Amines

<p>4-Amino-3-methylbenzoic acid is a chemical compound that can be synthesized from 4-Methylbenzoic acid and sodium carbonate. It has been used in the treatment of cervical cancer and leishmania. The synthesis of this drug is an example of a chemical reaction in which a carboxylic acid is reacted with sodium carbonate to give an ester and sodium bicarbonate. This process requires the use of trifluoroacetic acid. The resulting drug also has antiviral properties, as it inhibits HIV infection by blocking reverse transcriptase activity. 4-Amino-3-methylbenzoic acid was also shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>4-Amino-2-fluorobenzylamine dihydrochloride is a high quality, complex compound that can be used as a reagent, useful intermediate, or fine chemical. It is a versatile building block that can be used as a reaction component in the synthesis of speciality chemicals such as research chemicals and building blocks for drugs. It is also an important scaffold for drug design and development. 4-Amino-2-fluorobenzylamine dihydrochloride has CAS No. 2200281-02-1 and is useful in the synthesis of many different compounds.</p>

<p>4,4'-Diamino-3,3'-dimethyldiphenylmethane is a reactive dye that is used in the diagnosis of cervical cancer. It has been shown to suppress the expression of tumor suppressor genes by binding to DNA and interfering with transcription. This dye is also a polyvinyl compound that binds to proteins through an amine group. The bound form of 4,4'-Diamino-3,3'-dimethyldiphenylmethane can be detected using an electrode and hydroxyl group as a diode. Multivariate logistic regression was used to determine the relationship between the bound form of 4,4'-Diamino-3,3'-dimethyldiphenylmethane and women who have not had any symptoms of cervical cancer. A section was taken from each subject's cervix and stained with 4,4'-Diamino-3,3'-dimethyldiphenylmethane</p>

<p>(1R)-(1S,2S,3R,5S)-Pinanediol-N-(N-pyrazinylphenylalaninoyl)-1-amino-3-methyl-butane-1-boronate is a boronic acid derivative that has been shown to have an antiproliferative effect on cancer cells. It is a biodegradable, water soluble drug with a low toxicity profile. The maximum tolerated dose has been established in vivo studies and it can be used as an imaging agent for diagnosis. (1R)-(1S,2S,3R,5S)-Pinanediol-N-(N-pyrazinylphenylalaninoyl)-1-amino-3-methyl-butane-1-boronate may be used to treat cancers such as breast cancer or leukemia. This drug targets the proteasome and inhibits its activity by binding to the active site of the 20s</p>

<p>3-Amino-4-methoxybenzoic acid ethyl ester is a chemical building block that can be used in the synthesis of various organic compounds. It is an important reaction component, and can also be used as a reagent or useful scaffold. 3-Amino-4-methoxybenzoic acid ethyl ester is soluble in organic solvents and has a high quality. This chemical has been shown to be useful for research purposes.</p>

<p>Methyl 3-amino-5,6-dichloro-2-pyrazine carboxylate is a synthetic molecule that has been synthesized from dimethylamiloride. This chemical has been labeled and used for a variety of homologous and synthetic modifications. It may be used in labeling experiments to identify an unknown compound or to determine the structure of a known compound. The methyl 3-amino-5,6-dichloro-2-pyrazine carboxylate can also be used as a ligand to bind with subunits of proteins or nucleic acids. Photolabile methyl 3-amino-5,6-dichloro-2-pyrazine carboxylate can be synthesized by using light energy to cleave the ester bonds in the chemical. This chemical is useful for assays and techniques such as spectroscopy and nuclear magnetic resonance (NMR).</p>

<p>4-[(7-Chloro-4-quinolinyl)amino]-1-pentanol (QLT) is a drug that has been shown to be effective against both healthy volunteers and malaria patients. It is a prodrug that is metabolized by the liver into 7-chloroquinalone, which inhibits the growth of plasmodium falciparum. QLT has been shown to be safe and well tolerated in studies with healthy volunteers, and it does not appear to cause significant adverse effects. QLT also has an effect on T cells, which may be due to its ability to inhibit protein synthesis and cell division.</p>

<p>2-Aminoethoxyamine dihydrochloride is a cardiotonic, which is a chemical agent that acts on the heart to increase contractility. It has been shown to be more efficient and less toxic than other cardiotonics. 2-Aminoethoxyamine dihydrochloride has been found to act as an epoxidizing agent and can be used in the synthesis of istaroxime, an inhibitor of cholesterol biosynthesis.2-Aminoethoxyamine dihydrochloride also reacts with dehydroepiandrosterone to form 2-aminoethoxyamidine hydrochloride.</p>

