Amines

<p>(R)-3-(2-Amino-2-oxoethyl)-5-methylhexanoic acid (cis) is an intermediate in the synthesis of a chiral drug. It is prepared by a ring-opening reaction with an alkyl substituent, followed by asymmetric synthesis to provide optically pure cis stereoisomers. This compound has been shown to be active as a desymmetrizer of esters and as an intermediate in the synthesis of biologically active compounds.</p>

<p>4-Bromobutan-1-amine hydrobromide is a microtubule stabilizer that blocks the polymerization of tubulin and prevents cell division. It is activated by protonation and can be used to probe for cisplatin sensitivity. 4-Bromobutan-1-amine hydrobromide has been shown to have a high degree of specificity for cancer cells in culture, as well as sensitivity in animal models. This drug also has an excellent safety profile in humans and is an FDA approved chemotherapeutic agent.</p>

<p>3-Ethyl 1-adamantanamine hydrochloride is a versatile building block that is used as a research chemical. It is a reagent and speciality chemical, as well as an intermediate in the production of other compounds. 3-Ethyl 1-adamantanamine hydrochloride can be used as a high quality building block for the synthesis of other compounds. It has been shown to be useful in the synthesis of complex compounds.</p>

<p>4,6-Diaminopyrimidine is a potent inhibitor of epidermal growth factor receptor. It has been shown to inhibit the production of soluble guanylate cyclase and cGMP in vitro and in vivo. This drug has also been shown to inhibit cancer cell growth in vitro and in vivo. 4,6-Diaminopyrimidine has potential clinical relevance as an anticancer agent due to its ability to inhibit the kinases necessary for cancer proliferation. This drug also has pharmacokinetic properties that are favorable for anticancer drugs, including low plasma protein binding, high clearance rate, and short half-life. The activity of this drug was tested on hepg2 cells (human hepatoma) with an inhibitory effect on growth factor receptors such as EGFR and PDGFRs</p>

<p>N-(3-Methyl-2-propan-2-ylimidazol-4-yl)-N-oxidohydroxylamine is a chemical compound that has been shown to have antimicrobial activity in vitro. It interacts with the matrix effect and can be used as a chemotherapeutic agent. The molecule is also an analytical method for detection of cancer cells, which can be performed using a lc-ms/ms method.</p>

<p>(2-Aminophenyl)boronic acid hydrochloride is an analytical reagent that is used in the cross-coupling reaction between aryl bromides and organoboron compounds. It has been synthesized from 2-aminophenylboronic acid, which can be produced by the alkylation of phenol with 3-bromoquinoline. This compound has been shown to have antimalarial activity against the human malaria parasite Plasmodium falciparum in vitro. (2-Aminophenyl)boronic acid hydrochloride has also been shown to have a high intestinal absorption rate when given orally to rats. In vivo studies are needed to determine whether this chemical is safe for humans.</p>

<p>N-Boc-2-bromoethylamine is a chemical compound that is used as a gadolinium chelate. This molecule has been shown to be chemically stable and can be easily synthesized in high yield, which makes it an ideal candidate for use in cell culture experiments. The reaction solution of N-Boc-2-bromoethylamine with serine proteases, such as trypsin and chymotrypsin, has been shown to result in the formation of peptides with amide bonds at the C terminus. This process is called a "Michael addition." The 2-nitroimidazole group of N-Boc-2-bromoethylamine is potent inhibitor of protein kinases and has been shown to inhibit hypoxic tumor growth by inhibiting the uptake of glucose by cancer cells. It also has antimicrobial properties, acting as an affinity ligand for binding to bacterial or fungal cells.</p>

<p>2-(2-Methoxyphenoxy)ethylamine hydrochloride is a fine chemical with the CAS No. of 64464-07-9. It is a versatile building block that can be used as an intermediate for research chemicals, reaction components and specialty chemicals. This compound has been shown to work as a reagent in high quality synthesis.</p>

<p>4-Bromo-3-fluorobenzylamine hydrochloride (4BFBAH) is a compound that has been used in the past as a chemical intermediate. It is now being studied for use in boosting and stratigraphic research. This compound can be produced by reacting 4-bromo-3-fluorobenzoic acid with ammonia, and it has been shown to have waterlogging properties. 4BFBAH has also been shown to be useful in the analysis of infrastructures and socioeconomic conditions.</p>

<p>Quinolin-2-yl-methylamine is an amine that is used in the synthesis of other compounds. It can be prepared by protonation of quinoline with methylamine, followed by crystallization. The yield of this reaction is dependent on the purity of the starting materials and the reaction conditions. This compound has a molecular weight of 169.07 g/mol and a melting point at 217 °C. The infrared spectrum for Quinolin-2-yl-methylamine shows peaks at 2900 cm−1, 1670 cm−1, and 1590 cm−1. It also has x-ray crystallography data (space group P21/c).</p>

<p>Fmoc-12-amino-4,7,10-trioxadodecanoic acid is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Fmoc-12-amino-4,7,10-trioxadodecanoic acid is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>

