Список публикаций Лаборатории синтеза антибиотиков, преодолевающих резистентность (САПР)

 

  1. A.S. Tikhomirov, Y.B. Sinkevich, L.G. Dezhenkova, D.N. Kaluzhny, N.S. Ilyinsky, V.I. Borshchevskiy, D. Schols, A.E. Shchekotikhin, Synthesis and antitumor activity of cyclopentane-fused anthraquinone derivatives, European Journal of Medicinal Chemistry, 2024, 265, 116103, https://doi.org/10.1016/j.ejmech.2023.1161031
  2. M.I. Treshchalin, V.A. Polozkova, E.I. Moiseenko, A.E. Shchekotikhin, S.A. Dovzhenko, M.B. Kobrin, E.R. Pereverzeva, Experimental Evaluation of the Hypersensitivity Reactions of a New Glycopeptide Antibiotic Flavancin in Animal Models, Pharmaceuticals, 2023, 16(11), 1569; https://doi.org/10.3390/ph16111569 img

     

  3. V.A. Litvinova, A.S. Gostev, A.S. Tikhomirov, A.E. Shchekotikhin, New heteroarene-fused anthraquinones: Synthesis and PyBOP-mediated amination, Tetrahedron, 2023, 149, 4, 133722, https://doi.org/https://doi.org/10.1016/j.tet.2023.133722img

     

  4. A. Islam, X.C. Chen, C.-W. Weng, C.-Y. Chen, C.-W. Wang, M.-K. Chen, A.S. Tikhomirov, A.E. Shchekotikhin, P.J. Chueh, Water-soluble 4-(dimethylaminomethyl)heliomycin exerts greater antitumor effects than parental heliomycin by targeting the tNOX-SIRT1 axis and apoptosis in oral cancer cells, eLife, 2023, https://doi.org/10.7554/eLife.87873.1img

     

  5. В.А. Литвинова, А.С. Тихомиров, Методы синтеза 1,3-оксазолидин-2-онов, Методы синтеза 1,3-оксазолидин-2-онов, Химия гетероциклических соединений, 2023, 59(11/12), 733-735img

     

  6. K. Shapovalova, G. Zatonsky, N. Grammatikova, I. Osterman, E. Razumova, A. Shchekotikhin, A. Tevyashova, Synthesis of 6”-Modified Kanamycin A Derivatives and Evaluation of Their Antibacterial Properties. Pharmaceutics, 2023, 15, 1177. https://doi.org/10.3390/pharmaceutics15041177img

     

  7. A.A. Panov, Quantum-Chemical Study of Keto-Enol Equilibrium and Global Electrophilicity of Hydroxymaleimide Derivatives. Doklady Physical Chemistry, 2023, 508, 28–32, https://doi.org/10.1134/S001250162360002Ximg

     

  8. Levshin I.B., Simonov A.Y., Lavrenov S.N., Panov A.A., Grammatikova N.E., Alexandrov A.I., Ghazy E.S.M.O., Savin N.A., Gorelkin P.V., Erofeev A.S., Polshakov V.I. Antifungal Thiazolidines: Synthesis and Biological Evaluation of Mycosidine Congeners. Pharmaceuticals, 2022, 15, 5, 563-586. DOI: 10.3390/ph15050563тд1

     

  9. Treshchalin M.I., Polozkova V.A., Moiseenko E.I., Treshalina H.M., Shchekotikhin A.E., Pereverzeva E.R. Evaluation of Toxic Properties of New Glycopeptide Flavancin on Rats. Pharmaceuticals, 2022, 15, 661. DOI: 10.3390/ph15060661тл2

     

  10. A.N. Tevyashova, S.S. Efimova, A.I. Alexandrov, E.S.M.O. Ghazy, E.N. Bychkova, S.E. Solovieva, G.B. Zatonsky, N.E. Grammatikova, L.G. Dezhenkova, E.R. Pereverzeva, E.B. Isakova, O.S. Ostroumova, O.A. Omelchuk, V.V. Muravieva, M.M. Krotova, T.V. Priputnevich, A.E. Shchekotikhin, Semisynthetic Amides of Polyene Antibiotic Natamycin, ACS Infectious Diseases 2022, 2022, https://doi.org/10.1021/acsinfecdis.2c00237тл3
  11. A. Tevyashova, S. Efimova, A. Alexandrov, O. Omelchuk, E. Ghazy, E. Bychkova, G. Zatonsky, N. Grammatikova, L. Dezhenkova, S. Solovieva, O. Ostroumova, A. Shchekotikhin, Semisynthetic Amides of Amphotericin B and Nystatin A1: A Comparative Study of In Vitro Activity/Toxicity Ratio in Relation to Selectivity to Ergosterol Membranes, Antibiotics 2023, 12(1), 151; https://doi.org/10.3390/antibiotics12010151тл4