4-DAMP

4-DAMP
  • CAS No.:1952-15-4
  • Grade:99.96%
  • Formula:C21H26INO2
  • M.W.:451.34
  • Solvent:≥ 5 mg/mL (11.08 mM); Clear solution

Overview

4-DAMP (4-DAMP methiodide) is a potent and selective antagonist of M3 receptors and also has a high affinity for the closely-related M5 receptors . 4-DAMP combined with 5-Fluorouracil (5-Fu) ( HY-90006 ) could significantly reduce the cell viability and enhance apoptosis in MKN45 and BGC823 gastric cancer cells. 4-DAMP inhibits lipopolysaccharide (LPS)- and tobacco-induced pulmonary inflammation and reduces mucin 5AC ( MUC5AC ), oligomeric mucus/gel-forming secretion.

Application

Products | Products > Disease Areas > Cancer | Products > Disease Areas > Inflammation or Immune System Disease | Products > Signaling Pathways > GPCR/G Protein | Products > Signaling Pathways > Neuronal Signaling | Products > Signaling Pathways > Apoptosis | Products > Signaling Pathways > Metabolic Enzyme/Protease | Products > Signaling Pathways > Protein Tyrosine Kinase/RTK | Products > Signaling Pathways > JAK/STAT Signaling | Products > Signaling Pathways > Immunology/Inflammation | Products > Research Areas > Inflammation/Immunology | Products > Research Areas > Cancer | Products > Research Areas > Cancer > Cancer Targeted Therapy | Products > Research Areas > Cancer > Cancer Immunotherapy | Products > Research Areas > Cancer > Cancer Metabolism and Metastasis | Products > Signaling Pathways > Apoptosis | Products > Signaling Pathways > MMP | Products > Signaling Pathways > EGFR | Products > Signaling Pathways > Interleukin Related | Products > Signaling Pathways > mAChR

Product Information

  • Catalog No.: HY-100958
  • CAS No.: 1952-15-4
  • Molecular Formula: C21H26INO2
  • Molecular Weight: 451.34
  • Purity: 99.96%
  • Storage: 4°C, sealed storage, away from moisture and light * In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
  • Solubility: ≥ 5 mg/mL (11.08 mM); Clear solution
  • Availability: In-stock

Source

Original product source


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