Heterociclos con nitrógeno (N)

<p>Fentanyl is a synthetic opioid that is similar to morphine. It has been used in human studies for its analgesic effects. Fentanyl has been shown to have a high potential for abuse and can cause life-threatening respiratory depression. It can be administered orally, intravenously, or by inhalation. The drug is metabolized by the liver into several inactive metabolites. Fentanyl is an analog of the natural opioid peptide endorphin and binds to δ-opioid receptors in the central nervous system, which are involved in the regulation of pain. This drug also has antinociceptive properties at low doses and δ-opioid agonist activity at higher doses.</p>

<p>Please enquire for more information about 1-(Trifluoroacetyl)-4-piperidinone 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-(4-Fluorobenzoyl)piperidin-4-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromo-6-methoxypyridin-3-amine is a perovskite that has been shown to have a high photoluminescence quantum yield and can be used in solar cells. This compound interacts with both the ligands and the acceptors, boosting the efficiency of these compounds. The 2-bromo-6 methoxypyridin-3 amine is a semiconductor with an electron affinity of 1.9 eV and a band gap of 1.6 eV. It has been shown to be efficient as a photoluminescent material in nanocrystals.</p>

<p>N-Benzyl-4-piperidone is a potent antagonist of the histamine H1 receptor. It binds to the receptor in vivo, and it has been shown that this binding leads to a decrease in the release of neurotransmitters in the central nervous system. This drug is used for the treatment of hiv infection and for other conditions such as allergic rhinitis, chronic idiopathic urticaria, and vasomotor rhinitis. N-Benzyl-4-piperidone inhibits the reaction between propionyl chloride and dibutyltin oxide to form a dialkyl tin compound by an acylation reaction. The low energy released during this reaction may be due to hydrogen bonding between this drug and water molecules.</p>