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Structure-antifungal activity relationships of polyene antibiotics of the amphotericin B group.
Tevyashova AN, Olsufyeva EN, Solovieva SE, Printsevskaya SS, Reznikova MI, Trenin AS, Galatenko OA, Treshalin ID, Pereverzeva ER, Mirchink EP, Isakova EB, Zotchev SB, Preobrazhenskaya MN. Tevyashova AN, et al. Among authors: reznikova mi. Antimicrob Agents Chemother. 2013 Aug;57(8):3815-22. doi: 10.1128/AAC.00270-13. Epub 2013 May 28. Antimicrob Agents Chemother. 2013. PMID: 23716057 Free PMC article.
Chemical modification and biological evaluation of new semisynthetic derivatives of 28,29-Didehydronystatin A1 (S44HP), a genetically engineered antifungal polyene macrolide antibiotic.
Preobrazhenskaya MN, Olsufyeva EN, Solovieva SE, Tevyashova AN, Reznikova MI, Luzikov YN, Terekhova LP, Trenin AS, Galatenko OA, Treshalin ID, Mirchink EP, Bukhman VM, Sletta H, Zotchev SB. Preobrazhenskaya MN, et al. Among authors: reznikova mi. J Med Chem. 2009 Jan 8;52(1):189-96. doi: 10.1021/jm800695k. J Med Chem. 2009. PMID: 19055412
Synthesis and study of the antifungal activity of new mono- and disubstituted derivatives of a genetically engineered polyene antibiotic 28,29-didehydronystatin A1 (S44HP).
Preobrazhenskaya MN, Olsufyeva EN, Tevyashova AN, Printsevskaya SS, Solovieva SE, Reznikova MI, Trenin AS, Galatenko OA, Treshalin ID, Pereverzeva ER, Mirchink EP, Zotchev SB. Preobrazhenskaya MN, et al. Among authors: reznikova mi. J Antibiot (Tokyo). 2010 Feb;63(2):55-64. doi: 10.1038/ja.2009.118. Epub 2009 Dec 4. J Antibiot (Tokyo). 2010. PMID: 19960041
Synthesis and mode of action of hydrophobic derivatives of the glycopeptide antibiotic eremomycin and des-(N-methyl-D-leucyl)eremomycin against glycopeptide-sensitive and -resistant bacteria.
Printsevskaya SS, Pavlov AY, Olsufyeva EN, Mirchink EP, Isakova EB, Reznikova MI, Goldman RC, Branstrom AA, Baizman ER, Longley CB, Sztaricskai F, Batta G, Preobrazhenskaya MN. Printsevskaya SS, et al. Among authors: reznikova mi. J Med Chem. 2002 Mar 14;45(6):1340-7. doi: 10.1021/jm010460i. J Med Chem. 2002. PMID: 11882003
Modification of olivomycin A at the side chain of the aglycon yields the derivative with perspective antitumor characteristics.
Tevyashova AN, Shtil AA, Olsufyeva EN, Luzikov YN, Reznikova MI, Dezhenkova LG, Isakova EB, Bukhman VM, Durandin NA, Vinogradov AM, Kuzmin VA, Preobrazhenskaya MN. Tevyashova AN, et al. Among authors: reznikova mi. Bioorg Med Chem. 2011 Dec 15;19(24):7387-93. doi: 10.1016/j.bmc.2011.10.055. Epub 2011 Oct 25. Bioorg Med Chem. 2011. PMID: 22088308
Role of the acyl groups in carbohydrate chains in cytotoxic properties of olivomycin A.
Tevyashova AN, Durandin NA, Vinogradov AM, Zbarsky VB, Reznikova MI, Dezhenkova LG, Bykov EE, Olsufyeva EN, Kuzmin VA, Shtil AA, Preobrazhenskaya MN. Tevyashova AN, et al. Among authors: reznikova mi. J Antibiot (Tokyo). 2013 Sep;66(9):523-30. doi: 10.1038/ja.2013.39. Epub 2013 May 22. J Antibiot (Tokyo). 2013. PMID: 23695417
A modification of the N-terminal amino acid in the eremomycin aglycone.
Miroshnikova OV, Berdnikova TF, Olsufyeva EN, Pavlov AY, Reznikova MI, Preobrazhenskaya MN, Ciabatti R, Malabarba A, Colombo L. Miroshnikova OV, et al. Among authors: reznikova mi. J Antibiot (Tokyo). 1996 Nov;49(11):1157-61. doi: 10.7164/antibiotics.49.1157. J Antibiot (Tokyo). 1996. PMID: 8982345 Free article.
24 results