Synthesis of carbohydrate-scaffolded thymine glycoconjugates to organize multivalency

Scholarly Works

• Uspenskaia, A. A.; Doroshenko, I. A.; Popovicheva, K. A.; Shmychkov, N. V.; Pryakhina, E. V.; Shafikov, R. R.; Skvortsov, D. A.; Beklemishev, M. K.; Zaborova, O. V.; Podrugina, T. A.; Machulkin, A. E.; Beloglazkina, E. K. Pentamethine cyanine dyes with alkynyl group as perspective structure for conjugation with targeting moiety. Bioorganic & medicinal chemistry letters 2024, 115, 130025. doi:10.1016/j.bmcl.2024.130025
• Uspenskaia, A.; Doroshenko, I. A.; Popovicheva, K. A.; SHmychkov, N. V.; Pryakhina, E. V.; SHafikov, R. R.; Skvortsov, D. A.; Beklemishev, M. K.; Podrugina, T. A.; Machulkin, A. E.; Beloglazkina, E. K. Pentamethine Cyanine Dyes with Alkynyl Group as Perspective Structure for Conjugation with Targeting Moiety. Elsevier BV 2024. doi:10.2139/ssrn.4897969
• Uspenskaia, A. A.; Krasnikov, P. A.; Majouga, A. G.; Beloglazkina, E. K.; Machulkin, A. E. Fluorescent conjugates based on prostatic specific membrane antigen ligands as an effective visualization tool for prostate cancer. Биохимия 2023, 88, 1173–1190. doi:10.31857/s0320972523070084
• Uspenskaia, A. A.; Krasnikov, P. A.; Majouga, A. G.; Beloglazkina, E. K.; Machulkin, A. E. Fluorescent Conjugates Based on Prostate-Specific Membrane Antigen Ligands as an Effective Visualization Tool for Prostate Cancer. Biochemistry. Biokhimiia 2023, 88, 953–967. doi:10.1134/s0006297923070088
• Machulkin, A. E.; Uspenskaya, A. A.; Zyk, N. Y.; Nimenko, E. A.; Ber, A. P.; Petrov, S. A.; Shafikov, R. R.; Skvortsov, D. A.; Smirnova, G. B.; Borisova, Y. A.; Pokrovsky, V. S.; Kolmogorov, V.; Vaneev, A.; Ivanenkov, Y. A.; Khudyakov, A. D.; Kovalev, S. V.; Erofeev, A.; Gorelkin, P. V.; Beloglazkina, E. K.; Zyk, N. V.; Khazanova, E. S.; Majouga, A. G. PSMA-targeted small-molecule docetaxel conjugate: Synthesis and preclinical evaluation. European journal of medicinal chemistry 2021, 227, 113936. doi:10.1016/j.ejmech.2021.113936
• Jaeschke, S. O.; vom Sondern, I.; Lindhorst, T. K. Synthesis of regioisomeric maltose-based Man/Glc glycoclusters to control glycoligand presentation in 3D space. Organic & biomolecular chemistry 2021, 19, 7013–7023. doi:10.1039/d1ob01150b
• Brekalo, J.; Despras, G.; Lindhorst, T. K. Pseudoenantiomeric glycoclusters: Synthesis and testing of heterobivalency in carbohydrate-protein interactions. Organic & biomolecular chemistry 2019, 17, 5929–5942. doi:10.1039/c9ob00124g
• Ciuk, A. K.; Gloe, T.-E.; Lindhorst, T. K. Carbohydrate-Scaffolded Thymine Multimers: Scope and Limitations of the Allylation–Hydroboration Sequence. European Journal of Organic Chemistry 2018, 2018, 6971–6982. doi:10.1002/ejoc.201801387
• Freichel, T.; Eierhoff, S.; Snyder, N. L.; Hartmann, L. Toward Orthogonal Preparation of Sequence-Defined Monodisperse Heteromultivalent Glycomacromolecules on Solid Support Using Staudinger Ligation and Copper-Catalyzed Click Reactions. The Journal of organic chemistry 2017, 82, 9400–9409. doi:10.1021/acs.joc.7b01398
• Müller, C.; Despras, G.; Lindhorst, T. K. Organizing multivalency in carbohydrate recognition. Chemical Society reviews 2016, 45, 3275–3302. doi:10.1039/c6cs00165c
• Poplata, S.; Tröster, A.; Zou, Y.-Q.; Bach, T. Recent Advances in the Synthesis of Cyclobutanes by Olefin [2+2] Photocycloaddition Reactions. Chemical reviews 2016, 116, 9748–9815. doi:10.1021/acs.chemrev.5b00723
• Haag, R. Multivalency as a chemical organization and action principle. Beilstein journal of organic chemistry 2015, 11, 848–849. doi:10.3762/bjoc.11.94

Explore citations to this article at