Amines

<p>(S)-(-)-1-Boc-3-aminopyrrolidine is an inhibitor that inhibits the activity of phosphoinositide 3-kinase (PI3K) by binding to the ATP binding site and inhibiting PI3K. It has been shown to inhibit the activation of PI3Kδ, which plays a key role in tumorigenesis and metastasis. The drug also has metabolic stability and selectivity for PI3Kδ over other kinases, as well as high affinity for this enzyme. The drug was found to have low toxicity in vitro, but its effects on humans are unknown.</p>

<p>Please enquire for more information about [(6-Chloro-1-isopropyl-1H-benzimidazol-2-yl)methyl]amine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N,N,N',N'-Tetramethyl-p-phenylenediamine is a chemical compound that has been found to have a high affinity for proteins and nucleic acids. It interacts with these molecules by steric interactions and can change the phase transition temperature of water. N,N,N',N'-Tetramethyl-p-phenylenediamine reacts with surfactant sodium dodecyl (SDA) to produce protonated SDA species. These protonated SDA species are able to react with nucleophiles such as p-hydroxybenzoic acid (PHBA), which leads to an exchange reaction. The redox potentials of PHBA and N,N,N',N'-tetramethyl-p-phenylenediamine vary from -0.85 V to -1.05 V at pH 7.4, depending on the number of nitrogen atoms in the molecule. The x-ray</p>

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

<p>Please enquire for more information about 2-Imidazo[1,2-a]pyridin-2-yl-ethylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-5-bromobenzonitrile is a bioactive substance that belongs to the class of amines. It is used as an intermediate in the production of other industrial chemicals, such as polyurethanes and polyamides. 2-Amino-5-bromobenzonitrile can be found in faeces at a concentration of approximately 1 µg/g. The metabolic pathway for 2-amino-5-bromobenzonitrile has been shown to be cyp3a5 dependent.</p>

<p>O-(Tert-butyldimethylsilyl)hydroxylamine is a stereospecific, oxidized, insoluble, tautomeric hydroxamic acid. It is used as a reagent in organic synthesis to form lactams by reaction with hexamethylenetetramine. The compound can be prepared by treatment of hydroxylamine with diacetate in the presence of aluminium chloride. The product is an orange liquid that crystallizes from water, but is not soluble in most organic solvents.</p>

<p>(S)-tert-Butyl 3-(methylamino)pyrrolidine-1-carboxylate is a research chemical that can be used as a versatile building block for the synthesis of complex compounds. It is also a reaction component in the synthesis of speciality chemicals and useful scaffolds. It has been shown to have high quality, reagent grade and purity.</p>

<p>Please enquire for more information about N-[3-Fluoro-4-[(methylamino)carbonyl]phenyl]-2-methylalanine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 5-Amino-3,7-dimethylxanthine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Tetrahydro-a-(1-naphthalenylmethyl)-2-furanpropanoic Acid 2-(Diethylamino)ethyl Ester is a fatty acid analog that has antimicrobial properties. It is used in the treatment of bone cancer, and can be used to diagnose and treat other diseases such as glomerular filtration rate, receptor binding, and malonic acid. Tetrahydro-a-(1-naphthalenylmethyl)-2-furanpropanoic Acid 2-(Diethylamino)ethyl Ester binds to receptors on cells, which leads to an increase in the amount of monoamine neurotransmitters released by the cells.</p>

<p>5-Aminobenzooxazole is a cox-2 inhibitor that has been shown to inhibit the growth of cervical cancer cells. It acts by inhibiting ubiquitin ligases, which are enzymes that regulate protein degradation. 5-Aminobenzooxazole has shown anticancer activity in vitro and in vivo and induces cell cycle arrest and apoptosis (cell death) of cervical cancer cells. The mechanism for this effect may be due to the ability of 5-aminobenzooxazole to disrupt the acidic environment of the tumor microenvironment. This drug also inhibits glutamate neurotransmitter release, leading to neuronal death. 5-Aminobenzooxazole is not active against normal cells because they lack the enzyme needed for this reaction.</p>

