance can be prepared by reacting trimethylolpropane with methacrylates and magnesium in an organic solvent such as isopropyl alcohol or acetone. NNPA can also be synthesized by reacting zinc powder with ammonium bicarbonate, followed by carbamoylation with an organic amine such as isopropylcarbamate.</p>

<p>Capstone product B is a magnetic resonance spectroscopy agent that has been deacetylated. It can be broken down by photolysis, and is metabolized by hydrocarbon-degrading enzymes. Capstone product B contains a betaine group that is sensitive to light, and can be detected by resonance spectroscopy. The experiment was conducted on soil samples with the use of a surfactant to increase the solubility of the analyte in water.</p>

<p>Alpha-aminoisobutyric acid methyl ester hydrochloride (AABME) is an amino acid that is a metabolite of the neurotransmitter GABA. It has been shown to be transported across the blood-brain barrier by a carrier-mediated transport system and is taken up by neurons via a solute carrier family 38 member 2 transporter. AABME has been observed at physiological levels in maternal blood plasma, urine, cerebrospinal fluid, and brain tissue. It has also been studied in vitro using 3T3-L1 preadipocytes as a model for adipogenesis. In this context, it has been shown to increase cell proliferation and inhibit apoptosis.</p>

<p>1-Acetyl-1,2,3,4-tetrahydroquinolin-7-amine hydrochloride is a versatile building block that can be used in the synthesis of complex compounds with high quality and as a speciality chemical. This compound is useful as a reagent and reaction component in organic synthesis. It has been shown to be useful in the synthesis of new scaffolds for drug discovery.</p>

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

<p>4-Aminobenzaldehyde polymer is a crystalline solid that is soluble in organic solvents. It can be used as a reaction vessel for acylation reactions, such as the conversion of an acid chloride to the corresponding amide. 4-Aminobenzaldehyde polymer has been shown to react with diazonium salts to form the corresponding diazo compounds in high yields. The electron activity of the molecule was tested by measuring its oxidation potentials and reducing power. 4-Aminobenzaldehyde polymer is functionalized with both nucleophilic and electrophilic groups. This compound also has electrochemical properties, including optical properties and nmr spectra. The control experiments for this substance are sodium nitrate, which does not react with diazonium salts or react with 4-aminobenzaldehyde polymer at all.</p>

<p>3-Amino-4-carbomethoxybenzoic acid is a compound that has not yet been labeled with a function. It has been shown to be an intermediate in the synthesis of polymers, such as polyamides and polyesters. 3-Amino-4-carbomethoxybenzoic acid is involved in biological functions related to butyric acid, which is a metabolite of the amino acids phenylalanine and tyrosine, or from the degradation of proteins. It is also used as a precursor for amines and may be an intermediate in the synthesis of glycoconjugates. The compound was found to have anticancer properties when used in combination with other drugs, such as doxorubicin and etoposide. Furthermore, it was found to have anti-inflammatory activities by inhibiting prostaglandin synthesis.</p>

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<p>3-Amino-3-(4-bromophenyl)propanoic acid is a versatile building block that is used in the synthesis of many different compounds. It is a reagent, useful as a research chemical and as a speciality chemical. 3-Amino-3-(4-bromophenyl)propanoic acid has been used in the synthesis of a number of complex compounds, including pharmaceuticals and pesticides. This compound is a good choice for use in organic synthesis because it reacts readily with an array of functional groups, such as carboxylic acids and amines.</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>N-Benzylhydroxylamine HCl is a quinolizidine alkaloid with a hydroxamic acid group. It is used in the synthesis of various organic compounds and pharmaceuticals, such as hydroxamic acids, bisected tetrahydrofurans, and β-amino acids. N-Benzylhydroxylamine HCl is also a substrate for gelatinase. The reaction yield depends on the choice of solvent; methyl alcohol yields higher yields than does ethyl alcohol. The asymmetric synthesis of this compound is stereoselective and can be achieved through different methods, including bisection or tetrahydrofuran (THF) synthesis.</p>

<p>3-Aminopropyldiisopropylethoxysilane (APDS) is a monolayer chemical that is used to modify the surface properties of a variety of substrates. This chemical can be used for patterning, functionalization, and immobilization of biomolecules. APDS has been shown to have a protective effect on cells in culture by preventing oxidation and denaturation of proteins. APDS also has been used for detection methods such as electron microscopy and photoelectron spectroscopy.</p>

<p>3-Dansylaminophenylboronic acid is a boronic acid that forms reversible covalent bonds with dopamine. It can be used in the diagnosis of cancer, as it binds to histone lysine and magnetic particles. The fluorescence resonance of 3-Dansylaminophenylboronic acid can also be used in the diagnosis of cancer, as it produces a strong signal. This compound has been shown to have homogeneous assays for the detection of dopamine and lipoprotein lipase in urine samples. 3-Dansylaminophenylboronic acid has also been found to be effective against cancer cells in culture, although it is not active against polysialic-expressing cells.</p>

<p>Methyl 2-amino-4-bromobenzoate is an amide that has a potential use as a cross-coupling agent in organic synthesis. It is labile and must be handled with care; it can also be used as an additive to polymerize natural polymers. Methyl 2-amino-4-bromobenzoate has been shown to enhance the efficiency of chemical reactions, including those between carboxylic acid and amines, and has been used in the synthesis of peptides. This chemical has functional groups that are compatible with a wide range of sequences, allowing for its use as a toolkit in synthetic chemistry. Methyl 2-amino-4-bromobenzoate is an analog of methyl 4-(aminomethyl)benzoate (MAMB).</p>

