Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Emine Elçin Oruç Emre"'
Autor:
Yusuf Sıcak, Bedriye Seda Kurşun Aktar, Gizem Tatar Yılmaz, Fatma Aydoğmuş Öztürk, Mehmet Öztürk, Tuğba Taşkın Tok, Emine Elçin Oruç Emre
Publikováno v:
ACS Omega, Vol 8, Iss 41, Pp 38641-38657 (2023)
Externí odkaz:
https://doaj.org/article/cec71b6dd9e7449d93daee7d5b0fa361
Publikováno v:
International Journal of Chemistry and Technology. 6:7-14
A series of E-4-(3-oxo-3-(substituted)prop-1-en-1-yl)benzoic acid derivatives (1-5) were synthesized by the Claisen-Schmidt condensation of various ketones with 4-formylbenzoic acid. The anticholinesterase (AChE and BChE), tyrosinase, and urease inhi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9eea67339163cf5963db8314c5ecc62b
https://doi.org/10.32571/ijct.1003871
https://doi.org/10.32571/ijct.1003871
Publikováno v:
Pharmaceutical Chemistry Journal. 56:559-569
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f68c3117db145802e08fbb625158e9a8
https://doi.org/10.1007/s11094-022-02674-3
https://doi.org/10.1007/s11094-022-02674-3
Autor:
Yusuf Sıcak, Hüseyin Kekeçmuhammed, Ayşegül Karaküçük‐İyidoğan, Tuğba Taşkın‐Tok, Emine Elçin Oruç‐Emre, Mehmet Öztürk
Publikováno v:
Journal of Molecular Recognition.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a8575f595afd8119dccdb4a8cbe0064
https://doi.org/10.1002/jmr.3020
https://doi.org/10.1002/jmr.3020
Autor:
Demet Taşdemir Kahraman, Ayşegül Karaküçük-İyidoğan, Yasemin Saygideger, Emine Elçin Oruç-Emre, Tugba Taskin-Tok, Eyüp Başaran, Sedat İlhan, Burcu Saygıdeğer Demir, Aykut Üren, Hasan Bayram
Publikováno v:
New Journal of Chemistry. 46:2777-2791
Thirty-four chiral compounds having benzoxadiazole and sulfonamide moieties on the skeleton have been synthesized. The in vitro cytotoxic activity and apoptotic effects of these compounds have been evaluated using the A549 lung cancer cell line.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4b0543454f3803ebfe45225c1b4909b
https://doi.org/10.1039/d1nj03809e
https://doi.org/10.1039/d1nj03809e
Publikováno v:
International Journal of Chemistry and Technology.
Inhibitors of xanthine oxidase (XO) are effective and most major therapeutic drugs for the management of gout. Chalcone compounds are important in terms of biological activity and have great importance in enzyme studies in recent years. In the presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56e89e56de2346a4ae3f49076395f68c
https://doi.org/10.32571/ijct.1199221
https://doi.org/10.32571/ijct.1199221
Publikováno v:
Volume: 5, Issue: 1 52-58
International Journal of Chemistry and Technology
International Journal of Chemistry and Technology
The anticancer activities 3-(substituted phenyl)-1-[4-(morpholine-4-yl)phenyl]prop-2-en-1-one derivatives were investigated against PC3 (Human Prostate Carcinoma Cell) and HT29 (Human colon colorectal adenocarcinoma) cell lines. The anticancer activi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::227ee86a5c2fc0f22e6c83ae132eefc6
https://doi.org/10.32571/ijct.910580
https://doi.org/10.32571/ijct.910580
Publikováno v:
Journal of Heterocyclic Chemistry. 57:830-841
WOS: 000503097500001 Twenty-four pyrazolo derivatives (1-4)(a-f) were synthesized and characterized by FTIR, H-1, and C-13 NMR (Nuclear Magnetic Resonance), and elemental analysis. The synthesized compounds were also investigated for their antioxidan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10c5f0482df4e72fe8546327721f9793
https://doi.org/10.1002/jhet.3829
https://doi.org/10.1002/jhet.3829
Autor:
B Aydınöz, Emine Elçin Oruç-Emre, Tugba Taskin-Tok, Ayşegül Karaküçük-İyidoğan, Jan Balzarini
Publikováno v:
Pharmaceutical Chemistry Journal
Two series of new aromatic thiosemicarbazone derivatives were synthesized by condensation of N-(4-cyanophenyl)hydrazine carbothioamide (I) and N-(4-methylsulfanylphenyl)hydrazine carbothioamide (II) with appropriate aromatic aldehydes in order to inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12dcff35eb66a88bf93ad08b383b070f
http://europepmc.org/articles/PMC7089137
http://europepmc.org/articles/PMC7089137
Autor:
Aysegul Iyidogan, Fatih Tok, Selin Engür, Senem Sinem Yazici, Emine Elçin Oruç-Emre, Bedia Koçyiğit-Kaymakçıoğlu, Miriş Dikmen
Publikováno v:
Letters in Drug Design & Discovery. 16:522-532
WOS: 000464613300006
Background: Hydrazones, one of the important classes of organic molecules, are pharmaceutical agents comprising -CO-NH-N=CH- group in the structure therefore and exhibiting significant biological activity. Methods: 5-Chloro-
Background: Hydrazones, one of the important classes of organic molecules, are pharmaceutical agents comprising -CO-NH-N=CH- group in the structure therefore and exhibiting significant biological activity. Methods: 5-Chloro-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ca5729b83a87772417571d5944ee8c7
https://doi.org/10.2174/1570180815666180816124102
https://doi.org/10.2174/1570180815666180816124102