Zobrazeno 1 - 9
of 9
pro vyhledávání: '"J L, Rideout"'
Autor:
G B, Roberts, J A, Fyfe, S A, McKee, S G, Rahim, S M, Daluge, M R, Almond, J L, Rideout, G W, Koszalka, T A, Krenitsky
Publikováno v:
Biochemical pharmacology. 46(12)
The varicella-zoster virus (VZV) thymidine kinase (TK) EC 2.7.2.21) catalyzes the phosphorylation of many anti-VZV nucleosides. Purified, bacterially expressed VZV TK was characterized with regard to N-terminal amino acid sequence, pI value, pH optim
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 18(3)
A major metabolite of zidovudine (3'-azido-3'-deoxythymidine, AZT), which previously had not been observed in a variety of experimental animals, was identified in samples of plasma and urine from cynomolgus monkeys and a patient treated with AZT. The
Publikováno v:
Journal of Medicinal Chemistry. 26:1489-1494
Ribonucleosides of 4-(alkylthio)-1H-pyrazolo[3,4-d]pyrimidines have been shown to be useful anticoccidial agents [Krenitsky, T. A.; Rideout, J. L.; Koszalka, G. W.; Inmon, R. B.; Chao, E. Y.; Elion, G. B.; Latter, V. S.; Williams, R. B. J. Med. Chem.
Publikováno v:
Journal of Biological Chemistry. 251:6757-6766
2-Fluoroadenosine (F-Ado) is a potent inhibitor of lymphocyte-mediated cytolysis studied in vitro. The inhibition of cytolysis by F-Ado was potentiated markedly by an inhibiotr (Ro 20-1724) of adenosine 3':5'-monophosphate (cAMP) phosphodiesterase an
Publikováno v:
The Journal of biological chemistry. 251(21)
2-Fluoroadenosine (F-Ado) is a potent inhibitor of lymphocyte-mediated cytolysis studied in vitro. The inhibition of cytolysis by F-Ado was potentiated markedly by an inhibiotr (Ro 20-1724) of adenosine 3':5'-monophosphate (cAMP) phosphodiesterase an
Publikováno v:
ChemInform. 20
Autor:
T P, Zimmerman, G, Wolberg, G S, Duncan, J L, Rideout, L M, Beacham, T A, Krenitsky, G B, Elion
Publikováno v:
Biochemical pharmacology. 27(13)
Autor:
T A, Krenitsky, J V, Tuttle, G W, Koszalka, I S, Chen, L M, Beacham, J L, Rideout, G B, Elion
Publikováno v:
The Journal of biological chemistry. 251(13)
Kinetic constants were determined for 34 nucleoside substrates of deoxycytidine kinase (EC 2.7.1.74) from calf thymus. Substrate efficiency was assessed by the ratio of Vmax to Km. Inhibition constants were determined for 61 nonsubstrate nucleosides
Autor:
R L, Miller, D L, Adamczyk, W H, Miller, G W, Koszalka, J L, Rideout, L M, Beacham, E Y, Chao, J J, Haggerty, T A, Krenitsky, G B, Elion
Publikováno v:
The Journal of biological chemistry. 254(7)