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product name Gallamine Triethiodide


Description: Gallamine Triethiodide is a cholinergic receptor blocker with an IC50 of 68.0 ± 8.4 μM. Specifically, Gallamine Triethiodide is a mAChR M2 antagonist with pronounced cardioselectivity. It exerts its effects by combining with the cholinergic receptor sites in muscle and competitively blocking the transmitter action of acetylcholine. It is a synthetic non-depolarizing blocking drug. The actions of gallamine triethiodide are similar to those of tubocurarine but this agent blocks the cardiac vagus and may cause sinus tachycardia and, occasionally, hypertension and increased cardiac output. 

References: J Pharmacol Exp Ther. 1986 Jan;236(1):219-23.



Molecular Weight (MW)

891.53 
Formula

C30H60I3N3O3 
CAS No.

65-29-2 
Storage

-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)

DMSO: 100 mg/mL (112.2 mM)
Water: <1 mg/mL
Ethanol: 100 mg/mL (112.2 mM)
Solubility (In vivo)

 
Synonyms

 

other peoduct :References PubMed ID::http://www.ncbi.nlm.nih.gov/pubmed/19391041

In Vitro

In vitro activity


Kinase Assay:


Cell Assay

In Vivo  
Animal model  
Formulation & Dosage  
References  

ABT-199

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Author: Sodium channel

Share this post on:

product name Gallamine Triethiodide


Description: Gallamine Triethiodide is a cholinergic receptor blocker with an IC50 of 68.0 ± 8.4 μM. Specifically, Gallamine Triethiodide is a mAChR M2 antagonist with pronounced cardioselectivity. It exerts its effects by combining with the cholinergic receptor sites in muscle and competitively blocking the transmitter action of acetylcholine. It is a synthetic non-depolarizing blocking drug. The actions of gallamine triethiodide are similar to those of tubocurarine but this agent blocks the cardiac vagus and may cause sinus tachycardia and, occasionally, hypertension and increased cardiac output. 

References: J Pharmacol Exp Ther. 1986 Jan;236(1):219-23.



Molecular Weight (MW)

891.53 
Formula

C30H60I3N3O3 
CAS No.

65-29-2 
Storage

-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)

DMSO: 100 mg/mL (112.2 mM)
Water: <1 mg/mL
Ethanol: 100 mg/mL (112.2 mM)
Solubility (In vivo)

 
Synonyms

 

other peoduct :References PubMed ID::http://www.ncbi.nlm.nih.gov/pubmed/19391041

In Vitro

In vitro activity


Kinase Assay:


Cell Assay

In Vivo  
Animal model  
Formulation & Dosage  
References  

ABT-199

Share this post on:

Author: Sodium channel