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Antiangiogenic Activity and in Silico Cereblon Binding Analysis of Novel Thalidomide Analogs.

Megan L PeachShaunna L BeedieCindy H ChauMatthew K CollinsSuzana MarkolovicWeiming LuoDavid TweedieChristian SteinebachNigel H GreigMichael GütschowNeil VargessonMarc C NicklausWilliam Douglas Figg
Published in: Molecules (Basel, Switzerland) (2020)
Due to its antiangiogenic and anti-immunomodulatory activity, thalidomide continues to be of clinical interest despite its teratogenic actions, and efforts to synthesize safer, clinically active thalidomide analogs are continually underway. In this study, a cohort of 27 chemically diverse thalidomide analogs was evaluated for antiangiogenic activity in an ex vivo rat aorta ring assay. The protein cereblon has been identified as the target for thalidomide, and in silico pharmacophore analysis and molecular docking with a crystal structure of human cereblon were used to investigate the cereblon binding abilities of the thalidomide analogs. The results suggest that not all antiangiogenic thalidomide analogs can bind cereblon, and multiple targets and mechanisms of action may be involved.
Keyphrases
  • molecular docking
  • molecular dynamics simulations
  • binding protein
  • aortic valve
  • pulmonary hypertension