Building Blocks

<p>2-Amino-6-bromopyrazine is a versatile building block that can be used in the synthesis of complex compounds. It is also used as a reagent, speciality chemical and useful scaffold for the synthesis of pharmaceuticals and other chemicals. 2-Amino-6-bromopyrazine is available from Sigma Aldrich with CAS No. 54237-53-5.</p>

<p>Adamantane-2-carboxylic acid is a synthetic polymer that is used as a matrix in molecular electrostatic potential flow chromatography. Adamantane-2-carboxylic acid has been shown to form a polymeric matrix with trifluoromethyl groups and carbon tetrachloride, which can be used to separate neurotensin receptor agonists from dopamine antagonists. This compound also has the ability to cross the blood-brain barrier and bind to dopamine receptors, which may be useful for controlling diabetes. Adamantane-2-carboxylic acid is also an organic solvent and can be used as an alternative to chlorinated solvents such as carbon tetrachloride for environmental pollution control.</p>

<p>6-Amino-5-bromopyrimidine-2,4(1H,3H)-dione (6ABPD) is a purine derivative that functions as an inhibitor of phosphorylase kinase. It has been shown to inhibit tumor growth in vivo and in vitro and is used as a therapeutic agent for the treatment of cancer. 6ABPD inhibits the production of phosphorylase kinase by binding to the enzyme's active site with noncompetitive inhibition. Inhibition of phosphorylase kinase leads to a decrease in the levels of ATP and thus decreases the availability of substrates for tumor cell growth and proliferation. 6ABPD also binds to thymidine kinase and inhibits its activity, which may account for some of its antitumor effects.</p>

<p>6-Amino-2-pyrazinecarboxylic acid is a high quality reagent that is used as an intermediate for the synthesis of complex compounds. It is also a useful scaffold for the production of valuable speciality chemicals. This chemical is also used as a reaction component in research and development to produce versatile building blocks. 6-Amino-2-pyrazinecarboxylic acid has been shown to be useful for producing fine chemicals and speciality chemicals, which are often used in many industries.</p>

<p>4-Amino-N-(2-phenylethyl)benzenesulfonamide (4APBS) is a histone deacetylase inhibitor. It has been shown to inhibit the histone methyltransferase activity of EZH2, which is important for regulating gene expression, in cells treated with 4APBS. This inhibition leads to increased levels of the transcriptional coactivator β-catenin and reduced levels of tumor suppressor genes. These changes ultimately lead to an increase in cancer cell proliferation and decreased apoptosis. 4APBS also interacts with hormone receptors that are found on the surface of cells and can regulate cellular functions such as proliferation, differentiation, or apoptosis.</p>

<p>1-Amino-1-cyclopropanecarbonitrile hydrochloride (ACN) is a synthetic compound that has been shown to be effective against cancer and inflammatory diseases. It is an acidic compound that has been shown to inhibit the growth of tumor cells by inducing apoptosis. This drug also binds to chloride ions and inhibits the production of inflammatory cytokines, such as IL-6, TNFα, and IL-2. 1-Amino-1-cyclopropanecarbonitrile hydrochloride is soluble in water and acetonitrile with a melting point of about 157°C. The molecule's structure was determined through kinetic measurements and thermodynamic calculations.</p>

<p>2-(2-Aminophenyl)benzimidazole is a synthetic compound with the chemical formula C8H6N2. It has an intramolecular hydrogen bond and reacts with salicylaldehyde to form 2-aminobenzimidazole, which is a reaction product. 2-(2-Aminophenyl)benzimidazole may be used as an antimicrobial agent, but it also has other uses such as a reagent in organic synthesis. It is soluble in water and can be obtained through liquid chromatography.</p>

<p>2-Amino-4-fluoropyridine is an acylation reaction product of 2-amino-4-chloropyridine and a fatty acid. The diaminopyridine moiety is responsible for the inhibition of copper enzymes. In addition, fluorine substitution provides a higher operational stability. The synthesis of this compound is accomplished through the use of thionyl chloride in an operational procedure that includes heating at 180 °C for 4 hours. 2-Amino-4-fluoropyridine has been shown to be effective against some bacteria such as Mycobacterium tuberculosis and Legionella pneumophila, which are resistant to other agents. This drug also has antiplasmodial properties and can be used to treat malaria. The structure based design of this molecule was optimized by replacing chlorine with fluorine as well as introducing a n oxide group to provide a sterically more favorable conformation.</p>

<p>5,6,7,8-Tetrahydronaphthalene-2-carbaldehyde is an indole derivative that is used as a precursor to produce other compounds. It is an inducers of enzymes (e.g., hydroxylase) and has been shown to increase the production of toxic metabolites such as cyclized products. 5,6,7,8-Tetrahydronaphthalene-2-carbaldehyde can be synthesized from anthracene by reacting it with acetone and hydrochloric acid. This compound can be converted into a variety of derivatives including esters and zoxazolamine. 5,6,7,8-Tetrahydronaphthalene-2-carbaldehyde also has carcinogenic properties and has been shown to cause cancer in rats when injected or orally administered in high doses.</p>