<p>2,6-Dichloro-5-nitropyrimidin-4-amine is a chlorinating agent that reacts with aliphatic and aromatic amines to form substituted pyrimidines. The substitution pattern of the product depends on the regioselectivity of the reaction. 2,6-Dichloro-5-nitropyrimidin-4-amine is one of the few chlorinating agents that react with propylamine. Substitution at position 2 of the purine ring has been found to be more selective than substitution at position 6. The 2,6-dichloropyrimidine can also be used as a nitro group source in chemical synthesis or as an intermediate in production of other compounds.</p>

<p>Please enquire for more information about (R)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 1-(4-Amino-3,5-dichloro-phenyl)-2-bromo-ethanone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 1-(Boc-amino)-4,9-dioxa-12-dodecanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about [(4-Methyl-1H-imidazol-5-yl)methyl]amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Diethylaminosulfur trifluoride (DAST) is a reactive chemical that can be used as a methylating agent. It reacts with the hydroxyl group of carotenoids, including β-carotene, to produce x-ray crystal structures with the alcohol methanol solvent. DAST also reacts with 6alkyl and methyl glycosides, such as sucrose, producing a hydroxy derivative. DAST has been shown to have carcinogenic properties in tumor cell lines and is able to induce apoptosis in these cells by damaging their DNA. The use of DAST for cancer treatment can be done through laser ablation or injection into tumors.</p>

<p>Please enquire for more information about 1-(Fmoc-amino)-4,9-dioxa-12-dodecanamine·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Amino-5,6,7,8-tetrahydronaphthalene-2,3-diol is a potent dopamine D2 receptor antagonist. It has been shown to inhibit the light emission of dopamine in vitro. This compound also has a high affinity for 5-HT receptors and has been shown to be a potent agonist at these sites. 6-Amino-5,6,7,8-tetrahydronaphthalene-2,3-diol has been found to induce pluripotent stem cells from human fibroblasts. These cells can differentiate into virtually any cell type in the body and may be used to study diseases such as Parkinson's disease and cancer.</p>

<p>Please enquire for more information about N,N'-Di-(4-methyl-phenyl)-N,N'-diphenyl-1,4-phenylendiamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about N-[(1S)-1-(Aminocarbonyl)propyl]-4-chlorobutanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Allylamine HCl content - max 7%</p>

<p>1,4-Dichloro 6-carboxytetramethylrhodamine is a rhodamine-class fluorescent dye with excitation/emission wavelengths of 541/568 nm.</p>

<p>Please enquire for more information about DABCYL-(Asn670,Leu671)-Amyloid b/A4 Protein Precursor770 (669-674)-EDANS ammonium salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The process of asymmetric epoxidation is used to convert alkenes into epoxides in a single step. This reaction is catalyzed by the use of a chiral catalyst with an enantiomeric excess (ee) greater than 50%. The reactants are added to the catalyst and hydrogen peroxide, which oxidizes the alkenes. The resulting epoxides can be isolated from the reaction mixture by distillation or extraction. Factors that affect this reaction include the type of reactant, solvent, temperature, and pressure.</p>

<p>Please enquire for more information about Boc-N-Methyl-gaMMa-aMinobutyric acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Aminomethyl resin is a polymeric solid that is used in peptide synthesis. It has been shown to interact with peptides and peptide fragments with high efficiency. Aminomethyl resin also has the ability to form specific interactions with amino acids and other molecules that are involved in the chemical synthesis of peptides. This resin can be used for screening and purification of peptides.</p>

<p>2-Aminoethanesulphonamide monohydrochloride is a perovskite with a hexagonal shape. It has been shown to interact with the pharmacophore of the enzyme cytochrome P450, and it has been optimized for the reaction by altering its structure. This product is soluble in gaseous form, but can also be used as a solid. 2-Aminoethanesulphonamide monohydrochloride has an absorption maximum at 325 nm and emits fluorescence at 420 nm. It is used in devices that detect ionizing radiation.</p>

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

<p>Dithiobis(3-mercaptopropionate) is an analog of 3-[(2-Aminoethyl)dithio]propionic acid (DTA). It has been used as a cross-linking agent for the synthesis of polymers with acidic pH. Dithiobis(3-mercaptopropionate) is also used for the synthesis of conjugates and bifunctional molecules. Dithiobis(3-mercaptopropionate) can be synthesized by reacting bis(sulfanylmethyl)amine with sodium azide in an acidic solution. The cross-linking reaction will produce a disulfide bond, which is a covalent linkage between two cysteine residues in two different polypeptides or proteins. This crosslink is irreversible, so it cannot be broken down by chemical processes, but can be broken down by enzymatic digestion.</p>

