Ammine

<p>Applications 3-Aminocyclohexanol_x000D_(cis/trans mixture) (cas# 6850-39-1) is a compound useful in organic synthesis.<br></p>

<p>Applications 1,3-Diamino-2-propanol is a reagent used in the quantitative fluorescent detection of pyrophosphate with quinolin-ligated dinuclear zinc complexes.<br>References Mikata, Y., et al.: Inorg. Chem., 52, 10223 (2013)<br></p>

<p>Impurity Vildagliptin Impurity<br>Applications 1-Amino-3-nitroadamantane has potential application in co-catalyst for transition metal reactions and maybe a useful intermediate for the synthesis of Vildagliptin (V305000), an antidiabetic drug that inhibits dipeptidyl peptidase 4 (DPP-4). Vildagliptin exhibits antioxidant properties and may be an apoptotic compound against pancreatic cancer cells.<br>References Amritha, C., et al.: JCDR 9, FC14 (2015); Ahren, B., et al.: J. Clin. Endocrinol. Metab., 89, 2078 (2004), Ahren, B., et al.: Diabetes Care, 27, 2874 (2004), Barlocco, D., et al.: Curr. Opin. Invest. Drugs, 5, 1094 (2004)<br></p>

<p>Applications 2-Amino-2-butenediamide (cas# 18486-76-5) is a compound useful in organic synthesis.<br></p>

<p>Applications 3-(N,N-Dimethylamino)phenylboronic Acid (cas# 178752-79-9) is a compound useful in organic synthesis.<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></p>

<p>Applications Used in the preparation of homobifunctional rhodamine for labeling proteins.<br>References Corrie, J. et al.; Bioconjugate Chem. 9, 160 (1998)<br></p>

<p>Applications A potent γ-ketoaldehyde scavenger that has been shown to protects cardiac sodium channel (NaV1.5) from oxidant-induced inactivation<br>References Zagol-Ikapitte, I. et al.: Pharmaceutics, 2, 18 (2010); Nakajima, T. et al.: J. Mol. Cell. Cardiol., 48, 352 (2010); Davies, S.S. et al.: Biochem., 45, 15756 (2006);<br></p>

<p>Applications 4-(Ethylmethylamino)butanal Diethyl Acetal is a useful research chemical.<br></p>

<p>Applications N-[3-(4-Aminophenyl)propyl]-N,N-dimethylamine<br></p>

<p>Stability Volatile<br>Applications N-Ethylbutylamine is used as a reagent in the synthesis of substituted pyrimidines as corticotropin releasing factor (CRF) receptor ligands.<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 Kuppast, B., et al.: Eur. J. Med. Chem., 78, 1 (2014)<br></p>

<p>Applications 2-(Methylamino)benzamide (cas# 7505-81-9) is a useful research chemical.<br></p>

<p>Applications 3-Amino-1,2-propandiol is used in the synthesis of Decarbazolyl Carvedilol (D212720), a metabolite of Carvedilol (C184625) found in humans, rats, dogs and mice.<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 Schaefer, W.H. et al.: Drug. Metab. Dispos., 26, 958 (1998); Neugebauer, G. &amp; Neubert, P.: Eur. J. Drug. Metabol. Ph., 16, 257 (1991); Neugebauer, G. et al.: J. Cardiovasc. Pharm., 10, S85 (1987)<br></p>

<p>Applications Tetrabutylammonium Azide (cas# 993-22-6) is a useful research chemical.<br></p>

<p>Applications Used in the preparation of pyrimidine derivatives.<br></p>

<p>Applications Ethyl (2Z)-2-[(Acetyloxy)imino]-2-amino-acetic Acid Ester is an intermediate used in the synthesis of N-(2-Hydroxyethyl)-5-methyl-1,2,4-oxadiazole-3-carboxamide (H942278), which is a photolysis product of Metronidazole (M338880), an antibiotic.<br>References Moore, Douglas E., et al.: Radiation Phy. and Chem., 36(4), 547-50 (1990)<br></p>

