Cargando…
Induction of Cyp450 enzymes by 4-thiazolidinone-based derivatives in 3T3-L1 cells in vitro
4-Thiazolidinones and related derivatives are regarded as privileged structures in medicinal chemistry and a source of new drug-like compounds. To date it is known that thiazolidinones are able to induce CYP1A1 activity in 3T3-L1 cells. Therefore, to extend the knowledge of the mechanism of thiazoli...
Autores principales: | Szychowski, Konrad A., Skóra, Bartosz, Kryshchyshyn-Dylevych, Anna, Kaminskyy, Danylo, Rybczyńska-Tkaczyk, Kamila, Lesyk, Roman, Gmiński, Jan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102453/ https://www.ncbi.nlm.nih.gov/pubmed/33219472 http://dx.doi.org/10.1007/s00210-020-02025-7 |
Ejemplares similares
-
Evaluation of Anticancer and Antibacterial Activity of Four 4-Thiazolidinone-Based Derivatives
por: Skóra, Bartosz, et al.
Publicado: (2022) -
5-Ene-4-thiazolidinones – An efficient tool in medicinal chemistry
por: Kaminskyy, Danylo, et al.
Publicado: (2017) -
Synthesis and Anticancer Activity Evaluation of 5-[2-Chloro-3-(4-nitrophenyl)-2-propenylidene]-4-thiazolidinones
por: Buzun, Kamila, et al.
Publicado: (2021) -
Anticancer properties of 5Z-(4-fluorobenzylidene)-2-(4-hydroxyphenylamino)-thiazol-4-one
por: Szychowski, Konrad A., et al.
Publicado: (2019) -
A Facile Synthesis and Anticancer Activity Evaluation of Spiro[Thiazolidinone-Isatin] Conjugates
por: Kaminskyy, Danylo, et al.
Publicado: (2011)