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Pinokalant

Chemical Structure : Pinokalant

CAS No.: 149759-26-2

Pinokalant (LOE908, LOE-908)

Catalog No.: PC-25775Not For Human Use, Lab Use Only.

Pinokalant (LOE908, LOE-908) is an inhibitor of receptor-operated Ca(2+) channels (ROCCs) and non-selective cation channel inhibitor, inhibits store-operated Ca2+ entry (SOCE) induced by direct depletion of Ca2+ stores with 100 nM thapsigargin or 100 nM ionomycin with EC50 of 2 uM and 4 uM, respectively.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Pinokalant (LOE908, LOE-908) is an inhibitor of receptor-operated Ca(2+) channels (ROCCs) and non-selective cation channel inhibitor, inhibits store-operated Ca2+ entry (SOCE) induced by direct depletion of Ca2+ stores with 100 nM thapsigargin or 100 nM ionomycin with EC50 of 2 uM and 4 uM, respectively.
Pinokalant (LOE908, LOE-908) does not affect thapsigargin- or ionomycin-induced Ca2+ release from intracellular stores.
Pinokalant (LOE908, LOE-908) reversibly suppressed thapsigargin- as well as ionomycin-induced whole-cell membrane currents.

Physicochemical Properties

M.Wt 712.84
Formula C41H48N2O9
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

2-(6,7-dimethoxy-3,4-dihydroisoquinolin-1-yl)-2-phenyl-N,N-bis(2,3,4-trimethoxyphenethyl)acetamide

References

1. Krautwurst D, et al. Mol Pharmacol. 1993 May;43(5):655-9.

2. Krautwurst D, et al. Naunyn Schmiedebergs Arch Pharmacol. 1994 Mar;349(3):301-7.

3. Encabo A, et al. Br J Pharmacol. 1996 Oct;119(4):702-6.

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