<p>Applications 3-[(3-aminophenyl)amino]benzonitrile (cas# 1147094-81-2) is a useful research chemical.<br></p>

<p>Applications Ethyl 5-amino-1-benzofuran-2-carboxylate is used as an synthetic intermediate in the preparation of indolebutylpiperazines, a class of dual 5-HT1A receptor agonists and serotonin reuptake inhibitors. Ethyl 5-amino-1-benzofuran-2-carboxylate was also used as a potential radiolabelled analog for melanoma imaging and targeted radiotherapy.<br>References Chezal, J.M., et al.: J. Medn. Chem., 51, 3133 (2008); Heinrich, T., et al.: J. Medn. Chem., 47, 4684 (2004);<br></p>

<p>Applications Methyl (2S)​-​2-​Aminobutanoate is a general chemical reagent used in the synthesis of methylsulphonamide based small molecule legumain inhibitors.<br>References Ness, K. et al.: Bioorg. Med. Chem. Lett., 26, 413 (2016);<br></p>

<p>Applications N,N'-Bis(salicylidene)ethylenediamine is a common chelating ligand that is used in coordination chemistry. In particular it was used to form a new zinc(salen) nano complex which possess strong photoluminescence properties. Also used to form iron complexes which may possess anticancer properties.<br>References Mohammadikish, M., et al.: J. Cryst. Growth., 431, 39 (2015); Wani, W., et al.: New J. Chem., 40, 1063 (2016);<br></p>

<p>Applications Ethyl 4-[[(methylphenylamino)methylene]amino]benzoate<br></p>

<p>Applications 6-AMINO-2,2-DIMETHYL-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE (cas# 105807-84-9) is a useful research chemical.<br></p>

<p>5-[3-Methoxy-4-(4-methoxy-benzyloxy)-benzyl]-pyrimidine-2,4-diamine is a monoclonal antibody that blocks the signal of CTLA-4, a receptor on T cells. It has been shown to be effective in inhibiting skin cancer and primary breast cancers. This drug also has immunomodulatory effects and can be used to treat autoimmune diseases. 5-[3-Methoxy-4-(4-methoxy-benzyloxy)-benzyl]-pyrimidine-2,4-diamine binds to ctla-4 with high affinity and specificity, preventing the interaction of ctla-4 with its ligands such as CD80 (B7.1) and CD86 (B7.2). This prevents the activation of T cells by antigen presenting cells and suppresses the immune response.</p>

<p>3-Amino-5-fluoropyridine is a chiral amino acid that can be synthesized from butyronitrile and fluorine in the presence of an organocatalyst. The synthesis can be carried out with either a biodegradable or non-biodegradable catalyst. 3-Amino-5-fluoropyridine can be used as a precursor to prepare medicines such as fluoroquinolones, which are antibiotics that inhibit bacterial growth by binding to DNA-dependent RNA polymerase and preventing transcription and replication. Fluoroquinolones are also potent anti-inflammatory agents and have been shown to reduce inflammation in animal models of asthma, arthritis, and colitis. 3-Amino-5-fluoropyridine can be synthesized from nitro compounds with aluminium mediated reactions. Nitro compounds are toxic substances that have been used in explosives or as herbicides.</p>

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

<p>4-Ethyl-2,5-dimethoxy-benzeneethanamineHydrochloride is a metabolic substrate of CYP2D6. It is also an inhibitor of CYP1A2 and CYP3A4. The class of 4-Ethyl-2,5-dimethoxy-benzeneethanamineHydrochloride is not yet known. 4-Ethyl-2,5-dimethoxy-benzeneethanamineHydrochloride has been shown to cause toxicity in animal studies. Toxicity may be due to its inhibition of cytochrome P450 enzymes, which are involved in metabolism and detoxification.</p>

