Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Şafak Ulusoylar Yıldırım"'
Autor:
Zafer Asım Kaplancıklı, Fatih Demirci, Gamze Göger, Ömer Öztürk, Yusuf Özkay, Şafak Ulusoylar Yıldırım, Leyla Yurttaş, Usama Abu Mohsen
Publikováno v:
Volume: 38, Issue: 5 815-824
Turkish Journal of Chemistry
Turkish Journal of Chemistry
WOS: 000340769100013
Some thiazole derivatives bearing dithiocarbamic acid esters were synthesized in order to investigate their anticandidal activity and cytotoxicity. The structures of the obtained final compounds (6a-j) were confirmed by spec
Some thiazole derivatives bearing dithiocarbamic acid esters were synthesized in order to investigate their anticandidal activity and cytotoxicity. The structures of the obtained final compounds (6a-j) were confirmed by spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49d69aa03be1ffa1c5224785473b0c17
https://doi.org/10.3906/kim-1312-62
https://doi.org/10.3906/kim-1312-62
Autor:
Lütfi Genç, Gülşen Akalın Çiftçi, Şafak Ulusoylar Yıldırım, Halide Edip Temel, Mehlika Dilek Altıntop, Zafer Asım Kaplancıklı
Publikováno v:
Medicinal Chemistry Research. 22:3751-3759
WOS: 000320673200021
In this study, we aimed to study the apoptotic effects of 2-[(9-ethyl-9H-carbazol-3-yl)amino]-2-oxoethyl N,N-disubstituted dithiocarbamates on A549 lung carcinoma and C6 glioma cell lines. Cytotoxicity analyses of DNA synthe
In this study, we aimed to study the apoptotic effects of 2-[(9-ethyl-9H-carbazol-3-yl)amino]-2-oxoethyl N,N-disubstituted dithiocarbamates on A549 lung carcinoma and C6 glioma cell lines. Cytotoxicity analyses of DNA synthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::598b981e069b57b47f16bee358fbeec4
https://doi.org/10.1007/s00044-012-0325-2
https://doi.org/10.1007/s00044-012-0325-2
Autor:
Zafer Asım Kaplancıklı, Şafak Ulusoylar Yıldırım, Mehlika Dilek Altıntop, Gülşen Akalın Çiftçi
WOS: 000336742500010
Oxadiazoles have received much attention due to their wide range of biological activities including antitumor activity. In this study, we aimed to study apoptotic effects of some 1,3,4-oxadiazole derivatives on human lung ad
Oxadiazoles have received much attention due to their wide range of biological activities including antitumor activity. In this study, we aimed to study apoptotic effects of some 1,3,4-oxadiazole derivatives on human lung ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f7a850f98e1e371c71188b44a827766
https://hdl.handle.net/11421/12481
https://hdl.handle.net/11421/12481
Autor:
Şafak Ulusoylar Yıldırım, Gülhan Turan-Zitouni, Zafer Asım Kaplancıklı, Usama Abu Mohsen, Ahmet Özdemir, Gülşen Akalın Çiftçi, Leyla Yurttaş
WOS: 000330766600050
A new class of tetrazole-hydrazone derivatives including chloro-substituted phenyl moiety were synthesized to perform anticancer activity screening. The structural elucidation of the compounds was performed by IR, H-1 NMR, C
A new class of tetrazole-hydrazone derivatives including chloro-substituted phenyl moiety were synthesized to perform anticancer activity screening. The structural elucidation of the compounds was performed by IR, H-1 NMR, C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe63ca9a69f99670542f005ce94095e9
https://hdl.handle.net/11421/13538
https://hdl.handle.net/11421/13538
Autor:
Şeref Demirayak, Zafer Asım Kaplancıklı, Leyla Yurttaş, Şafak Ulusoylar Yıldırım, Gülsen Akalın Çiftçi
Publikováno v:
ChemInform. 44
Most of the synthesized title compounds (V) (16 examples), especially derivatives (Va)—(Vc), exhibit considerable activity and selectivity against C6 and MCF-7 cancer cell lines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::092d5497fb36b2bff690dfaa602c31bb
https://doi.org/10.1002/chin.201337154
https://doi.org/10.1002/chin.201337154
Autor:
Gülsen Akalın Çiftçi, Zafer Asım Kaplancıklı, Şeref Demirayak, Şafak Ulusoylar Yıldırım, Leyla Yurttaş
WOS: 000318810800008
PubMed ID: 23526768
The synthesis of some new 1-(2-aryl-2-oxoethyl)-2-[(morpholine-4-yl)thioxomethyl]benzimidazole derivatives and investigation of their anticancer activities were the aims of this work. 2-(Chloromethyl
PubMed ID: 23526768
The synthesis of some new 1-(2-aryl-2-oxoethyl)-2-[(morpholine-4-yl)thioxomethyl]benzimidazole derivatives and investigation of their anticancer activities were the aims of this work. 2-(Chloromethyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83fc1ee6d0d33d91ef9b8dd92c609b9d
https://hdl.handle.net/20.500.12511/840
https://hdl.handle.net/20.500.12511/840
Autor:
Zafer Asım Kaplancıklı, Şafak Ulusoylar Yıldırım, Mehlika Dilek Altıntop, G. Iscan, Guelsen Akalin, Guelhan Turan‐Zitouni, Ahmet Oezdemir
Publikováno v:
ChemInform. 43
From the new triazolothiadiazine derivatives (III), compound (IIId) is found to be the most potent derivative against Candida albicans.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b79f03630d7227186ee60caca1ec0603
https://doi.org/10.1002/chin.201211158
https://doi.org/10.1002/chin.201211158
Autor:
Gülhan Turan-Zitouni, Gülşen Akalın, Mehlika Dilek Altıntop, Ahmet Özdemir, Gökalp İşcan, Zafer Asım Kaplancıklı, Şafak Ulusoylar Yıldırım
WOS: 000298120500033
PubMed ID: 21959231
New triazolothiadiazine derivatives were synthesized via the ring closure reaction of 4-amino-5-substituted-2,4-dihydro-3H-1,2,4-triazol-3-thiones with phenacyl bromides. The compounds were tested in
PubMed ID: 21959231
New triazolothiadiazine derivatives were synthesized via the ring closure reaction of 4-amino-5-substituted-2,4-dihydro-3H-1,2,4-triazol-3-thiones with phenacyl bromides. The compounds were tested in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a574fe8e38ecc970a51d86f097635b6
https://hdl.handle.net/11421/13474
https://hdl.handle.net/11421/13474