Building Blocks

<p>N-(4-Aminobutyl)-1,4-butanediamine trihydrochloride (N(4)ABDAT) is a fine chemical and versatile building block. It can be used as an intermediate in the synthesis of pharmaceuticals and other organic chemicals. N(4)ABDAT is also a useful reagent for research purposes. The compound has a CAS number of 189340-78-1. It was originally synthesized by reacting 4-aminobutyric acid with 1,4-butanediamine, which yielded N(4)ABDAT as the major product. The chemical properties of N(4)ABDAT have been studied extensively including its reaction with potassium hydroxide, hydrochloric acid and sodium hydroxide to form different compounds.</p>

<p>Please enquire for more information about 1,6-Anhydrochitobiose 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 3-(Azidomethyl)-4-methyl-2,5-dihydrofuran-2,5-dione, 1M in acetonitrile 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 1,5-Anhydro-D-glucitol 6-dihydrogenphosphate disodium 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-Amino-1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-2(1H)-pyrimidinone  including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Aminobenzoic acid is a chemical compound that can be used as an antibacterial agent in wastewater treatment. It has been shown to be effective against Aerobacter aerogenes and other bacteria. 4-Aminobenzoic acid is a basic compound with an aromatic ring and four amine groups. It is often used in the synthesis of polymers, pharmaceuticals, dyes, and pigments. The polymerase chain reaction (PCR) technique uses 4-aminobenzoic acid as a cofactor for DNA synthesis. Electrochemical impedance spectroscopy (EIS) is another application of this chemical compound in which it acts as a redox mediator in the electrical circuit. 4-Aminobenzoic acid also has been shown to have toxic effects on bowel disease cells, which may be due to its ability to react with nucleophilic groups on cell surfaces or by inhibiting the production of essential proteins or enzymes within the cells</p>

<p>2-Aminoacridone is a fluorescent dye.  The applications of 2-Aminoacridone are extensive in biochemical and analytical research. It is commonly employed in glycoprotein and glycoconjugate studies, leveraging its high sensitivity and specificity in detecting saccharide structures. Researchers utilize this dye in various assays, including high-performance liquid chromatography (HPLC) and electrophoresis, to analyze carbohydrate content and structure. Its role is critical in advancing our understanding of carbohydrate-related biological processes, such as cell signaling and disease pathogenesis, facilitating developments in both diagnostics and therapeutic strategies.</p>

<p>6-Amino-9H-purine-9-propanoic acid is an acid lactam that belongs to the class of dihedral molecules. It is a colorless solid that crystallizes in plates, which have been shown to have a strong affinity for ammonium ions. 6-Amino-9H-purine-9-propanoic acid has been shown to be a substrate for the enzyme purine nucleoside phosphorylase, which catalyzes the phosphorolysis of nucleosides with the release of inorganic phosphate and ribose 5'-phosphate. The molecule can also react with electron radiation to form gamma rays, which may lead to its use as a molecular probe.</p>

<p>Arg-Gly-Asp TFA salt is a molecule that is used as a prodrug, meaning it is inactive until it has been converted to the active form. It has been shown to be effective when injected subcutaneously or intramuscularly and is hydrophilic. Arg-Gly-Asp TFA salt has been shown to have problematic effects on polymerization when exposed to heat. The molecule has an active form that can be absorbed into the body through injection sites and then hydrolyzed by esterases or glucuronidases, oxidized by cytochrome P450 enzymes, reduced by glutathione reductase, or conjugated with glucuronic acid. Arg-Gly-Asp TFA salt also specifically binds to markers expressed at high levels in Mycobacterium tuberculosis strains (e.g., ESX-1 secretion system protein) and inhibits cell growth in culture.</p>

<p>5-Amino-2-nitrobenzoic acid is a drug that has been shown to inhibit the activity of proteases. It has been used to detect the presence of protease activity in urine samples, as well as to study the inhibition of protease activity by other drugs. 5-Amino-2-nitrobenzoic acid is an inhibitor of chymotrypsin, trypsin, and elastase. This drug has been shown to be effective in inhibiting these enzymes at low concentrations, with a detection sensitivity of approximately 0.1 μM. 5-Amino-2-nitrobenzoic acid inhibits the growth of bacteria by binding to them and preventing protein synthesis. The compound also inhibits the enzyme dihydrolipoamide dehydrogenase in mitochondria, which is required for cellular respiration and energy production.</p>

<p>N-Acetyl-4-aminosalicylic acid is an active site directed probe for the detection of salicylic acid. It has a fluorescence emission maximum at 370 nm and a fluorescence quantum yield of 0.93. N-Acetyl-4-aminosalicylic acid can be used to analyze samples, such as wastewater and human urine, which contain salicylic acid. The probe is protonated in the presence of salicylic acid and then binds to the acceptor in the sample with a bimodal distribution. The fluorescence resonance energy transfer (FRET) process between the donor and acceptor leads to an increase in fluorescence intensity that can be detected by electrophoresis methods. This probe also has a conformational change when it binds to its target, which allows for easy separation from other components in the sample by size exclusion chromatography.</p>

