Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Timo Mack"'
Autor:
Daniel Fürniss, Timo Mack, Frank Hahn, Sidonie B. L. Vollrath, Katarzyna Koroniak, Ute Schepers, Stefan Bräse
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 56-63 (2013)
Sugar moieties are present in a wide range of bioactive molecules. Thus, having versatile and fast methods for the decoration of biomimetic molecules with sugars is of fundamental importance. The glycosylation of peptoids and polyamines as examples o
Externí odkaz:
https://doaj.org/article/833462c28308436a828a7ba9604f67d9
Publikováno v:
CHIMIA, Vol 63, Iss 5 (2009)
The attachment of photolabile groups to biologically active molecules offers a very versatile way to put a biological effect under the control of an external trigger signal and thus confers spatiotemporal and dose control to this effect. Over the las
Externí odkaz:
https://doaj.org/article/452f513720e545769d6340ae68600e6f
Autor:
Alexander Heckel, Timo Mack, Khashti Ballabh Joshi, Florian Schäfer, Martin B. Koeppel, Alexandre Rodrigues-Correia
Publikováno v:
Analytical and Bioanalytical Chemistry. 399:441-447
Nucleobase-caged oligonucleotide residues have photolabile "caging groups" that prevent the formation of Watson-Crick base pairs until the unmodified nucleobase is restored in a photolysis event. This principle can be used to put a growing variety of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5979c1a22b99cb00b6c792f4a95a1727
https://doi.org/10.1007/s00216-010-4274-7
https://doi.org/10.1007/s00216-010-4274-7
Autor:
Alexander Heckel, Thomas Höver, Günter Mayer, Jens Müller, Daniel F. Freitag, Timo Mack, Bernd Pötzsch
Publikováno v:
ChemBioChem. 10:654-657
Subtle change: Spatiotemporal modulation of individual protein subdomains with light as the trigger signal becomes possible by using bivalent aptamers and introducing photolabile "caging groups" to switch individual aptamer modules ON or OFF differen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::664086274eaef573a76b9d500543e9b2
https://doi.org/10.1002/cbic.200800814
https://doi.org/10.1002/cbic.200800814
Autor:
Alexander Heckel, Florian Schäfer, Khashti Ballabh Joshi, Timo Mack, Josef Wachtveitl, Manuela A. H. Fichte
Publikováno v:
Organic letters. 13(6)
Nitrodibenzofuran (NDBF) groups are used as photolabile “caging” groups to temporarily mask the Watson−Crick interaction of dA and dC residues. They show improved masking capabilities and are photodeprotected 12 times more efficiently than 1-(o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c4e650403cde4fad4eeb971022fda01
https://pubmed.ncbi.nlm.nih.gov/21341754
https://pubmed.ncbi.nlm.nih.gov/21341754
Publikováno v:
CHIMIA, Vol 63, Iss 5 (2009)
The attachment of photolabile groups to biologically active molecules offers a very versatile way to put a biological effect under the control of an external trigger signal and thus confers spatiotemporal and dose control to this effect. Over the las
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0f902c7497beb390bb3dd06846c8f29
https://www.chimia.ch/chimia/article/view/4662
https://www.chimia.ch/chimia/article/view/4662