> Шифр: ВУ18/2018/2 Журнал 2018г. № 2 Kolisnyk, S. V. The reactivity of ethyl esters of 2-(benzoylamino) (1-R-2-oxoindoline-3-ylidene) acetic acids / S. V. Kolisnyk [et al.]. - С.3-7 Другие авторы: Svechnikova O. M., Vinnyk O. F., Kolisnyk O. V., Altukhov O. O. Yusifova, D. Yu. Determination of a number of indicators of “Venocoryl” ointment / D. Yu. Yusifova, T. A. Suleymanov. - С.8-11 Kovalevska, I. V. The spectrophotometric study of thioctic acid solutions to develop the method of its quantitative determination / I. V. Kovalevska, O. A. Ruban, V. O. Grud’ko. - С.12-18 Kerimov, Yu. B. The pharmacognostic study of the aerial part of Prangos ferulacea lindl. at the stage of the beginning of vegetation / Yu. B. Kerimov [et al.]. - С.19-23 Другие авторы: Isaev D. I., Kerimli E. G., Akhmedov E. Yu. Redkin, R. G. The synthesis of spiro[indole-3,1’-pyrrolo[3,4-c]pyrrole]-2,4’,6’-trione derivatives, the study of their antimicrobial activity and the molecular docking on staphylococcal dehydrosqualene synthase / R. G. Redkin, K. V. Hlebova. - С.24-35 Sydora, N. V. The technological aspects for complex processing of hawthorn fruits / N. V. Sydora, A. M. Kovalyova, V. K. Iakovenko. - С.36-40 Kriukova, A. I. The study of the technological and microbiological parameters of a dietary supplement “Osteovert” / A. I. Kriukova, I. M. Vladymyrova. - С.41-47 Nemchenko, A. S. Analysis of approaches to pharmacotherapy of patients with cardiovascular diseases according to the data of the Ukrainian and British Formularies / A. S. Nemchenko, Yu. Ye. Kurylenko. - С.48-51 Kobets, M. M. A social significance of the pharmacogenetic testing in Ukraine on the example of the CYP2B6 gene participating in the nicotine metabolism / M. M. Kobets, O. V. Filiptsova, Yu. M. Kobets. - С.52-56 Syumka, Ye. I. The study of the antimicrobial activity of ethylene-N,N’- bis(spiroindole-3,3’-pyrrolo[3,4-c]pyrrole-2a’,5a’-dihydro-2,2’,6’(1H,1’H,5’H)-trione) derivatives / Ye. I. Syumka [et al.]. - С.57-62 Другие авторы: Osolodchenko T. P., Chernykh V. P., Shemchuk L. A. Имеются экземпляры в отделах: всего 1 Свободны: 1 |
Redkin, R. G. The synthesis of spiro[indole-3,1’-pyrrolo[3,4-c]pyrrole]-2,4’,6’-trione derivatives, the study of their antimicrobial activity and the molecular docking on staphylococcal dehydrosqualene synthase [Текст] / R. G. Redkin, K. V. Hlebova> // Вісн. фармації. - 2018. - № 2. - С. 24-35 MeSH-главная: (химический синтез) ПИРРОЛЫ -- PYRROLES (химический синтез) МОЛЕКУЛЯРНОЙ СТЫКОВКИ МОДЕЛИРОВАНИЕ -- MOLECULAR DOCKING SIMULATION (использование, методы) АНТИБАКТЕРИАЛЬНЫЕ СРЕДСТВА -- ANTI-BACTERIAL AGENTS (химический синтез) СТРУКТУРА-АКТИВНОСТЬ, ВЗАИМОСВЯЗЬ -- STRUCTURE-ACTIVITY RELATIONSHIP ИНДОЛЫ -- INDOLES (химический синтез) Аннотация: To synthesize the series of new spiro[indole-3,1’-pyrrolo[3,4-c]pyrrole]-2,4’,6’-trione derivatives, study their physicochemical characteristics, antibacterial activity and precision of the molecular docking on the model of staphylococcal dehydrosqualene synthase Доп.точки доступа: Hlebova, K. V. Свободных экз. нет |