Cargando…
Stereoselective Synthesis of the Isomers of Notoincisol A: Assigment of the Absolute Configuration of this Natural Product and Biological Evaluation
[Image: see text] The total syntheses of all stereoisomers of notoincisol A, a recently isolated natural product with potential anti-inflammatory activity, are reported. The asymmetric synthesis was conducted employing a lipase-mediated kinetic resolution, which enables easy access to all required c...
Autores principales: | Rycek, Lukas, Ticli, Vincenzo, Pyszkowski, Jakob, Latkolik, Simone, Liu, Xin, Atanasov, Atanas G., Steinacher, Theresa, Bauer, Rudolf, Schuster, Daniela, Dirsch, Verena M., Schnürch, Michael, Ernst, Margot, Mihovilovic, Marko D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society and American
Society of Pharmacognosy
2018
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256351/ https://www.ncbi.nlm.nih.gov/pubmed/30362739 http://dx.doi.org/10.1021/acs.jnatprod.8b00439 |
Ejemplares similares
-
Linked magnolol dimer as a selective PPARγ agonist – Structure-based rational design, synthesis, and bioactivity evaluation
por: Dreier, Dominik, et al.
Publicado: (2017) -
Magnolol dimer-derived fragments as PPARγ-selective probes
por: Dreier, Dominik, et al.
Publicado: (2018) -
Metal-assisted synthesis of unsymmetrical magnolol and honokiol analogs and their biological assessment as GABA(A) receptor ligands
por: Rycek, Lukas, et al.
Publicado: (2015) -
Corrigendum to “Metal-assisted synthesis of unsymmetrical magnolol and honokiol analogs and their biological assessment as GABA(A) receptor ligands” [Bioorg. Med. Chem. Lett. 25/2 (2015) 400–403]
por: Rycek, Lukas, et al.
Publicado: (2015) -
Structural Features Defining NF-κB Inhibition by Lignan-Inspired Benzofurans and Benzothiophenes
por: Dao-Huy, Toan, et al.
Publicado: (2020)