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The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity Научная публикация

Журнал Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Вых. Данные Год: 2020, Том: 56, Номер: 6, Страницы: 769-775 Страниц : 7 DOI: 10.1007/s10593-020-02729-x
Ключевые слова 3-phenacyluridine; alkylation; biological activity; hypnotics; uridine receptor
Авторы Novakov Ivan A. 1 , Brunilina Leila L. 1 , Kirillov Ivan A. 1 , Nawrozkij Maxim B. 1 , Robinovich Mariya D. 1,2 , Titova Evgeniya S. 1 , Sheikin Dmitry S. 1 , Ruchko Evsey A. 3 , Pavlova Alla, V 4 , Kotlyarova Anastasiya A. 4 , Tolstikova Tatyana G. 4
Организации
1 (Данные Web of science) Volgograd State Tech Univ, 28 Lenina Ave, Volgograd 400005, Russia
2 (Данные Web of science) JSC Volzhsky Orgsinthese, 100 Aleksandrova St, Volzhskiy 404117, Russia
3 (Данные Web of science) JSC Pharm Sintez, 2,Build 46 2nd Kabelnaya St, Moscow 111024, Russia
4 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, 9 Akad Lavrentieva Ave, Novosibirsk 630090, Russia

Реферат: New structural analogs of 3-phenacyluridine were obtained as a result of N(3)-alkylation of 1-(2-acetoxyethyl)- and 1-(2-acetoxyethoxymethyl)uracil. Biological studies of the title compounds in an acute in vivo experiment did not reveal their hypnotic properties and ability to enhance the effects of diazepam and chloral hydrate.
Библиографическая ссылка: Novakov I.A. , Brunilina L.L. , Kirillov I.A. , Nawrozkij M.B. , Robinovich M.D. , Titova E.S. , Sheikin D.S. , Ruchko E.A. , Pavlova A.V. , Kotlyarova A.A. , Tolstikova T.G.
The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
Chemistry of Heterocyclic Compounds. 2020. V.56. N6. P.769-775. DOI: 10.1007/s10593-020-02729-x WOS Scopus РИНЦ
Даты:
Опубликована в печати: 1 июн. 2020 г.
Опубликована online: 18 июл. 2020 г.
Идентификаторы:
Web of science WOS:000549786600005
Scopus 2-s2.0-85088151588
РИНЦ 45410782
OpenAlex W3043020827
Альметрики: