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Discovery of VU6008677: A Structurally Distinct Tricyclic M 4 Positive Allosteric Modulator with Improved CYP450 Profile.

Rory A CapstickSean R BollingerJulie L EngersMadeline F LongSichen ChangVincent B LuscombeAlice L RodriguezColleen M NiswenderThomas M BridgesOlivier BoutaudP Jeffrey ConnDarren W EngersDennis C LiottaKayla J Temple
Published in: ACS medicinal chemistry letters (2024)
This Letter details our efforts to develop novel tricyclic muscarinic acetylcholine receptor subtype 4 (M 4 ) positive allosteric modulator (PAM) scaffolds with improved pharmacological properties. This endeavor involved a "tie-back" strategy to replace the 3-amino-5-chloro-4,6-dimethylthieno[2,3- b ]pyridine-2-carboxamide core, which led to the discovery of two novel tricyclic cores: an 8-chloro-9-methylpyrido[3',2':4,5]thieno[3,2- d ]pyrimidin-4-amine core and 8-chloro-7,9-dimethylpyrido[3',2':4,5]furo[3,2- d ]pyrimidin-4-amine core. Both tricyclic cores displayed low nanomolar potency against human M 4 and greatly reduced cytochrome P450 inhibition when compared with parent compound ML253 .
Keyphrases
  • small molecule
  • endothelial cells
  • high throughput
  • binding protein