Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Amal M. Y. Mohsen"'
Autor:
Hans-Georg Breitinger, Darius P. Zlotos, Carmen Villmann, Christoph A. Sotriffer, Anders A. Jensen, Amal M. Y. Mohsen, Ulrike Holzgrabe, Yasmine M. Mandour, Mohamed Akmal Marzouk, Ulrike Breitinger
Publikováno v:
Journal of Natural Products. 82:2332-2336
(11S)-11-Aminostrychnine (1) and N-[(11S)-strychnine-11-yl]propionamide (2) were synthesized and characterized as antagonists of homomeric α1 and heteromeric α1β glycine receptors in a functional fluorescence-based assay and a patch-clamp assay an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6efdc1b829a35955cc90bab2aa51665
https://doi.org/10.1021/acs.jnatprod.9b00180
https://doi.org/10.1021/acs.jnatprod.9b00180
Autor:
Darius P, Zlotos, Amal M Y, Mohsen, Yasmine M, Mandour, Mohamed A, Marzouk, Ulrike, Breitinger, Carmen, Villmann, Hans-Georg, Breitinger, Christoph, Sotriffer, Anders A, Jensen, Ulrike, Holzgrabe
Publikováno v:
Journal of natural products. 82(8)
(11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::458c977f3b45ffabfe13ebbf9b9a3dcf
https://pubmed.ncbi.nlm.nih.gov/31385511
https://pubmed.ncbi.nlm.nih.gov/31385511
Autor:
Christoph A. Sotriffer, Carmen Villmann, Amal M. Y. Mohsen, Anders A. Jensen, Edita Sarukhanyan, Yasmine M. Mandour, Ulrike Holzgrabe, Hans-Georg Breitinger, Thomas Dandekar, Darius P. Zlotos, Ulrike Breitinger, Maha M. Banoub
Publikováno v:
Journal of natural products. 79(12)
A series of (E)-11-isonitrosostrychnine oxime ethers, 2-aminostrychnine, (strychnine-2-yl)propionamide, 18-oxostrychnine, and N-propylstrychnine bromide were synthesized and evaluated pharmacologically at human α1 and α1β glycine receptors in a fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94f525f80096ec47d5cee85f90bf7843
https://pubmed.ncbi.nlm.nih.gov/27966945
https://pubmed.ncbi.nlm.nih.gov/27966945
Publikováno v:
Chemistrybiodiversity. 11(8)
Nine strychnine derivatives including neostrychnine, strychnidine, isostrychnine, 21,22-dihydro-21-hydroxy-22-oxo-strychnine, and several hydrogenated analogs were synthesized, and their antagonistic activities at human α1 and α1β glycine receptor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4493aa3dd2a55a4fc6864191770bcfb
https://pubmed.ncbi.nlm.nih.gov/25146769
https://pubmed.ncbi.nlm.nih.gov/25146769
Autor:
Justin Julius, Shalini Sethi, Paula A. Witt-Enderby, Mira A. M. Behnam, Amal M. Y. Mohsen, David Heckman, Christian Markl, Mohamed I. Attia, Darius P. Zlotos
Publikováno v:
MedChemComm. 2:991
A synthesis and pharmacological evaluation of new melatonin receptor ligands obtained by 2-substitution of melatonin with (indol-1-yl)methyl, (isoindolin-2-yl)methyl, and (tetrahydroiso-quinolin-2-yl)methyl groups is reported. The isoindoline analogu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a3f133f4581404d8b535b941c64ac8c
https://doi.org/10.1039/c1md00149c
https://doi.org/10.1039/c1md00149c