<p>N,N-Dimethyldodecylamine N-oxide, also known as lauryldimethylamine oxide (LDAO), is an amine oxide nonionic surfactant with a C12 alkyl chain used widely in cosmetics, washing, cleaning and personal care products. LDAO has antimicrobial properties and is effective against common bacteria such as S. aureus and E. coli.</p>

<p>Please enquire for more information about 2-[(2,4-Dimethylphenyl)amino]nicotinic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3,5-Diaminosalicylic acid is a potent antibacterial agent that inhibits the synthesis of bacterial cell walls by inhibiting the enzyme transpeptidase. It is also used as a preservative and stabilizer in pharmaceutical formulations. 3,5-Diaminosalicylic acid has been shown to be active against cochliobolus at an optimum concentration of 2%. The solute is stable in water or dilute acids and alkalis. However, it can be hydrolyzed by strong bases such as sodium hydroxide and potassium hydroxide. Impurities such as nitro groups can be removed by washing with water or ethanol. The drug substance should be analyzed using high performance liquid chromatography (HPLC) methods to ensure stability and purity. 3,5-Diaminosalicylic acid forms crystalline needles that are colorless to white in solution. They will dissolve when heated but form precipitates when cooled. The crystals are</p>

<p>Ethoxy-Fluorophosphoryl-N-Methylmethanamine is a chemical that belongs to the class of nerve agents. It can be used as an antidote for sarin poisoning. This compound reacts with the enzyme butyrylcholinesterase, which breaks down acetylcholine in the synapses. In this way, it blocks the transmission of nerve impulses and causes muscle paralysis. Ethoxy-Fluorophosphoryl-N-Methylmethanamine acts as an antagonist of acetylcholine receptors in both animals and humans. It also inhibits cholinesterase activity in blood pressure regulation, which leads to increased blood pressure levels. When administered at sublethal doses, this compound induces a long lasting sensitization of the central nervous system to other cholinergic drugs such as atropine or nerve gases such as sarin.</p>

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<p>4-(N,N-Diethylamino)cinnamic acid is a dye-sensitized solar cell sensitizer that has been synthesized from thiophene and acrylic acid. This compound is efficient in dye-sensitized solar cells and can be used to produce solar cells with an efficiency of over 10%.</p>

<p>5-Aminophthalide is a chemical compound that can be found as an oxidation product in cellular structures. It has been shown to have cancer-inhibiting properties and may be used for the treatment of prostate carcinoma. 5-Aminophthalide is a molecule that has two isomers, one with two chlorine atoms and one with three chlorine atoms. The molecule contains functional groups such as carbonyl, amine, and nitro groups. These functional groups are important for its activity and can bind to the enzyme dehydrogenase in bacteria, which is involved in the biosynthesis of guanine nucleotides. 5-Aminophthalide inhibits bacterial growth by binding to this enzyme and preventing it from functioning normally. This causes an accumulation of guanine nucleotides within cells, which prevents them from dividing.</p>

<p>Aminopterin is an antineoplastic agent and antifolate, which is a synthetic derivative of pteroylglutamic acid. It functions as a chemotherapeutic agent by inhibiting dihydrofolate reductase, an enzyme crucial in the folic acid pathway, thereby preventing the conversion of dihydrofolate to tetrahydrofolate. This disruption leads to impaired synthesis of purine nucleotides and thymidylate, which are essential for DNA synthesis and cell division.</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>(6S)-5,6,7,8-Tetrahydro-6-[propyl[2-(2-thienyl)ethyl]amino]-1-naphthalenol is a potent and selective dopamine receptor agonist. It acts by binding to the dopamine receptors in the brain. This binding stimulates the release of dopamine and prevents it from being reabsorbed into the neurons, which in turn increases levels of extracellular dopamine in the synapse. (6S)-5,6,7,8-Tetrahydro-6-[propyl[2-(2-thienyl)ethyl]amino]-1-naphthalenol has been shown to have antidepressant effects in animal models of depression. It also has a long half life and can be administered as a transdermal patch for prolonged relief from depression symptoms.</p>

<p>Boc-L-4-Aminophenylalanine is an amino acid that has been shown to be synthesized by cancer cells in breast cancer cell lines, and can also be conjugated with anticancer drugs. It has been shown to have a high affinity for cancer cells. Boc-L-4-Aminophenylalanine is a substrate for L type amino acid transporters and can be used for the treatment of breast cancer. This compound may also be useful in the treatment of other cancers due to its ability to inhibit the uptake of endogenous amino acids.</p>

<p>4-Aminothiobenzamide (4ATB) is a chemical compound that is used as an anticancer agent and an antimicrobial agent. It has been shown to have antitumor activity against human liver cancer cells and anticancer activity against human adrenergic receptor-positive lung cancer cells. 4ATB binds to the chloride ion present in the cell membrane, which prevents the influx of chloride ions into the cell. This leads to an increase in intracellular pH and disruption of cellular functions. 4ATB has also been shown to inhibit methicillin-resistant Staphylococcus aureus (MRSA) infections by inhibiting bacterial growth and reducing the production of proteins vital for cell division.</p>

