Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Angelika Ullrich"'
Autor:
Tobias F. Primke, Rebecca Ingelfinger, Mohammed A. F. Elewa, Igor Macinkovic, Andreas Weigert, Matthias P. Fabritius, Christoph A. Reichel, Angelika Ullrich, Uli Kazmaier, Luisa D. Burgers, Robert Fürst
Publikováno v:
Cells, Vol 12, Iss 16, p 2112 (2023)
The anti-inflammatory effects of depolymerizing microtubule-targeting agents on leukocytes are known for a long time, but the potential involvement of the vascular endothelium and the underlying mechanistic basis is still largely unclear. Using the r
Externí odkaz:
https://doaj.org/article/0aefd39697be478ca324db28bd49dec4
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 1652-1656 (2012)
Thio-Ugi reactions are described as an excellent synthetic tool for the synthesis of sterically highly hindered endothiopeptides. S-Methylation and subsequent amidine formation can be carried out in an inter- as well as in an intramolecular fashion.
Externí odkaz:
https://doaj.org/article/63dc55d6a55445839d0ecd21f7cf5cd4
Autor:
Jennifer Herrmann, Yasser A Elnakady, Romina M Wiedmann, Angelika Ullrich, Manfred Rohde, Uli Kazmaier, Angelika M Vollmar, Rolf Müller
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e37416 (2012)
Pretubulysin is a natural product that is found in strains of myxobacteria in only minute amounts. It represents the first enzyme-free intermediate in the biosynthesis of tubulysins and undergoes post-assembly acylation and oxidation reactions. Pretu
Externí odkaz:
https://doaj.org/article/ac6d869997c4495c99858d23d48dca91
Autor:
Angelika Ullrich, Uli Kazmaier
Publikováno v:
Organic Reactions. :1-560
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59c5a21ff53ce0f6890d39035306e463
https://doi.org/10.1002/0471264180.or112.01
https://doi.org/10.1002/0471264180.or112.01
Autor:
Angelika Ullrich, Uli Kazmaier
Publikováno v:
Organic Reactions. :1051-1581
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a1e0ead47eb30758fb837443614e6bf
https://doi.org/10.1002/0471264180.or112.02
https://doi.org/10.1002/0471264180.or112.02
Publikováno v:
Methods in Molecular Biology ISBN: 9781071616888
Cyclic peptides, which often exhibit interesting biological properties, can be obtained by macrolactamization of adequately protected linear peptide chains. Because of the remarkable biological properties, methods for the efficient cyclization of pep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fffed2657c6ba3ffe86a6d780fee1e8d
https://doi.org/10.1007/978-1-0716-1689-5_4
https://doi.org/10.1007/978-1-0716-1689-5_4
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2371
Cyclic peptides, which often exhibit interesting biological properties, can be obtained by macrolactamization of adequately protected linear peptide chains. Because of the remarkable biological properties, methods for the efficient cyclization of pep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aee2346532cf65a46ae635aa22077ce7
https://pubmed.ncbi.nlm.nih.gov/34596843
https://pubmed.ncbi.nlm.nih.gov/34596843
Autor:
Kevin Bauer, Tamara Doroshenko, Andreas Grueter, Angelika Ullrich, Uli Kazmaier, Gregor Jung, Isabel Filbrich
Publikováno v:
Synthesis. 49:2743-2748
Coumaryl triflate can be used for a wide range of substitution reactions, either under Pd-catalyzed conditions or via direct nucleophilic substitutions, and is therefore an ideal substrate for the fluorescence labeling of functionalized compounds, su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e279b8320d4102de8138f1271825b74e
https://doi.org/10.1055/s-0036-1588159
https://doi.org/10.1055/s-0036-1588159
Publikováno v:
Oncotarget
Microtubule-targeting agents (MTAs) are the most widely used chemotherapeutic drugs. Pretubulysin (PT), a biosynthetic precursor of the myxobacterial tubulysins, was recently identified as a novel MTA. Besides its strong anti-tumoral activities, PT a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddeee334f34e0a9616129ebd1d31b27d
http://publikationen.ub.uni-frankfurt.de/files/44761/container.zip
http://publikationen.ub.uni-frankfurt.de/files/44761/container.zip
Autor:
Verena K. Kretzschmann, Angelika M. Vollmar, Uli Kazmaier, Donata Gellrich, Angelika Ullrich, Robert Fürst, Stefan Zahler
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 34:294-303
Objective— Pretubulysin (PT) is a novel, synthetically accessible myxobacterial compound that acts as a tubulin-depolymerizing agent and inhibits cancer cell growth in vitro and in vivo. Moreover, PT was found to attenuate tumor angiogenesis. Here,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27e53d90957a49e951e9e31690ecacc1
https://doi.org/10.1161/atvbaha.113.302155
https://doi.org/10.1161/atvbaha.113.302155