Novel pyrimido[1,2- a ]imidazole derivatives as potent Pks13-TE inhibitors: structure-based virtual screening and rational design
Abstract
Integrated virtual and biological screening guided the design and synthesis of 50 novel pyrimido[1,2- a ]imidazole derivatives, leading to the discovery of potent Pks13-TE inhibitor 34 (IC 50 = 0.23 μM).
Fields of Study & Subjects
Protein Kinase Regulation and GTPase Signaling
Cell death mechanisms and regulation
Protein Tyrosine Phosphatases
Publication details
- Journal / source
- RSC Medicinal Chemistry
- Volume
- 17
- Issue
- 2
- Pages
- 1066–1082
- Publication date
- 1 January 2026
- Language
- EN