Academic Journal

Synthesis and Pharmacological Evaluation of Novel 1′‐[2‐(Difluoromethoxy)benzyl]‐2′ H,5′ H‐spiro[8‐azabicyclo[3.2.1]octane‐3,4′‐imidazolidine]‐2′,5′‐diones and Their Derivatives

التفاصيل البيبلوغرافية
العنوان: Synthesis and Pharmacological Evaluation of Novel 1′‐[2‐(Difluoromethoxy)benzyl]‐2′ H,5′ H‐spiro[8‐azabicyclo[3.2.1]octane‐3,4′‐imidazolidine]‐2′,5′‐diones and Their Derivatives
المؤلفون: Madaiah, Malavalli, Prashanth, Maralekere K., Revanasiddappa, Hosakere D., Veeresh, Bantal
المصدر: Archiv der Pharmazie ; volume 347, issue 5, page 370-380 ; ISSN 0365-6233 1521-4184
بيانات النشر: Wiley
سنة النشر: 2014
المجموعة: Wiley Online Library (Open Access Articles via Crossref)
الوصف: A series of novel 1′‐[2‐(difluoromethoxy)benzyl]‐2′ H ,5′ H ‐spiro[8‐azabicyclo[3.2.1]octane‐3,4′‐imidazolidine]‐2′,5′‐dione substituted hydantoins ( 5 – 32 ) were synthesized using an appropriate synthetic route and characterized by elemental analysis and spectral data. The novel molecules were screened for anticonvulsant activity in mice by maximal electroshock (MES) and subcutaneous pentylenetetrazol (ScPTZ)‐induced seizure tests. The neurotoxicity was assessed using the rotarod method. Compounds 9 , 10 , 18 , 30 , and 31 exhibited anticonvulsant potency against MES seizure and in the ScPTZ model, with lesser neurotoxicity. Some title compounds showed lesser central nervous system depression compared to phenytoin.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1002/ardp.201300289
الاتاحة: http://dx.doi.org/10.1002/ardp.201300289
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fardp.201300289
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ardp.201300289
Rights: http://onlinelibrary.wiley.com/termsAndConditions#vor
رقم الانضمام: edsbas.43371E97
قاعدة البيانات: BASE