<p>4-Aminobenzanilide is an antimicrobial agent that is synthesized from 2-aminobenzamide and 4-aminophenol. It has been shown to be effective against a number of bacteria, including Staphylococcus aureus and Streptococcus pyogenes. 4-Aminobenzanilide has also been shown to inhibit the growth of Mycoplasma pneumoniae in mammalian cells, which may be due to its ability to block DNA replication and transcription. This compound can also disrupt the synthesis of amides by inhibiting the enzyme aminopeptidase N. The low energy required for this reaction makes it possible for this compound to work as an antimicrobial agent with minimal toxicity.</p>

<p>N-Methyldioctylamine is a biodegradable, water soluble, and non-toxic chemical that can be used as an alternative to caustic soda for wastewater treatment. It removes organic matter from industrial effluents by breaking down long chain hydrocarbons into smaller fragments and reacts with the hydroxyl group of proteins to form hydroxylamines. N-Methyldioctylamine has been shown to inhibit protease activity in wild-type strains of bacteria, such as Escherichia coli and Pseudomonas aeruginosa. It also inhibits hematopoietic cells from developing into mature cells by disrupting the biochemical composition of their membranes. N-Methyldioctylamine is reactive with fatty acids and amines found in mammalian tissue samples. This compound can be used as a sample preparation agent or analytical reagent for caproic acid, which is used in process optimization applications.</p>

<p>4,5-Diamino-6-chloropyrimidine is a glycosidic compound that has been used for the optimization of drug targets. It has been shown to have antimalarial activity against Plasmodium falciparum in vitro and in vivo. 4,5-Diamino-6-chloropyrimidine binds to the amine groups on nucleotides, specifically purines (adenine and guanine), and amidates the 6-chloropurine ring. This makes it a potential candidate for use in chemotherapy. The structure of 4,5-diamino-6-chloropyrimidine was determined by NMR and mass spectroscopy analysis.</p>

<p>Fosaprepitant is a drug that belongs to the class of drugs used for chemotherapy. It is a prodrug that is converted in vivo to aprepitant, its active form. Fosaprepitant acts as an antagonist of the neurokinin-1 receptor (NK-1R) and inhibits the binding of substance P, which leads to an anti-inflammatory effect. Fosaprepitant has been shown to inhibit the production of substance P in animal models, leading to a reduction in inflammation. In clinical trials, fosaprepitant has been shown to be safe and well tolerated when used with other drugs such as cisplatin and docetaxel in patients with cancer.</p>

<p>Giosiamine is a heterocyclic molecule that is used as a reaction component, reagent, and useful scaffold. It is also a high-quality research chemical with speciality use in the synthesis of other chemicals. Giosiamine is available at CAS No. 1815-02-7 and can be used as an intermediate for the production of complex compounds such as pharmaceuticals, pesticides, and fine chemicals. This product has been shown to be versatile in its applications and can serve as a building block for various types of reactions.</p>

<p>6-Carboxytetramethylrhodamine (TAMRA) is a widely employed fluorescent dye (orange-red) suitable for different uses. In PCR applications, it has been used both as a reporter at the 5’ or as a quencher at the 3’ end. TAMRA-labelled oligonucleotides have been used to study interactions with DNA or DNA/proteins interactions. It is an excellent fluorescent acceptor for FRET applications with a suitable dye pair. It is used as a protein/antibody labelling agent for structural studies, immunochemistry and flow cytometry. Bioconjugation is generally performed through coupling of the carboxylic acid to a primary amine at the N-terminus of a protein, on lysine side chains or amino-modified oligonucleotide. Carboxylic acids activated with succinimidyl esters react with primary amines.</p>

<p>5-Fluoro-2-(trifluoromethyl)pyridin-4-amine is a fine chemical that is used to create other organic compounds. This compound is an intermediate in the production of pharmaceuticals, pesticides, and herbicides. It can also be used as a reagent or a speciality chemical in research. 5-Fluoro-2-(trifluoromethyl)pyridin-4-amine can be used as a reaction component to synthesize other compounds and has been shown to have versatile functions as a building block for complex molecules. This compound is not classified by the Chemical Abstract Service (CAS) and does not have any reported toxic effects on humans.</p>

<p>4-Amino-3-nitrophenol is a reactive aminophenol that can be synthesized from hydrogen sulfate and diethyl ester. It is used in the synthesis of amines and other chemicals, as well as in analytical methods for determining the concentration of nitrates, nitrites, and aminophenols. 4-Amino-3-nitrophenol has been shown to have photocatalytic activity.</p>

