Hétérocycles azotés (N)

Please enquire for more information about 3-Phenyl-2-(pyridin-3-yl)propanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Ethyl 1-ethylpiperidine-4-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Impurity Terazosin EP Impurity M Applications 1,4-Di-2-furoyl-piperazine (Terazosin EP Impurity M) can be used in biological studies to examine the relationship of structure to parasiticide activity of nitrated derivatives. References Cavier, R., et al.: Chimica Therapeutica 5, 270 (1970)

Please enquire for more information about 5-Nitro-2-[(2,2,6,6-tetramethylpiperidin-4-yl)amino]benzonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 6-Fluoro-4-methyl-2-pyridinamine can be synthesized from 2,6-Dichloro-4-methylpyridine (39621-00-6).

Please enquire for more information about (3-Cyanopyridin-2-yl)cyanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4-(Pyrrolidin-1-ylmethyl)piperidin-4-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2,6-Difluoropyridine-3-carboxylic acid is a synthetic compound that has been shown to inhibit the activity of various enzymes. It has been found to be an effective inhibitor of 5-hydroxytryptamine 2c receptor (5-HT2c) and epidermal growth factor (EGF) receptors. This drug also has the ability to modulate depression, as it increases serotonin levels in the brain by inhibiting its reuptake. The inhibition of EGF receptor leads to an increase in epidermal growth factor and hyperproliferative diseases. In addition, this drug inhibits cancer cell proliferation by blocking the activation of factors that control cell division. Finally, 2,6-Difluoropyridine-3-carboxylic acid is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction

4,6-Dimethyl-2-mercaptopyrimidine is a protonated form of the compound 4,6-dimethylpyrimidine. It is a member of the group p2 of nitrogenous bases and has a hydrogen bond interaction with its base pair. The reaction mechanism for this molecule is similar to that of other tricyclic antidepressant drugs, as it involves an intermolecular hydrogen bonding reaction where the deprotonated hydroxyl group on one molecule transfers a proton to the adjacent nitrogen atom on another molecule. 4,6-Dimethyl-2-mercaptopyrimidine has been shown to be active in cervical cancer cells and is capable of inhibiting DNA synthesis and protein synthesis. This compound also has antihistamine effects which are likely due to its hydrogen bonding interactions with histamine receptors.