DPI 201-106
DPI 201-106 is a small molecule that enhances cardiac contractility by selectively inhibiting inactivation of the TTX-resistant h1 sodium channel. It also modulates potassium and L-type calcium currents, making it a useful research tool for studying cardiac electrophysiology and contractility in both in vitro and in vivo models.
Product Specifications
CAS Number
97730-95-5
Product Name Alternative
Inhibitor, SDZ 201106, SDZ201106, SDZ-201106, Na channels, Na+ channels, inhibit, DPI 201 106, DPI 201106, DPI 201-106, DPI-201-106, DPI201-106, Sodium Channel, SodiumChannel, Voltage-gated sodium channel
Field of Research
Pharmacology & Drug Discovery
Purity
97.26% (May vary between batches)
Solubility
10% DMSO+40% PEG300+5% Tween 80+45% Saline:5 mg/mL (10.72 mM) ; DMSO:250 mg/mL (535.83 mM)
Smiles
OC (COc1cccc2[nH]c (cc12) C#N) CN1CCN (CC1) C (c1ccccc1) c1ccccc1
Molecular Formula
C29H30N4O2
Molecular Weight
466.57
Storage Conditions
-20°C
Notes
For research use only.
Available Sizes
Frequently Asked Questions
More Discoveries
Explore Other Products
Browse additional items from our catalog
MR201779L2V 200 µL
Kras (NM_021284) Mouse Tagged ORF Clone Lentiviral Particle
Sign In for Pricing
View Details