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<p>Methyl 2-amino-4-(trifluoromethyl)benzoate is a non-steroidal anti-inflammatory drug that is structurally related to anthranilic acid. It has been shown to reduce the proliferation of human breast cancer cells in vitro. This drug inhibits the activity of cellular senescence, which has been implicated in aging and cancer progression. Methyl 2-amino-4-(trifluoromethyl)benzoate binds to receptor sites on the cell nucleus and prevents the binding of ligands to these receptors, thereby inhibiting transcriptional activity. This compound also increases cell sensitivity to radiation and chemotherapeutic agents by preventing DNA repair mechanisms from functioning properly. Methyl 2-amino-4-(trifluoromethyl)benzoate inhibits the production of reactive oxygen species by inducing oxidative stress in cells and may inhibit protein synthesis through its ability to bind tightly to proteins.</p>

<p>2-Amino-5-fluorobenzothiazole is a synthetic compound that is used as an agrochemical. It has low efficiency and can be found in tissue culture. The biological properties of this compound are not fully understood. It has been shown to have potential antitumor activity and may be able to inhibit tyrosine kinase. 2-Amino-5-fluorobenzothiazole is also found in the inorganic section of the periodic table. This compound is water soluble, but does not dissolve well in organic solvents such as acetone or chloroform. 2-Amino-5-fluorobenzothiazole also has agricultural applications, being used as a pesticide and for controlling tuberculosis in animals.</p>

<p>6-Fluorogramine is a synthetic compound that is metabolized by drug-metabolizing enzymes to form 6-fluorohydroxymethyltetrahydrofolate. This intermediate is then hydrolyzed to form 6-hydroxymethyltetrahydrofolate and monohydroxy methylene tetrahydrofolate. The reaction yield for this reaction is about 60%. 6-Fluorohydroxymethyltetrahydrofolate can also be converted to paraformaldehyde and dimethylamine, which are used in the synthesis of other compounds. The positional isomer of 6-fluoromethylenetetrahydropterin (6FMTP) can be synthesized from 6-fluoroformaldehyde and paraformaldehyde.</p>

<p>20-Deoxo-23-deoxy-5-O-[3,6-dideoxy-3-(dimethylamino)-beta-D-glucopyranosyl]-20,23-di-1-piperidinyltylonolide is an antimicrobial agent that belongs to the group of chemotherapeutic agents. It is a fluorinated analog of tilmicosin. The low dose group was treated with this drug for five days, and the high dose group received 20 times the amount of drug. Fluorescence spectrometry showed that there was no significant difference in the fluorescence intensity between these two groups after 24 hours. This drug has been shown to have pharmacokinetic properties in rats and mice, but further optimization may be required to improve its process.</p>

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

<p>(S)-2-Aminobutyramide hydrochloride is a strong acid that can be used in the synthesis of other compounds. It is made by dissociating acetic acid with hydrogen chloride, or by reacting ammonia with hydrochloric acid. (S)-2-Aminobutyramide hydrochloride is also known as 2-aminobutyric acid dihydrochloride and protonated aminobutyric acid. It can be used to synthesize many other compounds, including amino acids, pharmaceuticals, and polymers. The virulent properties of this compound make it useful for industrial purposes.</p>

<p>2,5-Dimethoxy-N-[(2-methoxyphenyl)methyl]-4-(trifluoromethyl)benzeneethanamine is a synthetic drug that belongs to the group of psychotropic drugs. It has been shown to cause death in rats, which is likely due to its ability to inhibit serotonin uptake by neurons. 2,5-Dimethoxy-N-[(2-methoxyphenyl)methyl]-4-(trifluoromethyl)benzeneethanamine also inhibits the enzyme monoamine oxidase and prevents the breakdown of monoamines such as serotonin. This drug has been shown to have both stimulant and depressant properties. 2,5-Dimethoxy-N-[(2-methoxyphenyl)methyl]-4-(trifluoromethyl)benzeneethanamine can be quantified in human blood samples using liquid chromatography with a</p>

<p>1,2,3,4-Tetrahydro-1-naphthylamine hydrochloride is a high quality reagent that can be used as an intermediate in the synthesis of various organic compounds. It has been shown to be a useful building block for the synthesis of complex compounds and speciality chemicals. Tetrahydro-1-naphthylamine hydrochloride is also a versatile building block for reactions involving amines or other nucleophiles. Tetrahydro-1-naphthylamine hydrochloride is an interesting scaffold for research chemicals due to its ability to react with various functional groups.</p>

