1. Membrane Transporter/Ion Channel Neuronal Signaling
  2. Potassium Channel Calcium Channel
  3. Lidoflazine

Lidoflazine is a high affinity blocker of the HERG (human ether-a-go-go-related gene) K+ channel. Lidoflazine is an antianginal calcium channel blocker that carries a significant risk of QT interval prolongation and ventricular arrhythmia.

For research use only. We do not sell to patients.

Lidoflazine Chemical Structure

Lidoflazine Chemical Structure

CAS No. : 3416-26-0

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Solution
10 mM * 1 mL in DMSO USD 946 Ask For Quote & Lead Time
Solid
5 mg USD 537 Ask For Quote & Lead Time
10 mg USD 860 Ask For Quote & Lead Time

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Description

Lidoflazine is a high affinity blocker of the HERG (human ether-a-go-go-related gene) K+ channel. Lidoflazine is an antianginal calcium channel blocker that carries a significant risk of QT interval prolongation and ventricular arrhythmia[1].

In Vitro

Lidoflazine inhibits potently HERG current (IHERG) recorded from HEK 293 cells stably expressing wild-type HERG (IC50 of ~16 nM).

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

491.62

Formula

C30H35F2N3O

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

O=C(NC1=C(C)C=CC=C1C)CN2CCN(CCCC(C3=CC=C(F)C=C3)C4=CC=C(F)C=C4)CC2

Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Purity & Documentation

Purity: ≥98.0%

References
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Lidoflazine
Cat. No.:
HY-112075
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