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Merck
  • Anthranilic sulfonamide CCK1/CCK2 dual receptor antagonists II: tuning of receptor selectivity and in vivo efficacy.

Anthranilic sulfonamide CCK1/CCK2 dual receptor antagonists II: tuning of receptor selectivity and in vivo efficacy.

Bioorganic & medicinal chemistry letters (2009-10-10)
Marna Pippel, Kristen Boyce, Hariharan Venkatesan, Victor K Phuong, Wen Yan, Terrance D Barrett, Guy Lagaud, Lina Li, Magda F Morton, Clodagh Prendergast, Xiaodong Wu, Nigel P Shankley, Michael H Rabinowitz
초록

In the previous article we demonstrated how certain CCK2R-selective anthranilic amides could be structurally modified to afford high-affinity, selective CCK1R activity. We now describe our efforts at modulating and optimizing the CCK1R and CCK2R affinities aimed at producing compounds with good pharmacokinetics properties and in vivo efficacy in rat models of gastric acid and pancreatic amylase secretion.

MATERIALS
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Sigma-Aldrich
Anthranil, 99%