<p>2-Amino-5-bromo-3-iodopyridine (2AB3IP) is a cacchi anthelmintic that is active against the trophozoites of Giardia lamblia. 2AB3IP also has antimicrobial properties, but is not active against bacteria. The high lipophilicity and pharmacokinetic properties of this drug make it a potential therapeutic candidate for the treatment of giardiasis. The mechanism of action of 2AB3IP is mediated by potassium t-butoxide, which activates the drug to form its reactive intermediate. This intermediate reacts with DNA in the parasite to form covalent adducts. This process leads to inhibition of RNA synthesis and subsequent cell death.</p>

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

<p>2-[1,2,4]Triazol-1-yl-benzylamine is a chemical compound that has been shown to be an excellent reagent in organic synthesis. It is also used as a building block for the synthesis of compounds related to pharmaceuticals, pesticides and other speciality chemicals. 2-[1,2,4]Triazol-1-yl-benzylamine is a versatile intermediate that can be used in the synthesis of complex compounds with good yields and high purity.</p>

<p>2-Cyano-1,5-dimethylpyrrole is a quinone antibiotic. It has been shown to have antibacterial activity against organisms such as Staphylococcus, Streptococcus, and Pyogenes. This chemical has been shown to be active in the gaseous phase and against test organisms in alcohol extracts. 2-Cyano-1,5-dimethylpyrrole also exhibits flavonoid and saponin properties that may contribute to its antimicrobial activity.</p>

<p>Trimethyl 1,3,5-benzene tricarboxylate is a chemical compound that belongs to the group of polycarboxylic acids. It is used as a polymerization agent in the manufacture of ionic polymers. The first step in this process is cationic polymerization, which involves the reaction between trimethyl 1,3,5-benzene tricarboxylate and sodium citrate to form an ion pair. This process can be followed by hydrolysis with hydrochloric acid and sodium carbonate to release the carboxylate anion from the polymer chain and regenerate trimethyl 1,3,5-benzene tricarboxylate. Trimethyl 1,3,5-benzene tricarboxylate has been shown to have optical properties that depend on its molecular weight and metal surface interactions. It can also be used as a chelating agent for zinc diethyld</p>

<p>2,5-Dichlorobenzonitrile is a chemical compound that contains a nitrile group. It is used as an intermediate in organic synthesis, as well as for the production of various pharmaceuticals and pesticides. 2,5-Dichlorobenzonitrile is oxidized to form 2,5-dichlorophenol which can be further converted to 2,5-dichloroquinone. This redox cycle is reversible and can be used to synthesize other compounds. The reaction time of this process is about one hour at room temperature. Maleate has been shown to inhibit the hepatic metabolism of 2,5-Dichlorobenzonitrile. This may lead to accumulation of 2,5-Dichlorobenzonitrile in the liver and potentially cause hepatitis or even liver cancer. Chloromethylation of 2,5-Dichlorobenzonitrile leads to the formation of chlor</p>

<p>2,4-Pyridinedicarboxylic acid diethyl ester is an aliphatic hydrocarbon that has been shown to be a potent active oxygen scavenger. It has also been shown to inhibit the uptake of fatty acids and organic anions by tubule cells in the liver, as well as to reduce collagen breakdown in the endoplasmic reticulum. This compound is converted into pyridinedicarboxylic acid, which inhibits hepcidin production and thus increases iron absorption. 2,4-Pyridinedicarboxylic acid diethyl ester also has a biochemical profile that is similar to that of a lipophilic fatty acid ester.</p>

<p>2-[(Phenylsulfonyl)amino]benzoic acid is a white crystalline solid that is soluble in water and ethanol. It has a melting point of 176°C and a boiling point of 280°C. 2-[(Phenylsulfonyl)amino]benzoic acid binds to DNA by an intercalative mechanism, forming covalent bonds with the bases on the DNA. This binding prevents the DNA from unwinding during replication and transcription, thus inhibiting the synthesis of RNA and protein. The dimers form between two molecules of 2-[(Phenylsulfonyl)amino]benzoic acid, due to hydrogen bonding between the carboxylic acid groups. The crystal structure has been determined for this compound as centrosymmetric with space group P2 1 /c. A benzene ring is found in the molecule, which can form a pyridine ring when exposed to heat or</p>

<p>1,2-Dimethoxy-4,5-dinitrobenzene is a fluorescent compound that can be used as a probe to study the response elements in DNA. It has been shown to inhibit HDAC activity and induce nuclear translocation of Nrf2 in wild-type mice. 1,2-Dimethoxy-4,5-dinitrobenzene has also been shown to decrease the level of plasma protein carbonyls in cancer patients. This molecule has analytical applications for determining the presence of it's target compounds in biological samples.</p>

<p>Non-proteinogenic amino acid; Inhibitor of glutamine synthetase</p>

<p>7,7,8,8-Tetracyanoquinodimethane is a quinoid compound that is used as an analytical chemical reagent. It has been shown to be a powerful reducing agent and can be used in the determination of trace amounts of metals. 7,7,8,8-Tetracyanoquinodimethane also reacts with cationic surfactants and hydroxyl groups to form stable compounds. The nitrogen atoms in this molecule are capable of multiple transfer reactions with other molecules.br&gt;br&gt; <br>The redox potentials of this substance are negative and it has been shown to have the ability to transport pharmaceutical preparations across cell membranes. Boron nitride (BN) has been shown to stabilize the structure of 7,7,8,8-tetracyanoquinodimethane by forming strong hydrogen bonds between the BN and hydroxyl groups on this molecule.</p>