Academic Journal

(1R,2S,5R)-5-Methyl-2-(propan-2-yl)cyclohexyl 4-amino-3-phenylbutanoate hydrochloride: Synthesis and anticonvulsant activity

التفاصيل البيبلوغرافية
العنوان: (1R,2S,5R)-5-Methyl-2-(propan-2-yl)cyclohexyl 4-amino-3-phenylbutanoate hydrochloride: Synthesis and anticonvulsant activity
المؤلفون: Nesterkina Mariia, Musatov Vladimir, Honcharova Olena, Kravchenko Iryna
المصدر: Open Chemistry, Vol 20, Iss 1, Pp 703-707 (2022)
بيانات النشر: De Gruyter, 2022.
سنة النشر: 2022
المجموعة: LCC:Chemistry
مصطلحات موضوعية: ester, l-menthol, phenibut, terpenoid, anticonvulsant activity, steglich esterification, Chemistry, QD1-999
الوصف: Ester based on l-menthol and phenibut ‒ (1R,2S,5R)-5-methyl-2-(propan-2-yl)cyclohexyl 4-amino-3-phenylbutanoate hydrochloride was obtained in 78% yield using N,N′-dicyclohexylcarbodiimide as a coupling reagent along with catalytic amount of 4-dimethylaminopyridine. The obtained product was characterized by FT-IR, fast-atom bombardment-mass spectrometry along with 1H-NMR and 13C-NMR spectral analysis; the purity was assessed using high-performance liquid chromatography. Phenibut ester has been examined on the models of chemically- and electrically-induced seizures for potential anticonvulsant profile.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2391-5420
2022-0189
Relation: https://doaj.org/toc/2391-5420
DOI: 10.1515/chem-2022-0189
URL الوصول: https://doaj.org/article/a068a88b3bb84af1990c1370b525cf9b
رقم الانضمام: edsdoj.068a88b3bb84af1990c1370b525cf9b
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:23915420
20220189
DOI:10.1515/chem-2022-0189