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

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

<p>Please enquire for more information about OM99-2trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>DDAVP is an analogue of vasopressin, which belongs to the class of inositol phosphates. It is a potent agonist for the V1 receptor and has a higher affinity for this receptor than vasopressin. DDAVP also has antagonist properties at the V2 receptor. The biological activity of DDAVP is mediated by its ability to increase phospholipase A2 activity and cause the release of arachidonic acid from membrane phospholipids. This activation causes an increase in prostaglandin synthesis, leading to increased vascular permeability and hypotension. DDAVP may also have antidiuretic effects due to its antagonism of oxytocin receptors.</p>

<p>Fencamine is a substrate molecule that is used in the synthesis of peptide hormones. It can be detected in urine samples and has been shown to be a synthetic cannabinoid. Fencamine can be used for diagnostic purposes. Fencamine has been shown to have matrix effects on the bowel disease, hepatitis, and hepatitis C., as well as exerting control analysis of the metabolite molecule. Fencamine has also been shown to have an effect on inflammatory bowel disease, hepatitis C., and toll-like receptor 2.</p>

<p>7-Diethylamino-4-methylcoumarin is a fluorescence probe that can be used in applications such as the study of hydrogen bonding interactions. It is excited by laser light and emits a red-shifted fluorescent light. 7-Diethylamino-4-methylcoumarin is a hydroxyl group analogue of coumarin, which has been shown to have physiological effects on the liver cells. The absorption spectrum of 7-Diethylamino-4-methylcoumarin is sensitive to changes in pH and chemical stability. A decrease in pH increases the intensity of the emission while an increase in pH decreases the intensity of the emission. This compound can also be used to label nucleic acids during polymerase chain reactions (PCR) or for sample preparation before analysis using nuclear magnetic resonance spectroscopy (NMR).</p>

<p>4-Amino-5-methoxy-2-methylbenzenesulfonic acid is a compound that has been used as an additive to analytical reagents in order to improve their sensitivity. This compound is used as the sodium salt, which is water soluble and has a high degree of reproducibility. 4-Amino-5-methoxy-2-methylbenzenesulfonic acid has also been used for the validation of analytical methods, including calibration and cytotoxicity testing. The validation procedure includes colorants, spectra analysis, impurities, and solvents.</p>

<p>(2R)-2-Aminopropanamide is a chemical compound that is classified as an amide. It has been shown to inhibit bacterial growth and induce apoptosis in mammalian cells, but not in bacteria. This drug has a number of hydrogen bonding interactions with the carbonyl group and amide functional groups and can bind to affinity ligands with hydrogen bonding interactions. (2R)-2-Aminopropanamide inhibits the activity of enzymes that are involved in the synthesis of d-alanine, which is a precursor for protein synthesis. It also inhibits the enzyme glutamine synthase, which plays a key role in building up nitrogen reserves in bacteria. The drug binds to DNA by forming hydrogen bonds with the phosphate backbone and intercalates into double-stranded DNA by forming van der Waals interactions with base pairs.</p>

<p>5-Aminopyridine-3-carboxylic acid (5APC) is a structural analog of nicotinic acid that has been shown to have anti-inflammatory effects. 5APC inhibits the production of inflammatory cytokines, such as IL-10 and IL-17, by inhibiting the activation of NFκB and MAPK pathways. This drug also has significant inhibitory activities against dextran sulfate sodium (DSS)-induced acute colitis in experimental models. 5APC is thought to act by interrupting the assembly of p38 mitogen activated protein kinase (MAPK) and nuclear factor kappa B (NFκB) signaling complexes.</p>

<p>N-Des(2-diethylamino) metoclopramide acetic acid is a benzyl ester of metoclopramide, a prodrug that is metabolized to the active form in the body. It has been shown to be effective against healthy human subjects and hplc analyses of biological samples have shown it to be a metabolite of metoclopramide. N-Des(2-diethylamino) metoclopramide acetic acid is used as a catalyst for catalytic hydrogenation reactions, such as the conversion of methyl esters into ethyl or butyl esters. It can also be used for catalytic hydrogenation reactions with diazomethane, such as those required for the synthesis of quinolones.</p>

