Identification and Biochemical Studies on Novel Non-Nucleoside Inhibitors of the Enzyme Adenosine Kinase |
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Authors: | Jae Park Gayathri Vaidyanathan Bhag Singh Radhey S Gupta |
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Institution: | (1) Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON, Canada, L8N 3Z5 |
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Abstract: | The enzyme adenosine kinase (AK) plays a key role in the regulation of intracellular and extracellular concentration of adenosine
(Ado), which exhibits potent hormonal activity in cardiovascular, nervous and immune systems. In view of the pharmacological
effects of Ado, there is much interest in identifying inhibitors of AK, which can augment its tissue-protective effects. In
this study, we have screened 1040 compounds from a chemical library of putative kinase inhibitors for their effect on purified
human recombinant AK. These studies have identified 8 novel, non-nucleoside AK inhibitors. Four of these compounds (viz. 2-tert-butyl-4H-benzo1,2,4]thiadiazine-3-thione
(2759–0749); N-(5,6-diphenyl-furo2,3-d]pyrimidin-4-yl)-propionamide (3998–0118); 3-5,6-Bis-(4-methoxy-phenyl)-furo2,3-d]pyrimidin-4-ylamino]-propan-1-ol
(4072–2732); and 2-2-(3,4-dihydroxy-phenyl)-5-phenyl-1H-imidazol-4-yl]-fluoren-9-one (8008–6198)), which inhibited human
AK in a concentration-dependent manner in a low micromolar range (IC50 = 0.38 ∼ 1.98 μM) were further studied. Kinetic and structural studies on these compounds provide evidence that inhibition
of AK by these compounds was competitive with respect to Ado and non-competitive for ATP. All of these compounds also inhibited
uptake of Ado and its metabolism in cultured mammalian cells at comparable concentrations indicating their efficient cellular
penetrability. These AK inhibitors, whose chemical structures differ significantly from all previously known inhibitors, provide
useful lead compounds for identification of more potent but less toxic AK inhibitors that may prove useful for therapeutic
purposes. |
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Keywords: | adenosine adenosine kinase adenosine kinase inhibitors kinetics studies drug screening structure-activity studies |
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