Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Milan, Vrabel"'
Autor:
Rastislav Dzijak, Juraj Galeta, Arcadio Vázquez, Jaroslav Kozák, Marika Matoušová, Helena Fulka, Martin Dračínský, Milan Vrabel
Publikováno v:
JACS Au, Vol 1, Iss 1, Pp 23-30 (2020)
Externí odkaz:
https://doaj.org/article/6971f460794d4de7971f6877cb460bae
Autor:
Michael Kugler, Martin Hadzima, Rastislav Dzijak, Robert Rampmaier, Pavel Srb, Lukáš Vrzal, Zdeněk Voburka, Pavel Majer, Pavlína Řezáčová, Milan Vrabel
Publikováno v:
RSC Medicinal Chemistry. 14:144-153
Here we show how different selection methods can be used for the discovery of a selective and potent carbonic anhydrase inhibitors. X-Ray and NMR structural studies were used to reveal the key binding interactions of the inhibitor with the enzyme.
Publikováno v:
ACS Omega. 7:21233-21238
Autor:
Milan Vrabel, Veronika Šlachtová, Simona Bellová, Agustina La-Venia, Juraj Galeta, Martin Dračínský, Karel Chalupský, Helena Mertlíková-Kaiserová, Peter Rukovanský, Rastislav Dzijak
The development of reagents that can selectively react in complex biological media is an important challenge. Here we show that N1-alkylation of 1,2,4-triazines yields the corresponding triazinium salts, which are three orders of magnitude more react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c1c48644cfc314998d73c80405b0695
https://doi.org/10.26434/chemrxiv-2023-75pjq
https://doi.org/10.26434/chemrxiv-2023-75pjq
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Chemistry – A European Journal
Chemistry – A European Journal
Fluorescent probes that light‐up upon reaction with complementary bioorthogonal reagents are superior tools for no‐wash fluorogenic bioimaging applications. In this work, a thorough study is presented on a set of seventeen structurally diverse co
Publikováno v:
ACS Synthetic Biology. 9:486-493
The site-specific chemical modification of proteins through incorporation of noncanonical amino acids enables diverse applications, such as imaging, probing, and expanding protein functions, as well as to precisely engineer therapeutics. Here we repo
Autor:
Rosaria Gitto, Claudiu T. Supuran, Federica Bucolo, Andrea Angeli, Francesca Mancuso, Clemente Capasso, Laura De Luca, Milan Vrabel
Publikováno v:
ChemMedChem
(2021): 3787–3794. doi:10.1002/cmdc.202100510
info:cnr-pdr/source/autori:Mancuso F.; De Luca L.; Bucolo F.; Vrabel M.; Angeli A.; Capasso C.; Supuran C.T.; Gitto R./titolo:4-Sulfamoylphenylalkylamides as Inhibitors of Carbonic Anhydrases Expressed in Vibrio cholerae/doi:10.1002%2Fcmdc.202100510/rivista:ChemMedChem (Print)/anno:2021/pagina_da:3787/pagina_a:3794/intervallo_pagine:3787–3794/volume
(2021): 3787–3794. doi:10.1002/cmdc.202100510
info:cnr-pdr/source/autori:Mancuso F.; De Luca L.; Bucolo F.; Vrabel M.; Angeli A.; Capasso C.; Supuran C.T.; Gitto R./titolo:4-Sulfamoylphenylalkylamides as Inhibitors of Carbonic Anhydrases Expressed in Vibrio cholerae/doi:10.1002%2Fcmdc.202100510/rivista:ChemMedChem (Print)/anno:2021/pagina_da:3787/pagina_a:3794/intervallo_pagine:3787–3794/volume
A current issue of antimicrobial therapy is the resistance to treatment with worldwide consequences. Thus, the identification of innovative targets is an intriguing challenge in the drug and development process aimed at newer antimicrobial agents. Th
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e96198 (2014)
Posttranslational modifications (PTMs) of proteins determine their structure-function relationships, interaction partners, as well as their fate in the cell and are crucial for many cellular key processes. For instance chromatin structure and hence g
Externí odkaz:
https://doaj.org/article/21c0c695a5054c3581627170b22d4422
Publikováno v:
Chemistry – A European Journal
Despite the great advances in solid-phase peptide synthesis (SPPS), the incorporation of certain functional groups into peptide sequences is restricted by the compatibility of the building blocks with conditions used during SPPS. In particular, the i
Publikováno v:
ChemPlusChem. 85(8)
Bioorthogonal cleavage reactions are gaining popularity in chemically inducible prodrug activation and in the control of biomolecular functions. Despite similar applications, these reactions were developed and optimized on different substrates and un