<p>4-(Methylnitrosoamino)-1-(3-pyridinyl)-1-butanone (NNK) is a carcinogenic chemical that has been identified in tobacco smoke. It induces squamous cell carcinomas in the respiratory tract of rodents and induces lung cancer in the offspring of pregnant rats exposed to NNK. This compound binds to double-stranded DNA, with high affinity for the minor groove, and inhibits DNA synthesis by binding to enzymes such as polymerase chain. In addition, it has been shown to cause transformation of epithelial cells into mesenchymal cells in vitro. 4-(Methylnitrosoamino)-1-(3-pyridinyl)-1-butanone binds to α7 nicotinic acetylcholine receptors and increases the response element activity.</p>

Please enquire for more information about [(1-Benzyl-1H-pyrazol-4-yl)methyl]amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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

<p>Please enquire for more information about 2-(4-Methoxyphenyl)-2-(1-hydroxycyclohexyl)ethylamineHydrochloride 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 [3-(1-Isopropyl-1H-benzimidazol-2-yl)propyl]amine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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

<p>1-Aminopiperidine is a hydrochloric acid derivative that is used to treat tuberculosis. It inhibits the enzyme catalysis of phospholipase A2 (PLA2) and blocks the release of arachidonic acid from cell membranes. 1-Aminopiperidine has been shown to have tuberculostatic activity in vivo by inhibiting PLA2 and blocking the release of arachidonic acid. This agent also exhibits antitumor properties, which may be due to its ability to inhibit the production of prostaglandin E2 (PGE2), an inflammatory mediator that can stimulate tumor growth. 1-Aminopiperidine binds to cannabinoid receptors, but does not bind to opioid or benzodiazepine receptors. This drug also exhibits antagonist activity against rimonabant, a type of receptor blocker for cannabinoid receptors.</p>

3,3'-Diaminodiphenylmethane is a diamine that is used in organic synthesis as an electron-deficient ligand. It is used to prepare metal complexes and as a catalyst for the preparation of various organic compounds. 3,3'-Diaminodiphenylmethane has been used as an imprinting agent to generate fluorescent labels on proteins, nucleotides, and peptides. 3,3'-Diaminodiphenylmethane also emits fluorescence when irradiated with ultraviolet light. This compound can be used to identify amines in urine samples by reacting with them under acidic conditions.

2-Methyltryptamine is a tryptamine derivative that binds to the 5-HT2 receptors in the brain and blocks the action of serotonin. It has been proposed as a possible treatment for human immunodeficiency, but more research is needed to determine its efficacy. 2-Methyltryptamine acts as an agonist at 5-HT2 receptors and can be used in plate tests to detect histones deacetylase activity.

<p>3-Aminobiphenyl is a biphenyl compound that is used in the production of dyes and pesticides. It has been detected in human urine samples using an analytical method based on chemical ionization. 3-Aminobiphenyl can be detoxified by conjugation with glutathione, but the conjugation process can be inhibited by the presence of amines such as caffeine, which competitively bind to glutathione. 3-Aminobiphenyl may also cause cancer, but there is no evidence for this theory at present.</p>

<p>2-Amino-6-chloropyrazine (2ACP) is an inhibitor that binds to the active site on human protein kinase C (PKC). It has been shown to inhibit PKC by hydrogen bonding with the hydroxide ion, which blocks its catalytic activity. 2ACP has been studied for its potential use in treating cancer and for inhibiting amine oxidases, which are enzymes associated with inflammation and chronic obstructive pulmonary disease. The inhibition of these enzymes may help to reduce stenosis in the lungs or other organs. 2ACP also has been shown to have antimycobacterial activity against Mycobacterium tuberculosis, M. avium complex, and M. leprae by inhibiting DNA synthesis and RNA synthesis. 2ACP inhibits the kinase receptor on the cell membrane that phosphorylates a water molecule into a chlorine atom, which then reacts with hydrogen peroxide to form free radicals that can kill bacteria</p>

<p>Please enquire for more information about (1S,3S)-Methyl 3-aminocyclobutane carboxylate hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about N-[4-(Aminosulfonyl)-2,1,3-benzoxadiazol-7-yl]-2-aminoethyl methanethiosulfonate 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-(5-chloro-2-methyl-1H-indol-3-yl)ethanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

