1. Membrane Transporter/Ion Channel Neuronal Signaling Anti-infection
  2. nAChR Parasite
  3. Levamisole

Levamisole  (Synonyms: (-)-Tetramisole)

Art. -Nr.: HY-A0106 Reinheit: 99.96%
Handling Instructions Technical Support

Levamisole ((-)-Levamisole), an anthelmintic agent with immunomodulatory properties. Levamisole acts as a positive allosteric modulator (PAM) for the α3β2 (EC50=300 μM) and α3β4 (EC50=100 μM) subtype of nAChRs. Orally active.

Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.

Levamisole

Levamisole Chemische Struktur

CAS. Nr. : 14769-73-4

Größe Preis Verfügbarkeit Menge
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
Auf Lager
Solution
10 mM * 1 mL in DMSO Auf Lager
Solid
100 mg Auf Lager
500 mg Auf Lager
1 g Auf Lager
5 g Auf Lager
10 g   Angebot einholen  
50 g   Angebot einholen  

* Bitte wählen Sie Menge, bevor Sie Artikel hinzufügen.

This product is a controlled substance and not for sale in your territory.

Kundenbewertung

Based on 14 publication(s) in Google Scholar

Other Forms of Levamisole:

Top Publications Citing Use of Products
  • Biologische Aktivität

  • Reinheit & Dokumentation

  • Verweise

  • Kundenbewertung

Beschreibung

Levamisole ((-)-Levamisole), an anthelmintic agent with immunomodulatory properties. Levamisole acts as a positive allosteric modulator (PAM) for the α3β2 (EC50=300 μM) and α3β4 (EC50=100 μM) subtype of nAChRs. Orally active[1][2].

Cellular Effect
Cell Line Type Value Description References
A549 IC50
> 100 μM
Compound: Levamisole
Cytotoxicity against human A549 cells assessed as cell growth inhibition after 24 hrs by MTT assay
Cytotoxicity against human A549 cells assessed as cell growth inhibition after 24 hrs by MTT assay
[PMID: 27376493]
CCRF-CEM IC50
> 250 μM
Compound: Levamisole
Cytotoxicity against human CEM cells after 72 hrs by Coulter counting method
Cytotoxicity against human CEM cells after 72 hrs by Coulter counting method
[PMID: 25064346]
HeLa IC50
250 μM
Compound: Levamisole
Cytotoxicity against human HeLa cells after 72 hrs by Coulter counting method
Cytotoxicity against human HeLa cells after 72 hrs by Coulter counting method
[PMID: 25064346]
HeLa IC50
96 μM
Compound: Levamisole
Cytotoxicity against human HeLa cells assessed as cell growth inhibition after 24 hrs by MTT assay
Cytotoxicity against human HeLa cells assessed as cell growth inhibition after 24 hrs by MTT assay
[PMID: 27376493]
L1210 IC50
206 μM
Compound: Levamisole
Cytotoxicity against mouse L1210 cells after 48 hrs by Coulter counting method
Cytotoxicity against mouse L1210 cells after 48 hrs by Coulter counting method
[PMID: 25064346]
MCF7 IC50
> 100 μM
Compound: Levamisole
Cytotoxicity against human MCF7 cells assessed as cell growth inhibition after 24 hrs by MTT assay
Cytotoxicity against human MCF7 cells assessed as cell growth inhibition after 24 hrs by MTT assay
[PMID: 27376493]
In Vivo

(S)-(-)-Levamisole (Levamisole) (50 μg/ml and 200 μg/ml; p.o.; 30 days) prevents weight gain in mice that were fed a high fat diet[2].

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

Klinische Studie
Molekulargewicht

204.30

Formel

C11H12N2S

CAS. Nr.
Appearance

Solid

Color

White to off-white

SMILES

C12=N[C@@H](C3=CC=CC=C3)CN1CCS2

Versand

Room temperature in continental US; may vary elsewhere.

Speicherung
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Lösungsmittel & Löslichkeit
In Vitro: 

DMSO : 100 mg/mL (489.48 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 4.8948 mL 24.4741 mL 48.9481 mL
5 mM 0.9790 mL 4.8948 mL 9.7896 mL
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. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

  • Molaritätsrechner

  • Verdünnungsrechner

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:

Select the appropriate dissolution method based on your experimental animal and administration route.

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
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:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: ≥ 2.5 mg/mL (12.24 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

    Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
  • Protocol 2

    Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

    Solubility: ≥ 2.5 mg/mL (12.24 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

    Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
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.
Please enter your animal formula composition:
%
DMSO +
+
%
Tween-80 +
%
Saline
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Calculation results:
Working solution concentration: mg/mL
Method for preparing stock solution: mg drug dissolved in μL  DMSO (Stock solution concentration: mg/mL).
The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only. If necessary, please contact MedChemExpress (MCE).
Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline.
 If the continuous dosing period exceeds half a month, please choose this protocol carefully.
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Reinheit & Dokumentation

Purity: 99.97%

Verweise

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. 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
DMSO 1 mM 4.8948 mL 24.4741 mL 48.9481 mL 122.3703 mL
5 mM 0.9790 mL 4.8948 mL 9.7896 mL 24.4741 mL
10 mM 0.4895 mL 2.4474 mL 4.8948 mL 12.2370 mL
15 mM 0.3263 mL 1.6316 mL 3.2632 mL 8.1580 mL
20 mM 0.2447 mL 1.2237 mL 2.4474 mL 6.1185 mL
25 mM 0.1958 mL 0.9790 mL 1.9579 mL 4.8948 mL
30 mM 0.1632 mL 0.8158 mL 1.6316 mL 4.0790 mL
40 mM 0.1224 mL 0.6119 mL 1.2237 mL 3.0593 mL
50 mM 0.0979 mL 0.4895 mL 0.9790 mL 2.4474 mL
60 mM 0.0816 mL 0.4079 mL 0.8158 mL 2.0395 mL
80 mM 0.0612 mL 0.3059 mL 0.6119 mL 1.5296 mL
100 mM 0.0489 mL 0.2447 mL 0.4895 mL 1.2237 mL
  • No file chosen (Maximum size is: 1024 Kb)
  • If you have published this work, please enter the PubMed ID.
  • Your name will appear on the site.
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.

Ihre kürzlich angesehenen Produkte:

Online-Anfrage

Your information is safe with us. * Required Fields.

Produktname

 

Requested Quantity *

Name des Antragstellers *

 

Anrede

E-Mail-Addresse *

 

Telefonnummer *

Department

 

Name der Organisation *

City

Bundesland

Country or Region *

     

Bemerkungen

Massenanfrage

Inquiry Information

Produktname:
Levamisole
Art. -Nr.:
HY-A0106
Menge:
MCE Japan Authorized Agent: