Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Adriana Ignat"'
Autor:
Victor Roller, Angela Ciuntu, Elena Țarcă, Nicolae Sebastian Ionescu, Teodora-Simina Drăgoiu, Jana Bernic, Eva Gudumac, Emil Ceban, Ana Mișina, Tatiana Băluțel, Adriana Ignat, Liliana Fuior-Bulhac, Dana Elena Mîndru
Publikováno v:
Diagnostics, Vol 14, Iss 19, p 2243 (2024)
Malformative uropathy in children is one of the most common pathological conditions, with an incidence of 5–14% in newborns. Recent research shows that even in the current conditions, they are often diagnosed only in the advanced stages, when Chron
Externí odkaz:
https://doaj.org/article/b5b058587acc4e9781226d928267c6b7
Autor:
Valentin Zaharia, Thomas Efferth, Luminita Silaghi-Dumitrescu, Victor Kuete, Luiza Gaina, Adriana Ignat (Grozav)
Publikováno v:
Molecules, Vol 18, Iss 4, Pp 4679-4688 (2013)
New aryl-hydrazinyl-1,3-selenazole and aroyl-hydrazonyl-1,3-selenazoles were synthesized via Hantzsch type condensation reactions of selenosemicarbazides with α-halogenocarbonyl derivatives, under classical versus microwave heating conditions. Excel
Externí odkaz:
https://doaj.org/article/705a0c5448724f6e86279d5f40a30ab2
Autor:
Tiberius Ignat, Adriana Ignat
Der Artikel enthält eine Zusammenfassung des Studienberichts "The Transformative Role of University Libraries and other Memory Institutions for Citizen Science and Open Science in the Baltics" (Die transformative Rolle von Universitätsbibliotheken
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5a59ab69d41d85df6616e93cf2ab564
Autor:
Thomas Efferth, Victor Kuete, Luminita Silaghi-Dumitrescu, Valentin Zaharia, Adriana Ignat, Luiza Gaina
Publikováno v:
Molecules
Molecules; Volume 18; Issue 4; Pages: 4679-4688
Molecules, Vol 18, Iss 4, Pp 4679-4688 (2013)
Molecules; Volume 18; Issue 4; Pages: 4679-4688
Molecules, Vol 18, Iss 4, Pp 4679-4688 (2013)
New aryl-hydrazinyl-1,3-selenazole and aroyl-hydrazonyl-1,3-selenazoles were synthesized via Hantzsch type condensation reactions of selenosemicarbazides with α-halogenocarbonyl derivatives, under classical versus microwave heating conditions. Excel
Autor:
Marlyse L. Moungang, Luminita Silaghi-Dumitrescu, Victor Kuete, Valentin Zaharia, M. Vasilescu, Nicolae Palibroda, Charles Fokunang, Bonaventure T. Ngadjui, Adriana Ignat, Bathelemy Ngameni, Castelia Cristea
Publikováno v:
Medicinal Chemistry Research. 22:5670-5679
A series of novel functionalized 1,3-selenazole was synthesized by Hantzsch-type condensation reaction and evaluated for their in vitro cytotoxic activity against two human cancer cell lines. The structures of the synthesized selenosemicarbazones and
Autor:
Victor Kuete, Valentin Zaharia, Armelle T. Mbaveng, Adriana Ignat, Bathelemy Ngameni, Bonaventure T. Ngadjui
Publikováno v:
BMC Pharmacology & Toxicology
Background Bacterial multidrug resistance (MDR) constitutes a major hurdle in the treatment of infectious diseases worldwide. The present study was designed to evaluate the antibacterial activities of synthetic p-toluenesulfonyl-hydrazinothiazoles ag
Autor:
Adriana Ignat, Tamas Lovasz, Corina Tatomir, Castelia Cristea, Luminiţa Silaghi-Dumitrescu, M. Vasilescu, Eva Fischer-Fodor, Valentin Zaharia
Publikováno v:
Archiv der Pharmazie. 345:574-583
A series of new phenothiazinyl-thiazolyl-hydrazine derivatives were synthesized by Hantzsch cyclization of 1-(10-ethyl-10H-phenothiazin-3-yl)-methylidene-thiosemicarbazide with α-halocarbonyl derivatives. Comparison between classical and microwave a
Publikováno v:
Journal of Chromatographic Science. 50:157-161
Using reversed-phase high-performance thin-layer chromatography and a methanol-water mixture as the mobile phase, the lipophilicity of 12 new synthesized derivatives is studied. The first eight compounds have as a basic chemical structure aryliden-hy
Autor:
Charles Fokunang, Marlyse L. Moungang, Bonaventure T. Ngadjui, Nicolae Palibroda, Bathelemy Ngameni, Victor Kuete, Adriana Ignat, Valentin Zaharia
Publikováno v:
European Journal of Medicinal Chemistry. 45:5080-5085
A series of novel p-toluenesulfonyl-hydrazinothiazoles and hydrazino-bis-thiazoles derivatives (2a-f, 3a-f and 5-8) were synthesized by initial condensation of p-toluenesulfonylthiosemicarbazide 1 with a series of α-halogenocarbonyls in acetone or d
Autor:
Luminita Silaghi-Dumitrescu, Tamas Lovasz, Adriana Ignat, M. Vasilescu, Corina Tatomir, Eva Fischer‐Fodor, Valentin Zaharia, Castelia Cristea
Publikováno v:
ChemInform. 43
Microwave-assisted Hantzsch cyclization leads to novel phenothiazinyl-thiazolyl-hydrazine derivatives (III) which are evaluated for their antiproliferative effect against hepatic HepG2 tumor cells and colon carcinoma CC531S cells.