| Makale Türü | Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale) | ||
| Dergi Adı | Chemistryselect (Q3) | ||
| Dergi ISSN | 2365-6549 Wos Dergi Scopus Dergi | ||
| Dergi Tarandığı Indeksler | SCI-Expanded | ||
| Makale Dili | İngilizce | Basım Tarihi | 04-2023 |
| Cilt / Sayı / Sayfa | 8 / 13 / – | DOI | 10.1002/slct.202300241 |
| Makale Linki | https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/slct.202300241 | ||
| UAK Araştırma Alanları |
Organik Kimya
Spektroskopi
Biyokimya
|
||
| Özet |
| In this study, it was planned to synthesize new members of fenamate isosteres and investigate its effect on some metabolic enzymes such as Acetylcholinesterase, Butyrylcholinesterase, α‐Glucosidase, Carbonic andyhrase I–II. The target compounds were obtained from the reaction of N‐subtituted anthranilic hydrazides with sulfonylated aldehyde derivatives. The structures of the compounds were characterized using Fourier‐transform Infrared, Nuclear Magnetic Resonance, and High‐resolution Mass Spectroscopy. Compounds had potent inhibitory strength with Ki values in the range of 0.23±0.03–7.12±0.41 μM against carbonic anhydrase‐I and 0.13±0.01–6.21±0.52 μM against carbonic anhydrase‐II. Compounds inhibited acetycholinesterase and butyrylcholinesterase with the Ki values in the range of 42.73±15.80 nM–977.52±32.67 nM and 25.84±4.09 nM–261.36±34.05 nM, respectively. All … |
| Anahtar Kelimeler |
| Anti-cholinesterase | anti-diabetic | fenamate isosteres | molecular docking | synthesis |
| Atıf Sayıları | |
| Web of Science | 38 |
| Scopus | 38 |
| Google Scholar | 44 |
| Dergi Adı | ChemistrySelect |
| Yayıncı | Wiley-Blackwell Publishing Ltd |
| Açık Erişim | Hayır |
| ISSN | 2365-6549 |
| E-ISSN | 2365-6549 |
| CiteScore | 3,0 |
| SJR | 0,366 |
| SNIP | 0,434 |