Aminas

<p>2-Amino-4,6-dihydroxypyrimidine is a chemical compound that is used in the synthesis of pemetrexed. It has been shown to inhibit the growth of cancer cells in cell culture by cross-coupling with nitrogen atoms in DNA and thereby inhibiting replication. 2-Amino-4,6-dihydroxypyrimidine also reacts with halides to form reaction intermediates that are capable of reacting with hydrogen bonds and other functional groups. This chemical compound has been shown to have radical scavenging activities in acidic environments and vibrational properties.</p>

Z-1,6-Diaminohexane·HCl is a versatile building block that can be used as a reagent, speciality chemical, or useful scaffold. This compound has been shown to be a useful intermediate in the synthesis of other compounds and can also react with metal ions to generate metal complexes. Z-1,6-Diaminohexane·HCl is a high quality compound that is stable and soluble in water, making it suitable for use in reactions at room temperature.

<p>Thiamine nitrate is a form of vitamin B1 that is used to treat thiamine deficiency. Thiamine nitrate is an oxidized form of thiamin, also known as vitamin B1. It can be synthesized by reacting thiamin hydrochloride with nitric acid. Thiamine nitrate has been shown to protect against neuronal death in the brain and restores cognitive function in patients with Wernicke-Korsakoff syndrome due to its ability to target enzymes involved in energy metabolism and calcium ion homeostasis. It also prevents acute alcohol intoxication and protects against neurotoxicity caused by nonsteroidal anti-inflammatory drugs.<br>Thiamine nitrate also has a fluorescence probe that can be used for detection and quantification of some proteins, such as DNA polymerase or ribonucleotide reductase, which are essential for cell growth or DNA synthesis.</p>

<p>3-(Difluoromethoxy)benzyl amine is a high-quality reagent that is used as an intermediate in the synthesis of complex compounds. 3-(Difluoromethoxy)benzyl amine is also a useful building block for the synthesis of speciality chemicals and research chemicals. This compound can be used as a versatile building block, which can be used to synthesize different functional groups. 3-(Difluoromethoxy)benzyl amine is soluble in many organic solvents and has a boiling point of 193 °C.</p>

<p>3-Methoxybenzenamine is a molecule that can be synthesized by an asymmetric reaction. It has carcinogenic potential and is classified as a chemical substance. 3-Methoxybenzenamine reacts with hydrochloric acid to form hydrogen chloride gas and methoxybenzene. The hydroxyl group on the molecule reacts with l-tartaric acid to form an ester, which then undergoes hydrolysis to produce 3-hydroxybutanoic acid. This reaction also produces water, which may result in a decrease of the concentration of the reactants. 3-Methoxybenzenamine can also react with amines to form quaternary ammonium salts, which are highly soluble in water and have a high detection sensitivity.</p>

4-(Aminomethyl)benzenesulfonamide acetate is a biocompatible polymer that is used in the treatment of infectious diseases. It has antibacterial efficacy against a range of microorganisms, including methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa. This polymer binds to sulfadiazine and antimicrobial peptides, which then act as antimicrobial agents. 4-(Aminomethyl)benzenesulfonamide acetate also exhibits good chemical stability in vivo and has been shown to inhibit the growth of skin cells.

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4,5-Diamino-1-(2-hydroxyethyl)pyrazolesulphate is a compound that is used as an intermediate in the production of ethoxymethylenemalonate. It is synthesized by hydrolysis of 4,5-diamino-1-(2-hydroxyethyl)pyrazole (DAP). In order to determine the purity and identity of this compound, it must be passed through a filter. The filtration process can be accomplished using analytical methods such as supercritical fluid chromatography or electrospray mass spectrometry. This compound has been shown to have a very high efficiency when recycled and can be used for the expansion of ethoxymethylenemalonate.

