KT-362 fumarate

CAS No. 105394-80-7

KT-362 fumarate( —— )

Catalog No. M34305 CAS No. 105394-80-7

KT-362 fumarate is a novel compound that acts as an antagonist of calcium channels, potassium channels and sodium channels.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 511 In Stock
5MG 426 In Stock
10MG 599 In Stock
25MG 889 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    KT-362 fumarate
  • Note
    Research use only, not for human use.
  • Brief Description
    KT-362 fumarate is a novel compound that acts as an antagonist of calcium channels, potassium channels and sodium channels.
  • Description
    KT-362 fumarate is a novel compound that acts as an antagonist of calcium channels, potassium channels and sodium channels.KT-362 fumarate causes vasodilation by affecting intracellular calcium mobilization in atrial muscle cells.KT-362 fumarate has a relaxing effect on femoral and basilar artery strips in rabbits.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    Calcium Channel
  • Recptor
    Calcium Channel | Potassium Channel | Sodium Channel
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    105394-80-7
  • Formula Weight
    516.61
  • Molecular Formula
    C26H32N2O7S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    C(=C/C(O)=O)\C(O)=O.C(CCNCCC1=CC(OC)=C(OC)C=C1)(=O)N2C=3C(=CC=CC3)SCCC2
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • Efonidipine

    Efonidipine (NZ-105) is a potent, dual T-type and L-type calcium channel blocker.

  • alpha-L-Rhamnose

    Addition of the Rhamnose-rich polysaccharide RROP-1 to normal human dermal fibroblasts (NHDFs) and human endothelial cells produced a dose-dependent stimulation of the calcium-signaling pathway inducing fast and transient increases in Ca2 influx and intracellular free Ca2 level.

  • Imagabalin hydrochlo...

    Imagabalin (PD 0332334) is a novel ligand for the α2δ subunit of the voltage-dependent calcium channel (VDCC) with some selectivity for the α2δ1 subunit over α2δ2.