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Structure-antifungal activity relationships of polyene antibiotics of the amphotericin B group.
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: treshalin id.
J Med Chem. 2009 Jan 8;52(1):189-96. doi: 10.1021/jm800695k.
J Med Chem. 2009.
PMID: 19055412
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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: treshalin id.
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
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Improved antifungal polyene macrolides via engineering of the nystatin biosynthetic genes in Streptomyces noursei.
Brautaset T, Sletta H, Nedal A, Borgos SE, Degnes KF, Bakke I, Volokhan O, Sekurova ON, Treshalin ID, Mirchink EP, Dikiy A, Ellingsen TE, Zotchev SB.
Brautaset T, et al. Among authors: treshalin id.
Chem Biol. 2008 Nov 24;15(11):1198-206. doi: 10.1016/j.chembiol.2008.08.009.
Chem Biol. 2008.
PMID: 19022180
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Eremomycin pyrrolidide: a novel semisynthetic glycopeptide with improved chemotherapeutic properties.
Olsufyeva EN, Shchekotikhin AE, Bychkova EN, Pereverzeva ER, Treshalin ID, Mirchink EP, Isakova EB, Chernobrovkin MG, Kozlov RS, Dekhnich AV, Preobrazhenskaya MN.
Olsufyeva EN, et al. Among authors: treshalin id.
Drug Des Devel Ther. 2018 Sep 10;12:2875-2885. doi: 10.2147/DDDT.S173923. eCollection 2018.
Drug Des Devel Ther. 2018.
PMID: 30237697
Free PMC article.
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Amides of pyrrole- and thiophene-fused anthraquinone derivatives: A role of the heterocyclic core in antitumor properties.
Tikhomirov AS, Litvinova VA, Andreeva DV, Tsvetkov VB, Dezhenkova LG, Volodina YL, Kaluzhny DN, Treshalin ID, Schols D, Ramonova AA, Moisenovich MM, Shtil AA, Shchekotikhin AE.
Tikhomirov AS, et al. Among authors: treshalin id.
Eur J Med Chem. 2020 Aug 1;199:112294. doi: 10.1016/j.ejmech.2020.112294. Epub 2020 May 6.
Eur J Med Chem. 2020.
PMID: 32428792
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Heterocyclic ring expansion yields anthraquinone derivatives potent against multidrug resistant tumor cells.
Tikhomirov AS, Tsvetkov VB, Volodina YL, Litvinova VA, Andreeva DV, Dezhenkova LG, Kaluzhny DN, Treshalin ID, Shtil AA, Shchekotikhin AE.
Tikhomirov AS, et al. Among authors: treshalin id.
Bioorg Chem. 2022 Oct;127:105925. doi: 10.1016/j.bioorg.2022.105925. Epub 2022 Jun 4.
Bioorg Chem. 2022.
PMID: 35728293
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