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Design and Identification of a Novel, Functionally Subtype Selective GABAA Positive Allosteric Modulator (PF-06372865).

Robert M OwenDavid BlakemoreLishuang CaoNeil FlanaganRebecca FishKarl R GibsonRachel GurrellChan Woo HuhJuha KammonenElisabeth Mortimer-CassenSarah A NickollsKiyoyuki OmotoDafydd OwenAndy PikeDavid C PrydeDavid S ReynoldsRosemarie RoeloffsColin RoseClara SteadMifune TakeuchiJoseph S WarmusChristine Watson
Published in: Journal of medicinal chemistry (2019)
The design, optimization, and evaluation of a series of novel imidazopyridazine-based subtype-selective positive allosteric modulators (PAMs) for the GABAA ligand-gated ion channel are described. From a set of initial hits multiple subseries were designed and evaluated based on binding affinity and functional activity. As designing in the desired level of functional selectivity proved difficult, a probability-based assessment was performed to focus the project's efforts on a single subseries that had the greatest odds of delivering the target profile. These efforts ultimately led to the identification of two precandidates from this subseries, which were advanced to preclinical safety studies and subsequently to the identification of the clinical candidate PF-06372865.
Keyphrases
  • small molecule
  • quality improvement
  • bioinformatics analysis
  • stem cells
  • cell therapy
  • bone marrow
  • mass spectrometry
  • clinical evaluation