3-Aminopyridine-4-carboxaldehyde (3APCA) is an acridone that is a colorless, crystalline solid. It has a molecular formula of C8H6N2O2 and a molecular weight of 174.14 g/mol. 3APCA can be synthesized by heating 2-pyridinecarboxylic acid with chloroacetyl chloride in the presence of pyridine as a solvent. The compound can be detected by nmr spectra, which are efficient methods for characterization of this chemical. The spectrum shows peaks at δ 8.22 ppm (1H), 7.61 ppm (1H), 6.99 ppm (2H), 5.87 ppm (1H), 4.06 ppm (2H). 3APCA has been shown to react with alkyl bromides to form carboxylic acids, which are shown by the peaks at δ 8.22 ppm and

<p>(N,N-Dimethyl)methyleneammonium iodide is a potent antagonist for the histamine H2 receptor that has been shown to inhibit gastric acid secretion. It is an enantiopure compound that can be prepared by asymmetric synthesis using palladium complexes. The methylene group in this molecule is activated with hydroxylamine and acrylates, which are then reacted with ethyl diazoacetate and amines to produce (N,N-dimethyl)methyleneammonium iodide. (N,N-Dimethyl)methyleneammonium iodide is a potent antagonist at the histamine H2 receptor, where it can inhibit gastric acid secretion and reduce stomach ulcers. It also has been shown to have anti-inflammatory effects.</p>

<p>Alanine,n,N'-[[5-[2-amino-5-(2,2-dimethyl-1-oxopropyl)-4-thiazolyl]-2-furanyl]phosphinylidene]bis[2-methyl-,1,1'-diethylester] is a metabolic inhibitor that is used in the treatment of type 2 diabetes. It inhibits gluconeogenesis by inhibiting the enzyme phosphoenolpyruvate carboxykinase (PEPCK), which catalyzes the conversion of oxaloacetate to phosphoenolpyruvate. This compound has been shown to reduce fasting blood glucose levels in diabetic animals and humans.</p>

<p>Diisopropylammonium dichloroacetate (DADCA) is a chemical that inhibits the metabolism of glucose. It has been shown to have a hypoglycemic effect in rats and is being investigated as a treatment for metabolic disorders such as diabetes and obesity. DADCA has also been shown to reduce liver lesions in animals with chronic viral hepatitis, and has been found to be effective in reducing tumor growth in mice. This drug can also be used to treat bowel disease by reducing the amount of ammonia released by bacteria. DADCA may also have physiological effects on humans, including an increase in blood pressure and fever, although these effects have not yet been studied.</p>

Please enquire for more information about 2-Amino-3-(1.2-dihydro-2-oxoquinoline-4-yl)propanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>7-Amino-4-(trifluoromethyl)coumarin is a coumarin derivative that has been used as a fluorescence probe for the study of enzyme activities. It can be used as a potential biomarker for autoimmune diseases, and has also been shown to have tyrosine kinase domain binding activity. 7-Amino-4-(trifluoromethyl)coumarin can bind to the hydroxyl group in tyrosine residues with high affinity, and binds to the nitrogen atoms in protein kinases with low affinity. This compound is able to form intermolecular hydrogen bonds and steric interactions with peptide hormones.</p>

<p>4-Aminophenyl methylcarbinol is a chemical compound that is used as an additive in the production of polyurethane. It accelerates the reaction between isocyanate and polyol, which enhances the rate of polymerization. 4-Aminophenyl methylcarbinol has been shown to increase the yield by about 30% when it was added to a reaction mixture. The activation energies for this reaction were found to be 29.6 kJ/mol for the nitro group and 29.8 kJ/mol for the carbonyl group. This chemical compound also has functional groups that are capable of forming hydrogen bonds with other molecules, which may help to bind them together during polymerization reactions.</p>

<p>2-Amino-5,6-dichlorobenzothiazole is an aminobenzothiazole derivative that has been shown to have antibacterial activity. It is a hydrophobic molecule with a skeleton consisting of alternating amines and carboxylic acids. 2-Amino-5,6-dichlorobenzothiazole binds to the fatty acid ester component of bacterial cell walls by hydrogen bonding or ionic interactions, disrupting the integrity of the cell wall and inhibiting the growth of bacteria. 2-Amino-5,6-dichlorobenzothiazole can be used to decolorize dyes and textiles that have been stained by oily materials. It is also used as a surfactant in personal care products such as shampoos and conditioners.</p>

