Evaluating Bis‐Phenacyl Bromide‐Based Bis‐Heterocyclic Templates as Anticancer Prototypes and Potential PARP1 Inhibitors

Documenti analoghi

• Dual Biological Potential: Anticancer and Antibacterial Activities of Bis‐ α, ω‐Bifunctional Sphingolipids from the Marine Sponge Oceanapia ramsayi
  di: Dele Abdissa Keneni, et al.
  Pubblicazione: (2025)
• Synthesis, Characterization, and Biological Activity of New 4‘‐Functionalized Bis‐Terpyridine Ruthenium(II) Complexes: Anti‐Inflammatory Activity Advances
  di: Mohamed M. Elnagar, et al.
  Pubblicazione: (2024)
• Expanding the Variety of Pyridinium‐Based Bis‐QACs with Antimicrobial Properties: Investigation into Linker Structure‐Activity Correlation
  di: Nikita A. Frolov, et al.
  Pubblicazione: (2025)
• Next‐Generation Bcl‐2 Inhibitors: Design and Evaluation of Indolyl‐Triazole Derivatives with Anticancer Potential
  di: Ahmed M. Almehdi, et al.
  Pubblicazione: (2025)
• Discovery of Potent Isoindolinone Inhibitors that Target an Active Conformation of PARP1 Using DNA‐Encoded Libraries
  di: Kelly A. McCarthy, et al.
  Pubblicazione: (2024)