<p>N-Acetyl-3-hydroxyindole is a colorless liquid that inhibits the activity of enzymes such as butyric acid, active methylene, and acyl halides. It is also used to inhibit the enzyme eosinophil peroxidase in clinical tests. N-Acetyl-3-hydroxyindole has been shown to be an efficient method for high-throughput analysis of enzymatic reactions. This chemical can be immobilized on porous supports and used to measure enzyme activities. N-Acetyl-3-hydroxyindole has been shown to have therapeutic effects in clinical data with a potent inhibitor of eosinophil peroxidase.</p>

<p>2-(Aminomethyl)benzamide hydrochloride is a research chemical with high quality and versatile building block properties. It is a useful intermediate in the synthesis of complex compounds, and can be used as a reagent for the production of speciality chemicals. 2-(Aminomethyl)benzamide hydrochloride is also an important reaction component in the synthesis of some fine chemicals, such as pharmaceuticals, dyes, pesticides, and perfumes. 2-(Aminomethyl)benzamide hydrochloride has CAS No. 1187927-15-6 and can be purchased from chemical suppliers worldwide.</p>

<p>D-Alanine benzyl ester p-toluenesulfonate salt is a fine chemical that is used in research and development. It is a versatile building block that can be used as an intermediate or a reaction component. D-Alanine benzyl ester p-toluenesulfonate salt has been shown to have high quality, which makes it useful for the production of complex compounds. This compound can be used as a speciality chemical or as a reagent in research.</p>

<p>4-Aminomethylbenzoic acid (4AMBA) is a metabolite that is formed from the amino acid methionine. It has been shown to inhibit the growth of prostate cancer cells in vitro and in vivo. 4-Aminomethylbenzoic acid inhibits the activity of polymerase chain reaction (PCR), which is an enzyme that catalyzes DNA replication. The hydroxyl group on 4-aminomethylbenzoic acid reacts with one of the phosphate groups on DNA, forming a covalent bond and inhibiting DNA synthesis. This inhibition occurs at the step called initiation, where DNA synthesis begins by binding of RNA polymerase to a specific sequence of DNA. In addition, 4-aminomethylbenzoic acid also inhibits the activity of x-ray diffraction data, which is an enzyme that catalyzes RNA transcription. Histological analysis shows that 4-aminomethylbenzoic acid causes congestive heart</p>

<p>N-Acetyl-L-alanine is the N-acetylated form of L-alanine and is a nonessential amino acid. It is an amide containing one nitrogen atom and two carbonyl groups. The nitrogen can be found in either the alpha or beta position on the amide. The biological properties of N-acetyl-L-alanine are similar to those of L-alanine, as it is used as a substrate for protein synthesis and has been shown to inhibit p21 and epidermal growth factor. The conformational properties of N-acetyl-L-alanine are different from that of L-alanine due to its changed shape, which may affect its biological activity.</p>

<p>N-Acetylglycine is an amide, which is a molecule with both a carboxylate and hydroxyl group. It belongs to the class of antimicrobial agents and has been shown to inhibit the growth of bacteria by inhibiting synthesis of folic acid and other metabolites. N-Acetylglycine also inhibits the formation of terminal residues from amino acids. The analytical method for this compound is based on the reaction between n-acetylglycine and hydrogen chloride in methanol. This produces picolinic acid, which can be detected using ultraviolet spectroscopy at a wavelength of 325 nm.</p>

<p>2-Amino-6-methoxybenzonitrile is an organic compound that belongs to a group of monosubstituted hydroxylamines. It has been used in the synthesis of various analogues, such as caprolactam and methoxyanthranilic acid. Hydrochloric acid reacts with 2-amino-6-methoxybenzonitrile to form 2-amino-6-hydroxybenzonitrile, which can be oxidized to 2-amino-6-(hydroxymethyl)benzonitrile. This reaction is catalyzed by copper or zinc metal.</p>

<p>2-Amino-4-fluorobenzamide is a catalyst that reacts with alcohols and cyclizes them to form quinazolinones. It has been shown to oxidize various alcohols including those with an electron-donating group, such as esters and nitro groups. 2-Amino-4-fluorobenzamide also reacts with electron-deficient alcohols, such as oximes and hydrazines. The mechanism of the oxidative cyclizations is not well understood but it is likely that they are initiated by a nucleophilic attack on the carbonyl carbon atom followed by a concerted or stepwise oxidation of the C=O double bond. The oxidative cyclization reactions are mechanistically similar to those of other catalytic oxidations, such as those used in the industrial production of acetic acid from methanol.</p>

<p>N-Acetyl-L-tyrosine is a tyrosine derivative with a chemical structure similar to that of an amino acid. It is used as a model system in biochemistry and molecular biology to study the transfer reactions of tyrosine, which are important for energy metabolism, protein synthesis, and metal chelation. N-Acetyl-L-tyrosine is also an effective substrate molecule for many analytical methods, such as thin layer chromatography or liquid chromatography.</p>