Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Tomáš Kraus"'
Publikováno v:
Chemical Science. 14:4059-4069
New lipid-linked 2′-deoxyribonucleoside triphosphates were synthesized and used for enzymatic construction of various lipid–oligonucleotide conjugates capable of efficient anchoring to plasma membranes.
Autor:
Ambra Spampinato, Erika Kužmová, Radek Pohl, Veronika Sýkorová, Milan Vrábel, Tomáš Kraus, Michal Hocek
Publikováno v:
Bioconjugate Chemistry.
Publikováno v:
Bioconjugate chemistry.
Nucleosides and 2'-deoxyribonucleoside triphosphates (dNTPs) bearing 3,3'-dimethoxy-2,2'-diphenyl-6-(4-hydroxyphenyl)-bodipy fluorophore attached through a propargyl or propargyl-triethylene glycol linker to position 5 of 2'-deoxycytidine were design
Autor:
Ján Matyašovský, Radek Pohl, Pedro Güixens-Gallardo, Attila Palágyi, Michal Hocek, Miroslav Kuba, Laure Tack, Tomáš Kraus
Publikováno v:
Organic & Biomolecular Chemistry. 19:9966-9974
We designed and synthesized nucleosides bearing aminophenyl- or aminonaphthyl-3-methoxychromone fluorophores attached at position 5 of cytosine or thymine and converted them to nucleoside triphosphates. The fluorophores showed solvatochromic fluoresc
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Thymidine triphosphate bearing benzylidene-tetrahydroxanthylium near-IR fluorophore linked to the 5-methyl group via triazole was synthesized through the CuAAC reaction and was used for polymerase synthesis of labelled DNA probes. The fluorophore lig
Publikováno v:
Analytical Biochemistry. 614:114002
The reported method allows for a simple and rapid monitoring of DNA replication and cell cycle progression in eukaryotic cells in vitro. The DNA of replicating cells is labeled by incorporation of a metabolically-active fluorescent (Cy3) deoxyuridine
Publikováno v:
Chemistry – A European Journal. 26:11911-11911
Autor:
Michal Hocek, Radek Pohl, Ján Matyašovský, Pedro Güixens-Gallardo, Tomáš Kraus, Dmytro Dziuba, Zbigniew Zawada
Publikováno v:
Bioconjugate chemistry. 29(11)
Synthesis of cytosine, uracil, and 7-deazaadenine 2′-deoxyribonucleosides and triphosphates (dNTPs) bearing hexamethylated phenyl-bodipy fluorophore attached at position 5 of pyrimidines or at position 7 of 7-deazapurine was developed. All the titl
Publikováno v:
Angewandte Chemie (International ed. in English). 57(31)
Chemically modified nucleoside triphosphates (NTPs) are widely exploited as unnatural metabolites in chemical biology and medicinal chemistry. Because anionic NTPs do not permeate cell membranes, their corresponding neutral precursors are employed in