Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Liudmila Kraeva"'
Autor:
Petr Snetkov, Elizaveta Rogacheva, Arina Kremleva, Svetlana Morozkina, Mayya Uspenskaya, Liudmila Kraeva
Publikováno v:
Pharmaceutics, Vol 14, Iss 6, p 1186 (2022)
Bacterial infections have accompanied humanity throughout its history and became vitally important in the pandemic area. The most pathogenic bacteria are multidrug-resistant strains, which have become widespread due to their natural biological respon
Externí odkaz:
https://doaj.org/article/5da74726642d4e479246c17e2a21468a
Autor:
Sergey Chuprun, Dmitry Dar’in, Elizaveta Rogacheva, Liudmila Kraeva, Oleg Levin, Olga Manicheva, Marine Dogonadze, Tatiana Vinogradova, Olga Bakulina, Mikhail Krasavin
Publikováno v:
Antibiotics, Vol 9, Iss 10, p 666 (2020)
Starting from the structure of antimycobacterial screening hit OTB-021 which was devoid of activity against ESKAPE pathogens, we designed, synthesized and tested two mutually isomeric series of novel simplified analogs, 2- and 4-(3-nitro-1,2,4-triazo
Externí odkaz:
https://doaj.org/article/9b4e8bcc2c3549e784e50624700c3436
Publikováno v:
Experimental and Сlinical Urology. 15:120-128
Introduction. Introduction Antibacterial therapy is the main line of treatment for lower urinary tract infections (LUTIs). At the same time, not always satisfactory efficacy and the growing problem of antibiotic resistance of the main uropathogens de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::628b4c0e4ac5dc8e2c9fd10bb4e90a43
https://doi.org/10.29188/2222-8543-2022-15-2-120-128
https://doi.org/10.29188/2222-8543-2022-15-2-120-128
Publikováno v:
Experimental and Сlinical Urology. 15:170-176
Introduction. The proportion of candidal balanoposthitis is 30-35% of all forms of infectious balanoposthitis. Diabetes mellitus is one of the main risk factors for the development of the disease. The purpose of the study was to conduct a comparative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27878d3fd7e136a41cf2c56dff4b098f
https://doi.org/10.29188/2222-8543-2022-15-1-170-176
https://doi.org/10.29188/2222-8543-2022-15-1-170-176
Autor:
Liudmila Kraeva
Publikováno v:
Infekcionnye bolezni. 19:85-91
In recent years, acute respiratory viral infections (ARVIs) and other acute respiratory diseases (ARDs) have acquired some new characteristics of the disease course. The structure of complications has changed, in particular, such complications as com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0394e4fd53137d22506fb1047b45e667
https://doi.org/10.20953/1729-9225-2021-3-85-91
https://doi.org/10.20953/1729-9225-2021-3-85-91
Autor:
Alexander N. Koronatov, Pavel A. Sakharov, Vladimir V. Sharoyko, Elizaveta V. Rogacheva, Alexander F. Khlebnikov, Mikhail S. Novikov, Nikolai V. Rostovskii, Tatiana B. Tennikova, Liudmila Kraeva, Artem G. Glukharev
Publikováno v:
RSC Advances. 9:37901-37905
Non-natural 2H-azirine-2-carboxylic acids were obtained in high yields by FeCl2-catalyzed isomerization of 5-chloroisoxazoles to azirine-2-carbonyl chlorides followed by their hydrolysis. The 3-aryl- and 3-heteroaryl-substituted acids are stable duri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f024b7db14c7c1382529ad23bab13578
https://doi.org/10.1039/c9ra09345a
https://doi.org/10.1039/c9ra09345a
Autor:
Alexandra A. Sysoeva, Mikhail V. Il’in, Vitalii V. Suslonov, Dmitrii S. Bolotin, Liudmila Kraeva, Alexander S. Novikov, Elizaveta Rogacheva, Vadim Yu. Kukushkin
Publikováno v:
New Journal of Chemistry. 43:17358-17366
The developed one-pot protocol to 5-amino-1,2,4-triazoles or 5-amino-1,2,4-oxadiazoles includes an interplay between aminonitrones R1C(NH2)N+(Me)O− (R1 = Alk, Ar, Het), isocyanides R2NC (R2 = Alk, Ar), Br2, and hydrazines (for the triazoles) or hyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4dfcdbab2c877746c26dccd4ec5fea0
https://doi.org/10.1039/c9nj04529e
https://doi.org/10.1039/c9nj04529e
Autor:
Alexander F. Khlebnikov, Anastasiya V. Agafonova, Alexander N. Koronatov, Pavel A. Sakharov, Mikhail S. Novikov, Nikolai V. Rostovskii, Liudmila Kraeva, Elizaveta V. Rogacheva
Publikováno v:
Organicbiomolecular chemistry. 18(46)
Azirine-containing dipeptides and depsipeptides with a wide range of substituents have been synthesized in high yields via the Passerini and Ugi multicomponent reactions (MCRs) using 2H-azirine-2-carboxylic acids as the acid component. The obtained M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a03e67a949f1c678cbba4e4bd07e6b8
https://pubmed.ncbi.nlm.nih.gov/33170920
https://pubmed.ncbi.nlm.nih.gov/33170920
Autor:
Alexander Kolobov, Vladimir A. Karasev, Viktor Luchinin, Yuri Orkhov, Natalia Shevchenko, Tatiana M. Zimina, Liudmila Kraeva, Ivan Mandrik, Nikita O. Sitkov
Publikováno v:
The 1st International Electronic Conference on Biosensors.
At the end of year 2019 the first reports appeared of a new coronavirus and on 31st December 2019 WHO declared a public health emergency of international concern. To date (as of 6:08 pm CET, 24th November 2020) according to WHO the new coronavirus, n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fc385149daf04ad09ecf02207649287
https://doi.org/10.3390/iecb2020-07059
https://doi.org/10.3390/iecb2020-07059
Autor:
Dmitry Dar'in, Elizaveta Rogacheva, Tatiana Vinogradova, Liudmila Kraeva, Oleg V. Levin, Marine Dogonadze, Mikhail Krasavin, Olga Manicheva, Sergey Chuprun, Olga Bakulina
Publikováno v:
Antibiotics
Volume 9
Issue 10
Antibiotics, Vol 9, Iss 666, p 666 (2020)
Volume 9
Issue 10
Antibiotics, Vol 9, Iss 666, p 666 (2020)
Starting from the structure of antimycobacterial screening hit OTB-021 which was devoid of activity against ESKAPE pathogens, we designed, synthesized and tested two mutually isomeric series of novel simplified analogs, 2- and 4-(3-nitro-1,2,4-triazo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f8fe446ef96b23b195b5b6a357d821c
https://doi.org/10.3390/antibiotics9100666
https://doi.org/10.3390/antibiotics9100666