Zobrazeno 1 - 10
of 72
pro vyhledávání: '"1-b][1"'
Publikováno v:
Бюллетень сибирской медицины, Vol 18, Iss 3, Pp 21-28 (2019)
Introduction. In the modern world people are exposed to the influence of adverse psychological and physical factors, escalating in intensity. The search for new pharmacodynamic effects of [1,3,5]-thiadiazine derivatives designated by significant biol
Externí odkaz:
https://doaj.org/article/2e60ea1c02894f95b21db4df182fa1bb
The subject of this dissertation is the search for new therapeutic strategies for pancreatic cancer and aims to implement a Drug Discovery process for the rational design and synthesis of molecules active in the modulation of pathways related to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4612::d57392e9f74a64eedd5649d75cfd63a2
https://research.vu.nl/en/publications/053bd79d-15bd-42aa-bd0f-bfab5f5d94f4
https://research.vu.nl/en/publications/053bd79d-15bd-42aa-bd0f-bfab5f5d94f4
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Randazzo, Ornella
Publikováno v:
Randazzo, O 2022, ' Design of SF3B1 subunit modulators of the SF3B spliceosome complex ', PhD, Vrije Universiteit Amsterdam .
Randazzo, O 2022, ' Design of SF3B1 subunit modulators of the SF3B spliceosome complex ', Doctor of Philosophy, Vrije Universiteit Amsterdam . < https://hdl.handle.net/1871.1/053bd79d-15bd-42aa-bd0f-bfab5f5d94f4 >
Randazzo, O 2022, ' Design of SF3B1 subunit modulators of the SF3B spliceosome complex ', Doctor of Philosophy, Vrije Universiteit Amsterdam . < https://hdl.handle.net/1871.1/053bd79d-15bd-42aa-bd0f-bfab5f5d94f4 >
The subject of this dissertation is the search for new therapeutic strategies for pancreatic cancer and aims to implement a Drug Discovery process for the rational design and synthesis of molecules active in the modulation of pathways related to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a1db90dcf5a5a71c518fef3703ad6daa
http://hdl.handle.net/10447/533610
http://hdl.handle.net/10447/533610
Autor:
Ivan Nekrasa, S. G. Krivokolysko, E. Yu. Bibik, Victor V. Dotsenko, A. V. Demenko, K. A. Frolov
Publikováno v:
Bûlleten' Sibirskoj Mediciny, Vol 18, Iss 3, Pp 21-28 (2019)
Introduction. In the modern world people are exposed to the influence of adverse psychological and physical factors, escalating in intensity. The search for new pharmacodynamic effects of [1,3,5]-thiadiazine derivatives designated by significant biol
Autor:
Pascal Sonnet, Jean Guillon, Solène Savrimoutou, Sandra Rubio, Stéphane Moreau, Mathieu Marchivie, François Hallé
Publikováno v:
Comptes Rendus. Chimie
Comptes Rendus. Chimie, Académie des sciences (Paris), 2018, 21 (11), pp.987-992. ⟨10.1016/j.crci.2018.09.013⟩
Comptes Rendus. Chimie, 2018, 21 (11), pp.987-992. ⟨10.1016/j.crci.2018.09.013⟩
Comptes Rendus. Chimie, Académie des sciences (Paris), 2018, 21 (11), pp.987-992. ⟨10.1016/j.crci.2018.09.013⟩
Comptes Rendus. Chimie, 2018, 21 (11), pp.987-992. ⟨10.1016/j.crci.2018.09.013⟩
International audience; The X-ray crystal structure of 2-(4,5-dihydro-5-phenoxymethyl-1,3-oxazol-2-ylamino)-7-(2-hydroxy-3-phenoxypropyl)hexahydro-2H,6H-pyrimido[6,1-b][1,3]oxazin-6-one (1), a structure of adduct formed by the reaction of 5-(phenoxym
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Giovanna Li Petri, Patrizia Diana, Elisa Giovannetti, Godefridus J. Peters, Stella Cascioferro, Barbara Parrino, Btissame El Hassouni, Girolamo Cirrincione, Daniela Carbone
Publikováno v:
Anticancer Research, 39(7), 3615-3620. International Institute of Anticancer Research
Li Petri, G, Cascioferro, S, el Hassouni, B, Carbone, D, Parrino, B, Cirrincione, G, Peters, G J, Diana, P & Giovannetti, E 2019, ' Biological Evaluation of the Antiproliferative and Anti-migratory Activity of a Series of 3-(6-Phenylimidazo[2,1-b][1,3,4]thiadiazol-2-yl)-1H-indole Derivatives against Pancreatic Cancer Cells* ', Anticancer Research, vol. 39, no. 7, pp. 3615-3620 . https://doi.org/10.21873/anticanres.13509
Li Petri, G, Cascioferro, S, el Hassouni, B, Carbone, D, Parrino, B, Cirrincione, G, Peters, G J, Diana, P & Giovannetti, E 2019, ' Biological Evaluation of the Antiproliferative and Anti-migratory Activity of a Series of 3-(6-Phenylimidazo[2,1-b][1,3,4]thiadiazol-2-yl)-1H-indole Derivatives against Pancreatic Cancer Cells* ', Anticancer Research, vol. 39, no. 7, pp. 3615-3620 . https://doi.org/10.21873/anticanres.13509
Heterocyclic rings are recognized as key components of many natural, semi-synthetic and synthetic molecules with a broad spectrum of biological activities. Among these molecules, the indole and imidazo[2,1-b][1,3,4]thiadiazole systems have recently b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::befd9a0f4921b003bef1c177b66e796e
https://research.vumc.nl/en/publications/7406b72f-5dc6-44f3-8d98-9d5cf83e1d41
https://research.vumc.nl/en/publications/7406b72f-5dc6-44f3-8d98-9d5cf83e1d41
Autor:
Elisa Giovannetti, Barbara Parrino, Maria Grazia Cusimano, Veronica Di Sarno, Girolamo Cirrincione, Patrizia Diana, Giovanna Li Petri, Stella Cascioferro, Domenico Schillaci, Simona Musella
Publikováno v:
European Journal of Medicinal Chemistry, 167, 200-210. Elsevier Masson SAS
Cascioferro, S, Parrino, B, Petri, G L, Cusimano, M G, Schillaci, D, di Sarno, V, Musella, S, Giovannetti, E, Cirrincione, G & Diana, P 2019, ' 2,6-Disubstituted imidazo[2,1-b][1,3,4]thiadiazole derivatives as potent staphylococcal biofilm inhibitors ', European Journal of Medicinal Chemistry, vol. 167, pp. 200-210 . https://doi.org/10.1016/j.ejmech.2019.02.007
Cascioferro, S, Parrino, B, Petri, G L, Cusimano, M G, Schillaci, D, di Sarno, V, Musella, S, Giovannetti, E, Cirrincione, G & Diana, P 2019, ' 2,6-Disubstituted imidazo[2,1-b][1,3,4]thiadiazole derivatives as potent staphylococcal biofilm inhibitors ', European Journal of Medicinal Chemistry, vol. 167, pp. 200-210 . https://doi.org/10.1016/j.ejmech.2019.02.007
A class of 36 new 2-(6-phenylimidazo[2,-1-b][1,3,4]thiadiazol-2-yl)-1H-indoles was efficiently synthesized and evaluated for their anti-biofilm properties against the Gram-positive bacterial reference strains Staphylococcus aureus ATCC 25923, S. aure