<p>2-Amino-5-iodobenzoic acid methyl ester (2AIBA) is a molecule that can be used as an activatable probe for imaging cancer. It has a profile suitable for radionuclide therapy and is also senescent. 2AIBA binds to DNA and inhibits the synthesis of proteins, leading to cell death. 2AIBA has potent inhibitory activity against murine melanoma cells and synergistic effects when combined with acridone. The section of tumour cells was shown to be reduced by 42% in mice when treated with 2AIBA, acridone, and radiation compared to mice treated with radiation alone.</p>

<p>Benfotiamine is a thiamine derivative that is structurally similar to thiamine. It has been shown to have pharmacological effects in experimental models of diabetic complications and may be a potential therapeutic agent for the treatment of these conditions. Benfotiamine binds to the response element on the nuclear DNA, which leads to an increase in calcium pantothenate, a cofactor necessary for energy metabolism in mitochondria. The enzyme activities of benfotiamine are also modulated by calcium and magnesium ions. Benfotiamine can be used as an analytical method for nonsteroidal anti-inflammatory drugs (NSAIDs) by measuring the levels of benzoquinone imines and fluoroquinolones in urine.</p>

<p>4-Aminobenzamide is a compound that is used as an anti-tuberculosis drug. It inhibits the activity of aminotransferase, which is an enzyme responsible for converting amino acids into other compounds. 4-Aminobenzamide has been shown to have antimicrobial properties against bacteria, fungi and protozoa. It also has a protective effect on human liver cells, but can cause damage to rat liver cells in vitro. 4-Aminobenzamide also shows some activity against microbial metabolism and can be hydrolyzed by hydrochloric acid to form phenylacetic acid and ammonia. This compound has been shown to inhibit the nervous system disease progression of Huntington's disease in mice.</p>

<p>N,N'-Di-2-naphthyl-1,4-phenylenediamine is a chemical compound that is used in the production of polyvinyl chloride (PVC). It can be used as an antimicrobial agent to prevent the growth of bacteria and fungi. It is also used as a crosslinking agent in the production of PVC. The reaction solution consists of hydrochloric acid and methyl ethyl chloride. The monochloride is then reacted with 2-naphthol, followed by reaction with benzalkonium chloride. The final product is N,N'-di-(2-naphthyl)-1,4-(phenylene) diamine monochloride.</p>

<p>3-Amino-2-pyrazinecarboxylic acid methyl ester (3APCME) is a potent anti-mycobacterial agent that inhibits the growth of Mycobacterium tuberculosis by inhibiting the synthesis of amines, which are necessary for its survival. 3APCME has also been shown to have an inhibitory effect on other bacteria that require amines for their survival, such as Escherichia coli. This agent binds to the receptor and inhibits the enzyme pyrazinase in the reaction of phenoxy with dimethylformamide. The molecular modeling studies show that 3APCME is able to bind to a hydrophobic region on the enzyme's surface and form a covalent bond through nucleophilic attack. The asymmetric synthesis results in the production of one enantiomer of 3APCME and allows for greater efficacy against mycobacteria than other agents.</p>

<p>Intermediate in the synthesis of rivastigmine</p>

<p>2-(Aminosulfonyl)benzoic acid is a chemical compound that can be found in urine samples. It is used to detect the presence of saccharin and other artificial sweeteners, which are commonly used as substitutes for sugar. 2-(Aminosulfonyl)benzoic acid is also used to measure the presence of calcium pantothenate in food products. The chemical structure of this compound contains a hydrogen bond between the sulfur atom and the amine group. Hydrochloric acid can be used to break down 2-(Aminosulfonyl)benzoic acid into its constituent parts, which are sulfuric acid and benzoic acid. Uv absorption studies have also shown that 2-(Aminosulfonyl)benzoic acid absorbs ultraviolet light at 280 nm with an extinction coefficient of 20,000 M-1cm-1. This compound has been shown to have toxic effects on diabetic patients when taken orally in doses that</p>

<p>Isopentylamine is a chemical compound that belongs to the class of amines. It has been shown to be an agonist of the nicotinic acetylcholine receptor, which is a type of neurotransmitter receptor found in the central and peripheral nervous systems. Isopentylamine has been shown to have clinical relevance for congestive heart failure. This drug binds to the hydroxyl group on the receptor and increases the rate of diffusion into cells by increasing membrane permeability. The basic structure of isopentylamine is shown below:</p>

<p>Please enquire for more information about 5-Amino-4-oxopentanoic acid benzyl ester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>7-Amino-5-chloro-2(3H)-benzoxazolone is a high quality, versatile building block that has been used in the synthesis of many complex compounds. It has been used as an intermediate for the synthesis of reagents and fine chemicals. 7-Amino-5-chloro-2(3H)-benzoxazolone can be used as a speciality chemical and research chemical. CAS No. 889884-60-0.</p>