<p>N-(4-Methoxyphenyl)ethane-1,2-diamine is a synthetic compound that has been shown to inhibit the activity of cathepsins. It can be used in the treatment of diseases caused by these enzymes, such as osteoarthritis and Alzheimer's disease. N-(4-Methoxyphenyl)ethane-1,2-diamine has a pharmacokinetic profile that is favorable for oral administration. The drug is absorbed from the gastrointestinal tract readily and undergoes extensive metabolism in the liver. This process leads to the formation of active metabolites which are excreted in urine or bile. N-(4-Methoxyphenyl)ethane-1,2-diamine also inhibits nitroalkanes with activated aromatic rings, such as 4-nitrobenzaldehyde and 2,4,6-trinitrobenzene.</p>

<p>N-Benzyloctylamine is a broad-spectrum antibacterial that is effective against gram-positive and gram-negative bacteria. It has been shown to inhibit the growth of Escherichia coli and Bacillus subtilis, as well as other bacterial strains. N-Benzyloctylamine inhibits the activity of aminopeptidases, which are enzymes that hydrolyze amino acids from the ends of peptides. This inhibition leads to an accumulation of peptides in cells, which may lead to cell death by proteolysis. N-Benzyloctylamine also inhibits fatty acid synthase, which is an enzyme involved in the synthesis of fatty acids. This inhibition leads to a decrease in fatty acid production, resulting in a reduction in lipid accumulation within cells.</p>

<p>5-Pyridin-2-yl-2H-pyrazol-3-ylamine is a chemical intermediate that can be used in the synthesis of many different compounds. This compound is a versatile building block that can be used to make complex substances, as well as being an excellent reagent for research purposes. It has been shown to be useful as a reactant in the preparation of high quality chemicals and speciality chemicals. 5-Pyridin-2-yl-2H-pyrazol-3-ylamine is a fine chemical with CAS No. 92352-29-9.</p>

1-Phenyl-3-aminopyrazol-5-one is a solvent that can be used in elemental analysis. It has a molecular weight of 137.12 and is soluble in water, methanol, ethanol, acetone, ether, benzene and chloroform. 1-Phenyl-3-aminopyrazol-5-one has been shown to react with amines and form tautomers with different chemical properties. The spectral data for this compound are presented as the absorption spectra of substituted 1-phenyl-3-aminopyrazol-5-ones with acetyl groups at C2 and C4 (1), the nuclear magnetic resonance spectrum of 1-(dimethylamino)ethyl 3-[2-(N,N'-dimethylamino)ethyl]pyrazole (2), the NMR spectrum of 2-(dimethylamino)ethyl 3-[2-(N,N'-dimethylamino)ethyl]

5-Amino-2-(4-aminophenyl)benzoxazole is a drug that has been shown to have anti-diabetic properties. It acts by activating the protein kinase B (PKB), which is a key regulator of insulin resistance and glucose metabolism. 5-Amino-2-(4-aminophenyl)benzoxazole also binds to heat shock proteins, which may be responsible for its effects on liver cells, and has been shown to reduce viscosity in deionized water. This drug also acts as an inhibitor of protozoan parasites such as Plasmodium falciparum and Leishmania major, through its ability to inhibit their aldehyde dehydrogenase enzyme. 5-Amino-2-(4-aminophenyl)benzoxazole has a crystalline structure similar to that of the active form of insulin.

2-Amino-4,6-dibromophenol is an organic compound that is used in research for the synthesis of benzoxazoles and related compounds. It is a lactam analog that can be synthesized from commercially available starting materials. 2-Amino-4,6-dibromophenol has been shown to have pharmacological activity against tumor cells. This compound has also been used to synthesize regiospecific skeletal analogs of natural products.