<p>Ethyl (3-amino-3-cyanopropyl)methylphosphinate is a versatile building block that can be used as a reagent, speciality chemical, or research chemical. It is useful as an intermediate for complex compounds and can be used as a reaction component in the synthesis of high quality compounds. Ethyl (3-amino-3-cyanopropyl)methylphosphinate is also a useful scaffold in organic synthesis.</p>

<p>1-Aminopyrene is a chemical compound that has been shown to be an optical sensor for the detection of skin cancer. The compound reacts with nitrite ions in the blood, leading to a change in its optical properties. 1-Aminopyrene can be used as a tracer molecule and has been shown to be effective in tracking and imaging tumor cells in mice. This chemical is stable under most conditions and does not react with other chemicals, which makes it suitable for use in biological systems.<br>1-Aminopyrene is also able to inhibit microbial metabolism by reacting with nitrite ions, thereby inhibiting enzyme activity. It has been shown that this reaction may be due to the transfer of electrons from 1-aminopyrene to nitrite ions and the protonation of 1-aminopyrene by a hydroxyl ion.</p>

<p>4-Amino-N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isobutylbenzenesulfonamide is an amide that is used to treat HIV infections. It has been shown to have potent anti-viral activity against HIV infected cells in the laboratory and can inhibit the replication of HIV by interfering with the virus's ability to use the reverse transcriptase enzyme. 4ABAB has been shown to bind to the enzyme ribonuclease H (crth2), which is responsible for breaking down viral RNA. This binding prevents crth2 from cleaving viral RNA, thus inhibiting DNA synthesis and preventing cell death. 4ABAB also interferes with a hydrogen bond between ethyl group and the hydroxyl group on crth2, leading to a decrease in activity.</p>

<p>Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>

<p>4-Isocyanato-N,N-dimethyl-benzenamine is a chemical compound that is used as an intermediate for the synthesis of dyes and pigments. It is also used as a reagent in analytical methods involving fatty acids or oxysterols. 4-Isocyanato-N,N-dimethyl-benzenamine can be detected using a variety of techniques, including chromatography with on-line mass spectrometric detection and gas chromatography with electron ionization mass spectrometry. This chemical compound can be found as two stereoisomers: <br>4-(1'-methylpropyl)phenyl isocyanate;<br>4-(2'-methylpropyl)phenyl isocyanate.</p>

<p>Ancamine T is an amine curing agent, which is derived from synthetic chemical processes, specifically developed for use in epoxy systems. Its mode of action involves catalyzing the cross-linking reaction between epoxide groups in epoxy resins, leading to the formation of a highly cross-linked, thermoset polymer network. This curing process is essential for achieving the desired mechanical, thermal, and chemical resistance properties of the final product.</p>

<p>3-Amino-4-chlorobenzamide is an organic compound that belongs to the class of aminobenzoic acids and is used as a coupling agent in organic synthesis. It reacts with aryl halides or halides to form 3-amino-4-chlorobenzonitrile, which can be converted into anilines by heating with ammonia and ammonium chloride. This reaction has been shown to be reversible with heat. 3-Amino-4-chlorobenzamide is also used as a water absorber in paper products, such as diapers and sanitary napkins.</p>

<p>2-Aminochrysene is a chemical that binds to DNA and causes a genotoxic effect. It has been shown to be carcinogenic to rats and is carcinogenic in humans. 2-Aminochrysene is metabolized by conjugation with glucuronic acid or glutathione, which are found in the liver, kidney, and other tissues. The binding constants for 2-aminochrysene were measured using the calf thymus DNA as a substrate and amines as ligands. Transfer of 2-aminochrysene from the plasma membrane to the cytosol was observed in cells treated with nitrous oxide (NO). The cytosolic enzyme binding assay showed that 2-aminochrysene binds to the S9 protein of hepatic microsomes.<br>2-Aminochrysene has also been shown to inhibit phospholipase A2 activity, which may be due to its ability to bind to the enzyme's active site.</p>

<p>Brompheniramine is a non-sedating antihistamine with a variety of uses. It has been shown to inhibit the release of histamine and other mediators from mast cells, thereby preventing allergic reactions, such as hay fever, asthma, and chronic urticaria. Brompheniramine is also used for its sedative properties in the treatment of insomnia. Brompheniramine is a versatile building block that can be used to create complex compounds for research purposes or as speciality chemicals for high-quality fine chemical production.</p>

<p>1-Boc-1,8-diaminooctane is a polymerase that is used in the synthesis of DNA. It has been shown to be able to cleave supercoiled DNA and bind to acidic surfaces. This compound is fluorescent and can form covalent adducts with nucleic acids. 1-Boc-1,8-diaminooctane also has a piperidine group, which can act as a linker for other molecules such as anthracene. 1-Boc-1,8-diaminooctane is a neutral pH compound that reacts well with biomolecules.</p>

<p>4-Aminobenzophenone is a molecule that is used in the synthesis of diazonium salts. It has been shown to be an effective UV absorber and light emitter. 4-Aminobenzophenone is also able to coordinate with amine groups and hydrogen bonding, which allow it to form intermolecular bonds with other molecules. 4-Aminobenzophenone can be used in surface methodology as a cavity or as a hole on the surface of a material. 4-Aminobenzophenone has been shown to have an immune reaction when exposed to sunlight and emit light at wavelengths between 300 nm and 400 nm. This compound also reacts with carbonyl groups, which are found in quinoline derivatives, forming hydrogen bonds.</p>

