Zobrazeno 1 - 10
of 178
pro vyhledávání: '"Şükrü BEYDEMİR"'
Autor:
Betül Kaya, Ulviye Acar Çevik, Bilge Çiftçi, Hatice Esra Duran, Cüneyt Türkeş, Mesut Işık, Hayrani Eren Bostancı, Zafer Asım Kaplancıklı, Şükrü Beydemir
Publikováno v:
ACS Omega, Vol 9, Iss 42, Pp 42905-42914 (2024)
Externí odkaz:
https://doaj.org/article/1bb0689b3ea74a0ca7631ddaf2802d68
Publikováno v:
Brazilian Journal of Cardiovascular Surgery, Vol 37, Iss 4, Pp 481-487 (2022)
ABSTRACT Introduction: Presenilin 1 (PSEN1), catalase (CAT), glutathione-S-transferase (GST) and paraoxonase 1 (PON1) play a vital role in prediction, diagnosis and therapy of metabolic disorders. Methods: Metabolic enzyme activities and lipid peroxi
Externí odkaz:
https://doaj.org/article/c2106508bc6f4195b7a73fd0a2bf5fd4
Publikováno v:
Marine Science and Technology Bulletin, Vol 9, Iss 2, Pp 92-101 (2020)
In this study, the in vitro effects of some metal ions (Ag+, Cd2+, Cu2+, Fe2+, Ni2+ and Pb2+) on freshwater fish Capoeta umbla liver and gill glucose 6-phosphate dehydrogenase (G6PD) have been investigated. For this purpose, C. umbla liver and gill G
Externí odkaz:
https://doaj.org/article/a688aa41da3a4753b57f15b1c2cb9881
Autor:
Mustafa Durgun, Cüneyt Türkeş, Mesut Işık, Yeliz Demir, Ali Saklı, Ali Kuru, Abdussamat Güzel, Şükrü Beydemir, Suleyman Akocak, Sameh M. Osman, Zeid AlOthman, Claudiu T. Supuran
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 35, Iss 1, Pp 950-962 (2020)
Sulphonamides are biologically important compounds with low toxicity, many bioactivities and cost-effectiveness. Eight sulphonamide derivatives were synthesised and characterised by FT-IR, 13C NMR, 1H NMR, LC-MS and elemental analysis. Their inhibito
Externí odkaz:
https://doaj.org/article/eee04bfa1cfc44a4853cd06f8fde7298
Autor:
Samet Mert, Zuhal Alım, Mehmet Mustafa İşgör, Barış Anıl, Rahmi Kasımoğulları, Şükrü Beydemir
Publikováno v:
Arabian Journal of Chemistry, Vol 12, Iss 8, Pp 2740-2748 (2019)
In this study a series of pyrazole-3,4-dicarboxamide (3–10) derivatives bearing sulfonamide moiety were synthesized starting from 1-(3-nitrophenyl)-5-phenyl-1H-pyrazole-3,4-dicarboxylic acid (1). The structures of synthesized molecules were charact
Externí odkaz:
https://doaj.org/article/32185a467bad469294f52c733d20fdd2
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 277-284 (2017)
Aldose reductase (AR) inhibitors have vital importance in the treatment and prevention of diabetic complications. In this study, rat kidney AR was purified 19.34-fold with a yield of 3.49% and a specific activity of 0.88 U/mg using DE-52 Cellulose an
Externí odkaz:
https://doaj.org/article/f251f389503c4c19a8ee41e641da5d53
Autor:
İlhami Gulçin, Malahat Abbasova, Parham Taslimi, Zübeyir Huyut, Leyla Safarova, Afsun Sujayev, Vagif Farzaliyev, Şükrü Beydemir, Saleh H. Alwasel, Claudiu T. Supuran
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 1174-1182 (2017)
Compounds containing nitrogen and sulfur atoms can be widely used in various fields such as industry, medicine, biotechnology and chemical technology. Therefore, the reactions of aminomethylation and alkoxymethylation of mercaptobenzothiazole, mercap
Externí odkaz:
https://doaj.org/article/872df0176cda46e882aa4c001dd30491
Publikováno v:
Journal of Dental Sciences, Vol 10, Iss 2, Pp 123-127 (2015)
Background/purpose: Carbonic anhydrase (CA) VI is a unique salivary isoenzyme that regulates the pH in the oral environment. Its increased levels result in a more-alkaline saliva, hence it was hypothesized to contribute to dental calculus formation t
Externí odkaz:
https://doaj.org/article/d78360a577104e259a46f1cf1119c519
Publikováno v:
Biochemistry Research International, Vol 2017 (2017)
Phenolic compounds and flavonoids are known by their antioxidant properties and one of the most important sources for humans is the diet. Due to the harmful effects of synthetic antioxidants such as BHA and BHT, natural novel antioxidants have become
Externí odkaz:
https://doaj.org/article/1792966467b540af8ab01be1f5047917
Publikováno v:
Asian Pacific Journal of Tropical Biomedicine, Vol 4, Iss 8, Pp 603-609 (2014)
Objective: To investigate the in vitro effects of the antibacterial drugs, meropenem trihydrate, piperacillin sodium, and cefoperazone sodium, on the activity of human serum paraoxonase (hPON1). Methods: hPON1 was purified from human serum using simp
Externí odkaz:
https://doaj.org/article/abfe08c0e348430e8f04beb65f5969bf