Zobrazeno 1 - 8
of 8
pro vyhledávání: '"J E, Starrett"'
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 51:1672-1675
The structure of the title compound, C34H33BrO4, de- termined using direct methods and refined including the anomalous scattering from the Br atoms, shows that the absolute configuration at the C14 atom is R. High dis- placement parameters of several
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 291(1)
Synchronous hippocampal electroencephalographic activity occurring in a frequency range of 3 to12 Hz (i.e., hippocampal theta rhythm) has been associated with mnemonic processes in vivo. However, this link is tenuous and theta rhythm may be secondary
Publikováno v:
Advances in pharmacology (San Diego, Calif.). 37
Autor:
V K, Gribkoff, J T, Lum-Ragan, C G, Boissard, D J, Post-Munson, N A, Meanwell, J E, Starrett, E S, Kozlowski, J L, Romine, J T, Trojnacki, M C, Mckay, J, Zhong, S I, Dworetzky
Publikováno v:
Molecular pharmacology. 50(1)
Through expression of the cloned mouse (mSlo) or human (hSlo) large-conductance (BK) Ca(2+)-activated K+ channel in Xenopus laevis oocytes and HEK 293 cells, we characterized the effects of reported blockers and openers of BK channels to initiate the
Autor:
Patrick Balaguer, Jia-Yang Chen, Michel Pons, J E Starrett, Pierre Chambon, J Ostrowski, Silvana Penco, Hinrich Gronemeyer, P Reczek
Using retinoic acid receptor (RAR) reporter cells specific for either RAR alpha, beta or gamma, we have identified synthetic retinoids which specifically induce transactivation by RAR beta, while antagonizing RA-induced transactivation by RAR alpha a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4802f71b24d1e09b538f1f173f2fcf0f
https://europepmc.org/articles/PMC398196/
https://europepmc.org/articles/PMC398196/
Autor:
D R, Tortolani, J W, Russell, V J, Whiterock, M J, Hitchcock, I, Ghazzouli, J C, Martin, M M, Mansuri, J E, Starrett
Publikováno v:
Journal of pharmaceutical sciences. 83(3)
A series of 5’-derivatives and modified pyrimidine analogues of 2’,3’-didehydro-3’-deoxythymidine (d4T, stavudine, 1) were synthesized to determine their potential as oral prodrugs of d4T. Utilizing a screen developed for the rapid evaluation
Autor:
G. S. Poindexter, J. E. Starrett
Publikováno v:
Current Pharmaceutical Design. 11:3327-3327
Autor:
M M, Mansuri, J E, Starrett, I, Ghazzouli, M J, Hitchcock, R Z, Sterzycki, V, Brankovan, T S, Lin, E M, August, W H, Prusoff, J P, Sommadossi
Publikováno v:
Journal of medicinal chemistry. 32(2)
The nucleoside analogue 1-(2,3-dideoxy-beta-D-glycero-pent-2-enofuranosyl)thymine (d4T, 1) was prepared by ring opening of the 3',5'-anhydro compound 5. This method has been refined such that it can be used to prepare d4T on a large scale. The tripho