Zobrazeno 1 - 10
of 66
pro vyhledávání: '"S, Chumpradit"'
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 44:S225-S227
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 44:S524-S526
Autor:
Diana Bray, Michael E. Clark, Kenneth K. Andersen, S. Chumpradit, Colin D. Hubbard, Kathleen M. Young, Gregory J. Habgood
Publikováno v:
ChemInform. 23
Autor:
Kenneth K. Andersen, S. Chumpradit, Michael E. Clark, Kathleen M. Young, Colin D. Hubbard, Gregory J. Habgood, Diana Bray
Publikováno v:
The Journal of Organic Chemistry. 56:6508-6516
Publikováno v:
Neuropharmacology. 36(7)
Recently, [125I]S(-)5-OH-PIPAT [5-hydroxy-2-(N-n-propyl-N-3'-iodo-2'-propenyl)aminotetralin], a derivative of S(-)5-OH-DPAT (5-hydroxy-N,N-di-n-propyl-aminotetralin), was reported to be a better radioiodinated dopamine D2-like receptor ligand than th
Autor:
P D, Mozley, J B, Stubbs, H J, Kim, W, McElgin, S, Chumpradit, M P, Kung, G, Romaniello, H F, Kung
Publikováno v:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 36(7)
FIDA-2 (R-(+)-2,3-dimethoxy-5-iodo-N-[(1-4'-fluorobenzyl)-2-pyrrolidinyl) methyl] benzamide) is a simultaneously fluorinated and iodinated D2/D3 dopamine receptor antagonist. The purpose of this study was to measure its biodistribution and radiation
Autor:
J M, Vessotskie, M P, Kung, S, Chumpradit, G, Romaniello, W, McElgin, D, Frederick, R T, Malison, H F, Kung
Publikováno v:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 36(7)
R(+)-FIDA2, (R)-(+)-2,3-dimethoxy-5-iodo-N-[(1-(4'-fluorobenzyl)-2-pyrrolid iny l)- methyl]benzamide, is a new dopamine D2-like receptor imaging agent that can be labeled with either 123I or 18F for SPECT or PET imaging. The purpose of this study was
Publikováno v:
The Journal of Organic Chemistry. 53:4667-4675
Lorsque la substitution se fait par un mecanisme a 4 ou 6 centres, la reaction est endocyclique et intramoleculaire pour les exemples choisis dans l'article
Publikováno v:
ChemInform. 20
Lorsque la substitution se fait par un mecanisme a 4 ou 6 centres, la reaction est endocyclique et intramoleculaire pour les exemples choisis dans l'article
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 45:537-538