Zobrazeno 1 - 10
of 38
pro vyhledávání: '"H. J. Teschendorf"'
Autor:
W. Lubisch, H. G. Lemaire, H. J. Teschendorf, Berthold Behl, T. Höger, D. Seemann, H. Lehmann, G. Groß, Wolfgang Löscher, H. P. Hofmann
Publikováno v:
European Journal of Neuroscience. 11:250-262
Antagonists at the ionotropic non-NMDA [AMPA (amino-methyl proprionic acid)/kainate] type of glutamate receptors have been suggested to possess several advantages compared to NMDA (N-methyl-D-aspartate) receptor antagonists, particularly in terms of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34dc3705af31441aaeac7c99937eee85
https://doi.org/10.1046/j.1460-9568.1999.00432.x
https://doi.org/10.1046/j.1460-9568.1999.00432.x
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 7:2441-2446
Pyrrolylquinoxalinediones carrying carboxylates at the pyrrole side-chain were synthesized and evaluated for AMPA receptor binding and for selectivity over other glutamate receptors. Particularly dicarboxy derivatives represent selective and highly p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46e331beb0f9acd6e3d1e78af7c1d6c5
https://doi.org/10.1016/s0960-894x(97)00428-9
https://doi.org/10.1016/s0960-894x(97)00428-9
Publikováno v:
ChemInform. 29
Pyrrolylquinoxalinediones carrying carboxylates at the pyrrole side-chain were synthesized and evaluated for AMPA receptor binding and for selectivity over other glutamate receptors. Particularly dicarboxy derivatives represent selective and highly p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a78058e56032d8f24a6ed7c14e98d7ae
https://doi.org/10.1002/chin.199804242
https://doi.org/10.1002/chin.199804242
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 290(2)
LU-111995 is a novel antipsychotic drug in clinical development. It has a clozapine-like receptor profile and affinities for dopamine D(4) and 5-hydroxytryptamine(2A) receptors. The effects of LU-111995 were examined in three models of disrupted prep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3ebf901b185489f4c8e67a8b87a1d53a
https://pubmed.ncbi.nlm.nih.gov/10411583
https://pubmed.ncbi.nlm.nih.gov/10411583
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 288(3)
The anticonvulsant activity of inhibitors of monoamine oxidase (MAO) was reported early after the development of irreversible MAO inhibitors such as tranylcypromine, but was never clinically used because of the adverse effects of these compounds. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::559d6ba3b0c1eee0c860de5648455ef7
https://pubmed.ncbi.nlm.nih.gov/10027835
https://pubmed.ncbi.nlm.nih.gov/10027835
Autor:
F.J. Garcia-Ladonat, G. Greger, G. Steiner, Remy Luthringer, Paul Bailey, L. Unger, G. Gross, Mark A. Geyer, S. Bialojant, Jean-Paul Macher, B. Rendenbach-Müller, M. Traut, K. Wicket, H.-J. Teschendorf, P. Needham
Publikováno v:
European Neuropsychopharmacology. 8:S252-S253
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92c09ad362c278d05d34e0d5100c5aa8
https://doi.org/10.1016/s0924-977x(98)80453-7
https://doi.org/10.1016/s0924-977x(98)80453-7
Autor:
B. Neumann, A. Bach, R. Munschauer, T. Hogen, G. Steiner, H.-G. Hege, K. Jochims, G. Greger, G. Gross, H.-J. Teschendorf, S. Bialojan, L. Unger, M. Traut
Publikováno v:
Drugs of the Future. 23:0191
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::790abd93e905fd336eefe694a188f947
https://doi.org/10.1358/dof.1998.023.02.485880
https://doi.org/10.1358/dof.1998.023.02.485880
Autor:
W. Worstmann, Albrecht Franke, H P Hofmann, H.-J. Teschendorf, E Hädicke, G. Steiner, H. Kreiskott, Dieter Lenke
Publikováno v:
Journal of Medicinal Chemistry. 29:1877-1888
The synthesis and pharmacological activity of new (E),(Z)-[6-(alkylamino)-11H-dibenz[b,e]azepin-11- ylidene]acetonitriles 12-45 and (E),(Z)-[6-(aminoalkoxy)-11H-dibenz[b,e]azepin-11-ylidene] acetonitriles 46-51 are described. The introduction of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea9e0cba7f2e7e95f96966a2773e783a
https://doi.org/10.1021/jm00160a015
https://doi.org/10.1021/jm00160a015
Autor:
du Mesnil de Rochemont, H. Hruszek, null Eggert, G. Beyer, null Vilmar, H. J. Teschendorf, Otto Dyes, null Heise, null Wette, null Tapfer, null Hoffmann, Georg Lange
Publikováno v:
Zeitschrift für Krebsforschung. 47:474-480
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a05c3967cdeef24bd289028c1d830035
https://doi.org/10.1007/bf01620887
https://doi.org/10.1007/bf01620887
Autor:
Franz Sørensen, H. J. Teschendorf, null Sponholz, null Böhmig, null Schmierer, null Stöhr, H. Brach, null Stelzer, null Wurm, null Schairer, Heinz Lossen, W. Teschendorf
Publikováno v:
Zeitschrift für Krebsforschung. 48:5-11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ec54c288f067d385c1c3d739354d8e2
https://doi.org/10.1007/bf01637356
https://doi.org/10.1007/bf01637356