Zobrazeno 1 - 10
of 26
pro vyhledávání: '"E. A. Yurtaeva"'
Autor:
A. E. Pozdnyakova, S. L. Adzhiakhmetova, E. O. Sergeeva, D. I. Pozdnyakov, E. A. Yurtaeva, I. O. Borodina, D. V. Kompantsev
Publikováno v:
Фармация и фармакология (Пятигорск), Vol 11, Iss 6, Pp 482-493 (2024)
Earwaxes lead to a decrease in the quality of life. A rational and effective way to eliminate earwaxes without a participation of medical personnel is to use ear drops and solutions to dissolve sulfur masses. In this regard, therapeutic and hygienic
Externí odkaz:
https://doaj.org/article/1db814a5855b48beacb629c9b5da94d9
Autor:
S. A. Luzhnova, M. Yu. Yushin, A. V. Voronkov, S. A. Osychenko, N. M. Gabitova, E. A. Yurtaeva
Publikováno v:
Журнал микробиологии, эпидемиологии и иммунобиологии, Vol 0, Iss 5, Pp 18-22 (2016)
Aim. Study anti-leprosy activity of a 1.3-diazinon-4 compound derivative under the laboratory code PYaTd 1 on the model of intra-plantar infection of mice and evaluate the character of its antibacterial effect. Materials and methods. Study of specifi
Externí odkaz:
https://doaj.org/article/83843fccf44d49a0a97849b751c062e8
Publikováno v:
"Medical & pharmaceutical journal "Pulse". :38-43
One of the ways to solve the problem of drug resistance in the therapy of infectious diseases is to develop herbal preparations with high antibacterial activity, which have a good drug safety profile, is extremely significant for long-term therapy, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::addc57dcd323498e8474c95d2181407c
https://doi.org/10.26787/nydha-2686-6838-2021-23-7-38-43
https://doi.org/10.26787/nydha-2686-6838-2021-23-7-38-43
Autor:
A. G. Tyrkov, E. A. Yurtaeva
Publikováno v:
Russian Journal of Organic Chemistry. 56:1407-1411
A method for the synthesis of 2-(1,3-diphenyl-1H-1,2,4-triazol-5-yl)-2,2-dinitroacetonitrile was developed, and its reaction with diazomethane was investigated to show the reaction involves 1,3-dipolar cycloaddition and forms a separable mixture of 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94d8b6d6fd631acb635bc5d8a4cbd25b
https://doi.org/10.1134/s1070428020080114
https://doi.org/10.1134/s1070428020080114
Autor:
A. G. Tyrkov, E. A. Yurtaeva
Publikováno v:
Russian Journal of Organic Chemistry. 55:978-982
5-(Arylmethylidene)pyrimidine-2,4,6(1H,3H,5H)-triones reacted with substituted benzaldehyde oximes in the presence of N-bromosuccinimide and triethylamine to give 1,4-diaryl-2-oxa-3,7,9-triazaspiro-[4.5]dec-3-ene-6,8,10-triones and 3,4-diaryl-1,2,5-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f4b7c9ef04ad3675c1c1170e2314328
https://doi.org/10.1134/s1070428019070108
https://doi.org/10.1134/s1070428019070108
Autor:
E. A. Yurtaeva
Publikováno v:
Informatics in school. 1:29-35
Today education system is being modernized to meet the requirements of modern times, reflected in educational and professional standards. Platforms for working out the requirements are various contests. The article describes one of the most popular c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e544668496e576611c29fa75e7a5fbca
https://doi.org/10.32517/2221-1993-2019-18-1-29-35
https://doi.org/10.32517/2221-1993-2019-18-1-29-35
Publikováno v:
Russian Journal of Organic Chemistry. 55:269-272
The reactions of 5-(arylmethylidene)-2,4,6-pyrimidine-2,4,6(1H,3H,5H)-triones with arenecarbaldehyde phenylhydrazones in the presence of sodium N-chlorobenzenesulfonamide give 2,3,7,9-tetraasaspiro-[4.5]dec-1-ene-6,8,10-triones in yields of 30–45%.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ab1aff35cc1e8ee6c13f47328d5bfa8
https://doi.org/10.1134/s1070428019020222
https://doi.org/10.1134/s1070428019020222
Synthesis and Antimicrobial Activity of 5-(Arylmethylidene)-2,4,6-Pyrimidine-2,4,6(1H,3H,5H)-Triones
Publikováno v:
Pharmaceutical Chemistry Journal. 52:506-509
A series of 5-(arylmethylidene)-2,4,6-pyrimidine-2,4,6(1H,3H,5H)-triones were synthesized and tested for antimicrobial activity against Staphylococcus and Streptococcus bacteria strains.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b1fd538b963f2c8a1614c003558230d
https://doi.org/10.1007/s11094-018-1849-7
https://doi.org/10.1007/s11094-018-1849-7
Publikováno v:
Russian Journal of Organic Chemistry. 53:1071-1074
Previously unknown substituted 4-aryl-2,7,9-triazaspiro[4.5]decane-6,8,10-triones were synthesized in 50–70% yield by heating 5-(arylmethylidene)barbituric acids with N-methyl- or N-phenylglycine and para-formaldehyde or 4-methoxybenzaldehyde in bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f5e3e036816bc330c6d685eac45452a
https://doi.org/10.1134/s1070428017070181
https://doi.org/10.1134/s1070428017070181
Publikováno v:
Pharmaceutical Chemistry Journal. 50:436-439
Aseries of 5-(heterylmethylene)hexahydropyrimidin-2,4,6-triones was synthesized and their activities against Staphylococcus aureus, Bacillus subtilis, and Escherichia coli were assessed, with determination of minimum inhibitory concentrations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3aacc60dc39d6812cf73d6b31d4bc6e1
https://doi.org/10.1007/s11094-016-1465-3
https://doi.org/10.1007/s11094-016-1465-3