<p>1-(3-Aminopropyl)pyridin-2(1H)-one HCl is a fine chemical that belongs to the group of heterocyclic compounds. It is a versatile building block that can be used as an intermediate or a scaffold in chemical synthesis. 1-(3-Aminopropyl)pyridin-2(1H)-one HCl is soluble in water and has been shown to react with a variety of other compounds, including amines, alcohols, thiols, and phenols. This compound also has high quality and can be used for research purposes.</p>

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

<p>2-Methylthiopyrimidine-4,6-diamine is a potent inhibitor of the enzyme DNA polymerase. It has shown to be effective against hepg2 cells and other cancer cells. The compound binds covalently to the active site of the enzyme, where it stabilizes the transition state and deshields the electrostatic field around the nucleophilic nitrogen atom. This interaction leads to a decreased affinity for ATP, which is required for DNA synthesis. 2-Methylthiopyrimidine-4,6-diamine also has antimalarial activity and inhibits amide bond formation in hepg2 cells.</p>

<p>Triethylamine hydrochloride is a potential drug target and can be used to treat infectious diseases. Triethylamine hydrochloride inhibits the polymerase chain reaction, which is an important analytical technique for the detection of DNA sequences. It also has been shown to have antibacterial activity against Escherichia coli by inhibiting protein synthesis in bacteria. This may be due to its ability to form metal chelates with Fe3+, Cu2+, and Mn2+. Triethylamine hydrochloride has also been shown to inhibit the growth of Shigella flexneri and Mycobacterium tuberculosis by regulating transcription elongation through interaction with the RNA polymerase.</p>

<p>N-(tert-Butoxycarbonyl)-1,4-diaminobutane is a cationic polymer that is used for transfection. It has been shown to have high efficiency in the transfection of DNA into cells and polymers that are biodegradable and can be dissolved in water. This chemical compound also has an acidic pH range, which makes it useful for the treatment of intracellular environments with a low pH. N-(tert-Butoxycarbonyl)-1,4-diaminobutane has been shown to cause cytotoxicity in cells at high concentrations, but has no effects on cells at lower concentrations. The disulfide bonds of this compound make it endosomal-lytic and nonviral.</p>

<p>4-(Dimethylamino)pyridine, polymer-bound (4DAP-P), is a chemical compound that belongs to the aminopyridine class of compounds. 4DAP-P has been shown to have antibacterial efficacy against bacteria such as Escherichia coli and Klebsiella pneumoniae in vitro assays. It also has anti-inflammatory properties and can be used for the treatment of inflammatory bowel disease. 4DAP-P is not absorbed through the skin or mucus membranes, but can be taken orally with food or liquid. The polymer-bound form of 4DAP-P has been shown to be more stable than its free form, which may make it a better choice for some applications.</p>

<p>Methyl trioctyl ammonium chloride is a quaternary ammonium compound that is used as a surfactant in a variety of applications. It has been shown to have an adsorption isotherm with a Langmuir type of behavior and it can be used as an optical sensor for water vapor. Methyl trioctyl ammonium chloride has covalent links with other molecules, such as chloride ions. The chemical composition of the nanoparticles of this chemical are determined by surface methodology, such as plasma mass spectrometry or electrochemical impedance spectroscopy. Methyl trioctyl ammonium chloride has been shown to reduce nitrite ion and sodium citrate in wastewater treatment systems. This agent also exhibits physiological effects on animals and humans, including toxic effects on the central nervous system, liver toxicity, and reproductive toxicity.</p>

<p>3,5-Dihydroxybenzylamine hydrochloride is a high quality chemical used as a reagent for organic synthesis. It has also been used as an intermediate for the production of other chemicals and in the synthesis of complex compounds. 3,5-Dihydroxybenzylamine hydrochloride is also a useful scaffold for drug design and development. It can be used to make fine chemicals with various applications such as research chemicals, versatile building blocks, reaction components, and speciality chemicals.</p>

<p>Fmoc-beta-Ala-4-amino-D-Phe(Boc)-OH is a fine chemical that can be used as a building block in research, as a reagent for chemical synthesis, or as a speciality chemical. It is also a versatile building block that can be used to create other compounds. Fmoc-beta-Ala-4-amino-D-Phe(Boc)-OH is an intermediate compound and scaffold. This compound has been shown to react with ethyl chloroformate to yield the corresponding beta amino ester.</p>

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

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<p>N,N-Diallyl-5-methoxytryptamine (DMAT) is a synthetic cannabinoid that has been shown to produce effects similar to those of tetrahydrocannabinol. It has been used in clinical studies to study the effects of cannabinoids on the central nervous system. DMAT binds with high affinity to 5-HT2A receptors and low affinity to histamine H1 receptors. DMAT also binds moderately with 5-HT1A receptors, which are serotonin receptors found in the cerebral cortex and hippocampus regions of the brain. DMAT is a potent monoamine neurotransmitter reuptake inhibitor, which means it prevents the reuptake of monoamines such as dopamine, norepinephrine, and serotonin by blocking their transporters. This results in an increase in extracellular concentrations of these monoamines. DMAT is structurally similar to other drugs that have been shown to cause seizures, such as meprobamate, benzodiazepines,</p>

