1. Membrane Transporter/Ion Channel Neuronal Signaling Apoptosis Anti-infection
  2. Potassium Channel nAChR Apoptosis Bacterial Parasite
  3. Dequalinium Chloride

Dequalinium chloride is an Apamin (HY-P0256)-sensitive potassium channel selective blocker. Dequalinium chloride is a cationic, lipophilic mitochondrial poison. Dequalinium chloride is also an antagonist pf α7 nAChR, and an anti-microbial antiseptic agent with a broad bactericidal and fungicidal activity.

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

Dequalinium Chloride Chemical Structure

Dequalinium Chloride Chemical Structure

CAS No. : 522-51-0

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Customer Review

Based on 1 publication(s) in Google Scholar

Other Forms of Dequalinium Chloride:

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  • Biological Activity

  • Purity & Documentation

  • References

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Description

Dequalinium chloride is an Apamin (HY-P0256)-sensitive potassium channel selective blocker. Dequalinium chloride is a cationic, lipophilic mitochondrial poison. Dequalinium chloride is also an antagonist pf α7 nAChR, and an anti-microbial antiseptic agent with a broad bactericidal and fungicidal activity[1][2][3][4].

Cellular Effect
Cell Line Type Value Description References
Astrocyte EC50
1.418 μM
Compound: 29
Antiproliferative activity against mouse astrocyte cells by MTT assay
Antiproliferative activity against mouse astrocyte cells by MTT assay
[PMID: 17417631]
HEK293 IC50
1.3 μM
Compound: 15
Inhibition of Kca2.3 channel expressed in HEK293 cells by thallium flux assay
Inhibition of Kca2.3 channel expressed in HEK293 cells by thallium flux assay
[PMID: 18774291]
HEK293 IC50
2 μM
Compound: 15
Inhibition of Kca2.3 channel expressed in HEK293 cells by electrophysiology assay
Inhibition of Kca2.3 channel expressed in HEK293 cells by electrophysiology assay
[PMID: 18774291]
Sympathetic neuron IC50
0.74 μM
Compound: dequalinium (4)
The SKCa-blocking action was assessed by its ability to inhibit the after hyperpolarization (AHP) in cultured rat sympathetic neurones
The SKCa-blocking action was assessed by its ability to inhibit the after hyperpolarization (AHP) in cultured rat sympathetic neurones
[PMID: 7658440]
Sympathetic neuron IC50
0.9 μM
Compound: Dequalinium
Compound was tested for its ability to inhibit the after hyperpolarization which follows the action potential in rat sympathetic neurons.
Compound was tested for its ability to inhibit the after hyperpolarization which follows the action potential in rat sympathetic neurons.
[PMID: 8784458]
Sympathetic neuron IC50
1 μM
Compound: 22(dequalinium)
SKCa-blocking activity by its ability to inhibit after hyperpolarization (AHP) in cultured rat sympathetic neurons
SKCa-blocking activity by its ability to inhibit after hyperpolarization (AHP) in cultured rat sympathetic neurons
[PMID: 8558503]
Sympathetic neuron IC50
570 nM
Compound: Deq
Compound was tested for SKCa blocking action by measuring its ability to inhibit after hyperpolarization (AHP) in cultured rat sympathetic neurones
Compound was tested for SKCa blocking action by measuring its ability to inhibit after hyperpolarization (AHP) in cultured rat sympathetic neurones
[PMID: 9438015]
Sympathetic neuron IC50
900 nM
Compound: Dequalinium
Inhibition of after hyperpolarization (AHP) of cultured rat sympathetic neurons as SKCa channel blocking activity
Inhibition of after hyperpolarization (AHP) of cultured rat sympathetic neurons as SKCa channel blocking activity
[PMID: 15261276]
In Vitro

Dequalinium chloride blocks angiotensin II (100 nM)-evoked K+ loss in guinea-pig hepatocytes, with an IC50 of 1.5 μM[5].
Dequalinium (0-100 μg/mL, 72 h) chloride inhibits cell growth in human Pca cell lines (PC3, DU145, LNCaP, MDA-PCA-2B), and induces cell apoptosis in PC3 cells (0.9 μM, 4 h)[7].

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

In Vivo

Dequalinium chloride shows a LD50 of 18.3 mg/kg in mice (i.p., a single time)[2].
Dequalinium chloride (2 mg/kg, i.p., daily for 10 days) inhibits the tumor growth of mouse bladder carcinoma MB49[3].
Dequalinium chloride (2 mg/kg, s.c.) reduces Diisopropylfluorophosphate-induced tremors (organophosphate poisoning) in mice[6].

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

Clinical Trial
Molecular Weight

527.57

Formula

C30H40Cl2N4

CAS No.
Appearance

Solid

Color

Off-white to light yellow

SMILES

CC1=[N+](C2=CC=CC=C2C(N)=C1)CCCCCCCCCC[N+](C3=CC=CC=C3C(N)=C4)=C4C.[Cl-].[Cl-]

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

4°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

Solvent & Solubility
In Vitro: 

H2O : 0.99 mg/mL (1.88 mM; ultrasonic and warming and adjust pH to 3 with 1 M HCL and heat to 60°C)

DMSO : < 1 mg/mL (insoluble or slightly soluble)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.8955 mL 9.4774 mL 18.9548 mL
5 mM --- --- ---
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

  • Molarity Calculator

  • Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass
=
Concentration
×
Volume
×
Molecular Weight *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

×
Volume (start)

V1

=
Concentration (final)

C2

×
Volume (final)

V2

In Vivo:

For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

  • Protocol 1

    Add each solvent one by one:  50% PEG300    50% Saline

    Solubility: 2 mg/mL (3.79 mM); Suspended solution; Need ultrasonic

In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
Purity & Documentation

Purity: 99.91%

References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
H2O 1 mM 1.8955 mL 9.4774 mL 18.9548 mL 47.3871 mL

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

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Help & FAQs
  • Do most proteins show cross-species activity?

    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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Dequalinium Chloride
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