Synthesis and Anticonvulsant Activity of SomeN-Phenyl-2-phtalimidoethanesulfonamide Derivatives

التفاصيل البيبلوغرافية
العنوان: Synthesis and Anticonvulsant Activity of SomeN-Phenyl-2-phtalimidoethanesulfonamide Derivatives
المؤلفون: Ozlem Akgul, Fatma Sultan Kilic, Kevser Erol, Varol Pabuccuoglu
المصدر: Archiv der Pharmazie. 340:656-660
بيانات النشر: Wiley, 2007.
سنة النشر: 2007
مصطلحات موضوعية: Male, Electroshock, Sulfonamides, Magnetic Resonance Spectroscopy, Stereochemistry, Chemistry, medicine.medical_treatment, Pharmaceutical Science, Phthalimides, Dose level, Ring (chemistry), Mice, Structure-Activity Relationship, Taltrimide, Anticonvulsant, Seizures, Drug Discovery, Nitro, medicine, Animals, Pentylenetetrazole, Moiety, Molecule, Anticonvulsants, Pharmacophore
الوصف: In this study, inspired by the structures of the taltrimide, 2-phthalimidoethanesulphonamide, and the anilide pharmacophore known to be synthetically produced anticonvulsant compounds, fifteen N-phenyl-2-phtalimidoethanesulfonamide derivatives bearing substituents with diverse electronic and hydrophobic features on N-phenyl ring were synthesized. The structural confirmation of the title compounds was achieved by interpretation of spectral and analytical data. The anticonvulsant activity of the title compounds was determined against maximal electroshock seizure in mice at a dose level of 100 mg/kg. The preliminary screening results indicated that the exchange of the N-isopropyl moiety for an N-phenyl ring in the taltrimide molecule abolished the anticonvulsant activity. However, introducing certain substituents, such as nitro, methyl, and chloro, into the N-phenyl ring lead to more active compounds in comparison to the unsubstituted derivatives.
تدمد: 1521-4184
0365-6233
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53ddbe70eaa5747c29680f88f858f9c7
https://doi.org/10.1002/ardp.200700166
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....53ddbe70eaa5747c29680f88f858f9c7
قاعدة البيانات: OpenAIRE