<p>Trimipramine is an antidepressant drug of the tricyclic type. It is used in the treatment of depression, anxiety, and insomnia. Trimipramine also possesses anti-cancer effects and has been shown to inhibit prostate cancer cells. In addition, trimipramine inhibits the accumulation of cholesterol by inhibiting its synthesis.<br>Trimipramine maleate salt is a maleate salt of trimipramine that is soluble in water and alcohols. The biological properties and pharmacological treatments are similar to those of trimipramine.</p>

<p>Methyl 2-amino-3,4-diethoxybenzoate is a chemical compound that is used as a reagent for the preparation of other complex compounds. Methyl 2-amino-3,4-diethoxybenzoate has a CAS number of 1017083-69-0 and can be found in fine chemicals, research chemicals, and speciality chemicals. This chemical is also an intermediate for the synthesis of other compounds and has been shown to have many uses as a building block for more complex compounds. As a versatile building block, methyl 2-amino-3,4-diethoxybenzoate has been used in organic synthesis reactions to produce new compounds with unique properties.</p>

<p>Rhodamine B is a fluorescent dye that has been used as a model system to study the effects of drugs on P-glycoprotein (P-gp) function. It has been shown to inhibit P-gp function by binding to the transporter protein, which is responsible for pumping drugs and other compounds out of cells. Rhodamine B can be used as a probe for P-gp activity in cell lines, including squamous carcinoma cells, and can also be used to measure drug efflux from cells.<br>Rhodamine B was found to have an optimum concentration of 10 μM and a structural analysis showed it forms a complex with the transporter protein.</p>

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

<p>4-Amino-3-chloro-a-[(1,1-dimethylethyl)amino]methyl]-5-(trifluoromethyl)benzenemethanol (4ACBEM) is a fluorescent probe for the detection of intracellular Ca2+ levels. It binds to ryanodine receptors in the plasma membrane and can be used as a marker for Ca2+ mobilization in cells. 4ACBEM is used in flow cytometry and has been shown to bind to human serum albumin and other proteins with high affinity. The pharmacokinetics of 4ACBEM has been studied in rats, showing that it is eliminated by hepatic metabolism. This compound has also been shown to have no toxic effects on fetal bovine liver cells in vitro, although it does exhibit some interactions with the matrix that are dependent on the concentration of Ca2+.</p>

<p>3-Aminobutan-1-ol is an amine that is synthesized industrially by the reduction of soybean trypsin with borohydride. This chemical has been used as a substrate in asymmetric synthesis and can be detected by high detection sensitivity. 3-Aminobutan-1-ol binds to the carbonyl group of amino acid residues and causes a reaction with chloride ions for detection. The product of this reaction is an enantiomer, which can be separated from other reaction products by purified chiral stationary phases. 3-Aminobutan-1-ol is also involved in the biosynthesis of proteins and enzymes. It reacts with hydrochloric acid to form a salt, which can then be used as an enzyme inhibitor.</p>

<p>5-Aminoisophthalic acid is a molecule that belongs to the group of compounds classified as p2, which are characterized by a hydrogen bond. The molecule is synthesized from n-dimethylformamide and glycol ester. It can be used in the synthesis of other compounds, such as 5-aminoisophthalic acid, which has been shown to have hemolytic activity. FTIR spectroscopy analysis reveals that the structure of 5-aminoisophthalic acid has nitrogen atoms in its side chain. This molecule also has an ultraviolet absorption range of about 225 nm to about 300 nm and shows strong absorption bands at around 290 nm and 350 nm.</p>

<p>6-Amino-7-hydroxy-4-methylcoumarin is an antibacterial agent that has been shown to be effective against a range of Gram-positive and Gram-negative bacteria. It is synthesized from coumarins in nature, but also can be synthesized in the laboratory. This compound has been shown to inhibit bacterial growth by forming a covalent bond with the bacterial enzyme DNA gyrase, preventing the synthesis of DNA. 6-Amino-7-hydroxy-4-methylcoumarin has also been shown to have anti cancer properties.</p>

<p>4-Bromo-2-methylbenzylamine hydrochloride is a high quality, versatile building block that can be used in the synthesis of many different compounds. It is a reagent that can be used as an intermediate in the production of other compounds. 4-Bromo-2-methylbenzylamine hydrochloride is also a fine chemical and speciality chemical that can be used for research purposes. This compound has been shown to be useful as a reaction component in the synthesis of complex compounds.</p>

<p>4-N-Hexylbenzylamine is a fine chemical that is useful as a building block in the synthesis of complex compounds. It can be used as an intermediate in research chemicals, reaction components, and speciality chemicals. 4-N-Hexylbenzylamine has many uses in chemistry, including being a reagent to synthesize other compounds. This compound is also a versatile building block for the preparation of various amines and amides.</p>

