Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ivan D. Treshalin"'
Autor:
Alexander S. Tikhomirov, Vladimir B. Tsvetkov, Yulia L. Volodina, Valeria A. Litvinova, Daria V. Andreeva, Lyubov G. Dezhenkova, Dmitry N. Kaluzhny, Ivan D. Treshalin, Alexander A. Shtil, Andrey E. Shchekotikhin
Publikováno v:
Bioorganic chemistry. 127
Chemical modifications of anthraquiones are aimed at novel derivatives with improved antitumor properties. Emergence of multidrug resistance (MDR) due to overexpression of transmembrane ATP binding cassette transporters, in particular, MDR1/P-glycopr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08da249b320fa186ce71529aae5a2074
https://pubmed.ncbi.nlm.nih.gov/35728293
https://pubmed.ncbi.nlm.nih.gov/35728293
Autor:
Lyubov G. Dezhenkova, Alla A. Ramonova, Alexander A. Shtil, Alexander S. Tikhomirov, Ivan D. Treshalin, Dmitry N. Kaluzhny, Mikhail M. Moisenovich, Yulia L. Volodina, Dominique Schols, Andrey E. Shchekotikhin, Daria V. Andreeva, Valeria A. Litvinova, Vladimir B. Tsvetkov
Publikováno v:
European journal of medicinal chemistry. 199
Heteroarene-fused anthraquinone derivatives represent a class of perspective anticancer drug candidates capable of targeting multiple vital processes including drug resistance. Taking advantage of previously demonstrated potential of amide derivative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b730424d5acd17a5d8d86fce3043996
https://pubmed.ncbi.nlm.nih.gov/32428792
https://pubmed.ncbi.nlm.nih.gov/32428792
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:
Olga Volokhan, Trond E. Ellingsen, Sergey B. Zotchev, Håvard Sletta, Alexander Dikiy, Ingrid Bakke, Olga N. Sekurova, Kristin F. Degnes, Ivan D. Treshalin, Aina Nedal, Elena P. Mirchink, Trygve Brautaset, Sven Even F. Borgos
Publikováno v:
Chemistry & Biology. 15:1198-1206
Summary Seven polyene macrolides with alterations in the polyol region and exocyclic carboxy group were obtained via genetic engineering of the nystatin biosynthesis genes in Streptomyces noursei . In vitro analyses of the compounds for antifungal an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fa8d1a68a629091925eece5109469df
https://doi.org/10.1016/j.chembiol.2008.08.009
https://doi.org/10.1016/j.chembiol.2008.08.009
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:
Svetlana E. Solovieva, Ivan D Treshalin, M. I. Reznikova, Svetlana S. Printsevskaya, Eugenia N. Olsufyeva, Elena P. Mirchink, Maria N. Preobrazhenskaya, E. R. Pereverzeva, Anna N. Tevyashova, Sergey B. Zotchev, O. A. Galatenko, Trenin As
Publikováno v:
The Journal of antibiotics. 63(2)
Mono- and disubstituted novel derivatives of the heptaene nystatin analog 28,29-didehydronystatin A(1) (S44HP, 1) were obtained by chemical modification of the exocyclic C-16 carboxyl and/or an amino group of mycosamine moiety. The strategy of prepar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da08d5134f8ff0005c70ba9859516e4b
https://pubmed.ncbi.nlm.nih.gov/19960041
https://pubmed.ncbi.nlm.nih.gov/19960041
Autor:
Elena P. Mirchink, Vladimir M. Bukhman, Ivan D. Treshalin, Evgenia N. Olsufyeva, Svetlana E. Solovieva, Maria N. Preobrazhenskaya, Marina I. Reznikova, Olga A. Galatenko, Yuryi N. Luzikov, Sergey B. Zotchev, Larisa P. Terekhova, Håvard Sletta, Aleksei S. Trenin, Anna N. Tevyashova
Publikováno v:
Journal of medicinal chemistry. 52(1)
Twenty-three new derivatives of the heptaene nystatin analogue 28,29-didehydronystatin A(1) (1) (S44HP) were obtained by chemical modification of C16 carboxyl and amino groups of mycosamine. These derivatives comprised 15 carboxamides, 4 N-alkyl deri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bd35deeea5a533b6c9ae741160a50d8
https://pubmed.ncbi.nlm.nih.gov/19055412
https://pubmed.ncbi.nlm.nih.gov/19055412
Autor:
Maria N. Preobrazhenskaya, Evgenia N. Olsufyeva, Svetlana E. Solovieva, Anna N. Tevyashova, Marina I. Reznikova, Yuryi N. Luzikov, Larisa P. Terekhova, Aleksei S. Trenin, Olga A. Galatenko, Ivan D. Treshalin, Elena P. Mirchink, Vladimir M. Bukhman, Håvard Sletta, Sergey B. Zotchev
Publikováno v:
Journal of Medicinal Chemistry; Jan2009, Vol. 52 Issue 1, p189-196, 8p