Heterociclos com Nitrogénio (N)

The drug, 10-[2-(1-methyl-2-piperidinyl)ethyl]-2-(methylthio)-10H-phenothiazine hydrochloride (CGP 46660), is a competitive antagonist at the human histamine H3 receptor. It has been shown to bind to the histamine H3 receptor in the range of 0.001 to 1 μM and is selective for this receptor over other receptors. CGP 46660 is an optical sensor that can be used in titration calorimetry experiments to measure changes in heat production when it binds to histamine H3 receptors. The drug also has been shown to inhibit guanine nucleotide-binding protein (G protein) signaling pathways and brain functions such as memory formation, learning, and attention span. These effects were demonstrated in humans by measuring EEG activity. The optimum concentration of CGP 46660 for these effects was found to be between 0.01 and 10 μM.

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a-Tripiperideine is an enolate that can be used as a catalyst to catalyze the formation of carbinols and cyclic compounds. It is also used in the synthesis of trimeric products, such as platelets and erythrocytes. The reaction product of a-tripiperideine with magnesium yields trimerizing agents, which are used in the production of vinylene.

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Applications Intermediate for heterocyclic compounds as tyrosine kinase inhibitors and anticancer agents. References McLean, A., et al.: J. Chem. Phys., 72, 5639 (1980), Watts, J., et al.: J. Biol. Chem., 276, 43197 (2001),

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Please enquire for more information about 1-Pyridin-3-yl-1-tosylmethyl isocyanide including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Chloro-3-hydroxypyridine is a reactive chemical that can be synthesized from hydrochloric acid and ammonia. It has a high melting point, which is an indication of its strength. 2-Chloro-3-hydroxypyridine has been used in the kinetic and population growth studies for bacteria. The reaction of 2-chloro-3-hydroxypyridine with sodium hydrogen is exothermic and has a red shift, which indicates that the activation energy for this reaction is low. Activation energies are important because they indicate the stability of molecules.

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5-Bromo-2-iodopyrimidine is a nitrogen heterocycle that has been found to have potential for use in the treatment of cancer. It is an asymmetric synthesis product of the photophysical reaction, which can be achieved by using an in vivo model. The compound's structure was determined by X-ray crystallography and nuclear magnetic resonance spectroscopy, and it has been shown to have a formyl group with a palladium-catalyzed cross-coupling reaction. 5-Bromo-2-iodopyrimidine can also be used as an acceptor molecule for the potential therapy of cancer. The optical properties of this compound are also noteworthy, with absorption maxima at 330 nm and emission maxima at 385 nm.

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Applications 4-(6-hydrazinylpyrimidin-4-yl)morpholine (cas# 5767-36-2) is a useful research chemical.

4-Chloro-1H-imidazo[4,5-c]pyridine (4CI) is a nucleoside analog that inhibits the replication of RNA and DNA. It has significant inhibitory activity against herpes simplex virus type 1 and human immunodeficiency virus type 1 (HIV-1). 4CI inhibits the synthesis of adenosine, an important component in the synthesis of RNA and DNA. This drug also has antiviral properties against influenza A and B viruses. 4CI's effect on plasma cholesterol levels is thought to be due to inhibition of 3-hydroxy-3-methylglutaryl coenzyme A reductase.

Please enquire for more information about 2-Chloro-N-[(5-cyano-2,4-dimethyl-6-oxo-1,6-dihydropyridin-3-yl)methyl]acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Kinetin is a chemical compound that is used in research as a reagent, useful scaffold, and an intermediate. It has been shown to be an effective building block for the synthesis of complex compounds. Kinetin is also a versatile building block that can be used to synthesize many different types of compounds. Kinetin has a CAS number 525-79-1 and is classified as a speciality chemical.