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<p>Sodium ammonium hydrogen phosphate is a salt that has genotoxic effects. The genotoxic potential of this compound is dependent on the concentration and duration of exposure. This substance can interact synergistically with other substances, such as inorganic acids or hydrochloric acid. Sodium ammonium hydrogen phosphate has been shown to cause malonic acid in the presence of an appropriate carbon source, and to form diammonium phosphate, which is a genotoxic agent. It also interacts with collagen and particle substrates, forming a carbonyl group which may be responsible for its genotoxicity. br&gt;br&gt; Sodium ammonium hydrogen phosphate is acidic and reacts with proteins to form amide bonds. This reaction may lead to biochemical pathways that are associated with DNA damage.</p>

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Please enquire for more information about 2-Amino-7-methyl-5-oxo-4-(2-thienyl)-4,6,7,8-tetrahydro2H-chromene-3-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Sulfo-Cy3 diacid NHS ester is a CY3-derived dye. CY3 is an amine-reactive cyanine orange dye for fluorescent labelling of proteins and nucleic acids.

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<p>2-Amino-5-methyl-4-phenylthiazole is an organic compound that is a reactive intermediate. It can be used in treatments such as second order rate constants, stabilization, and kinetic. This chemical has a dimethylamine group, which is an amine with two methyl groups attached to it. 2-Amino-5-methyl-4-phenylthiazole has chloride and thiazolone groups, which are both heterocyclic rings of carbon atoms with nitrogen and sulfur atoms attached to them. The phenyl isothiocyanate group is also a heterocyclic ring of carbon atoms with sulfur attached to it. 2-Amino-5-methyl-4-phenylthiazole has the constant of K = 1.2 x 10 M^sup -1 <br>s^{sup -1} at 25 degrees Celsius. It reacts with acetonitrile and ethylpyridine</p>

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3-Amino-2-cyclohexen-1-one is a synthetic chemical that has been shown to have significant cytotoxicity and to be a powerful nitrosating agent. It was synthesized by the reaction of nitrite ion with two equivalents of acetonitrile in the presence of diazonium salt. 3-Amino-2-cyclohexen-1-one reacts with nucleophiles such as thiols, amines, or alcohols to produce nitrosamines. Nitrosamines are highly reactive chemicals that may cause a number of adverse effects, including cancer. 3-Amino-2-cyclohexen-1-one can also be used for postsynthetic modification reactions on other organic compounds. The mechanism for this process is not yet fully understood but it is believed that the trifluoromethyl group plays an important role in these reactions.

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

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Aluminum is an antifungal agent that has been used reliably for many years. It is a water-soluble, colorless solid that has been used for the treatment of yeast and other fungal infections. Aluminum is also used to treat bacterial infections. It does this by blocking the formation of new cell walls in fungi and bacteria, which may be due to its ability to bind catechols. Aluminum chloride binds to cyclic catechols such as protocatechuic acid and gallic acid, preventing them from combining with aluminum ions to form crystals that can cause kidney stones. This process prevents the formation of new cell walls in fungi and bacteria, which may be due to its ability to bind catechols.

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<p>2-((5,5-Dimethyl-3-oxocyclohex-1-enyl)amino)benzoic acid (DMACBA) is a channel inhibitor that blocks the voltage-gated sodium channels in neurons. It has been shown to be effective against malignant brain tumors. DMACBA inhibits the conformational changes of the channel caused by glycols and microwave irradiation. It also stabilizes the open state of the channel, preventing it from closing again after being opened by an action potential. This agent is stable in water and forms dimers with benzoic acid. DMACBA binds to pyrimidine in DNA, inhibiting bacterial replication and transcription.</p>

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<p>Ethyl 2-(4-(((phenylcarbonylamino)thioxomethyl)amino)-3,5-thiazolyl)acetate is a benzoic acid ethyl ester that belongs to the group of benzoyl derivatives. It is an antifungal agent with broad spectrum activity against a variety of fungi and yeasts. The chemical structure includes an aromatic ring, which can be substituted with a phenyl group at position 4 (e.g., chlorophenyl), and a 3,5-thiazolyl group at position 2. The thiazole moiety is found in many pharmaceuticals as it has been shown to inhibit the synthesis of DNA, RNA, and protein in cells by binding to the ribosomes on the endoplasmic reticulum of the cell. This inhibition leads to cell death.</p>

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