Heterociclos com Nitrogénio (N)

The 2,4-difluoropyrimidine molecule is an iterative molecule with a fluorine atom at the 2,4 position. It has potential for several applications, including photochemical reactions and ionization. This molecule has been studied in detail by correlating its photoelectron spectra with theoretical calculations. The 2,4-difluoropyrimidine can be used as a starting material for other molecules of interest.

1,4-Dihydro-2,6-dimethyl-4-[2-(trifluoromethyl)phenyl]-3,5-pyridinedicarboxylic acid 3-ethyl 5-[2-[[4-[3-(trifluoromethyl)-3H-diazir in-3-yl]benzoyl]amino]ethyl] ester is an anticancer drug that inhibits the glycoside hydrolase enzyme. This drug also binds to a transporter protein and blocks its function. 1,4-Dihydro-2,6-dimethyl-4-[2-(trifluoromethyl)phenyl]-3,5-pyridinedicarboxylic acid 3-ethyl 5-[2-[(4-[3-(trifluoromethyl)-3H--diazir in--3--yl]benzoyl)

Please enquire for more information about 5-(N-Methylcarbamoyl)pyridine-3-boronic acid, pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Chloro-6-cyanopyrazine is a compound that has been shown to have antimycobacterial activity against Mycobacterium avium. It may also have tuberculostatic activity and be useful for the treatment of tuberculosis. 2-Chloro-6-cyanopyrazine inhibits bacterial growth by binding to DNA, RNA, and protein synthesis in mycobacteria. The antibacterial effect is due to its ability to inhibit amidation and alkylation reactions, as well as its nucleophilic properties. 2-Chloro-6-cyanopyrazine is an acidic compound with a pKa of 3.2, which makes it more soluble in water than hydrophobic compounds such as alkanoic acids.

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2,4,6-Trichloropyrimidine-5-carboxaldehyde is a synthetic compound that is aniline derivative. It has been shown to inhibit the nucleophilic substitutions of flavin and metal ions. 2,4,6-Trichloropyrimidine-5-carboxaldehyde also has reactive properties and can react with chloride to form chloropyrimidines. 2,4,6-Trichloropyrimidine-5-carboxaldehyde inhibits xanthine oxidase (XO) by reacting with the hydroxyl group of the cofactor FAD. This leads to the formation of a covalent bond between XO and the substrate Xanthine. The reaction product is then released from XO, which prevents it from catalyzing the oxidation of hypoxanthine to xanthine and xanthine to uric acid.

5-Methoxy-1-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-2-(methylsulfinyl)-1H benzodimidazole (MMZ) is a chromatographic sample that is available in sodium hydrogen magnesium n-oxide form. MMZ is an antidiabetic drug that has shown to be effective in the treatment of type 2 diabetes mellitus and insulin resistance. This drug binds to ATPase alpha subunit, which inhibits the enzyme’s ability to pump sodium ions out of cells and increase intracellular sodium ion levels. The long half life of this drug makes it well suited for use as an oral medication. The impurities of this drug are methyl alcohol, benzimidazole derivative, and industrialized synthetic preparations. MMZ has prognostic properties that can be used to predict the progression of type 2 diabetes mellitus and insulin resistance.

Pyrazolo[4,3-c]pyridine is a lead compound that has been shown to inhibit the activity of kinases and pyridine nucleotidases. This drug has been shown to have anti-cancer effects in vitro and in vivo in a dose-dependent manner. Pyrazolo[4,3-c]pyridine has also been shown to be an inhibitor of atrial fibrillation by prolonging the QT interval and inhibiting cellular potency.

Pyridine-2-carbonyl chloride hydrochloride is a compound that can be used in the synthesis of picolinic acid. It has been shown to inhibit the proliferation of cancer cells and inflammatory diseases, such as arthritis. The mechanism of action is not fully understood, but it may involve inhibition of glutamate receptor subtype and amido hiv infection. Pyridine-2-carbonyl chloride hydrochloride also inhibits the growth of bacteria by binding to nuclear hormone receptors, which prevents transcription and replication. This drug is capable of inhibiting glutamic acid release by acting on its receptors.