Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Natalia Yuan Chen"'
Autor:
Elisabeth Jeanclos, Jan Schlötzer, Kerstin Hadamek, Natalia Yuan-Chen, Mohammad Alwahsh, Robert Hollmann, Stefanie Fratz, Dilan Yesilyurt-Gerhards, Tina Frankenbach, Daria Engelmann, Angelika Keller, Alexandra Kaestner, Werner Schmitz, Martin Neuenschwander, Roland Hergenröder, Christoph Sotriffer, Jens Peter von Kries, Hermann Schindelin, Antje Gohla
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-18 (2022)
Targeting cellular glucose metabolism is a therapeutic strategy in human diseases such as autoimmunity or cancer. Here, the authors demonstrate the druggability of phosphoglycolate phosphatase, and validate an alternative approach to control glycolys
Externí odkaz:
https://doaj.org/article/fece9c1dab514555a6b20fa9b7dd7974
Publikováno v:
Journal of Chemical Information and Modeling. 63:3186-3197
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26285365635045ecccbce1952040899e
https://doi.org/10.1021/acs.jcim.3c00061
https://doi.org/10.1021/acs.jcim.3c00061
Autor:
Feng, He, C James, Chou, Matthias, Scheiner, Eleonora, Poeta, Natalia, Yuan Chen, Sandra, Gunesch, Matthias, Hoffmann, Christoph, Sotriffer, Barbara, Monti, Tangui, Maurice, Michael, Decker
Publikováno v:
Journal of medicinal chemistry. 64(7)
The structures of melatonin and ferulic acid were merged into tertiary amide-based histone deacetylase 6 (HDAC6) inhibitors to develop multi-target-directed inhibitors for neurodegenerative diseases to incorporate antioxidant effects without losing a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::318f23c7d12113691eaa9ef111cb5032
https://pubmed.ncbi.nlm.nih.gov/33769811
https://pubmed.ncbi.nlm.nih.gov/33769811
Autor:
Michael Decker, Matthias Hoffmann, Sandra Gunesch, Tangui Maurice, Feng He, Barbara Monti, Christoph A. Sotriffer, C. James Chou, Eleonora Poeta, Matthias Scheiner, Natalia Yuan Chen
The structures of melatonin and ferulic acid were merged into tertiary amide-based histone deacetylase 6 (HDAC6) inhibitors to develop multi-target-directed inhibitors for neurodegenerative diseases to incorporate antioxidant effects without losing a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74825e016c60aeb9d52712e97936a7fe
http://hdl.handle.net/11585/845023
http://hdl.handle.net/11585/845023
Autor:
Marco, Maspero, Daniela, Volpato, Davide, Cirillo, Natalia, Yuan Chen, Regina, Messerer, Christoph, Sotriffer, Marco, De Amici, Ulrike, Holzgrabe, Clelia, Dallanoce
Publikováno v:
Bioorganic chemistry. 96
We synthesized a set of new hybrid derivatives (7-C8, 7-C10, 7-C12 and 8-C8, 8-C10, 8-C12), in which a polymethylene spacer chain of variable length connected the pharmacophoric moiety of xanomeline, an M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fd8567dd409e4e2770f8be1b430860d8
https://pubmed.ncbi.nlm.nih.gov/32032848
https://pubmed.ncbi.nlm.nih.gov/32032848
Autor:
Clelia Dallanoce, Ulrike Holzgrabe, Marco Maspero, Marco De Amici, Regina Messerer, Natalia Yuan Chen, Christoph A. Sotriffer, Davide Cirillo, Daniela Volpato
Publikováno v:
Bioorganic Chemistry. 96:103633
We synthesized a set of new hybrid derivatives (7-C8, 7-C10, 7-C12 and 8-C8, 8-C10, 8-C12), in which a polymethylene spacer chain of variable length connected the pharmacophoric moiety of xanomeline, an M1/M4-preferring orthosteric muscarinic agonist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb232453abed55c027a83968ccead37f
https://doi.org/10.1016/j.bioorg.2020.103633
https://doi.org/10.1016/j.bioorg.2020.103633