<p>Tritylamine is an inorganic acid that is synthesized by the reaction of trifluoroacetic acid with ammonia. It can be used to treat autoimmune diseases, such as rheumatoid arthritis, and has been shown to have a beneficial effect on collagen synthesis. Tritylamine has also been studied as a fluorescent probe for the detection of metal ions in biological systems. Tritylamine has been used in asymmetric synthesis and can also inhibit enzymes that catalyze metabolic reactions.</p>

<p>Please enquire for more information about 3-[[[2-[(Aminoiminomethyl)amino]-4-thiazolyl]methyl]sulfinyl]-N-(aminosulfonyl)propanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 12-(Boc-aminooxy)-dodecanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about PAL resin (200-400 mesh) 4-Alkoxy-2,6-dimethoxybenzylamine resin including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fmoc-S-trityl-L-penicillamine is a coordination compound that contains a thiolate and amide group. It has been used as a model system for studying the interaction between proteins and metal ions, with the cyclic structure mimicking the active site of enzymes. The coordination of Fmoc-S-trityl-L-penicillamine to proteins is affected by trypsin, an enzyme that cleaves peptides at carboxyl side chains. Trypsin can also lead to dehydration of Fmoc-S-trityl-L-penicillamine, forming an eliminations product. This compound also reacts with lysine residues in proteins, resulting in an alkene byproduct that can be removed by hydrogenation.</p>

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

<p>Please enquire for more information about (2S)-2-Amino-4-methyl-1-[(2R)-2-methyloxiranyl]-1-pentanone trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-[(3,3-Diphenylpropyl)methylamino]-2-methyl-2-propanol is an epoxy that can be synthesized from benzene and lercanidipine. It has been used in the production of cinnamic acid and other molecules. This molecule can be prepared by reacting cinnamic acid with chloromethyl methyl ether in a ring-opening reaction. The chloride ion is utilized as a nucleophile to react with the amide nitrogen atom of the cinnamic acid molecule to form the amide bond. The large-scale production of 1-[(3,3-diphenylpropyl)methylamino]-2-methyl-2-propanol utilizes refluxing to remove water and other byproducts that are formed during the process.</p>

<p>Please enquire for more information about 3-Aminoazepan-2-one hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-6-fluorobenzoic acid ethyl ester is a chemical that can be used as a building block in the synthesis of more complex compounds. It is a versatile intermediate and can be used to synthesize other important compounds, such as pharmaceuticals. This compound has been shown to be useful for the preparation of 2-amino-4,6-difluorobenzoic acid ethyl ester and many other derivatives. The colorless solid is soluble in ether and dichloromethane.</p>

<p>Please enquire for more information about (3R)-3-[(tert-Butoxycarbonyl)amino]-4-(2,4-difluorophenyl)butanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<p>Please enquire for more information about DABCYL-(Asn670,Leu671)-Amyloid b/A4 Protein Precursor770 (667-675)-EDANS ammonium salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (S,S)-(-)-Bis(a-methylbenzyl)amine Hcl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-(2-Aminoethyl)-3-(trimethoxysilyl)propylamine (NAP) is a cationic surfactant that is used as a fluorescent probe to study the binding of proteins to cell surface integrin receptors. The adsorption mechanism is based on the interaction between the hydrophobic parts of the protein and the hydrophobic parts of NAP. This interaction leads to an increase in the concentration of NAP at the interface and thus an increase in fluorescence. NAP has been shown to bind human serum albumin, fatty acids, and monoclonal antibodies with high affinity. It also has been shown to bind to plasma proteins through hydrogen bonding. The optimum concentration for NAP adsorption is 1mM.</p>

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

<p>2-Amino-5-fluorobenzonitrile is a molecule that belongs to the class of amines. The vibrational spectroscopies and diffraction experiments show that this molecule has a strong dipole moment, which is due to the carbamic acid group. 2-Amino-5-fluorobenzonitrile has been shown to be chiral, which means it can exist in two different forms, one with a left and one with a right orientation of the atoms. This molecule can be used as an analyte for thermodynamic measurements and can be used as a reagent in organic synthesis reactions. It also has functional groups that are useful for vibrational spectroscopies.</p>

