1. 2024
  2. A Convenient Oligonucleotide Conjugation via Tandem Staudinger Reaction and Amide Bond Formation at the Internucleotidic Phosphate Position

    Klabenkova, K. V., Zhdanova, P. V., Burakova, E. A., Bizyaev, S. N., Fokina, A. A. & Stetsenko, D. A., 7 Feb 2024, In: International Journal of Molecular Sciences. 25, 4, 2007.

    Research output: Contribution to journalArticlepeer-review

  3. 2023
  4. Template-Assisted Assembly of Hybrid DNA/RNA Nanostructures Using Branched Oligodeoxy- and Oligoribonucleotides

    Fokina, A., Poletaeva, Y., Dukova, S., Klabenkova, K., Rad'kova, Z., Bakulina, A., Zatsepin, T., Ryabchikova, E. & Stetsenko, D., 5 Nov 2023, In: International Journal of Molecular Sciences. 24, 21, 15978.

    Research output: Contribution to journalArticlepeer-review

  5. 2021
  6. New hybrid compounds combining fragments of usnic acid and thioether are inhibitors of human enzymes TDP1, TDP2 and PARP1

    Dyrkheeva, N. S., Filimonov, A. S., Luzina, O. A., Orlova, K. A., Chernyshova, I. A., Kornienko, T. E., Malakhova, A. A., Medvedev, S. P., Zakharenko, A. L., Ilina, E. S., Anarbaev, R. O., Naumenko, K. N., Klabenkova, K. V., Burakova, E. A., Stetsenko, D. A., Zakian, S. M., Salakhutdinov, N. F. & Lavrik, O. I., 1 Nov 2021, In: International Journal of Molecular Sciences. 22, 21, 11336.

    Research output: Contribution to journalArticlepeer-review

  7. Chemistry of peptide-oligonucleotide conjugates: A review

    Klabenkova, K., Fokina, A. & Stetsenko, D., Sept 2021, In: Molecules. 26, 17, 5420.

    Research output: Contribution to journalReview articlepeer-review

  8. 2018
  9. Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors

    Zakharova, O., Luzina, O., Zakharenko, A., Sokolov, D., Filimonov, A., Dyrkheeva, N., Chepanova, A., Ilina, E., Ilyina, A., Klabenkova, K., Chelobanov, B., Stetsenko, D., Zafar, A., Eurtivong, C., Reynisson, J., Volcho, K., Salakhutdinov, N. & Lavrik, O., 15 Aug 2018, In: Bioorganic and Medicinal Chemistry. 26, 15, p. 4470-4480 11 p.

    Research output: Contribution to journalArticlepeer-review

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