Ipidacrine

Ipidacrine
  • CAS No.:62732-44-9
  • Grade:99.81%
  • Formula:C12H16N2
  • M.W.:188.27
  • Solvent:≥ 2.5 mg/mL (13.28 mM); Clear solution

Overview

Ipidacrine is orally active and brain-penetrant AChE and BuChE inhibitors with IC 50 values of 1 μM and 1.9 μM, respectively, which is also a partial agonist of M2-cholinergic receptors and a reversible cholinesterase inhibitor. Ipidacrine has a stimulating effect on neuromuscular transmission and excitation along the nerve fibres with a moderately anti-pain effect. Ipidacrine is an aminopyridines and is structurally similar to Tacrine ( HY-111338 ). Ipidacrine is effective in various amnesia models, improves erectile function and inhibits K + and Na + -channels in the neuronal membrane in diabetic rats. Ipidacrine is promising for research of Alzheimer’s disease, ischaemic stroke, idiopathic neuropathy of the facial nerve, diabetes mellitus-induced erectile dysfunction and other deficits in central or peripheral cholinergic deseases.

Application

Products | Products > Disease Areas > Glucose Metabolism | Products > Disease Areas > Alzheimer's Disease | Products > Disease Areas > Neurological, Eye or Ear Disease | Products > Disease Areas > Metabolic or Endocrine Disease | Products > Disease Areas > Neurodegenerative Disease | Products > Signaling Pathways > Neuronal Signaling | Products > Signaling Pathways > Membrane Transporter/Ion Channel | Products > Research Areas > Neurological Disease | Products > Research Areas > Metabolic Disease | Products > Signaling Pathways > Cholinesterase (ChE) | Products > Signaling Pathways > Potassium Channel | Products > Signaling Pathways > Sodium Channel

Product Information

  • Catalog No.: HY-W027553
  • CAS No.: 62732-44-9
  • Molecular Formula: C12H16N2
  • Molecular Weight: 188.27
  • Purity: 99.81%
  • Storage: 4°C, protect from light * In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
  • Solubility: ≥ 2.5 mg/mL (13.28 mM); Clear solution
  • Availability: In-stock

Source

Original product source


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