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

<p>L-2,3-Diaminopropionic acid is a diamine with an asymmetric carbon atom. It has been used to synthesize antimicrobial peptides and has also shown hemolytic activity in vitro. L-2,3-Diaminopropionic acid is stable when exposed to water vapor, which may make it useful for the treatment of cancer tissues. This molecule has been shown to have significant cytotoxicity against human leukemia cells and is able to inhibit the growth of various bacteria by inhibiting protein synthesis in the ribosome. L-2,3-Diaminopropionic acid also inhibits the enzyme enolase and reduces the production of ATP in cells.</p>

<p>Please enquire for more information about (4-((2-Methylphenyl)aminocarbonyl)-aminophenyl)acetyl-Fibronectin CS-1 Fragment (1980-1983) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Used in treatment of nonspecific ulcerative colitis</p>

<p>Please enquire for more information about 4-Piperidylformylaminomethyl resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<p>(3S)-3-(tert-Butoxycarbonyl)amino-1-chloro-4-phenyl-2-butanone is an organic compound that belongs to the class of carbonyl reductase. It is used as a catalyst for the transformation of secondary alcohols to ketones or aldehydes, including isopropyl alcohol. The reaction proceeds via an intermediate carboxylic acid. The enzyme has been found in various microorganisms, and can be purified from Bacillus megaterium and Streptomyces lividans. The enzyme’s activity can be inhibited by steric effects, metal ions, or other compounds. (3S)-3-(tert-Butoxycarbonyl)amino-1-chloro-4-phenyl-2-butanone crystallizes in two forms: one with the chiral center at the 3 position and one with it at the 4 position.</p>

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

<p>N'-Nitrosopentyl-(3-picolyl)amine is a research chemical that can be used as a reaction component, reagent, or intermediate. It is a high quality and versatile building block for the synthesis of complex compounds. N'-Nitrosopentyl-(3-picolyl)amine has been shown to be useful as an intermediate in the synthesis of drugs such as pentoxifylline and lodoxamide, which are used to treat respiratory diseases. This chemical is also used to synthesize other compounds that have speciality applications such as pharmaceuticals and rubber additives.</p>

<p>Please enquire for more information about Imidazo[1,2-a]pyridin-7-amine hydrobromide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Z-L-alpha-aminobutyric acid is a homogeneous, optically active, linear phosphinic analogue of alpha-aminobutyric acid. It has been used in the synthesis of phosphinic analogues of cyclosporin and undecapeptides with high yields. The coupling reaction between Z-L-alpha-aminobutyric acid and benzaldehyde was carried out in two steps to produce the desired product. A stepwise condensation between Z-L-alpha-aminobutyric acid and 3,4,5,6 tetrahydropyrimidine was also successful.</p>

<p>2-Amino-4-fluorobenzaldehyde is a plant growth regulator that has been shown to be effective at increasing the yield of flowers and fruit crops. It is used as an intermediate in the synthesis of agrochemicals, such as 2-aminobenzaldehyde and anthranilic acid. The biosynthesis of 2-amino-4-fluorobenzaldehyde starts from methanol and intermediates such as anthranilic acid, aminoaldehydes, or alcohols. It can also be produced by oxidative coupling of 2-aminobenzaldehyde with phenylacetone in the presence of sodium hydroxide. 2-Amino-4-fluorobenzaldehyde has been shown to be more efficient than other plant growth regulators such as robinia or aminocyclopentane carboxylic acid (ACC).</p>

<p>4-Hydroxybenzylamine is a reactive compound that belongs to the class of amides. It is found in dietary sources and has been shown to have antihypertensive effects. 4-Hydroxybenzylamine is also used as a chemical intermediate in the synthesis of other compounds, such as 4-hydroxybenzoic acid. The mechanism of this reaction involves hydroxylation of the amide nitrogen by an oxidizing agent, such as trifluoroacetic acid, followed by replacement of hydrogen atoms on the carbonyl carbon with a hydroxyl group. The bioavailability of 4-hydroxybenzylamine is low because it is rapidly metabolized in erythrocytes, liver cells, and lung tissue. This metabolite may be responsible for some side effects seen with 4-hydroxybenzylamine therapy, including cardiac arrhythmias and lysinuria.</p>

