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TRPM4 inhibitor 8

CAS No. 1353979-43-7

TRPM4 inhibitor 8( —— )

Catalog No. M28894 CAS No. 1353979-43-7

TRPM4 inhibitor 8 is an inhibitor of Transient receptor potential melastatin 4(TRPM4) which contributes to viability, migration, cell cycle shift, and adhesion.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 35 Get Quote
10MG 53 Get Quote
25MG 87 Get Quote
50MG 170 Get Quote
100MG 267 Get Quote
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Biological Information

  • Product Name
    TRPM4 inhibitor 8
  • Note
    Research use only, not for human use.
  • Brief Description
    TRPM4 inhibitor 8 is an inhibitor of Transient receptor potential melastatin 4(TRPM4) which contributes to viability, migration, cell cycle shift, and adhesion.
  • Description
    TRPM4 inhibitor 8 is an inhibitor of Transient receptor potential melastatin 4(TRPM4) which contributes to viability, migration, cell cycle shift, and adhesion.
  • In Vitro
    NMDAR/TRPM4-IN-2 free base (compound 8) (0-10 μM) reduces the interactions of GluN2A and GluN2B with TRPM4 in a dose-dependent manner.NMDAR/TRPM4-IN-2 free base eliminates the CREB shutoff pathway and restores ERK1/2 activation and IEG induction while sparing the synaptic activity-driven, transcription-promoting activities of NMDARs.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    TRP/TRPV Channel
  • Recptor
    Endothelin A receptor|Endothelin B receptor
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1353979-43-7
  • Formula Weight
    257.175
  • Molecular Formula
    C11H17BrN2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (388.85 mM)
  • SMILES
    CCN(CCN)Cc1cccc(Br)c1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Balwierczak JL, et al. Characterization of a potent and selective endothelin-B receptor antagonist, IRL 2500.J Cardiovasc Pharmacol. 1995;26 Suppl 3:S393-6.
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