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

<p>3-(Dimethylamino)phenol is a chemical that is used as an additive in cosmetics. It has been shown to inhibit the production of epidermal growth factor and to have a growth-inhibiting effect on cells. 3-(Dimethylamino)phenol is found in many different types of products, including sunscreens, hair dyes, shampoos, and skin lotions. It has also been used as a preservative in food products, although it can be toxic at high doses. 3- (Dimethylamino)phenol has been shown to inhibit the production of fatty acids by inhibiting the activity of the enzyme lipoxygenase.</p>

<p>2-Aminohept-6-ynoic acid is a useful building block and can be used as a reagent in organic synthesis. It is a versatile building block, and can be used as an intermediate or scaffold in the preparation of complex compounds. CAS No. 211054-03-4</p>

<p>3-Methoxybenzylamine is a fatty acid amide that is synthesized from benzylamine derivatives. The compound is a viscosity enhancer and antioxidant, and has been shown to inhibit the reaction of 3-hydroxybutyric acid with hydrochloric acid. 3-Methoxybenzylamine has also been used as a dietary supplement in tissue samples to reduce the effects of oxidation on the fatty acid chains. This compound has an asymmetric synthesis, which can be achieved by reacting an amine with an acyl chain.</p>

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<p>Cyclohexylamine is a basic organic compound with the molecular formula CH(NH). It can be synthesized by the reaction of anhydrous sodium with p-nitrophenyl phosphate. Cyclohexylamine has been shown to have synergistic effects when combined with metal hydroxides and metal carbonyls, which may be due to its ability to reduce their potential for oxidation. Cyclohexylamine has been used as a model compound in an electrochemical impedance spectroscopy study of the interaction between enzyme activity and metal ions. In addition, cyclohexylamine has been found to have carcinogenic properties in cell line studies.</p>

<p>Serotonin reuptake inhibitor; anorectic</p>

<p>N-[(2-Fluorophenyl)methyl]-4-iodo-2,5-dimethoxybenzeneethanamine (25I-NBOMe) is a synthetic drug that acts as a potent agonist of the serotonin receptor 5-HT2A. It has been used in bioassays to study the function of this receptor and has been shown to be able to inhibit human liver metabolism. 25I-NBOMe is also an analytical tool for the detection and identification of cannabinoid derivatives, which are often found in synthetic cannabinoids. This compound can be analyzed by liquid chromatography tandem mass spectrometry (LC/MS/MS) methods with modifications that allow for the detection of metabolites.</p>

<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.<br>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>

<p>3-Amino-4-fluoroacetanilide is a white crystalline solid that is soluble in polar organic solvents. It has been used as a reaction component for the synthesis of heterocyclic compounds and as a reagent in organic synthesis. 3-Amino-4-fluoroacetanilide is also useful scaffold for the synthesis of high quality research chemicals and specialty chemicals. This compound can be used as an intermediate to synthesize more complex compounds, such as amino acid derivatives, amides, esters, and thioesters. 3-Amino-4-fluoroacetanilide is also a versatile building block with a broad range of uses in pharmaceuticals, agrochemicals, dyes, pigments, explosives and other fine chemicals.</p>

<p>(PEO)4-bis-amine is a thermodynamic data set. It is an amine with four amino groups and two amide groups that form stable complexes with metal ions. These complexes are amphiphilic, which means they can dissolve in both water and organic solvents. They have been shown to form micelles and paracrine complexes in the cell. The (PEO)4-bis-amine has also been shown to have a protective effect on age-related macular degeneration (AMD), as well as growth factor activity. (PEO)4-bis-amine has been shown to inhibit the production of surfactant sodium dodecyl and basic fibroblast growth factor, which may be due to its ability to form triplexes at high concentrations.</p>

<p>2-Aminoethyl diphenylborinate (2-APB) is a pharmacological agent that has been shown to be an effective inhibitor of growth factor-β1. This compound also has minimal toxicity, and it is a natural product. 2-APB inhibits the activity of borate channels in cell membranes and blocks intracellular calcium channels, which prevents the influx of calcium into cells. This compound has been shown to act as an inhibitor molecule by blocking the channel or 2-aminoethoxydiphenyl borate, which is an intracellular inhibitor molecule.</p>

<p>Tetramethylammonium bisulfate hydrate is an inorganic acid that is used as a reagent for analytical chemistry. It can be found in urine samples and has been used to determine the concentration of metal hydroxides in these samples. Tetramethylammonium bisulfate hydrate has been shown to inhibit the growth of bacteria, including polycarboxylic acid-producing strains, at concentrations of 100 mM. This property may be due to its ability to chelate metal ions required for bacterial growth. The magnesium salt of tetramethylammonium bisulfate hydrate is also used as a pharmaceutical dosage form. A chromatographic method involving co2 flow has been developed for the analysis of tetramethylammonium bisulfate hydrate.</p>

<p>L-2,4-Diaminobutyric acid, dihydrochloride is a chemical compound that is a non-protein amino acid. It is used in the production of gamma-aminobutyric acid (GABA) and has been shown to be able to penetrate the blood-brain barrier. However, it also has many other health effects such as increasing fatty acids in the brain and decreasing GABA uptake. L-2,4-Diaminobutyric acid, dihydrochloride can be used for diagnostic purposes or animal health.</p>

<p>(S)-(-)-3-tert-Butylamino-1,2-propanediol is a hydrophobic liquid that has been used as a stationary phase in chromatography. It interacts with nonaromatic compounds and has been used for the validation of high performance liquid chromatography (HPLC) detection sensitivity. It is also used as a ligand for ternary complexes and as an anion in chromatographic science. This compound's interactions are studied using evaporative light scattering, which can be used to determine the molecular weight of the compound.</p>

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