Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Evgenia N Olsufyeva"'
Autor:
Svetlana S Efimova, Anna N Tevyashova, Evgenia N Olsufyeva, Evgeny E Bykov, Olga S Ostroumova
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0188573 (2017)
A series of amides of the antifungal antibiotic amphotericin B (AmB) and its conjugates with benzoxaboroles was tested to determine whether they form pores in lipid bilayers and to compare their channel characteristics. The tested derivatives produce
Externí odkaz:
https://doaj.org/article/a124d1e6a4c04342adc642a4cc5441c1
Publikováno v:
Antibiotics, Vol 12, Iss 5, p 894 (2023)
A significant increase of microbial resistance to glycopeptides (especially vancomycin-resistant enterococci and Staphylococcus aureus) prompted researchers to design new semisynthetic glycopeptide derivatives, such as dual-action antibiotics that co
Externí odkaz:
https://doaj.org/article/1ea4532cf3e04970acb86dd876501600
Publikováno v:
Russian Chemical Reviews
This review summarizes main advances achieved by Russian researchers in the synthesis and characterization of semi-synthetic antibiotics of a new generation in the period from 2004 to 2019. The following classes of compounds are considered as the bas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b6fc5de04b7a31466aa19f591168b2b
https://doi.org/10.1070/rcr4892
https://doi.org/10.1070/rcr4892
Eremomycin pyrrolidide: a novel semisynthetic glycopeptide with improved chemotherapeutic properties
Autor:
E. N. Bychkova, Ivan D. Treshalin, Andrey V. Dekhnich, Elena P. Mirchink, Evgenia N Olsufyeva, Maria N. Preobrazhenskaya, Mikhail G Chernobrovkin, Elena B. Isakova, Andrey E. Shchekotikhin, E. R. Pereverzeva, Roman S. Kozlov
Publikováno v:
Drug Design, Development and Therapy. 12:2875-2885
Evgenia N Olsufyeva,1 Andrey E Shchekotikhin,1,2 Elena N Bychkova,1 Eleonora R Pereverzeva,1 Ivan D Treshalin,1 Elena P Mirchink,1 Elena B Isakova,1 Mikhail G Chernobrovkin,3 Roman S Kozlov,4 Andrey V Dekhnich,4 Maria N Preobrazhenskaya1,† 1Gause I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db7c79871fed548796c58b17e15d4493
https://doi.org/10.2147/dddt.s173923
https://doi.org/10.2147/dddt.s173923
Autor:
Evgenia N Olsufyeva, Olga S. Ostroumova, E. E. Bykov, Svetlana S. Efimova, Anna N. Tevyashova
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0188573 (2017)
PLoS ONE
PLoS ONE
A series of amides of the antifungal antibiotic amphotericin B (AmB) and its conjugates with benzoxaboroles was tested to determine whether they form pores in lipid bilayers and to compare their channel characteristics. The tested derivatives produce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b280b151d828c50d71e8db25b5a7348
http://europepmc.org/articles/PMC5706719?pdf=render
http://europepmc.org/articles/PMC5706719?pdf=render
Autor:
Evgenia N Olsufyeva, Lyubov G. Dezhenkova, Oleg Yu Savelyev, Trenin As, Alexander A. Shtil, Vladimir I. Polshakov, Anna N. Tevyashova, Alexander M. Korolev
Publikováno v:
The Journal of antibiotics. 69(7)
A novel series of conjugates of the antifungal antibiotic amphotericin B (AmB) with benzoxaboroles was synthesized. Antifungal activity of new compounds was tested on yeastβ Candida albicans and Cryptococcus humicolus and filamentous fungi Aspergill
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d93fd2f348f28e7d597e625229a4c67
https://pubmed.ncbi.nlm.nih.gov/27005557
https://pubmed.ncbi.nlm.nih.gov/27005557
Autor:
Miroshnikova Ov, Svetlana S. Printsevskaya, Evgenia N Olsufyeva, Daniel Chu, Jake J Plattner, Maria N. Preobrazhenskaya
Publikováno v:
The Journal of Antibiotics. 60:235-244
The acylation of unprotected vancomycin or eremomycin with activated esters of N(alpha)-protected amino acids or N(alpha)-alkyl-N(alpha)-Fmoc-amino acids is directed selectively to the amino group of the disaccharide branch (N') and after Fmoc-group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7069ccd53d91ee7f4de3fb767e03f10
https://doi.org/10.1038/ja.2007.28
https://doi.org/10.1038/ja.2007.28
Autor:
Evgenia N Olsufyeva, Andrey Y. Pavlov, Svetlana S. Printsevskaya, Elena P. Mirchink, Maria N. Preobrazhenskaya
Publikováno v:
Journal of Medicinal Chemistry. 46:1204-1209
The antibacterial properties of glycopeptide antibiotics are based on their interaction with the d-Ala-d-Ala containing pentapeptide of bacterial peptidoglycan. The hydrophobic amides of vancomycin (1), teicoplanin (2), teicoplanin aglycon (3), and e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17596f137a4221403286b979c4b47944
https://doi.org/10.1021/jm020320o
https://doi.org/10.1021/jm020320o
Autor:
Anna N. Tevyashova, Ivan D. Treshalin, E. R. Pereverzeva, Maria N. Preobrazhenskaya, Svetlana S. Printsevskaya, Sergey B. Zotchev, O. A. Galatenko, Svetlana E. Solovieva, M. I. Reznikova, Aleksei S. Trenin, Elena P. Mirchink, Evgenia N Olsufyeva, Elena B. Isakova
A comprehensive comparative analysis of the structure-antifungal activity relationships for the series of biosynthetically engineered nystatin analogues and their novel semisynthetic derivatives, as well as amphotericin B (AMB) and its semisynthetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16e1a2ef3f2408f70d966590e48af902
https://europepmc.org/articles/PMC3719701/
https://europepmc.org/articles/PMC3719701/
Autor:
Alexander M. Korolev, M. I. Reznikova, G. B. Lapa, Jacob J. Plattner, Maria N. Preobrazhenskaya, Evgenia N Olsufyeva, Yong Kang Zhang, Svetlana S. Printsevskaya
Publikováno v:
Future medicinal chemistry. 5(6)
Background: The ability of boron-containing compounds to undergo a number of novel binding interactions with drug target functional groups has recently been described. In an extension of this work, we have incorporated a boron-containing scaffold, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17e4e4a6918173e442e7dcecc0ca5f3f
https://pubmed.ncbi.nlm.nih.gov/23617428
https://pubmed.ncbi.nlm.nih.gov/23617428