Publications by authors named "F Erturk"
This study aims to evaluate the influences of ultraviolet radiation A and B (UVA + B) exposure on the liver and heart organs of albino rats. Female Wistar Albino rats, whose hair of the dorsal skin was shaved, were exposed to a combined UVA + B radiation for 2 h/day, for 4 weeks in order to be compared with the control group. Histopathological findings in vital organs (liver and heart) were evaluated.
View Article and Find Full Text PDFNovel enamine derivatives were synthesized from the reaction of lactone and chalcones and their antiproliferative and cytotoxic activities against six cancer cell lines (e. g., HeLa, HT29, A549, MCF7, PC3 and Hep3B) and one normal cell lines (e.
View Article and Find Full Text PDFObjectives: The aim of this study is to evaluate the efficacy of greater occipital nerve (GON) blockage in patients with migraine and fibromyalgia (FM) comorbidity.
Patients And Method: 20 patients who were diagnosed as FM according to 2010 American College of Rheumatology (ACR) diagnostic criteria and migraine according to International Classification of Headache Disorers II criteria and did not recieve any medication or GON block for both disorders were included for the study. GON blocks were repeated every week in the first month and repeated montly for the following 2 months.
The new 1-(4-(3-(aryl)acryloyl)phenyl)-1H-pyrrole-2,5-diones (5a-g) were prepared from 4'-aminchalcones (3a-g) and screened for biological activities. All compounds (3a-g and 5a-g), except 3d and 3e displayed good cytotoxic activities with IC values in the range of 7.06-67.
View Article and Find Full Text PDFArticle Synopsis
- The study focuses on new hybrid compounds combining chalcone and methanoisoindole units, which were synthesized and tested for their anticancer and antimicrobial properties.
- Six of these compounds showed strong anticancer effects, with inhibition rates between 80.51% and 97.02% compared to the standard drug 5-FU.
- Additionally, the compounds exhibited inhibitory effects on human carbonic anhydrase isoenzymes, suggesting potential for various biomedical applications.