A series of pyrazolo[3,4-d]pyrimidine derivatives was synthesized and evaluated for the Src kinase inhibitory activities. Compound 6e and 10c exhibited inhibition of Src kinase with an IC50 value of 5.6 and 5.1 μM, respectively. Hydroxamate derivative 15a was found to be a metal-mediated inhibitor for human Csk with an IC50 value of 2.0 μM showing 56-fold selectivity over Src kinase inhibition.

Investigations of the mechanism of pyrimidine nucleotide formation from orotic acid led to the isolation and characterization of an activated ribose phosphate derivative which serves as an intermediate in the overall process. In earlier communications (1) we have described briefly the enzymatic synthesis of this new intermediate, identified as PRPPI (equation (I)), and the occurrence of enzymes...

The title pyrimidine derivative, C7H8N4S, is essentially planar, with a maximum deviation of 0.029 (2) Å from the mean plane of the non-H atoms. In the crystal, mol-ecules are linked by an inter-molecular bifurcated N-H⋯N hydrogen bond between the cyano N atom and the two amino groups, an N-H⋯N hydrogen bond between the two amino groups and a weak C-H⋯π inter-action, forming a three-dimensional...

On the basis of 102 assigned frequencies to in plane vibrations of pyrimidine, pyrimidine-2-d2, pyrimidine-2, 5-d2, pyrimidine-4,6-d2, pyrimidine-2,4,6-d3 and pyrimidine-d4, 35 valance force field constants including 14 principals and 21 interaction force constants are calculated. New assignments are suggested for n<su...

In this reaction, an additional compound (X) should be formed in amounts equal to that of riboflavin. It has been shown (2) that all of the atoms of the pyrimidine portion, nitrogen atom 8, and the ribityl moiety of 6,7-dimethyl8.ribityllumazine are retained in the unknown compound. Furthermore, during isolation by column chromatography, the unknown compound was cleaved into ribitylamine and a ...

A pyrimidine-based sensor () has been synthesized through the facile one pot reaction of pyrrole-2-carboxaldehyde, 2-aminobenzimidazole and 1, 3-dimethylbarbituric acid in methanol using a few drops of HCl as a catalyst. Further, compound was fabricated into its fluorescent organic nanoparticles (FONPs) and characterized using DLS and SEM. The photophysical evaluation of the FONPs was done agai...

Ribonuclease A and ribonuclease S-protein have been investigated for their ability to catalyze the preparative synthesis of dinucleoside monophosphates and trinucleoside diphosphates of specific base composition and sequence. Kinetic analysis of identical reactions catalyzed by ribonuclease A and S-protein suggests that the synthetic activity of the native protein and the derivative differ with...

To investigate the influence of the pyrimidine 2-keto group on selection of nucleotides for incorporation into DNA by polymerases, we have prepared two C nucleoside triphosphates that are analogues of dCTP and dTTP, namely 2-amino-5-(2'-deoxy-beta-d-ribofuranosyl)pyridine-5'-triphosphate (d*CTP) and 5-(2'-deoxy- beta-d-ribofuranosyl)-3-methyl-2-pyridone-5'-triphosphate (d*TTP) respectively. Bot...

In the title pyrimidine-2,4-dione derivative, C14H16N2O2S, the dihedral angle between the six-membered rings is 77.81 (10)°. The mol-ecule is twisted about the Cp-S (p = pyrimidine) bond, with a C-S-C-N torsion angle of -59.01 (17)°. An intramolecular C-H⋯S hydrogen bond generates an S(5) ring motif. In the crystal, bifurcated acceptor N-H⋯O and C-H⋯O hydrogen bonds generate inversion-related d...

In this reaction, an additional compound (X) should be formed in amounts equal to that of riboflavin. It has been shown (2) that all of the atoms of the pyrimidine portion, nitrogen atom 8, and the ribityl moiety of 6,7-dimethyl8.ribityllumazine are retained in the unknown compound. Furthermore, during isolation by column chromatography, the unknown compound was cleaved into ribitylamine and a ...