73202-50-3Relevant academic research and scientific papers
Synthesis and structure-activity relationships of uracil nucleotide derivatives and analogues as agonists at human P2Y2, P2Y4, and P2Y6 receptors
El-Tayeb, Ali,Qi, Aidong,Müller, Christa E.
, p. 7076 - 7087 (2006)
A series of UTP, UDP, and UMP derivatives and analogues were synthesized and evaluated at the human pyrimidinergic P2Y receptor subtypes P2Y2, P2Y4, and P2Y6 stably expressed in 1321N1 astrocytoma cells. Substituents at N3
SYNTHESIS OF TRITIUM-LABELED NUCLEOSIDE 5'-TRIPHOSPHATES AND NUCLEOSIDE 5'-DIPHOSPHATES
Gordeeva, L. S.,Kaminskii, Yu. L.,Rumyantseva, L. N.,Patokina, N. A.,Korsakova, N. A.,et al.
, p. 729 - 733 (2007/10/02)
Tritium-labeled nucleoside 5'-triphosphates (NTPs) nucleoside 5'-diphosphates (NDPs) containing the tritium label in position 8 (in the purine nucleus) and 5 (in the pyrimidine nucleus) have been obtained by the dehalogenation of the corresponding bromine derivatives with gasous tritium.The dehalogenation of the Br-NTPs and Br-NDPs was carried out at atmospheric pressure in an aqueous alkaline medium using palladium catalysts (5percent Pd/BaSO4 or α-Pd).The possibility of introducing a tritium label into nucleotides of adenine series by the heterogeneous isotope exchange reaction with gaseous tritium in the presence of 5percent Pd/BaSO4 has been investigated.For the compounds synthesized, the compositions of the eluents used for the chromatographic isolation of the desired products are given.The molar activities of the compounds synthesized were between 370 and 740 TBq/mole (10-20 kCi/mole).
