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Synthesis and Structure-Activity Relationships of DCLK1 Kinase Inhibitors Based on a 5,11-Dihydro-6H-benzo[e]pyrimido[5,4-b][1,4]diazepin-6-one Scaffold.

Fleur M FergusonYan LiuWayne HarshbargerLing HuangJinhua WangXianming DengStephen J CapuzziEugene N MuratovAlexander TrospshaSenthil MuthuswamyKenneth D WestoverNathanael S Gray
Published in: Journal of medicinal chemistry (2020)
Doublecortin-like kinase 1 (DCLK1) is a serine/threonine kinase that is overexpressed in gastrointestinal cancers, including esophageal, gastric, colorectal, and pancreatic cancers. DCLK1 is also used as a marker of tuft cells, which regulate type II immunity in the gut. However, the substrates and functions of DCLK1 are understudied. We recently described the first selective DCLK1/2 inhibitor, DCLK1-IN-1, developed to aid the functional characterization of this important kinase. Here we describe the synthesis and structure-activity relationships of 5,11-dihydro-6H-benzo[e]pyrimido[5,4-b][1,4]diazepin-6-one DCLK1 inhibitors, resulting in the identification of DCLK1-IN-1.
Keyphrases
  • protein kinase
  • induced apoptosis
  • tyrosine kinase
  • oxidative stress
  • signaling pathway
  • endoplasmic reticulum stress
  • tissue engineering