<p>4-Amino-3-chlorobenzoic acid is a white solid with a molecular weight of 170.1 g/mol, melting point of 158.5°C and boiling point of 267°C. It has the molecular formula C6H5ClNO2 and the IUPAC name 4-(aminomethyl)-3-chlorobenzoic acid. The chemical structure of this compound is shown in Figure 1.</p>

<p>3-Aminophthalic acid hydrochloride is a diazonium salt that emits light when it reacts with chloride. This compound has been shown to be photophysically active in the presence of human serum, tumor tissue, and micelles. 3-Aminophthalic acid hydrochloride has also been found to be cytotoxic in a number of cancer models. It may also cause death by chemiexcitation of tissues. Furthermore, 3-aminophthalate and acetyl derivatives have shown anticancer activity.</p>

<p>3-(Aminomethyl)adamantan-1-ol HCl is a chemical substance that can be used as a reaction component, reagent, and useful scaffold in the synthesis of pharmaceuticals. It is also a speciality chemical with versatile building block and useful intermediate properties. 3-(Aminomethyl)adamantan-1-ol HCl has been shown to be an effective building block for complex compounds, such as those used in the synthesis of anti-inflammatory drugs.</p>

<p>3-Fluorophenylpropan-2-amine (3FPPA) is a synthetic, nonselective dopamine and serotonin reuptake inhibitor. 3FPPA has been shown to inhibit the growth of cancer cells in vitro, and enhances the release of growth factors from nerve endings in rat brain slices. 3FPPA can be used as a test compound for investigating the effects of psychostimulants on neural cell division.<br>3FPPA binds to fatty acids and can be used as a medication to treat obesity or cancer. 3FPPA is not selective for either dopamine or serotonin, but is an analog of both amines.</p>

<p>CCT 241533 is a Chinese herb that has been shown to have anti-cancer properties. It has been demonstrated to inhibit the growth of HL-60 cells and induce apoptosis in these cells. CCT 241533 also inhibits the proliferation of epidermal growth factor (EGF) and induces cell death in response to radiation. This drug also binds to toll-like receptors, which are proteins on the surface of cells that detect pathogens and initiate an immune response. CCT 241533 has been shown to inhibit polymerase chain reactions by competitive inhibition or by binding to DNA, preventing transcription or replication. CCT 241533 may be useful for the treatment of infectious diseases, such as tuberculosis, because it can bind to bacterial 16S ribosomal RNA and inhibit protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division.<br>CCT 241533 has been shown in animal studies to be effective against cervical cancer due to its ability to bind</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>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>

<p>Ticarcillin is a bactericidal antibiotic that is used to treat many types of infections caused by gram-positive bacteria, such as Streptococcus pneumoniae, Enterococcus faecalis and Enterococcus faecium. Ticarcillin has been shown to be effective against antibiotic-resistant strains of bacteria, including multidrug efflux pumps. This drug also has been shown to inhibit the growth of gram-negative bacteria such as Escherichia coli and Pseudomonas aeruginosa. Ticarcillin is used in combination with clavulanic acid for the treatment of infections caused by beta-lactamase producing organisms. It is also used in wastewater treatment to inhibit the growth of gram-negative bacteria that are resistant to other antibiotics. Ticarcillin can interfere with other medications by inhibiting their metabolism through cytochrome P450 enzymes or through competition for protein binding sites.</p>

<p>4-(3-Bromophenyl)-1,3-thiazol-2-amine is an inhibitor of enzymes such as cholinesterase and covalent binding. It has been shown to inhibit the activity of cholinesterase in vitro. This drug is not active against erythromycin or lincomycin. 4-(3-Bromophenyl)-1,3-thiazol-2-amine also has a phenylthiazole linkage that can be conjugated with other molecules for use as a therapeutic agent.</p>

<p>2,3-Diaminopropionic acid is an antimicrobial peptide with significant cytotoxicity against cancer cells. This compound has two amine groups that are able to form hydrogen bonds with each other. The x-ray crystal structures of this molecule reveal that it forms a beta sheet structure and an alpha helix, which is essential for the stability of this compound. 2,3-Diaminopropionic acid has been shown to have strong antibacterial activity against Gram-positive bacteria and good activity against Gram-negative bacteria such as Escherichia coli and Salmonella enterica. This compound also inhibits the synthesis of proteins in bacterial cells by inhibiting the enzyme protein synthesis. 2,3-Diaminopropionic acid is stable under normal conditions but can be hydrolyzed in water vapor or ester hydrochloride. It reacts with nitrogen atoms on the surface of biological molecules to form amides.</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>

