Zobrazeno 1 - 10
of 39
pro vyhledávání: '"E N, Bychkova"'
Autor:
E. E. Bykov, E. P. Mirchink, E. B. Isakova, E. N. Bychkova, E. N. Olsufyeva, A. N. Tevyashova
Publikováno v:
Антибиотики и Химиотерапия, Vol 62, Iss 3-4, Pp 10-17 (2020)
Antibacterial activity of hybrid antibiotics vancomycin-azithromycin (C11, C12-carbonate) and eremomycin-azitromycin (C11, C12-carbonate) was evaluated. Quantum chemical calculations of complexes of hybrid antibiotics with a model tripeptide ligand a
Externí odkaz:
https://doaj.org/article/6c541ce8cc114b3bae93328cdf91c18f
Publikováno v:
Антибиотики и Химиотерапия, Vol 60, Iss 9-10, Pp 7-11 (2020)
Amidation of the end carboxyl group of eremomycin and vancomycin by pinacolinic 4- or 3-amino methyl phenyl boron acids esters in the presence of the condensing reagent PyBOP resulted in formation of novel carboxamides of the antibiotics (IIIa-VIa).
Externí odkaz:
https://doaj.org/article/28dec7c29e9241d79f6dea09ad8de075
Publikováno v:
Pharmaceutical Chemistry Journal. 53:1018-1021
Amphotericin B (AmB) remains a drug of first choice for treatment of most severe mycoses despite significant toxicity and solubility problems. Screening of a series of new semisynthetic polyene macrolide derivatives identified AmB N-(2-aminoethyl)ami
Autor:
Anna N. Tevyashova, E. N. Bychkova, S. E. Solov’eva, Andrey E. Shchekotikhin, Natalya E Grammatikova
Publikováno v:
Pharmaceutical Chemistry Journal. 53:976-980
The search for new antifungal agents with improved chemotherapeutic properties has produced the semisynthetic polyene macrolide amphotericin B derivative amphamide, which has a number of clear advantages over the starting antibiotic. The development
Publikováno v:
материалы конференции.
Publikováno v:
Pharmaceutical Chemistry Journal. 52:930-935
Methods for selective chemical modification of the antitumor antibiotic olivomycin A(OA) were developed at GINA. The compound olivamide with advantages over starting OA was selected from series of OA analogs. The goal of the present work was to devel
Autor:
Anna N. Tevyashova, George V. Zatonsky, Evgeny E. Bykov, Svetlana E. Solovieva, Olga S. Ostroumova, Treshchalin Ivan D, Andrey E. Shchekotikhin, E. R. Pereverzeva, Elena B. Isakova, Natalia E. Grammatikova, Elena P. Mirchink, Svetlana S. Efimova, E. N. Bychkova
Publikováno v:
ACS infectious diseases. 6(8)
Amphotericin B (AmB, 1) is the drug of choice for treating the most serious systemic fungal or protozoan infections. Nevertheless, its application is limited by low solubility in aqueous media and serious side effects such as infusion-related reactio
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
Autor:
E. N. Bychkova, Ilya A. Osterman, Réka Erdei, Gyula Batta, Anna N. Tevyashova, Alexander M. Korolev, Elena B. Isakova, Zsolt Szücs, Elena P. Mirchink
One of the promising directions of the combined approach is the design of dual-acting antibiotics - heterodimeric structures on the basis of antimicrobial agents of different classes. In this study a novel series of azithromycin-glycopeptide conjugat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0127ae3d01e60af3e27529856ebe826c
Publikováno v:
Antibiotiki i khimioterapiia = Antibiotics and chemoterapy [sic]. 60(9-10)
Amidation of the end carboxyl group of eremomycin and vancomycin by pinacolinic 4- or 3-amino methyl phenyl boron acids esters in the presence of the condensing reagent PyBOP resulted in formation of novel carboxamides of the antibiotics (IIIa-VIa).