Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Tamas Hamori"'
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 10:899-902
Some 5-methyl analogues (14a-e) of the non-competitive AMPA antagonists 3-acylated 1-(4-aminophenyl)-4-methyl-7,8-methylenedioxy-4,5-dihydro-3H-2,3-benzodi azepines (2,3) have been synthesized. Generally they show diminished or low biological activit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33bbfb847443a1aa7e71fa4b5e67207e
https://doi.org/10.1016/s0960-894x(00)00117-7
https://doi.org/10.1016/s0960-894x(00)00117-7
Autor:
Tamas Hamori, Edit Horvath, Márton I.K. Fekete, Miklós Palkovits, Katalin Horvath, Sandor Solyom
Publikováno v:
Progress in Neurobiology. 60:309-342
Over the past 20 years, several members of the 2,3-benzodiazepine family have been synthesized. Some of these compounds—tofisopam (Grandaxin®), girisopam, nerisopam—exert significant anxiolytic and antipsychotic activities. Sites where actions o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55fac91f14bdd4069a6a9d69ea05ecb4
https://doi.org/10.1016/s0301-0082(99)00020-9
https://doi.org/10.1016/s0301-0082(99)00020-9
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :1423-1427
A highly specific enantioselective reduction, elaborated for the reduction of the 3,4-carbon–nitrogen double bond of 4-methyl-7,8-methylenedioxy-1-(4-nitrophenyl)-4,5-dihydro-3H-2,3-benzodiazepine 4 made possible the synthesis of the enantiomers of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b57b74becc7e28aa60ad3d41a453f7f7
https://doi.org/10.1039/p19950001423
https://doi.org/10.1039/p19950001423
Autor:
Peter Botka, Jeno Korosi, Pal Berzsenyi, István Tarnawa, Ferenc Andrasi, István Ling, Tamas Hamori
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 3:99-104
A series of N-substituted 1-(4'-aminophenyl)-4-methyl-3,4-dihydro-7,8-methylene-dioxy5H-2,3-benzodiazepines, structural analogues of the selective non-NMDA antagonist GYKI 52466, has been synthesized and tested for biological activity, in vivo and in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::149ab7aa7c949969375c61807045455b
https://doi.org/10.1016/s0960-894x(00)80100-6
https://doi.org/10.1016/s0960-894x(00)80100-6
Publikováno v:
ChemInform. 26
A highly specific enantioselective reduction, elaborated for the reduction of the 3,4-carbon–nitrogen double bond of 4-methyl-7,8-methylenedioxy-1-(4-nitrophenyl)-4,5-dihydro-3H-2,3-benzodiazepine 4 made possible the synthesis of the enantiomers of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6d0d0dfe2f99bb6d559256c3ab2024a
https://doi.org/10.1002/chin.199538210
https://doi.org/10.1002/chin.199538210
Publikováno v:
ChemInform. 31
Some 5-methyl analogues (14a-e) of the non-competitive AMPA antagonists 3-acylated 1-(4-aminophenyl)-4-methyl-7,8-methylenedioxy-4,5-dihydro-3H-2,3-benzodi azepines (2,3) have been synthesized. Generally they show diminished or low biological activit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::009d30d10d61b0aa8c90d8dd6ee88e48
https://doi.org/10.1002/chin.200036171
https://doi.org/10.1002/chin.200036171
Autor:
Gizella Ábrahám, István Tarnawa, Laszlo Gabor Harsing, Miklós Patthy, István Ling, Ferenc Andrasi, Tamas Hamori, K.M. Horvath, Pal Berzsenyi, Sandor Solyom, Istvan Kiraly, Istvan Pallagi, Gabor Kapus, Gyula Horváth, Emese Csuzdi
Publikováno v:
Bioorganicmedicinal chemistry. 8(8)
New halogen atom substituted 2,3-benzodiazepine derivatives condensed with an azole ring on the seven membered part of the ring system of type 3 and 4 as well as 5 and 6 were synthesized. It was found that chloro-, dichloro- and bromo-substitutions i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60573fb97ce642879a397296ab8620c5
https://pubmed.ncbi.nlm.nih.gov/11003158
https://pubmed.ncbi.nlm.nih.gov/11003158
Publikováno v:
Metszetek, Vol 7, Iss 4 (2018)
A humánerőforrás iránti kereslet igen erősen megváltozott az elmúlt évtizedben és átrendeződött a munkaerőpiac keresleti és kínálati oldala egyaránt. A 2000-es évek első évtizedére a munkaerő túlkínálat volt jellemző globál
Externí odkaz:
https://doaj.org/article/14c012baf2f94e3cb005c16fc7919654