Heterocycles with Nitrogen (N)

Please enquire for more information about 3-Bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,6-Diethyl-3-bromopyridine is a type of mycolic acid that is produced by Mycobacterium. It has been shown to be involved in the regulation of galactose metabolism and lipid synthesis. 2,6-Diethyl-3-bromopyridine has also been found to be an inhibitor of DNA g+c synthesis and functions as a connecting molecule between two phosphatidylethanolamines. This compound is also involved in the production of unsaturated fatty acids, which are essential for bronchial function.

5-Benzyloxyindole-3-glyoxylamide is a versatile building block that can be used in the synthesis of complex compounds. It has been shown to have a high quality and is useful as a reagent for research purposes. 5-Benzyloxyindole-3-glyoxylamide can be used as a reaction component and is useful as an intermediate in organic synthesis. 5BIGA has CAS number 22424-62-0 and is also known as 3-(benzyloxy)-5-(2,2,2-trifluoroethoxy)indole glyoxamide.

5-Bromo-2-iodopyridine is an antibiotic that is used to treat bacterial infections. It has been shown to inhibit the growth of bacteria by binding to the 50S ribosomal subunit. This drug also has a toxic effect on respiratory system cells, which may be due to its ability to induce apoptosis. 5-Bromo-2-iodopyridine interacts with DNA in a triazine ring and inhibits bacterial growth by inhibiting protein synthesis. The drug binds to the 50S ribosomal subunit at a site that is different from that of rifampin and other antibiotics. The reaction is catalyzed by palladium at high temperatures and takes place in organic solvents such as chloroform or benzene. This synthetic process can be made more efficient by using inexpensive starting materials, such as bromine, iodine, and acetone, rather than expensive starting materials like platinum or gold salts.

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5-Methoxypyrazine-2-carboxylic acid (5MPCA) is a diastereoselective inhibitor of β-amyloid peptide aggregation. It has been shown to reduce the formation of β-amyloid in a pharmacodynamic study with significant reduction of Aβ40 and Aβ42 levels in cerebral spinal fluid. 5MPCA inhibits the enzyme β-secretase, which cleaves the amyloid precursor protein (APP) at the β site, leading to reduced production of β-amyloid. The inhibition of β-secretase by 5MPCA prevents Aβ from being generated and thereby reduces its level in cerebral spinal fluid.

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Applications Urazole derivative.

Applications 2,5-Dioxopyrrolidin-1-yl dodecanoate (cas# 14565-47-0) is a useful research chemical.

Please enquire for more information about 4-(4-Benzyloxy-phenyl)-1-(1-phenyl-ethyl)-1,2,3,6-tetrahydro-pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Phenyl-Pyridin-3-Yl-Amine is a versatile synthetic reagent that can be used in the synthesis of a variety of organic compounds. It is an important precursor for the preparation of heterocyclic compounds, such as carbolines and n-oxides. Phenyl-Pyridin-3-Yl-Amine has been shown to have biological properties, including antioxidant activity. It also features a mesomeric structure which allows it to be used in strategies involving radical reactions. Phenyl-Pyridin-3-Yl-Amine exhibits chloride ion affinity and can be used as a salt, such as sodium salts.

This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Pyrimidine-2,5-diamine (PD) is a molecule that has been synthesized by molecular modeling and photophysical studies. PD is a molecule that has been validated for its hematopoietic cell enhancing properties. PD counteracts the phosphorylation of pyrimidine-2,5-diamine and prevents the binding to ribulose. This molecule also enhances the biosynthesis of ribulose. Pyrimidine-2,5-diamine is recycled by dephosphorylation in order to be reused as a hematopoietic cell booster.

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Please enquire for more information about [(1-Benzyl-1H-pyrrolo[3,2-c]pyridin-4-yl)thio]acetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications Piperonylic Acid is a compound closely mimicking the structure of transcinnamic acid involved in the phenylpropanoid pathway in plant physiology. References Schalk, M. et al.: Plant Physiol., 118, 209 (1998);

Applications 2-(n-Butyl-d9-amino)-4-chloro-6-cyclopropylamino-1,3,5-triazine (cas# 1189997-37-2) is a compound useful in organic synthesis.

1-Phenylsulfonyl-1H-indole is a synthetic, non-naturally occurring compound that belongs to the class of indole alkaloids. It is an asymmetrical molecule with a dihedral angle of 12.2° and a molecular weight of 226.11 g/mol. The compound has two benzyl groups that are attached to the phenylsulfonyl group at C4 and C5 positions, which are both hydrogen bonded to the indole group at C3 position. 1-Phenylsulfonyl-1H-indole is used as a starting material in organic reactions. It can be reacted with organolithium reagents to form sulfonamides or with Friedel-Crafts reaction to produce ketones.

Please enquire for more information about [1-(2-Furylmethyl)piperidin-3-yl]methanol hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Methyl piperidin-4-ylacetate is a chemical compound that belongs to the group of amides. It has been shown to have inhibitory activity against mosquitoes, animals, and infectious diseases. The active form of methyl piperidin-4-ylacetate inhibits the synthesis of molecules containing amines and quinquefasciatus by inhibiting dehydrogenase, which is an enzyme that catalyzes the conversion of amino acids into amines. The molecule also inhibits the synthesis of proteins by binding to ribonucleic acid (RNA).

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Please enquire for more information about 6-(1,3-Dioxo-1,3-dihydro-2H-pyrrolo[3,4-c]pyridin-2-yl)hexanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Intermediate in the synthesis of ibrutinib

5-Bromo-6-chloro-1H-indole is a fine chemical that is used as a building block for research chemicals, reagents, and speciality chemicals. It is soluble in chloroform and benzene, but insoluble in water. This product can be used as a reaction component or a useful intermediate in the production of complex compounds. 5-Bromo-6-chloro-1H-indole has been reported to be an effective scaffold for the synthesis of many novel compounds with potential applications such as pharmaceuticals, agrochemicals, and dyes.

Fmoc-O-tert-butyl-L-serine 3,4-dihydro-3-hydroxy-4-oxo-1,2,3-benzotriazine ester is a pharmacological agent that inhibits the enzymolysis of peptide chains. It is a reaction product and has been shown to have antiallergic properties in animal studies. Fmoc-O-tert - butyl - L - serine 3,4 - dihydro - 3 - hydroxy - 4 - oxo - 1,2,3 - benzotriazine ester binds to the carboxyl group of amino acids and blocks the carboxyl group from reacting with hydrogen ions. This prevents the release of carbon dioxide and ammonia from amino acids. The pharmacological activity of this agent has not been confirmed in humans.

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