<p>N-Methyl-2-fluoro-4-aminobenzamide is a toxic compound that is commonly used as a reagent in chemical synthesis and research. It has been studied for its potential use in medicine, particularly in the treatment of castration-resistant prostate cancer. N-Methyl-2-fluoro-4-aminobenzamide acts as a nucleophilic agent, participating in reactions that involve the addition of an acyl group to a target molecule. Its stable formyl group allows for efficient reaction yields and reliable results. However, due to its toxic nature, caution must be exercised when handling this compound.</p>

<p>DL-3-Amino-3-phenylpropionic acid is an amino acid that is synthesized by the reaction of malonic acid and ethyl ester. This compound is a competitive inhibitor of the enzyme pyruvate carboxylase and inhibits this enzyme in the conversion of pyruvic acid to acetyl CoA, which plays a key role in metabolism. DL-3-Amino-3-phenylpropionic acid has been shown to inhibit the growth of bacteria such as Escherichia coli, Salmonella typhimurium and Staphylococcus aureus. The inhibition of pyruvate carboxylase by DL-3-Amino-3-phenylpropionic acid prevents the production of acetaldehyde from pyruvate, which is toxic to cells.</p>

<p>Tenofovir is a nucleoside analog reverse transcriptase inhibitor that binds to the RNA-dependent polymerase. This compound is used in combination with other antiviral agents for the treatment of HIV-1 infection and for prophylaxis against HIV-1 infection. Tenofovir has been shown to be effective against infections caused by strains of HIV-1, such as the drug resistant virus. Tenofovir is absorbed rapidly after oral administration, with a bioavailability of over 80%. The prodrug fumarate is hydrolyzed to tenofovir in vivo and this conversion occurs more efficiently in acidic conditions. Alafenamide, a prodrug of tenofovir, has been approved by the FDA as an alternative to tenofovir disoproxil fumarate (TDF) for the treatment of HIV-1 infection. Alafenamide is an acyclic nucleoside phosphonate that inhibits viral replication by inhibiting reverse</p>

<p>2-(5-Bromo-2-pyridylazo)-5-(diethylamino)phenol is a chemical that is used for the detection of hydrochloric acid in water vapor. It reacts with zirconium oxide, which generates a red fluorescing complex. The reaction can be detected by using a fluorescence spectrometer with a test sample. 2-(5-Bromo-2-pyridylazo)-5-(diethylamino)phenol is also used to detect the presence of nitrogen atoms and sodium citrate in samples by reacting with them. This chemical reacts with an acid complex to form stable complexes. The analytical method is based on measuring the redox potential of this reaction. The flow system of this technique allows for dehydration of dehydroascorbic acid (DHA).</p>

<p>Please enquire for more information about (1S,2R)-Fmoc-aminocyclohexane carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 4-(2',4'-Dimethoxyphenyl-Fmoc-aminomethyl)-phenoxymethyl-polystyrene resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Dibromobenzene-1,2-diamine (DBD) is a chemical compound that belongs to the group of diamines. It is used in cancer research as an anticancer drug, inhibiting the growth of cancer cells by blocking intracellular calcium levels. DBD has been shown to be effective against pancreatic cancer cells and human cancer cells. The photophysical properties of DBD are determined by its neutral structure and electron deficiency, which makes it a suitable candidate for use in radiation treatment.</p>

<p>N-Benzoyl-(2R,3S)-3-amino-2-hydroxy-3-phenylpropionic acid (BAPA) is a substance that is used in the manufacture of various drugs. It is also a potent anticancer drug that can be used for the treatment of cancer. BAPA has been shown to be an effective chemotherapeutic agent against many types of cancer cells. This drug is synthesized through an asymmetric synthesis process and has been shown to have potent cytotoxic effects against cancer cells with low levels of glutathione peroxide reductase. BAPA also inhibits the growth of bacteria by hydrolyzing or oxidizing proteins or by binding to DNA and RNA.</p>

