JNJ-54082730

JNJ-54082730
  • CAS No.:2097493-39-3
  • Grade:99.98%
  • Formula:C20H22F2N6O
  • M.W.:400.43

Overview

JNJ-54082730 (Compound 1) is the orally active inhibitor for phosphodiesterase ( PDE ) that inhibits PDE2A , PDE3B , and PDE10A2 with IC 50 s of 0.95 nM, 6.17 μM (pIC 50 =5.21) and 87.1 nM (pIC 50 =7.06), respectively. JNJ-54082730 modulates the activity of AMPA receptor , enhance the synaptic plasticity and promotes the learning and memory function in rats models. JNJ-54082730 can cross blood-brain barrier.

Application

Products | Products > Disease Areas > Neurological, Eye or Ear Disease | Products > Signaling Pathways > Metabolic Enzyme/Protease | Products > Signaling Pathways > Neuronal Signaling | Products > Signaling Pathways > Membrane Transporter/Ion Channel | Products > Research Areas > Neurological Disease | Products > Signaling Pathways > Phosphodiesterase (PDE) | Products > Signaling Pathways > iGluR

Product Information

  • Catalog No.: HY-168966
  • CAS No.: 2097493-39-3
  • Molecular Formula: C20H22F2N6O
  • Molecular Weight: 400.43
  • Purity: 99.98%
  • Storage: Please store the product under the recommended conditions in the Certificate of Analysis.

Source

Original product source


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