نتایج جستجو برای: pyridinyl

تعداد نتایج: 490  

Journal: :Chimica techno acta 2023

Herein, we report a convenient one-pot synthesis of 1,2,4-triazinyl derivatives benzocoumarins. The proposed approach consists in the nucleophilic addition tetrahydrobenzo annulated dimethoxycoumarin to 1,2,4-triazines followed by double oxidation both dihydrotriazine and groups with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ). was carried out presence three-fold excess methanesulfonic acid...

Journal: :The Journal of pharmacology and experimental therapeutics 2016
Robert A Owens Bogna Ignatowska-Jankowska Mohammed Mustafa Patrick M Beardsley Jenny L Wiley Abdulmajeed Jali Dana E Selley Micah J Niphakis Benjamin F Cravatt Aron H Lichtman

Whereas the inhibition of fatty acid amide hydrolase (FAAH) or monoacylglycerol lipase (MAGL), the respective major hydrolytic enzymes of N-arachidonoyl ethanolamine (AEA) and 2-arachidonoylglycerol (2-AG), elicits no or partial substitution for Δ(9)-tetrahydrocannabinol (THC) in drug-discrimination procedures, combined inhibition of both enzymes fully substitutes for THC, as well as produces a...

2013
Saleha B. Vuyyuri Jacob Rinkinen Erin Worden Hyekyung Shim Sukchan Lee Keith R. Davis

Ascorbic acid (AA) exhibits significant anticancer activity at pharmacologic doses achievable by parenteral administration that have minimal effects on normal cells. Thus, AA has potential uses as a chemotherapeutic agent alone or in combination with other therapeutics that specifically target cancer-cell metabolism. We compared the effects of AA and combinations of AA with the glycolysis inhib...

Journal: :Molecular pharmacology 2001
Z G Gao J E Van Muijlwijk-Koezen A Chen C E Müller A P Ijzerman K A Jacobson

Allosteric modulators of A(1) and A(2A) adenosine receptors have been described; however, for the A(3) adenosine receptor, neither an allosteric site nor a compound with allosteric effects has been described. In this study, the allosteric modulation of human A(3) adenosine receptors by a series of 3-(2-pyridinyl)isoquinoline derivatives was investigated by examining their effects on the dissoci...

Journal: :Dalton transactions 2014
Marcel A H Moelands Daniel J Schamhart Emma Folkertsma Martin Lutz Anthony L Spek Robertus J M Klein Gebbink

A series of new chiral pyridinyl prolinate (RPyProR) ligands and their corresponding Fe(II) triflate and chloride complexes are reported. The ligands possess an NN'O coordination motif, as found in the active site of non-heme iron enzymes with the so-called 2-His-1-carboxylate facial triad. The coordination behaviour of these ligands towards iron turned out to be dependent on the counter ion (c...

Journal: :Dalton transactions 2012
Ana de Bettencourt-Dias Sebastian Bauer Subha Viswanathan Brandi C Maull Ayuk M Ako

A new ligand family based on picoline, bipyridine and terpyridine containing a nitro moiety has been synthesized and its coordination and sensitization ability for lanthanide ions has been studied. Three new complexes were characterized by X-ray single crystal diffraction and all three show uncommon coordination of the nitro moiety to the lanthanide ion. 5cTb, a terpyridine-nitro derivative wit...

1997
DANIEL S. COWEN PERRY B. MOLINOFF DAVID R. MANNING

The regulation in expression of human 5-hydroxytryptamine1A (5-HT1A) receptors by agonists and antagonists was studied in a stable transfected Chinese hamster ovary cell line expressing the human 5-HT1A receptor. Receptor density and affinity were measured with [I]4-(29-methoxyphenyl)-1-[29-[N-(29-pyridinyl)-p-iodobenzamido]ethyl]piperazine ([I]p-MPPI), a selective antagonist of 5-HT1A receptor...

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