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Quininib

Axon 2620
CAS:  143816-42-6
Purity:  99%
  • Soluble in DMSO
  • MF:  C17H13NO
  • MW:  247.29

Description

Quininib is a potent cysteinyl leukotriene (CysLT) antagonist with IC50 values of 1.4 μM and 38.5 μM at CysLT1 and cysLT2 receptors, respectively. Quininib inhibits downstream p-ERK signaling to reduce pro-inflammatory cytokines like IL-6 and IL-8. Mechanistically, it suppresses pathological neovascularization and tumor growth via a distinct pathway completely independent of classical VEGF signaling.

CysLT pharmacology is highly relevant to cancer biology. Quininib serves as a vital tool to support mechanistic studies of CysLT receptors, VEGF-independent pathways, and LTD4 signaling across biochemical, cellular, and disease-model assays.

Key Features

  • CysLT antagonist
  • IC50 values 1.4 μM (CysLT1) and 38.5 μM (CysLT2)
  • Supports focused CysLT pathway studies in biochemical and cellular systems
  • Suppresses pathological neovascularization independently of VEGF pathways

Applications

  • CysLT pharmacology and target-validation studies
  • CysLT pathway and signaling assays
  • Disease-model research related to cancer
  • Receptor signaling, ligand profiling and functional response assays

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