Results 131 to 140 of about 14,200 (182)
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Highly regioselective methylation of inosine nucleotide: an efficient synthesis of 7-methylinosine nucleotide

Nucleosides, Nucleotides & Nucleic Acids, 2020
A facile, straightforward, reliable, and an efficient chemical synthesis of inosine nucleotides such as 7-methylinosine 5'-O-monophosphate, 7-methylinosine 5'-O-diphosphate, and 7-methylinosine 5'-O-triphosphate, starting from the corresponding inosine nucleotide is delineated.
Annamalai, Senthilvelan   +2 more
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Inosine incorporation into myocardial nucleotides

Journal of Molecular and Cellular Cardiology, 1972
Abstract Inosine and hypoxanthine, degradative products of adenine nucleotides are released and also taken up by the heart. In order to determine whether inosine can be incorporated into adenine nucleotides by direct phosphorylation or whether initial degradation to hypoxanthine is necessary, isolated guinea pig hearts were perfused with non ...
V T, Wiedmeier, R, Rubio, R M, Berne
openaire   +2 more sources

An efficient protection-free chemical synthesis of inosine 5'-nucleotides

Nucleosides, Nucleotides & Nucleic Acids, 2020
A facile, straightforward, reliable, and efficient chemical synthesis of inosine nucleotides such as inosine-5'-monophosphate, inosine-5'-diphosphate, and inosine-5'-triphosphate, starting from inosine is delineated. The inosine-5'-monophosphate is achieved by the highly regioselective monophosphorylation of inosine using the Yoshikawa procedure.
Annamalai, Senthilvelan   +2 more
openaire   +2 more sources

Raman spectroscopic determination of inosine nucleoside in nucleotides

Talanta, 1999
Raman spectroscopy has been applied to the analytical determination of inosine nucleoside in nucleotides. Spectral characteristics of aqueous solutions of lithium, potassium and magnesium salts of inosine 5'-monophosphoric acid are described. Two characteristic bands located at 1553 and 1593 cm(-1) whose frequencies are not sensitive either to the ...
R, Escobar   +3 more
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The nucleotide derivatives inosine and inosinic acid inhibit intestinal absorption of mizoribine in rats

European Journal of Pharmacology, 2006
Inosine is absorbed via a N1 transporter that is selective for purine nucleosides. It is conceivable that inosine and inosinic acid might affect the intestinal absorption of mizoribine, an imidazole nucleoside that inhibits the de novo production pathway of guanine ribonucleotide.
Makoto, Okada   +4 more
openaire   +2 more sources

Analysis of adenine and inosine nucleotides

Analytica Chimica Acta, 1957
Abstract Different methods are described for the separation and determination of adoninc, hypoxanthine, adenosine, inoaineandtheir phosphorylated derivatives, and inorganic ortho-and pyrophosphatc: i) chromatographie procedures on paper, cellulose powder column and paper roll, 2) electrophurctic procedures on paper and cellulose powder column.
P. Cerletti, P.L. Ipata, N. Siliprandi
openaire   +1 more source

Inhibition of inosinic acid dehydrogenase by 6-chloropurine nucleotide

Biochemical Pharmacology, 1969
Abstract The inactivation of IMP dehydrogenase of sarcoma 180 ascites tumor cells by 6-chloroinosine 5'-phosphate (ClIMP) has been examined. In the absence of substrates the inhibition of enzymatic activity by this purine nucleotide analog is progressive with time and is not reversed by dialysis.
J H, Anderson, A C, Sartorelli
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Guanine and inosine nucleotides/nucleosides suppress murine T cell activation

Biochemical and Biophysical Research Communications, 2018
Damaged tissues and cells release intracellular purine nucleotides, which serve as intercellular signaling factors. We previously showed that exogenously added adenine nucleotide (250 μM ATP) suppressed the activation of murine splenic T lymphocytes. Here, we examined the effects of other purine nucleotides/nucleosides on mouse T cell activation. First,
Yuria, Shinohara, Mitsutoshi, Tsukimoto
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Inhibition of inosinic acid dehydrogenase by 8-substituted purine nucleotides

Journal of Medicinal Chemistry, 1981
A series of 8-substituted derivatives of adenosine monophosphate (AMP) and inosine monophosphate (IMP) were synthesized and examined for their ability to inhibit Escherichia coli IMP dehydrogenase. All compounds studied were competitive inhibitors in IMP-dependent competition studies and lacked substrate activity.
E B, Skibo, R B, Meyer
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