Zobrazeno 1 - 7
of 7
pro vyhledávání: '"NAZAN İNCELER"'
Autor:
Rengul Cetin-Atalay, Sultan Nacak Baytas, Nazan Inceler, Deniz Cansen Kahraman, Nilüfer N. Turan, Yeşim Özkan
With the aim of achieving new compounds possessing both anti-inflammatory and antiplatelet activities, we synthesized (E)-3-[3-(pyridin-3/4-yl)-1-(phenyl/sulfonylmethylphenyl)-1H-pyrazol-4-yl]acrylamides, and evaluated their COX-1 and COX-2 inhibitor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4968113d94c45b940a62d938d2437b67
https://avesis.gazi.edu.tr/publication/details/df0bd09b-b3eb-4c1e-9fca-3912b3585b1b/oai
https://avesis.gazi.edu.tr/publication/details/df0bd09b-b3eb-4c1e-9fca-3912b3585b1b/oai
Publikováno v:
Medicinal Chemistry Research. 22:5922-5933
(E)-3-[3-(pyridin-4-yl)-1-phenyl-1H-pyrazole-4-yl]acryl amides were evaluated for their antiplatelet activities. Compounds 4o and 4r were found as active derivatives showing a potent inhibitory activity on the arachidonic acid-induced aggregation, wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c605502bce2c37223052e517620213a0
https://doi.org/10.1007/s00044-013-0580-x
https://doi.org/10.1007/s00044-013-0580-x
Publikováno v:
Medicinal Chemistry Research. 22:3109-3118
A series of novel thiophene containing 1,3-diarylpyrazole derivatives were synthesized and the structures were determined by IR, H-1-NMR, and HRMS analysis. The anticancer activity of the title compounds against MCF7, MDA-MB-231, HeLa, Raji, and HL60
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c95a04c788654f3edc2f56246be5a568
https://doi.org/10.1007/s00044-012-0317-2
https://doi.org/10.1007/s00044-012-0317-2
Autor:
Abdurrahman Olğaç, Ernest Hamel, Sevda Menevse, Erden Banoglu, Akin Yilmaz, Nazan Inceler, Sultan Nacak Baytas, Giampietro Viola, Roberta Bortolozzi
Publikováno v:
Bioorganicmedicinal chemistry. 22(12)
In this study, we synthesized a series of trans-indole-3-acrylamide derivatives (3a-k) and investigated their activity for inhibition of cell proliferation against five human cancer cell lines (HeLa, MCF7, MDA-MB-231, Raji and HL-60) by MTT assay. Co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::938a969de0c3046e7d28d23ce0d63a89
https://pubmed.ncbi.nlm.nih.gov/24816066
https://pubmed.ncbi.nlm.nih.gov/24816066
Synthesis, cytotoxicity, and molecular properties prediction of novel 1,3-diarylpyrazole derivatives
A novel combinatorial library of ester and amide derivatives of 1,3-diarylpyrazoles was designed and synthesized. Anticancer activities of these compounds were assessed against MCF7, MDA-MB-231, HeLa, Raji, and HL60 human cancer cells by MTT assay. O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ba476da902986d43d64cac06b6cc265
https://avesis.gazi.edu.tr/publication/details/92b3a02e-d542-4d3d-b3fd-9101334a7b41/oai
https://avesis.gazi.edu.tr/publication/details/92b3a02e-d542-4d3d-b3fd-9101334a7b41/oai
Autor:
MEHTAP GÖKÇE, NURETTİN ABACIOĞLU, MECİT ORHAN ULUDAĞ, KHATEREH FATTAHPOUR MAVANEH, NAZAN İNCELER, SULTAN BAYTAŞ
Eleven antipyrine/pyridazinone hybrids were synthesized and evaluated for their in vivo analgesic and anti-inflammatory activities by p-benzoquinone-induced writhing test and carrageenan-induced paw edema model, respectively. The test results indicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd64938f61d6c9c05bcc0ab2f31f3b2a
https://avesis.gazi.edu.tr/publication/details/dc8a2ea5-8a6a-4c14-8ff1-0d518303e6df/oai
https://avesis.gazi.edu.tr/publication/details/dc8a2ea5-8a6a-4c14-8ff1-0d518303e6df/oai
Autor:
Mehtap Gokce, khatereh fattahpour mavaneh, Nazan Inceler, M. Orhan Uludag, Sultan Nacak Baytas, Nurettin Abacioglu
Publikováno v:
The FASEB Journal. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::add3c3fd4c34eb9013926395e0ab23eb
https://doi.org/10.1096/fasebj.25.1_supplement.lb388
https://doi.org/10.1096/fasebj.25.1_supplement.lb388