<p>3-Amino-4-bromophenol is an industrial chemical that is used in the diazotization and reduction reactions. 3-Amino-4-bromophenol can be synthesized by reacting hydrazine with iron oxide and nitrite in a condition of acetone and sodium nitrite. The product yield for this reaction is about 90%. 3-Amino-4-bromophenol crystallizes from acetone as a white powder.</p>

<p>5-Fluorotryptamine hydrochloride (5FTH) is a chlorinating agent that is used to treat oxidative injury. It has been shown to inhibit tumor growth in animal models. 5FTH is taken up by tissues and reacts with hypochlorous acid to form 5-fluoro-2,4-diaminobenzoic acid and chloride ions. The chloride ions react with the molecule or the radiotracer to produce the thermodynamic depolarization of hydrogen atoms, which leads to hyperpolarization of the molecule and positron emission.</p>

<p>cis-(+/-)-2-[(N-Benzyl-N-methyl)aminomethyl]-1-(3-methoxyphenyl)cyclohexanol hydrochloride is a versatile building block that can be used in the synthesis of complex compounds. This compound is also a useful reagent, speciality chemical, and reaction component. cis-(+/-)-2-[(N-Benzyl-N-methyl)aminomethyl]-1-(3-methoxyphenyl)cyclohexanol hydrochloride has been shown to be a valuable scaffold for research chemicals with high quality.</p>

<p>4-Amino-3-chlorobenzonitrile is a ligand that binds to the heme of cytochrome P450 (CYP) enzymes. It has been shown to have a pharmacokinetic profile in rats and mice with lung diseases, which is similar to that of 4-amino-2-bromobenzonitrile. This ligand inhibits CYP enzymes by competing with endogenous substrates for binding sites on the heme, leading to an increase in the metabolism of drugs such as carbonyl drugs. 4-Amino-3-chlorobenzonitrile also has potent inhibitory effects on efflux pumps in cells and may be used to treat drug resistant bacteria.</p>

<p>Boc-1,4-trans-diaminocyclohexane hydrochloride is a versatile building block that can be used to synthesize complex compounds and research chemicals. It has been used as a reagent, specialty chemical and useful intermediate in many different reactions. Boc-1,4-trans-diaminocyclohexane hydrochloride is also a high quality building block that can be utilized to produce pharmaceuticals, agrochemicals and other speciality chemicals. This compound is also an important scaffold for the synthesis of biologically active molecules.</p>

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<p>Propyl 4-aminobenzoate is an anti-angiogenic agent that inhibits the production of angiogenic factors. It has been shown to be effective in vivo with a kinetic data analysis and solubility data. Propyl 4-aminobenzoate reduces the size of angiogenic tumors and prevents new tumor formation. It also suppresses tumor growth by inhibiting the production of vascular endothelial growth factor (VEGF), thereby inducing apoptotic cell death. The induction of apoptotic cell death by propyl 4-aminobenzoate may be due to its ability to bind to and activate apoptosis protein, leading to a decrease in collagen synthesis and an increase in hyaluronic acid production.</p>

<p>2-Amino-5-nitro-2'-fluorobenzophenone is a prodrug that is activated by thiourea, a chemical agent that is used to break down the drug. It is an anti-inflammatory drug that acts as a selective COX inhibitor and has been shown to be effective in vivo against primary tumors. 2-Amino-5-nitro-2'-fluorobenzophenone has also been shown to have antiangiogenic properties and has been used to treat inflammatory diseases such as arthritis and psoriasis. This drug can be radiolabeled with carbon, fluorine, or iodine isotopes for use in positron emission tomography (PET) imaging of primary tumors. The drug binds to response elements on cells through electrostatic interactions between the molecular orbitals of the 2 amino groups and the nucleophilic centers of these molecules.</p>

<p>N-Methyl-N-phenylazetidin-3-amine hydrochloride is a white solid with a melting point of 175°C. It is soluble in water, ethanol, and ether. N-Methyl-N-phenylazetidin-3-amine hydrochloride is an intermediate for the synthesis of chemical compounds that are used in research and development. This compound can be used as a building block to create complex compounds with biological activity. It can also be used as a scaffold to create novel chemical compounds that have not been observed before. The quality of this chemical is high, making it suitable for research purposes.</p>

<p>2-Ethoxybenzylamine is a hydrophobic organic compound. It is an amine that is used as a reagent for the oxidation of primary, secondary, and tertiary amines to their corresponding aldehydes, ketones, and quinones. 2-Ethoxybenzylamine is used in the synthesis of glycopeptides and has been shown to be effective as a surrogate for benzylamine derivatives. This compound may also be an optimised enzyme complex with chloride ions that can activate certain oxidases.</p>

