Cargando…
Design, synthesis and molecular docking of new fused 1H-pyrroles, pyrrolo[3,2-d]pyrimidines and pyrrolo[3,2-e][1, 4]diazepine derivatives as potent EGFR/CDK2 inhibitors
A new series of 1H-pyrrole (6a–c, 8a–c), pyrrolo[3,2-d]pyrimidines (9a–c) and pyrrolo[3,2-e][1, 4]diazepines (11a–c) were designed and synthesised. These compounds were designed to have the essential pharmacophoric features of EGFR Inhibitors, they have shown anticancer activities against HCT116, MC...
Autores principales: | Belal, Amany, Abdel Gawad, Nagwa M., Mehany, Ahmed B. M., Abourehab, Mohammed A. S., Elkady, Hazem, Al‐Karmalawy, Ahmed A., Ismael, Ahmed S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9272933/ https://www.ncbi.nlm.nih.gov/pubmed/35801486 http://dx.doi.org/10.1080/14756366.2022.2096019 |
Ejemplares similares
-
Annellation of Triazole and Tetrazole Systems onto Pyrrolo[2,3-d]pyrimidines: Synthesis of Tetrazolo[1,5-c]-pyrrolo[3,2-e]-pyrimidines and Triazolo[1,5-c]pyrrolo-[3,2-e]pyrimidines as Potential Antibacterial Agents
por: Dave, Chaitanya G., et al.
Publicado: (2002) -
Going beyond the borders: pyrrolo[3,2-b]pyrroles with deep red emission
por: Tasior, Mariusz, et al.
Publicado: (2021) -
Targeting of the Mitochondrial TET1 Protein by Pyrrolo[3,2-b]pyrrole Chelators
por: Antonyová, Veronika, et al.
Publicado: (2022) -
Deciphering the unusual fluorescence in weakly coupled bis-nitro-pyrrolo[3,2-b]pyrroles
por: Poronik, Yevgen M., et al.
Publicado: (2020) -
Method for the Large-Scale
Synthesis of Multifunctional
1,4-Dihydro-pyrrolo[3,2-b]pyrroles
por: Tasior, Mariusz, et al.
Publicado: (2020)