Prediction of pharmacokinetics and molecular docking of new 1,2,3,4-tetrahydropyrimidine derivatives linked to carbohydrazide by aromatic and heteroaromatic linkers
The potential of 1,2,3,4-tetrahydropyrimidine–carbohydrazide hybrids as promising scaffolds for the design of selective HDAC8 inhibitors is demonstrated and provides valuable insights for further structural optimization and synthesis.