Tetrandrine Calcium Channel inhibitor

Cat.No.S2403

Tetrandrine, a bis-benzylisoquinoline alkaloid derived from Stephania tetrandra, is a calcium channel blocker.
Tetrandrine Calcium Channel inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 622.75

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 622.75 Formula

C38H42N2O6

Storage (From the date of receipt)
CAS No. 518-34-3 Download SDF Storage of Stock Solutions

Solubility

In vitro
Batch:

DMSO : 12 mg/mL (19.26 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 3 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Mechanism of Action

Targets/IC50/Ki
Calcium channel [1]
In vitro

Tetrandrine inhibits voltage-gated Ca2+ currents with an IC50 of 10.1 mM in isolated nerve terminals of the rat neurohypophysis. This compound is a high-affinity blocker of the type II, maxi-Ca(2+)-activated K+ channel of the rat neurohypophysial terminals with an IC50 of 0.21 mM. [1] Another study shows that it also inhibits Ca(2+)-activated Cl- currents (I(Cl,Ca)) with an IC50 of 5.2 mM. [2] This chemical inhibits the proliferation of human leukemic HL-60 cells via induction of apoptosis. [3]

References

Applications

Methods Biomarkers Images PMID
Western blot p-ASK1 / ASK1 / p-SEK1 / SEK1 / p-JNK1/2 / JNK1/2 Atg7 p-GSK3β / GSK3β / p-β-catenin / β-catenin S2403-WB3 25181458
Growth inhibition assay Cell viability S2403-viability1 29285984
Immunofluorescence p-STAT3 E-cadherin / Vimentin S2403-IF2 28332288

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