Clicked and long spaced galactosyl- and lactosylcalix[4]arenes: new multivalent galectin-3 ligands

Scholarly Works

• Vlachová, M.; Tran, V. N.; Červený, J.; Dolníček, F.; Petrásková, L.; Pelantová, H.; Kundrát, O.; Cvačka, J.; Bosáková, Z.; Křen, V.; Lhoták, P.; Viktorová, J.; Bojarová, P. Galectin-targeting glycocalix[4]arenes can enter the cells. Chemical communications (Cambridge, England) 2023, 59, 10404–10407. doi:10.1039/d3cc02905k
• Konvalinková, D.; Dolníček, F.; Hovorková, M.; Červený, J.; Kundrát, O.; Pelantová, H.; Petrásková, L.; Cvačka, J.; Faizulina, M.; Varghese, B.; Kovaříček, P.; Křen, V.; Lhoták, P.; Bojarová, P. Glycocalix[4]arenes and their affinity to a library of galectins: the linker matters. Organic & biomolecular chemistry 2023, 21, 1294–1302. doi:10.1039/d2ob02235d
• Nayak, M.; Samal, K.; Pati, A. Synthesis and characterization of the rccc-isomer of dodecatriazolo-resorcin[4]arene cavitand. In AIP Conference Proceedings, AIP Publishing, 2023; pp 60006 ff. doi:10.1063/5.0127510
• Ou, C.; Li, C.; Feng, C.; Tong, X.; Vasta, G. R.; Wang, L.-X. Synthesis, binding affinity, and inhibitory capacity of cyclodextrin-based multivalent glycan ligands for human galectin-3. Bioorganic & medicinal chemistry 2022, 72, 116974. doi:10.1016/j.bmc.2022.116974
• Cristófalo, A. E.; Cagnoni, A. J.; Uhrig, M. L. Synthesis of N-acetylglucosamine and N-acetylallosamine resorcinarene-based multivalent β-thio-glycoclusters: unexpected affinity of N-acetylallosamine ligands towards Wheat Germ Agglutinin. Organic & biomolecular chemistry 2020, 18, 6853–6865. doi:10.1039/d0ob01498b
• Bertuzzi, S.; Quintana, J. I.; Ardá, A.; Gimeno, A.; Jiménez-Barbero, J. Targeting Galectins With Glycomimetics. Frontiers in chemistry 2020, 8, 593. doi:10.3389/fchem.2020.00593
• Tavares, M. R.; Bláhová, M.; Sedláková, L.; Elling, L.; Pelantová, H.; Konefał, R.; Etrych, T.; Křen, V.; Bojarová, P.; Chytil, P. High-Affinity N-(2-Hydroxypropyl)methacrylamide Copolymers with Tailored N-Acetyllactosamine Presentation Discriminate between Galectins. Biomacromolecules 2020, 21, 641–652. doi:10.1021/acs.biomac.9b01370
• Knyazeva, I. R.; Matveeva, V. I.; Khrizanforova, V. V.; Syakaev, V. V.; Budnikova, Y. H.; Habicher, W. D.; Burilov, A. R. Click reaction in the synthesis of novel thiophosphorylated ligands for electrochemical hydrogen evolution. Mendeleev Communications 2019, 29, 388–390. doi:10.1016/j.mencom.2019.07.009
• Gorbunov, A.; Kuznetsova, J.; Puchnin, K.; Kovalev, V.; Vatsouro, I. Triazolated calix[4]arenes from 2-azidoethylated precursors: is there a difference in the way the triazoles are attached to narrow rims?. New Journal of Chemistry 2019, 43, 4562–4580. doi:10.1039/c8nj06464d
• Rahkila, J.; Ekholm, F. S.; Ardá, A.; Delgado, S.; Savolainen, J.; Jiménez-Barbero, J.; Leino, R. Novel Dextran-Supported Biological Probes Decorated with Disaccharide Entities for Investigating the Carbohydrate–Protein Interactions of Gal-3. Chembiochem : a European journal of chemical biology 2018, 20, 203–209. doi:10.1002/cbic.201800423
• Latxague, L.; Gaubert, A.; Barthélémy, P. Recent Advances in the Chemistry of Glycoconjugate Amphiphiles. Molecules (Basel, Switzerland) 2018, 23, 89. doi:10.3390/molecules23010089
• Stel, M.; Pieters, R. J. Multivalency; Wiley, 2017; pp 345–380. doi:10.1002/9781119143505.ch14
• Knyazeva, I. R.; Abdrafikova, D. K.; Mukhamedyanova, K. M.; Syakaev, V. V.; Gabidullin, B.; Gubaidullin, A. T.; Habicher, W. D.; Burilov, A. R.; Pudovik, M. A. Synthesis of novel highly functionalized triazole-linked calix[4]resorcinols via click reaction. Mendeleev Communications 2017, 27, 556–558. doi:10.1016/j.mencom.2017.11.005
• Sathiyajith, C.; Shaikh, R. R.; Han, Q.; Zhang, Y.; Meguellati, K.; Yang, Y.-W. Biological and related applications of pillar[n]arenes. Chemical communications (Cambridge, England) 2017, 53, 677–696. doi:10.1039/c6cc08967d
• Matthews, S. E. Calixsugars: Finally Reaching Their Therapeutic Potential?. Calixarenes and Beyond; Springer International Publishing, 2016; pp 559–600. doi:10.1007/978-3-319-31867-7_22
• Bojarová, P.; Křen, V. Sugared biomaterial binding lectins: achievements and perspectives. Biomaterials science 2016, 4, 1142–1160. doi:10.1039/c6bm00088f
• Stejskal, F.; Eigner, V.; Dvořáková, H.; Cuřínová, P.; Lhoták, P. Direct C–H azidation of calix[4]arene as a novel method to access meta substituted derivatives. Tetrahedron Letters 2015, 56, 5357–5361. doi:10.1016/j.tetlet.2015.08.002
• Casnati, A.; Sansone, F. Calixarene Ligands for Biomacromolecule Recognition. Reference Module in Chemistry, Molecular Sciences and Chemical Engineering; Elsevier, 2015. doi:10.1016/b978-0-12-409547-2.10827-3

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