Zobrazeno 1 - 10
of 14
pro vyhledávání: '"R H, Dodd"'
Autor:
J. Braudeau, L. Dauphinot, A. Duchon, A. Loistron, R. H. Dodd, Y. Hérault, B. Delatour, M. C. Potier
Publikováno v:
Advances in Pharmacological Sciences, Vol 2011 (2011)
Decrease of GABAergic transmission has been proposed to improve memory functions. Indeed, inverse agonists selective for α5 GABA-A-benzodiazepine receptors (α5IA) have promnesiant activity. Interestingly, we have recently shown that α5IA can rescu
Externí odkaz:
https://doaj.org/article/e7d457cc58184dafa204b2ca4a157715
Publikováno v:
Molecules, Vol 5, Iss 3, Pp 443-444 (2000)
11α,12α-aziridinosteroids (2a, b, c) were prepared from 5β-H-11-pregnene-3,20-dione (1) using different iminophenyliodinanes and cloramine aziridination reagents.
Externí odkaz:
https://doaj.org/article/daa98bf0ad8340deabe442333b1a9143
Autor:
J, Braudeau, L, Dauphinot, A, Duchon, A, Loistron, R H, Dodd, Y, Hérault, B, Delatour, M C, Potier
Publikováno v:
Adv Pharmacol Sci
Adv Pharmacol Sci, 2011, 2011, pp.e-153218. ⟨10.1155/2011/153218⟩
Advances in Pharmacological Sciences
Adv Pharmacol Sci, 2011, 2011, pp.e-153218. ⟨10.1155/2011/153218⟩
Advances in Pharmacological Sciences
International audience; Decrease of GABAergic transmission has been proposed to improve memory functions. Indeed, inverse agonists selective for α5 GABA-A-benzodiazepine receptors (α5IA) have promnesiant activity. Interestingly, we have recently sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::57ae50b3a7a8ce0ff2040abce73a0c38
https://hal.science/hal-00764914
https://hal.science/hal-00764914
Publikováno v:
British journal of pharmacology. 131(4)
(+)-ROD188 was synthesized in the search for novel ligands of the GABA binding site. It shares some structural similarity with bicuculline. (+)-ROD188 failed to displace [(3)H]-muscimol in binding studies and failed to induce channel opening in recom
Autor:
X, Doisy, M, Dekhane, M, Le Hyaric, J F, Rousseau, S K, Singh, S, Tan, V, Guilleminot, H, Schoemaker, M, Sevrin, P, George, P, Potier, R H, Dodd
Publikováno v:
Bioorganicmedicinal chemistry. 7(5)
Based on the structure of ZK91296 (4d), a high affinity partial agonist of the central benzodiazepine (omega) receptor, a series of pyrrolo[2,3-c]pyridine-5-carboxylate derivatives having mainly aralkyl and aralkyloxy substituents at C-3 was synthesi
Publikováno v:
Molecules 2000;5(3):443-444
Biblioteca Digital (UBA-FCEN)
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
Molecules
Volume 5
Issue 3
Pages 443-444
Scopus-Elsevier
Molecules, Vol 5, Iss 3, Pp 442-443 (2000)
Molecules, Vol 5, Iss 3, Pp 443-444 (2000)
Biblioteca Digital (UBA-FCEN)
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
Molecules
Volume 5
Issue 3
Pages 443-444
Scopus-Elsevier
Molecules, Vol 5, Iss 3, Pp 442-443 (2000)
Molecules, Vol 5, Iss 3, Pp 443-444 (2000)
11α,12α-aziridinosteroids (2a, b, c) were prepared from 5β-H-11-pregnene-3, 20-dione (1) using different iminophenyliodinanes and cloramine aziridination reagents. Fil:Di Chenna, P. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Natur
Autor:
E. Sigel, R. H. Dodd
Publikováno v:
Drugs of the Future. 26:1191
Publikováno v:
HETEROCYCLES. 36:435
The 1,3-dipolar cycloaddition reaction of 3,4-dihydro-β-carboline azomethine ylide (4) with dimethyl fumarate (5) and fumaronitrile (5') is described. The resulting hexahydroindolizine products (6) and (6') were dehydrogenated stepwise (-H 2 , -2H 2
Publikováno v:
Bulletin de l'Academie nationale de medecine. 167(7)
Autor:
L, Prado de Carvalho, P, Venault, E, Cavalheiro, M, Kaijima, A, Valin, R H, Dodd, P, Potier, J, Rossier, G, Chapouthier
Publikováno v:
Advances in biochemical psychopharmacology. 38