Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Martina Hlaváčková"'
Selectivity of original C-hexopyranosyl calix[4]arene conjugates towards lectins of different origin
Autor:
Jitka Moravcová, Eva Fujdiarová, Martina Hlaváčková, Martina Kašáková, Lenka Malinovská, Hana Dvořáková, Olga Maťátková, Michaela Wimmerová, Pavel Lhoták, Zdeňka Rottnerová, Tomáš Klejch
Publikováno v:
Carbohydrate Research. 469:60-72
As a part of ongoing activities towards the design of ligands against pathogenic lectins, a synthesis of original α-C-galacto/α-C-manno/α-C-fucopyranosyl glycomimetics based on a calix[4]arene scaffold and their binding evaluation is described. Th
Autor:
Martina Hlaváčková, Jitka Moravcová, Franck Fieschi, Martina Kašáková, Renato Ribeiro-Viana, Benedetta Bertolotti, Javier Rojo, Kamil Parkan, Ieva Sutkeviciute, Hana Dvořáková, Martino Ambrosini, Kateřina Nováková
Publikováno v:
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2017, 15 (18), pp.3995-4004. ⟨10.1039/c7ob00322f⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2017, 15 (18), pp.3995-4004. ⟨10.1039/c7ob00322f⟩
Organic & Biomolecular Chemistry, 2017, 15 (18), pp.3995-4004. ⟨10.1039/c7ob00322f⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2017, 15 (18), pp.3995-4004. ⟨10.1039/c7ob00322f⟩
The C-Type lectin DC-SIGN expressed on immature dendritic cells is a promising target for antiviral drug development. Previously, we have demonstrated that mono-and divalent C-glycosides based on d-manno and l-fuco configurations are promising DC-SIG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01628e7c4e5239ce5483a5765af10dd7
https://hal.science/hal-01538823
https://hal.science/hal-01538823
Publikováno v:
Carbohydrate Research. 340:161-166
4-Nitrophenyl 3,4,6-tri- O -acetyl-2-azido-2-deoxy-α- and β- d -mannopyranosides were prepared from methyl 4,6- O -benzylidene-α- d -glucopyranoside and 1,3,4,6-tetra- O -acetyl-α- d -glucopyranose, respectively. Chemoselective reduction of both
Publikováno v:
Carbohydrate research. 360
Two novel nonisosteric UDP-Gal analogues, (2-deoxy-2-fluoro- and 4-deoxy-4-fluoro-α-D-galactopyranosyl) phosphonoyl phosphates, were synthesized by optimized multistep procedures starting from 3,4,6-tri-O-benzyl-D-galactal and allyl 2,3,6-tri-O-benz
Autor:
Jitka Moravcová, Helena Heissigerová, Valerie Chazalet, Martina Hlaváčková, Petr Kočalka, Anne Imberty, Christelle Breton
Publikováno v:
Czech. Chem. Commun.
Czech. Chem. Commun., 2006, pp.1659-1672
Czech. Chem. Commun., 2006, pp.1659-1672
Employing the Michaelis-Arbuzov reaction of 1-O-acetyl-2,3,4,6-tetra-O-benzyl-D-galactopyranose with triethyl phosphite and trimethylsilyl trifluoromethanesulfonate, α- and β-D-galactopyranosylphosphonic acids were prepared in 33 and 28% yields, re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a3ca882833b85f0614736436e0f4832
https://hal.archives-ouvertes.fr/hal-00305773
https://hal.archives-ouvertes.fr/hal-00305773