| Yazarlar |
Esra Nur Çakmak
|
|
Prof. Dr. Mahmut GÜR
Kastamonu Üniversitesi, Türkiye |
|
Bayram Kıran
Türkiye |
| Özet |
| The aim of this study is to examine the effects of drug active compounds, which are widely used in the treatment of epilepsy, on voltage-gated Na+ channels are important channels that advance the action potential in the excitation direction by molecular docking method. These molecules have been selected considering the physiopathological effect mechanisms of epilepsy disease. When the action potential is stimulated, Na+ channels allow sodium ion entry into the cell and cause epilepsy seizures. For this reason, PDB ID: 4PA6 receptor, which acts as an antagonist according to its activity on the canal in the formation of epileptic seizures, was chosen for molecular docking study. As a result of molecular docking studies; Phenytoin gave the best binding affinity for 4PA6 with a value of -7.7 kcal/mol. Other results in descending order (as kcal/mol); Mesuximide (-7.5), Remacemide (-7.3), Tiagabine (-7.1), Ethotoin and Mephenytoin (-7.0), Primidone (-6.9), Topiramate (-6.6), Oxcarbazepine and Lamotrigine (-6.3), Felbamate (-6.0), Lacosamide (-5.9), Zonisamide (-5.8), Levetirecetam and Gabapentin (-5.7), Ethosuximide (-5.6), Trimethadion (-5.1), Valproic Acid (-5.0), Vigabatrin (-4.0), determined as. |
| Anahtar Kelimeler |
| Makale Türü | Özgün Makale |
| Makale Alt Türü | Ulusal alan endekslerinde (TR Dizin, ULAKBİM) yayımlanan tam makale |
| Dergi Adı | Hittite Journal of Science and Engineering |
| Dergi ISSN | 2148-4171 |
| Dergi Tarandığı Indeksler | TR DİZİN |
| Makale Dili | İngilizce |
| Basım Tarihi | 06-2022 |
| Cilt No | 9 |
| Sayı | 2 |
| Sayfalar | 89 / 102 |
| Doi Numarası | 10.17350/HJSE19030000259 |
| Makale Linki | https://dergipark.org.tr/en/pub/hjse/issue/70658/1047636 |
| Atıf Sayıları |