<p>2-Cyclohexyl-1-methylethyl)methylamine is a monoethyl ether of (2-cyclohexyl-1-methylethyl)amine. It is used as a nasal decongestant and has been shown to be effective against respiratory disorders such as bronchitis, sinusitis, and allergies. The drug can also be used for the diagnosis and prognosis of congestive heart failure. 2-Cyclohexyl-1-methylethyl)methylamine has been shown to bind to calcium ions in the nasal mucosa, thereby inhibiting the production of inflammatory mediators such as prostaglandins and leukotrienes. This drug also has an inhibitory effect on receptor activity for histamine, which leads to relief from allergic symptoms by reducing inflammation in the nose.</p>

<p>4-(2-Aminoethyl)benzene sulfonamide is a small-molecule drug that inhibits the activity of proteases, including serine and cysteine proteases. It has been shown to inhibit the growth of human renal cell cancer cells, as well as subcutaneous tumors in mice. 4-(2-Aminoethyl)benzene sulfonamide also inhibits the proliferation of Hl-60 cells and shows antitumor activity in a mouse model system. This drug is an inhibitor of prostaglandin endoperoxide synthase (PGHS), which is involved in tumorigenesis by causing inflammation and oxidative stress. 4-(2-Aminoethyl)benzene sulfonamide has been shown to be effective for treating colorectal adenocarcinoma, with no significant side effects on other organs.</p>

Bis(2,2,2-trifluoroethyl)amine is a colorless liquid that is soluble in water. It has a molecular weight of 122.11 and a boiling point of 217°C. Bis(2,2,2-trifluoroethyl)amine reacts with tetramethylammonium to form a dimer. The reaction is reversible and the bis(2,2,2-trifluoroethyl)amine can be regenerated by the addition of fluoride or an acid such as hydrochloric acid or sulfuric acid. Bis(2,2,2-trifluoroethyl)amine has an anion that can accept a proton from another molecule. This anion is also known as the bisulfite ion which reacts with hydrogen peroxide to form bisulfate and water.

<p>(R)-(-)-2-Aminoheptane is a lipase inhibitor that can be used as an immobilized or soluble protein. This compound has been shown to inhibit monoamine oxidase, which is an enzyme that breaks down neurotransmitters in the brain, and helps maintain their levels. (R)-(-)-2-Aminoheptane also inhibits electron ionization, and can be used to study the chemical properties of amines.</p>

<p>Please enquire for more information about cis-Dichloro(N,N,N',N'-tetramethylethylenediamine)palladium(II) 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(2-hydroxyethyl)propane-1,3-diamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>4,6-Diaminobenzene-1,3-dicarboxylic acid is an inorganic copper compound that is used as a copper salt. It has been shown to be effective as a chelating agent for the treatment of copper toxicity. 4,6-Diaminobenzene-1,3-dicarboxylic acid binds to metal ions and forms a complex with them. This complex can then be excreted from the body through urine or bile.</p>

Please enquire for more information about N-2,3-Dihydro-1H-inden-2-yl-N-ethylamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Diclofenac epolamine is a nonsteroidal anti-inflammatory drug that belongs to the class of diclofenac. It has been shown in clinical studies, with statistically significant results, to be effective against allergic reactions. Diclofenac epolamine is a film-forming polymer that can be used as a matrix for microcapsules containing diclofenac or other NSAIDs. This drug was designed to target tissue and provide effective analgesia at low doses. Diclofenac epolamine has an experimental model that uses monoclonal antibody-mediated delivery of diclofenac into the target tissue through microcapsules, which are then degraded by proteases present in the target tissue.