<p>Boc-N-Me-1,3-diaminopropane is a small molecule inhibitor of the hepatitis C virus. It interacts with the viral RNA polymerase and prevents translation of the viral genome into proteins. Boc-N-Me-1,3-diaminopropane also inhibits the assembly of new ribosomes from preformed subunits in cells infected with HIV. This drug binds to the ribosomal protein L11 and blocks interactions between this protein and other components of the ribosome. Boc-N-Me-1,3-diaminopropane has been shown to be effective against small molecule inhibitors that are resistant to traditional antiviral drugs, such as protease inhibitors and nucleotide analogues.</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>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>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>3-Amino-1-adamantanol hydrochloride (3AAAH) is a versatile building block that can be used for the synthesis of complex compounds. It has been shown to have a high quality and is useful as a reagent, research chemical, speciality chemical, or useful scaffold in organic synthesis.</p>

<p>6-amino-3-methyl-4-(4-nitrophenyl)-4H-pyrano[3,2-d]pyrazole-5-carbonitrile is a compound that has been shown to have correlations with energies and regression. It also has a linear regression, polarities, photophysical properties, and dipole. The fluorescence and excited state of this compound are singlet and hydrogen bonding interactions with solvents.</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(6)-Carboxytetramethylrhodamine succinimidyl ester is a chemical that can be used as a research chemical, speciality chemical, or a building block in the synthesis of other compounds. It is a high quality product and has been shown to be useful in the synthesis of complex compounds. This compound reacts with amines to form N-hydroxysuccinimide esters and is an excellent reagent for the production of fluorescamine derivatives. 5(6)-Carboxytetramethylrhodamine succinimidyl ester is also an excellent scaffold for the production of other chemicals such as peptides, proteins, and drugs. CAS No: 246256-50-8</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>4-Aminobenzoic acid sodium salt is an aminobenzoic acid that is used as a pharmaceutical intermediate. It is soluble in water and alcohol and has a pH of 4.5. The compound has been shown to inhibit the growth of bacteria by binding to enzymes involved in fatty acid synthesis, which prevents the formation of fatty acids and results in cell death. The compound also inhibits allergic reactions through its inhibition of histamine release from mast cells. 4-Aminobenzoic acid sodium salt has been found to have anti-inflammatory properties, which may be due to its ability to bind to epidermal growth factor receptors on the surface of keratinocytes, leading to increased cell proliferation and less inflammation.</p>

<p>Sulfur trioxide triethylamine complex is a second-order rate constant for the reaction of ester hydrochloride with carbapenem. It has been shown to have anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis. Sulfur trioxide triethylamine complex has also been shown to be an effective inhibitor of pyrazoles and chromatographic analysis at nmr spectra. It has been found to act as a substrate for hydroxyl group, fetal bovine serum, and metabolic disorders in urine samples. Disulfate is a byproduct of this reaction.</p>

<p>3-Amino-2,5,6-trifluorobenzoic acid is a pharmaceutical agent that can be used in the synthesis of dyestuffs and as a matrix for laser desorption/ionization (LDI) mass spectrometry. 3-Amino-2,5,6-trifluorobenzoic acid has been shown to form crystals that are insoluble in water or organic solvents. The crystal morphology was determined by using XRD and FTIR. 3-Amino-2,5,6-trifluorobenzoic acid also has high concentrations of impurities such as 2,4,6-trichloroaniline and 2-(3,4 dichlorophenyl) ethyl amine.</p>

<p>3-Aminoisoxazole is a chemical compound that belongs to the class of quinoline derivatives. It has potent antitumor activity and has been shown to inhibit the growth of cancer cells in vitro. 3-Aminoisoxazole is also an inhibitor of inflammatory disease, and has been shown to inhibit the production of cytokines (e.g., TNF-α) and nitric oxide, which are key mediators of inflammation. The mechanism by which 3-aminoisoxazole inhibits the production of inflammatory cytokines and nitric oxide may be due to its ability to react with nucleophilic groups on proteins and deactivate them, or by inhibiting the formation of reactive oxygen species through chemical reactions.</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>Rotigotine is a drug that is used to treat Parkinson's disease. It is a dopamine agonist that stimulates the release of dopamine in the brain. Rotigotine has been shown to be effective in controlling symptoms of Parkinson's disease, such as tremors and stiffness, and improving motor skills. This drug has also been shown to have a good tolerability profile, with few side effects reported. Rotigotine is rapidly absorbed from the gastrointestinal tract and metabolized by CYP2D6 into desalkyl rotigotine, which are pharmacologically inactive compounds. The mean terminal half-life for rotigotine is about 2 hours.</p>