<p>Fmoc-(S)-4-amino-2-carboxymethyl-1,3,4,5-tetrahydro-2H-[2]benzazepin-3-one is a specialized chemical compound, which is an Fmoc-protected amino acid derivative. This compound is synthesized through a series of organic synthesis steps that incorporate chiral precursors to ensure enantiomeric purity. As a building block for peptide synthesis, it acts by introducing a protected amino function into the peptide chain, providing stability and selectivity during the synthesis process.The primary applications of Fmoc-(S)-4-amino-2-carboxymethyl-1,3,4,5-tetrahydro-2H-[2]benzazepin-3-one are in the fields of medicinal chemistry and drug discovery, where it plays a crucial role in the development of novel peptide-based therapeutics. This compound is particularly valuable due to its ability to enhance the bioavailability and metabolic stability of peptides, allowing for the exploration of new therapeutic pathways and functions. Its use is integral in the design of peptides with specific biological activities, facilitating research into new pharmacological agents and treatments.</p>

<p>2,6-Pyridinediyldimethanamine is a reactive molecule that can be used in clinical studies. It has been shown to have an effect on mammalian cells, and it can also be used for structural studies of the molecule. This compound is mainly used as a chelate ligand in hydrogen bonding reactions. The kinetic of the reaction between 2,6-pyridinediyldimethanamine and chloride has been studied experimentally and found to follow second-order kinetics. X-ray crystal structures show that this compound forms a hydrogen bond with chloride ions.</p>

<p>4-Phenoxybenzylamine is a cardiac stimulant that belongs to the group of l-type calcium channel blockers. It is a highly potent and selective blocker of voltage-gated L-type calcium channels in myocytes, which are cells that make up the muscle tissue of the heart. 4-Phenoxybenzylamine has been shown to be effective against resistant strains and can be used to optimize sodium channels in recombinant cells. This drug also blocks potassium channels, which may lead to an antiseizure effect. 4-Phenoxybenzylamine is hydrophobic and can be given orally.<br>END&gt;&gt;</p>

<p>Rhodamine B isothiocyanate (RBITC) is a fluorescent dye that can be synthesized by reacting 2,4-dinitrobenzene with aniline. RBITC fluoresces in the visible spectrum, but has also been shown to fluoresce in the near infrared region of the electromagnetic spectrum. The microstructural and morphological properties of RBITC have been studied using simulations methods such as molecular dynamics and Monte Carlo techniques. RBITC has a spinodal decomposition behavior when heated or cooled, which can be used to study transport pathways in solids. These pathways are motivated by connectivity and topological techniques.</p>

<p>Tetrahexylammonium hydrogensulfate is a salt that is used in analytical chemistry to separate 3-mercaptopropionic acid from fatty acids. It is also used as a buffer in the chemical ionization mass spectrometry method for detection of cyclohexane ring. The separation of 3-mercaptopropionic acid from fatty acids can be achieved by using chromatographic science, which involves a co2 flow and chloride gas. This process has been shown to be effective for the analysis of urine samples, human serum, and hydrochloric acid. The reaction products are fatty acids and their derivatives, which are separated by chromatographic methods.</p>

<p>2,4-Diaminobenzaldehyde is a chemical compound that is used as an intermediate in the synthesis of drugs and other organic chemicals. It can be oxidized with periodate to produce 2,4-diaminophenol. This reaction system can then be desilyated to produce 2,4-diaminoanisole. Reaction time has a significant effect on the yield of this reaction system. The optimal dosage of periodate for this reaction system is 0.5 mM for 2,4-diaminophenol and 0.1 mM for 2,4-diaminoanisole. This reaction system can also be carried out using lavendamycin or tosyl chloride instead of periodate. The conversion efficiency of this reaction system is dependent on the presence or absence of methyl esters in the starting material and product.<br>END&gt;</p>

<p>D-alpha-Aminosuberic acid is a tetrapeptide with transcriptional regulatory properties. It has been shown to have minimal toxicity and lacks enzymatic inactivation, making it an attractive candidate as a drug for the treatment of cancer. D-alpha-Aminosuberic acid has been found to activate rat striatal cells in vitro and may have immunomodulatory effects that could be beneficial in infectious diseases. Clinical studies are needed before this drug can be used for these purposes.</p>

<p>Aminomethylphosphonic acid has proven action as a mimetic of both D- and L-alanine; it acts as an inhibitor of cell wall enzymes such as D-Ala-D-Ala synthetase, alanine racemase (JAA02406), and UDP-N-acetylmuramyl-L-alanine synthetase</p>

<p>2-Amino-4-(trifluoromethyl)benzoic acid (2ATB) is a fluorescent compound that is used in assays to study the function of cells. It is a functional theory that 2ATB binds to the skeleton of cells, which are then subjected to optical properties testing. Fluorescence resonance energy transfer has been shown to occur between 2ATB and retinoic acid molecules in the cell nucleus, which may be related to cellular senescence. The structure of 2ATB has been determined by X-ray crystallography and it has been synthesized by halogenation.</p>

<p>The molecular formula of methylamine is CH3NH2. It has an intramolecular hydrogen bond that stabilizes the molecule. Methanol is a good solvent for methylamine, and its ph optimum is 10. Methylamine reacts with hydrochloric acid to form a molecule consisting of two hydrogen atoms and one nitrogen atom (H3N-HCl). The locomotor activity of rats was reduced by methylamine after administration at doses greater than 200 mg/kg. The uptake of methylamine in human serum was increased by α-tocopherol, an antioxidant. Methylamine reacts with amines to form products with different properties, including alkanoic acid and fatty acid. Methylamine binds to the type strain receptor but not other strains or species of bacteria.</p>

