Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Ebru Mete"'
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 189-192 (2017)
4-(3-(4-Substituted-phenyl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl) benzenesulfonamides (9–16) were successfully synthesized and their chemical structures were confirmed by 1H NMR, 13C NMR, and HRMS spectra. Carbonic anhydrase I and II inhibitory eff
Externí odkaz:
https://doaj.org/article/3df16b74650445eaad5f140c0e9e32c1
Autor:
Halise Inci Gul, Ebru Mete, Sakip Emre Eren, Hiroshi Sakagami, Cem Yamali, Claudiu T. Supuran
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 169-175 (2017)
In this study, 4-[3-(4-hydroxyphenyl)-5-aryl-4,5-dihydro-pyrazol-1-yl]benzenesulfonamide (1–9) types compounds were synthesized and their chemical structures were confirmed by 1H NMR, 13C NMR and HRMS spectra. Cytotoxic and carbonic anhydrase (CA)
Externí odkaz:
https://doaj.org/article/07b5424b884d4990987515c2a246034b
Autor:
Mehmet Emin Topaloglu, Medine Gulluce, Oztekin Algul, Ebru Mete, Halise Inci Gul, Cavit Kazaz, Sinan Bilginer
Publikováno v:
Molecules, Vol 16, Iss 6, Pp 4660-4671 (2011)
The development of resistance to current antifungal therapeutics drives the search for new effective agents. The fact that several acetophenone-derived Mannich bases had shown remarkable antifungal activities in our previous studies led us to design
Externí odkaz:
https://doaj.org/article/7b16f98269464cfabff5a541995f5b66
Publikováno v:
Molecules, Vol 12, Iss 12, Pp 2579-2588 (2007)
1-Aryl-3-phenethylamino-1-propanone hydrochlorides 1-10, which are potentialpotent cytotoxic agents, were synthesized via Mannich reactions using paraformaldehyde,phenethylamine hydrochloride as the amine component and acetophenone, 4’-m
Externí odkaz:
https://doaj.org/article/512af28aa1044a8a9a21fc6dd613f303
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 9, Pp o2702-o2703 (2012)
In the title salt, C12H18NO+·Cl−, N—H...Cl interactions between the free chloride anions and the organic cations connect the molecules into hydrogen-bond dimers, forming a R22(8) motif. The dimers are linked by C—H...O hydrogen bonds into chai
Externí odkaz:
https://doaj.org/article/041f47ba0b3346deb922bd61d6de1c5f
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 9, Pp o2706-o2707 (2012)
In the title compound, C13H20NO+·Cl−, the protonated amino N atom is hydrogen bonded to the chloride anion. N—H...Cl hydrogen bonds link the anions and cations into dimers, which are connected by C—H...O hydrogen bonds, forming supramolecular
Externí odkaz:
https://doaj.org/article/19e382255e764dbc8bddb5e8d51a3ac8
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 1, Pp o71-o71 (2012)
The crystal structure of the title compound, C12H17BrNO+·Cl−, is stabilized by N—H...Cl and C—H...O hydrogen bonds, forming a three-dimensional network. The interactions framework is completed by C—H...π contacts between a methylene group a
Externí odkaz:
https://doaj.org/article/052804fa53f34e5aa59d740cd47bb4d1
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 6, Pp o1447-o1448 (2011)
In the title compound, C26H25Cl2NO2, the piperidine ring adopts a chair conformation with a cis configuration of the carbonyl and hydroxy substituents. The dihedral angle between the aromatic rings of the chlorobenzene groups is 24.3 (2)°. The pheny
Externí odkaz:
https://doaj.org/article/006de0c750b04826b54c0c6e2848bf00
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 352:35-42
Pyrazoline derivatives are among solvatochromic dyes and they are the most widely used in many fields such as sensors, labeling agent and optoelectronic devices. Therefore, synthesis of new pyrazoline derivatives and determination of their optical be
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 189-192 (2017)
Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry
4-(3-(4-Substituted-phenyl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl) benzenesulfonamides (9-16) were successfully synthesized and their chemical structures were confirmed by H-1 NMR, C-13 NMR, and HRMS spectra. Carbonic anhydrase I and II inhibitory eff