<p>5,5'-Diamino-2,2'-bipyridine is an acidic metalloporphyrin that has been shown to react with epoxides to form nucleophilic adducts. This compound can be used as a ligand for lanthanide ions and reacts with aminopyridine to form bromoethane. 5,5'-Diamino-2,2'-bipyridine has been shown to have carcinogenic properties and may induce bromoethane mutagenicity in the liver. This compound is also mutagenic when added to propylene carbonate. 5,5'-Diamino-2,2'-bipyridine is luminescent in air or water when exposed to UV light.</p>

<p>(2S)-N-Boc-2-amino-4-azido-butanoic acid methyl ester is a high quality, reagent, complex compound, useful intermediate, fine chemical that is used as a building block in the synthesis of speciality chemicals.</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-(Aminooxy)ethanol is an organic compound that has the chemical formula CH3NOCH2CH2OH. It belongs to the group of cyclic ketones and is a colorless liquid with a boiling point of 78°C. This substance can be produced by dehydrogenation of ethylene oxide or by reaction of formamide with sodium hydroxide and hydrochloric acid. The product can also be prepared from 2-hydroxyethanol, which reacts with ethylene in presence of HCl. The reaction time for this process is around 1 hour at room temperature. The chemical formula for 2-(Aminooxy)ethanol is C4H11NO2O.</p>

<p>4-Dimethylaminostilbene is a stilbene derivative that is used in the laboratory as an inhibitor of protein synthesis. 4-Dimethylaminostilbene inhibits the activity of enzymes such as acid conjugates, which are enzymes that catalyze reactions involving the addition of an acid to a molecule. This drug has been shown to inhibit sarcoma cells and to be active against animals. 4-Dimethylaminostilbene reacts with proteins by forming adducts with amino groups on the side chains of lysine or arginine residues in proteins, thereby inhibiting their function. The reaction products are excreted from the body through urine and bile. 4-Dimethylaminostilbene can be administered orally, but it must be taken with acidic foods or drinks to prevent its destruction.</p>

<p>2,3-Diaminobenzamide is a synthetic aromatic compound that is used as a radiation stabilizer. It is also an effective antimicrobial agent with reactive properties against bacteria and fungi. 2,3-Diaminobenzamide has been shown to have anti-cancer properties and can be used to treat inflammatory diseases such as rheumatoid arthritis or ulcerative colitis. The intramolecular hydrogen bond between the amide group and the benzene ring in 2,3-diaminobenzamide contributes to its stability and biological activity.</p>

<p>3-Aminophenylacetylene is a colorless liquid that is soluble in water. It has a molecular weight of 123.14 and a chemical formula of C6H5CHNH2. The transport rate of 3-aminophenylacetylene can be determined by FT-IR spectroscopy, and the epidermal growth factor can be used for the determination of 3-aminophenylacetylene. The anhydrous sodium copper complex is formed by the reaction of 3-aminophenylacetylene with hydrochloric acid. There are two possible mechanisms for this reaction: one involves the formation of a diazonium salt, while the other involves an analytical method that uses hydrogen bond or molecular docking analysis to determine the structure of 3-aminophenylacetylene. High values are obtained when 3-aminophenylacetylene reacts with malonic acid and protein synthesis.</p>

<p>2-(3,5-Dimethyl-1H-pyrazol-1-yl)quinolin-8-amine is a fine chemical that belongs to the group of versatile building blocks. It can be used as a reagent or as a speciality chemical in research and development. 2-(3,5-Dimethyl-1H-pyrazol-1-yl)quinolin-8-amine is also a useful scaffold for the synthesis of complex compounds and has been shown to be an effective inhibitor of protein tyrosine kinases.</p>

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

<p>4-Benzyloxybenzylamine is a synthetic analogue of the amino acid phenylalanine. It is a potent inhibitor of the enzyme tyrosinase and has been shown to be effective in inhibiting cell proliferation and inducing apoptosis in melanoma cells. The drug also has a potential for use as an anti-aging agent, which may be due to its ability to block tyrosinase activity, thereby preventing the formation of melanin. 4-Benzyloxybenzylamine also shows strong antimicrobial effects against both gram-positive and gram-negative bacteria. This drug is being investigated for use as a skin protectant, especially in cases where there are immunosuppressive conditions such as human immunodeficiency virus (HIV) or organ transplantation.</p>

<p>2-Amino-6-morpholin-4-ylpyrimidin-4(3H)-one (2AP) is a versatile building block for the synthesis of complex compounds. It is used as a reaction component in organic chemistry, as well as a reagent for the synthesis of other chemical substances. 2AP is also useful as an intermediate in the production of pharmaceuticals, agrochemicals, and other research chemicals. 2AP has been shown to be useful in the synthesis of fine chemicals, such as amorphous silicon dioxide and polystyrene sulfonic acid. This substance can be used to make a variety of products with different properties, which makes it an excellent scaffold for research purposes.<br>2AP can be found under CAS number 37409-97-5.</p>