Please enquire for more information about 1-(2-Phenylethyl)piperidin-4-amine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>4-[4-(Dimethylamino)-1-(4-fluorophenyl)-1-hydroxybutyl]-3-(hydroxymethyl)benzonitrile hydrobromide is an antagonist of the nicotinic acetylcholine receptor (nAChR) that has been shown to be prophylactic against mediated nitrogen. It was isolated from a marine sponge and shows high affinity for nAChRs, with low nanomolar binding constants. The prophylactic properties of 4-[4-(dimethylamino)-1-(4-fluorophenyl)-1-hydroxybutyl]-3-(hydroxymethyl)benzonitrile hydrobromide are mediated by its ability to antagonize the function of nAChRs and prevent the release of neurotransmitters such as acetylcholine.</p>

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

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

<p>Nitrosobis(2-hydroxyethyl)amine (NBEA) is an inhibitor of nitrite reductase, an enzyme that catalyzes the reduction of nitrite to ammonia. Nitrite reductase is used in wastewater treatment and is also involved in the metabolism of some carcinogens. NBEA has been shown to inhibit the activity of nitrite reductase by binding to its active site, preventing the enzyme from reducing nitrite to ammonia. NBEA has genotoxic effects on E. coli K-12 cells and increases DNA damage with prolonged exposure, which may be due to the production of reactive oxygen species such as superoxide radical anion and hydrogen peroxide.</p>

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

Please enquire for more information about N-alpha-Trityl-Nbeta-Fmoc-L-2,3-diaminopropionic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Aminopyridine is a compound with the chemical formula C6H5N3. It is used in biological studies as a model for the hydrogen bond, and has been shown to be effective against some bacteria and fungi. 3-Aminopyridine may also have antimicrobial activity. The mechanism of action of 3-aminopyridine is not well understood, but it is thought that this compound might bind to the active site of an enzyme or receptor and deactivate it. 3-Aminopyridine has been found to inhibit dinucleotide phosphate (DNP) reductase, which may play a role in carcinogenesis. There are two nitrogen atoms in 3-aminopyridine, one in the amine group and one in the pyridine ring. The hydroxyl group on the molecule can form hydrogen bonds with other molecules such as hydrochloric acid or hydrogen tartrate, which may be why it reacts with these substances so easily.

Please enquire for more information about N-Methyl-1-(3,4,5-trimethoxyphenyl)methanamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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<p>N-Nitroso-di-n-butylamine is a nitrosamine that is a product of wastewater treatment. It has been shown to inhibit mitochondrial function and induce liver lesions in rats at high doses. N-Nitroso-di-n-butylamine is structurally similar to the natural substrate ribose, which leads to inhibition of xanthine oxidase, an enzyme involved in purine metabolism. The structural analysis revealed the presence of reactive sites that are susceptible to attack by nucleophiles, such as hydroxyl radicals or hydrogen peroxide. This indicates that N-Nitroso-di-n-butylamine may be a precursor for other carcinogenic compounds. NADH is reduced by NADH dehydrogenase (complex I) in mitochondria to produce NAD+, which subsequently donates electrons to the electron transport chain and generates ATP. The ability of NNDB to inhibit complex I activity was assessed using hl60</p>

<p>Please enquire for more information about N,N-Bis[3-(methylamino)propyl]methylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<p>5-Aminoorotic acid is an antimicrobial agent that has been shown to have anticancer activity. It has a nitrogen atom and two oxygen atoms in the molecule. The chemical structure of 5-aminoorotic acid can be determined using NMR spectroscopy and its biological properties are dependent on hydrogen bonding interactions with other molecules. 5-Aminoorotic acid is a chelate ring, which means it can bind to metal ions such as lanthanum (La3+). 5-Aminoorotic acid has been shown to inhibit the glycol oxidation reaction and may also be able to inhibit other enzymatic reactions. This drug is stable for use in model systems and may also be used for cancer treatment.</p>

