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Publikace

2019

20. Faltinek, L.; Fujdiarová, E.; Melicher, F.; Houser, J.; Kašáková, M.; Kondakov, N.; Kononov, L.; Parkan, K.; Vidal, S.; Wimmerová, M. Lectin PLL3, a Novel Monomeric Member of the Seven-Bladed β-Propeller Lectin Family. Molecules 2019, 24, 4540. Odkaz

19. Jančaříková, G.; Houser, J.; Kašáková, M.; Oroszová, B.; Bertolotti, B.; Parkan, K.; Moravcová, J.; Wimmerová, M. Fucosylated inhibitors of recently identified bangle lectin from Photorhabdus asymbiotica. Sci Rep, 2019, 9, 14904. Odkaz

2018

18. Choutka J., Pohl R., Parkan K.: MOP and EE Protecting Groups in Synthesis of α- or β-Aryl-C-Glycosides from Glycals. ACS Omega 2018, 3, 7875-7887Odkaz

17. Vaňková K., Šimák O., Kettelhoit K., Parkan K.: One Step Transformation of Glycals into 1-Iodo Glycals. V knize: Proven Synthetic Methods, Vol 5 (P. Kosma eds.), str. XXX, ISBN: XXX. CRC Press, Taylor & Francis Group, 2018, in press.

2017

16. Raich, I.; Lövyová, Z.; Trnka, L.; Parkan, K.; Kessler, J.; Pohl, R.; Kaminský, J. Limitations in the description of conformational preferences of C-disaccharides: The (1 → 3)-C-mannobiose case. Carbohydr. Res. 2017, 451, 42-50.  Odkaz

15. olyvalent C-glycomimetics based on L-fucose or D-mannose as potent DC-SIGN antagonists. Org. Biomol. Chem. 2017, 15, 3995-4004. Odkaz

2016

14. Bertolotti, B.; Oroszová, B.; Sutkeviciute, I.; Kniežo, L.; Fieschi, F.; Parkan, K.; Lovyová, Z.; Kašáková, M.; Moravcová, J. Nonhydrolyzable C-disaccharides, a new class of DC-SIGN ligands. Carbohydr. Res. 2016, 435, 7-18. Odkaz

13. Kožíšek, M.; Štěpánek, O.; Parkan, K.; Albiñana, B. C.;  Pávová, M.; Weber, J.;a, Hans-Georg Krӓusslich, H.-G.; Konvalinka, J.; Machara,  A. Synthesis and evaluation of 2-pyridinylpyrimidines as inhibitors of HIV-1 structural protein assembly. Bioorg. Med. Chem. Lett. 2016, 26 , 3487–3490. Odkaz

12. Machara, A.; Lux, V.; Kožíšek, M.; Grantz, Šašková, K.; Štěpánek, O.; Kotora, M.; Parkan, K.; Pávová, M.; Glass, B.; Sehr, P.; Lewis, J.; Mueller, B.; Kraeusslich, H.-G.; Konvalinka J.; Specific inhibitors of HIV capsid assembly binding to the C-terminal domain of the capsid protein: evaluation of 2-arylquinazolines as potential virostatics. J. Med. Chem. 201659, 545-558. Odkaz

2015

11. Šnajdr, I.; Parkan, K.; Hessler, F.; Kotora M. Cross-metathesis Reaction of α- and β-Vinyl C-glycosides with Alkenes. Beilstein J. Org. Chem. 2015, 11, 1392–1397. Odkaz

10. Oroszová, B.; Choutka, J.; Pohl, R.; Parkan, K. Modular Stereoselective Synthesis of (1→2)-C-Glycosides based on the sp2–sp3 Suzuki–Miyaura Reaction. Chem. Eur. J. 2015, 21, 7043-7047. Odkaz

2014

9. Kraeusslich, H.; Sticht, J.; Wildova, M.; Lux, V.; Konvalinka, J.; Kotora, M.; Grantz, Saskova, K.; Kozisek, M.; Stepanek, O.; Parkan, K.; Machara, A. Use of substituted fused heterocyclic compounds for inhibiting HIV capsid assembly to treat HIV. WO 2014128206-A1, Aug 28, 2014. Odkaz

8. Kraeusslich, H.; Sticht, J.; Wildova, M.; Lux, V.; Konvalinka, J.; Kotora, M.; Grantz, Saskova, K.; Kozisek, M.; Stepanek, O.; Parkan, K.; Machara, A. 2,4-Substituted or 4,6-substituted pyrimidine compound useful for inhibiting HIV capsid assembly for treating a patient suffering from HIV. WO 2014128213-A1, Aug 28, 2014. Odkaz

7. Kraeusslich, H.; Sticht, J.; Wildova, M.; Lux, V.; Konvalinka, J.; Kotora, M.; Grantz, Saskova, K.; Kozisek, M.; Stepanek, O.; Parkan, K.; Machara, A. 2,4-Substituted or 4,6-substituted pyrimidine compound useful for inhibiting HIV capsid assembly for treating a patient suffering from HIV. EP 2769722-A1, Aug 27, 2014. Odkaz

6. Kraeusslich, H.; Sticht, J.; Wildova, M.; Lux, V.; Konvalinka, J.; Kotora, M.; Grantz, Saskova, K.; Kozisek, M.; Stepanek, O.; Parkan, K.; Machara, A. Use of substituted fused heterocyclic compounds for inhibiting HIV capsid assembly to treat HIV. EP 2769723-A1, Aug 27, 2014. Odkaz

5. Parkan, K.; Pohl, R.; Kotora, M. Cross-Coupling Reaction of Saccharide-Based Alkenyl Boronic Acids with Aryl Halides: The Synthesis of Bergenin, Chem. Eur. J. 201420, 4414 – 4419. Odkaz

2011

4. Lovyova, Z.; Parkan, K.; Kniezo, L. Stereoselective preparation of four 3-C-mannosylated D- and L-glucals from a single starting compound, Tetrahedron 2011, 67, 4967 – 4979. Odkaz

3. Olive, A.; Parkan, K.; Givelet, C.; Michl, J. Covalent Stabilization: A Sturdy Molecular Square from Reversible Metal-Ion-Directed Self-Assembly, J. Am. Chem. Soc. 2011, 133, 20108 – 20111. Odkaz

2010

2. Parkan, K.; Werner, L.; Lovyova, Z.; Prchalova, E.; Kniezo, L. An approach to stereoselective preparation of 3-C-glycosylated D- and L-glucals. Carbohydr. Res. 2010345, 352–362. Odkaz

2008

1. Parkan, K.; Vich, O.; Dvorakova, H.; Kniezo, L. Stereoselective preparation of 2,3-dideoxy-3-C-[(α-D-galactopyranosyl)methyl]-D-arabino-hexopyranose and 2,3-dideoxy-3-C-[(α-D-galactopyranosyl)methyl]-L-arabino-hexopyranose.  Collect. Czech. Chem. Commun. 200873, 690–700. Odkaz

 

 

Aktualizováno: 8.1.2020 08:46, Autor: Kamil Parkan

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