Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ferenc Andrasi"'
Publikováno v:
Brain Research Bulletin. 66:43-49
Cerebroprotection after administration of glutamate receptor antagonists has been well documented. The present study is intended to determine whether the non-competitive alpha-amino-3-hydroxy-methyl-4-isoxazolyl-propionic acid (AMPA) receptor antagon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7704d53b0429d336c7869a14b6851a38
https://doi.org/10.1016/j.brainresbull.2005.03.012
https://doi.org/10.1016/j.brainresbull.2005.03.012
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:
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. 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:
Ferenc Andrasi
Publikováno v:
ChemInform. 32
The development of therapeutic agents against peptic ulcer at the Institute for Drug Research at Budapest is reviewed. Among others, the genesis of the omeprazole molecule is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20566fdb9a126aef01c02415c8ddc214
https://doi.org/10.1002/chin.200150273
https://doi.org/10.1002/chin.200150273
Publikováno v:
Brain research bulletin. 68(4)
The neuroprotective effect of talampanel, a negative allosteric modulator of alpha-amino-3-hydroxy-methyl-4-isoxazolyl-propionic acid (AMPA) receptors has been described previously. However, in these studies the histological changes and not the funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a086b65810655eaa12d898de89318d3
https://pubmed.ncbi.nlm.nih.gov/16377432
https://pubmed.ncbi.nlm.nih.gov/16377432
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
Autor:
J. Lango, E. K. Bozo, Ferenc Andrasi, T. Somorai, J. Janaky, Géza Szilágyi, Jozsef Reiter, G. Nagy
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76cb561ac8e2ab25830f527615129082
https://doi.org/10.1002/chin.199026198
https://doi.org/10.1002/chin.199026198
Publikováno v:
European Journal of Pharmacology. 183:295-296
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8569ce9f58599ce6dac547aae5797cdc
https://doi.org/10.1016/0014-2999(90)93150-o
https://doi.org/10.1016/0014-2999(90)93150-o
Publikováno v:
European Journal of Pharmacology. 183:1416-1417
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::227e941ca521a9e86b527b652abfb907
https://doi.org/10.1016/0014-2999(90)94548-c
https://doi.org/10.1016/0014-2999(90)94548-c