Please enquire for more information about 2-Amino-1-tetralone hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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>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>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>1-Amino-2,4-imidazolidinedione-13C3 is an antibiotic that belongs to the group of nitrofurans. It is used for the treatment of infections caused by bacteria that are resistant to other antibiotics. The LC-MS/MS analysis showed that 1-aminohydantoin was formed as a degradation product of chloramphenicol and that this metabolite had been detected in urine samples from patients treated with chloramphenicol. Nitrofuran is also a possible degradation product. A reaction monitoring experiment using ionization monitoring and monitoring on the precursor ion at m/z 287 confirmed the presence of 1-aminohydantoin in a sample containing both chloramphenicol and nitrofuran. Quantification was performed using calibration curves obtained from pure standards.</p>

<p>Dicyclohexylamine is a trifluoromethanesulfonic acid (TFSA) scavenger that inhibits HIV infection by blocking the reaction solution. TFSA is a by-product of the industrial production of solanum tuberosum, and has been shown to inhibit plant enzyme activity. Dicyclohexylamine has been shown to be an effective inhibitor of enzymes such as phosphodiesterase, lipases, and proteases in detergent compositions. It also inhibits the activity of a number of enzymes in organic solutions and chemical reactions.</p>

N-Phenylhydroxylamine is a chemical compound that is used in wastewater treatment. It is a hydrophobic compound that has been shown to irreversibly inhibit the nitrite reductase enzyme, which is responsible for converting nitrite ions into nitrate ions. This reaction mechanism was studied using in vitro assays with picolinic acid and nitrobenzene. N-Phenylhydroxylamine binds to the active site of the enzyme and blocks access by the substrate, preventing it from being converted into its product. The reaction can be reversed by adding hydrogen fluoride, which displaces the N-phenylhydroxylamine molecule from its binding site. N-Phenylhydroxylamine also binds to nitrogen atoms and participates in transfer reactions with other molecules, making it reactive and capable of reacting with other compounds. The sample preparation process should include separating N-phenylhydroxylamine from water samples after extraction because it will react with

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

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<p>Silyl protecting group for alcohols; reagent for introducing protected C atom</p>

<p>(R)-(-)-a-[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]benzeneacetic Acid is an inhibitor of the enzyme histamine N-methyltransferase (HNMT), which is responsible for the synthesis of histamine. The inhibition of HNMT leads to a decrease in histamine levels and therefore has been used as a treatment for chronic prostatitis, lacrimal gland, and energy efficiency. Histamine N-methyltransferase also participates in the regulation of apoptosis by methylating proapoptotic proteins like Bax, so inhibition can lead to an increase in apoptosis. This chemical is also able to bind with chloride ions and form diphenyl ethers through a reaction solution, which are known to have anticancer properties.</p>

<p>2-Amino-5-chloropyridine is an organic compound that is a metabolite of nicotinic acid. 2-Amino-5-chloropyridine has been detected in urine samples and can be extracted from urine with hydrochloric acid. It can also be prepared by the reaction of picolinic acid and malonic acid, which are both found in the human body. The compound has been shown to have pharmacokinetic properties, including a half life of approximately 1 hour and a volume of distribution of 0.3 L/kg. 2-Amino-5-chloropyridine has also been shown to have structural analysis and binding properties with hydrogen bonding interactions. The structure was determined by X-ray crystal structures, which revealed the presence of a reactive group p2 and the absence of any other reactive groups. 2-Amino-5-chloropyridine is used as an analytical method for fluorescence detection in combination</p>

<p>4-(Aminomethyl)pyridin-2-amine is a reversible inhibitor of the cytochrome P450 system, which is responsible for the metabolism of drugs. It inhibits the activity of cytochrome P450 enzymes and prevents the conversion of prodrugs to active metabolites. This drug has been shown to inhibit myocardial injury caused by ischemia-reperfusion or overload. 4-(Aminomethyl)pyridin-2-amine has also been shown to have inhibitory activities on myocardial cells in culture, as well as on cardiomyocytes in vivo. In addition, it appears that this drug may be useful for reversing cardiac hypertrophy and heart failure, which are associated with a number of diseases including hypertension and diabetes mellitus. The pharmacokinetic profile of 4-(aminomethyl)pyridin-2-amine has been studied in humans. The half-life is short (1</p>