<p>Tetramethylammonium acetate monohydrate is an on-line, inorganic acid that reacts with other reagents to form hydrogen bonds. Tetramethylammonium acetate monohydrate is used as a reactive solvent for organic solutes and has been used in hydrophilic interaction chromatography to separate fatty acids and phenolic acids. This compound has been shown to be effective in the treatment of chronic bronchitis due to its ability to break down mucus.</p>

<p>Thiamine monophosphate chloride dihydrate is a form of the vitamin thiamine. It has been used in control analysis to measure the activity of enzymes that require thiamine as a cofactor, such as transketolase and pyruvate kinase. Thiamine monophosphate chloride dihydrate has also been studied in biochemical properties, where it was found that this compound can be cleaved by picolinic acid to form thiazole phosphate. The matrix effect is an important factor in polymerase chain reactions and has been shown to be dependent on the presence of dinucleotide phosphate. This compound is an essential component of energy metabolism and plays a role in protein synthesis. Thiamine monophosphate chloride dihydrate also has toxicological studies, including a model system using wild-type strains of yeast. These studies have shown that this compound leads to physiological effects such as inhibition of glycolysis and lactic acid production.</p>

<p>(1-tert-Butylcyclopropyl)amine hydrochloride is a ciprofloxacin analog that inhibits the growth of bacteria by binding to the enzyme DNA gyrase. It also prevents the cleavage of RNA and protein synthesis which blocks the production of new cells in bacterial colonies. The drug has a broad spectrum of activity against Gram-positive and Gram-negative organisms, including methicillin-resistant Staphylococcus aureus (MRSA). The drug has been shown to be effective against isolates resistant to ciprofloxacin, such as Enterobacteriaceae, Pseudomonas aeruginosa, Acinetobacter baumannii, and Klebsiella pneumoniae. <br>(1-tert-Butylcyclopropyl)amine hydrochloride binds to microtubules and disrupts the cell division process during mitosis. This drug has been shown to inhibit spindle formation in</p>

<p>Tris(dimethylamino)sulfonium difluorotrimethylsilicate is a solute that is used in synthetic chemistry. It has been shown to stimulate bone growth in vitro and to inhibit the metastasis of cancer cells in animal studies. Tris(dimethylamino)sulfonium difluorotrimethylsilicate has also been shown to be an effective treatment for bladder cancer. This compound has been shown to bind to cortistatin, an active substance that inhibits the proliferation of human bladder cancer cells. The compound binds to benzyl groups on cortistatin and prevents it from binding with its receptors on the bladder cancer cells, leading to cell death.</p>

<p>2,3,5-Trifluorobenzylamine hydrochloride is an important chemical building block that is used in a variety of chemical reactions. It can be used as a reagent to form 2,3,5-trifluorobenzaldehyde and other useful chemicals. The compound also has the ability to be used as a versatile building block in synthetic organic chemistry. 2,3,5-Trifluorobenzylamine hydrochloride is an intermediate in the synthesis of various pharmaceuticals and pesticides. The compound also has potential use as a scaffold in drug design applications.</p>

<p>5-Amino-1,3,4-thiadiazole-2-sulfonamide is a chemical compound that inhibits the growth of skin cancer cells. It has inhibitory properties against choroidal neovascularization induced by dorzolamide hydrochloride and other pharmacological agents. 5-Amino-1,3,4-thiadiazole-2-sulfonamide has also been shown to have antiangiogenic activity in vitro and in vivo assays. 5ATTS inhibits the growth of bacteria and fungi by inhibiting fatty acid synthesis. The drug also has been shown to be effective in treating diabetic neuropathy and fluorescein angiography associated with itchy eyes.</p>

<p>1-Aminoindane HCl is an inhibitor of the enzyme aminotransferase, which is involved in the metabolism of amines. It binds to the active site of this enzyme and prevents it from catalyzing its usual reaction. 1-Aminoindane HCl has been shown to inhibit 5-hydroxytryptamine uptake and release in rat brain synaptosomes. This drug also inhibits the binding of a number of drugs (e.g., amphetamine) to their receptors on plasma membranes and blocks the binding of drugs such as pargyline and α-methylparatyrosine to their receptors on mitochondria. 1-Aminoindane HCl is also a competitive inhibitor for primary amines such as tyramine and phenylethylamine.</p>

<p>(R)-2-Amino-1-phenylethanol is a molecule that has antimicrobial activity. It binds to the active site of bacterial enzymes, such as those involved in the synthesis of cell walls, and inhibits the growth of bacteria through competitive inhibition. This molecule also has a dihedral angle that is similar to that of other molecules with antibacterial activity. (R)-2-Amino-1-phenylethanol is an enantiomer, which means it can be synthesized from either (S)- or (R)-1-phenylethanol. The racemic form is more active than any individual enantiomer.</p>