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

<p>Please enquire for more information about Biotinyl-epsilon-aminocaproyl-D-Phe-Pro-Arg-chloromethylketone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-2-oxoethoxy)acetic acid is a product that can be used as a transport agent in the process of extracting glycosides. It has been shown to have strong adsorption properties and is able to extract glycosides from plant material. 2-Amino-2-oxoethoxy)acetic acid has a high affinity for calcium, which is an important component in the adsorption mechanism.</p>

<p>Please enquire for more information about (2R,4S)-1-tert-Butyl 2-methyl4-aminopyrrolidine-1,2-dicarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (S)-3-Amino-3-(4-chlorophenyl)-propan-1-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-((5-Bromopyridin-2-yl)amino)-4-oxobutanoic acid (BABA) is a potent photosynthetic inhibitor that inhibits light-driven electron transport in chloroplasts. This inhibition of electron transport leads to the accumulation of reactive oxygen species and cellular dysfunction. BABA is used to induce dormancy in plants and is also used as a chemical inhibitor for arabidopsis thaliana, a type of plant commonly used in molecular biology research. Studies have shown that BABA inhibits the growth of fat cells, which may be due to its ability to inhibit protein synthesis, leading to decreased fat deposition. In addition, this drug has been shown to reduce eye disorders such as retinal degeneration and cataracts by inhibiting the production of reactive oxygen species, which causes oxidative stress.</p>

<p>Please enquire for more information about 4-(Fmoc-hydrazino)-benzoylaminomethyl resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Tetrabutylammonium acetate is a complex of tetrabutylammonium with the trifluoroacetate anion. It has been used as a reagent for the preparation of α-hydroxylated ketones, including natural products. Tetrabutylammonium acetate can be used in titration calorimetry to measure the heat evolved during the reaction between hydroxyl group and sodium salts. The heat released corresponds to the amount of water produced from this reaction. In this way, it can be determined whether or not a molecule contains an active hydrogen atom. Tetrabutylammonium acetate also reacts with reactive compounds such as dpp-iv inhibitors, forming a reactive intermediate that cannot be isolated due to its instability. This intermediate is detected by analytical methods such as plasma mass spectrometry or infrared spectroscopy. Tetrabutylammonium acetate also reacts with asymmetric synthesis, forming an intram</p>

<p>Ethylammonium tetrafluoroborate is an ionic liquid that is a colorless, nonvolatile liquid at room temperature. It has a melting point of -9 °C and a boiling point of 230 °C. This compound is soluble in water and organic solvents, but insoluble in diethyl ether. Ethylammonium tetrafluoroborate can be used as an electrolyte for lithium-ion batteries. The reversible oxidation reaction of ethylammonium tetrafluoroborate can be catalyzed by the addition of fluorine or carbonyl groups to the molecule. The NMR spectra of ethylammonium tetrafluoroborate show that it contains an alcohol group with a phase transition temperature near 35 °C and an activation energy near 15 kJ/mol. This compound also undergoes polymerization reactions with various types of monomers, such as vinyl acetate and methyl methacrylate,</p>

<p>Aminoguanidine hydrochloride is a basic compound that can be used as an anti-inflammatory drug. It has been shown to have a hypoglycemic effect, which may be due to its ability to increase the activity of glutathione peroxidase and glutathione reductase in experimental models. Aminoguanidine hydrochloride also inhibits the production of inflammatory cytokines such as TNF-α, IL-1β and IL-6. Experiments with transfected cells have shown that aminoguanidine hydrochloride induces neuronal death, which may be due to its ability to inhibit protein synthesis by interfering with ribosomal function.</p>

<p>Boc-15-amino-4,7,10,13-tetraoxapentadecanoic 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. Boc-15-amino-4,7,10,13-tetraoxapentadecanoic 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>Tetra-n-propylammonium hydrogen sulfate (TPAS) is a pharmaceutical dosage that consists of tetra-n-propylammonium ions and hydrogen sulfate anions. It has a diameter of about 2 nm, and can be detected by fluorescence techniques. TPAS has shown to have pharmacologic activities, including the ability to react with hydrogen fluoride in solution to form a precipitate that can be used as a sample preparation reagent. TPAS also has been shown to produce dehydrating effects on chloride in an alicyclic system.</p>