<p>Please enquire for more information about 2-[[(4-Acetylphenyl)amino]methylene]-5,5-dimethyl-1,3-cyclohexanedione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Boc-ethylenediamine is a chemical compound that belongs to the group of peptide hormones. It is historically used as a building block for peptides, such as luteinizing hormone releasing hormone (LHRH), which control reproduction and regulate the release of hormones. N-Boc-ethylenediamine has been shown to inhibit dpp-iv, an enzyme that breaks down proteins needed for cell growth and survival. This inhibition leads to cell death by apoptosis, or programmed cell death. N-Boc-ethylenediamine has also been shown to be an antimicrobial peptide against gram negative bacteria. The synthesis of this compound can be accomplished through several methods, including using diazonium salt or histone proteins. The analytical method involves hydrogen bonding between the amines and trifluoroacetic acid in order to produce the desired product.</p>

<p>5-Amino-4,6-dichloropyrimidine is a fluorescent probe that can be used in the detection of nucleophiles. It has been shown to inhibit the growth of cells infected with herpes simplex virus and hl-60 cells. This compound has also been shown to have nicotinic acetylcholine receptor activity and can be used as an analog for purines. The nitrogen atoms in this molecule are responsible for its anti-cancer properties. 5-Amino-4,6-dichloropyrimidine binds to epidermal growth factor (EGF) and blocks its binding site on the cell surface, reducing cancer cell proliferation. Benzyl groups on either end of this molecule act as a protective group against acid hydrolysis, making it stable in acidic environments such as stomach acid. This drug also contains chlorine atoms that make it easy to synthesize and purify by reacting with trifluoroacetic acid.</p>

<p>[2-(3-Methylphenoxy)ethyl]amine hydrochloride is a fine chemical that is a versatile building block. It can be used as a reaction component in the synthesis of complex molecules and as a reagent for the synthesis of speciality chemicals and research chemicals. This compound has been shown to react with nitric acid to form an amine salt, which is useful for the manufacture of pharmaceuticals. [2-(3-Methylphenoxy)ethyl]amine hydrochloride can also be reacted with chloroacetic acid to form an amine salt, which is useful for the manufacture of pesticides. The high quality and versatility of this compound make it a useful scaffold for many types of reactions.</p>

<p>4-Aminobenzotrifluoride is a chemical compound that belongs to the group of nitroso compounds. It has been shown to have antiproliferation activity in vitro and in vivo. 4-Aminobenzotrifluoride is synthesized by reacting sodium nitrite with p-hydroxybenzoic acid in the presence of an organic acid, such as acetic acid or formic acid, to produce diazonium salt. The diazonium salt is then reacted with an inorganic acid, such as hydrochloric acid or sulfuric acid. This reaction produces 4-aminobenzotrifluoride and water.</p>

<p>5-Aminotetramethyl rhodamine is a chemical that is used as a reagent, intermediate, and building block in the synthesis of organic compounds. This compound is useful as an intermediate in the synthesis of complex compounds, such as pharmaceuticals, agrochemicals, and other fine chemicals. 5-Aminotetramethyl rhodamine can also be used as a speciality chemical or research chemical. It has been shown to be a versatile building block in the synthesis of new compounds with potential use in applications such as medicine and electronics.</p>

<p>The heptafluoro-N,N-bis(1,1,2,2,2-pentafluoroethyl)propane-1-amine is a chemical compound that is used as an additive. This additive has been shown to be efficient in the removal of organic compounds such as benzene and toluene from water. It can also be used for the treatment of biofuel waste water. The heptafluoro-N,N-bis(1,1,2,2,2-pentafluoroethyl)propane-1-amine has shown to have a wavelength absorbance profile with a maximum at 370 nm in the ultraviolet region of the electromagnetic spectrum. This compound can also be used for barcoding and identification purposes in applications where human contact is required.</p>

<p>4-Bromo-6-amino-m-xylene is a chemical that is used to synthesize other chemicals. It is a versatile building block and can be used as an intermediate in organic synthesis. It has been shown to react with nucleophiles, such as alcohols, amines, and thiols. 4-Bromo-6-amino-m-xylene also reacts with metal halides to form complexes. This compound has been shown to have high quality and can be used in research or as a reagent for further reactions.</p>

<p>A 2-aminopyridine substituent is added to the 3-position of benzonitrile to form 2-amino-3-fluorobenzonitrile. The hydrogenolysis of this compound at low temperatures yields indoles. Cyanogen bromide can be used as a catalyst for the reaction, but it must be removed before the product is purified. This reaction also produces a cyano group, which can be used in other reactions such as nitration or reduction. The glycinate molecule can also be formed by this process, and it is a neutral functional group that is capable of forming esters with carboxylic acids.</p>

<p>Bromotrimethylammoniumbimane bromide is a fluorescent molecule that can be used as a probe for protease activity. It is also used to study the α1 subunit of the human histone deacetylase (HDAC) complex, which plays an important role in HIV infection and autoimmune diseases. The redox potential of Bromotrimethylammoniumbimane bromide has been shown to be dependent on its basic structure, with the disulfide bond being the most reactive. This chemical has been shown to have cytosolic Ca2+-dependent effects on cell signaling pathways, including induction of apoptosis and modulation of protein phosphatases.</p>