Gallamine Triethiodide - Moligand™, 10mM in DMSO , Muscle-type nicotinic acetylcholine receptor antagonist, CAS No.65-29-2, Muscle-type nicotinic acetylcholine receptor antagonist

CAS: 65-29-2 Cat. No.: G408368 Molecular Weight: 891.53 EC Number: 200-605-1 PubChem CID: 6172
AVAILABLE TO ORDER
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. 10mM in DMSO
Synonyms
2,​2',​2''-​[1,​2,​3-​benzenetriyltris(oxy​)​]​tris[N,​N,​N-​triethyl-ethanaminium, iodide (1:3)
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1ml
G408368-1ml
2

$37.90

$55.90
Save $18.00 (32.20%)
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Why this grade

Moligand™, 10mM in DMSO Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Information

Gallamine Triethiodide Gallamine Triethiodide is a cholinergic receptor blocker with an IC50 of 68.0 ± 8.4 μM.
In vitro


In vivo


Cell Data

cell lines:

Concentrations:

Incubation Time:

Powder Purity:≥97%

Specifications

Synonyms
2, ​2', ​2''-​[1, ​2, ​3-​benzenetriyltris(oxy​)​]​tris[N, ​N, ​N-​triethyl-ethanaminium, iodide (1:3)
Specifications & Purity
Moligand™, 10mM in DMSO
Biochemical and Physiological Mechanisms
Gallamine Triethiodide is a cholinergic receptor blocker with an IC50 of 68.0 ± 8.4 μM.
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Moligand™
Action Type
ALLOSTERIC MODULATOR, ANTAGONIST, CHANNEL BLOCKER
Mechanism of action
Muscle-type nicotinic acetylcholine receptor antagonist
Names and Identifiers
Isomeric SMILES CC[N+](CC)(CC)CCOC1=C(C(=CC=C1)OCC[N+](CC)(CC)CC)OCC[N+](CC)(CC)CC.[I-].[I-].[I-]
WGK Germany 3
RTECS BS1100000
PubChem CID 6172
Molecular Weight 891.53

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Associated Targets(Human)
CHRNA1 Tclin Acetylcholine receptor subunit alpha (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
Melt Point(°C)235 °C
Citations of This Product
References
1. Lin Huang, Weixia Zhang, Difei Tong, Lingzheng Lu, Weishang Zhou, Dandan Tian, Guangxu Liu, Wei Shi.  (2023)  Triclosan and triclocarban weaken the olfactory capacity of goldfish by constraining odorant recognition, disrupting olfactory signal transduction, and disturbing olfactory information processing.  WATER RESEARCH,      [PMID:36801581] [10.1016/j.watres.2023.119736]
2. Petrus Siregar, Gilbert Audira, Ling-Yi Feng, Jia-Hau Lee, Fiorency Santoso, Wen-Hao Yu, Yu-Heng Lai, Jih-Heng Li, Ying-Ting Lin, Jung-Ren Chen, Chung-Der Hsiao.  (2021)  Pharmaceutical Assessment Suggests Locomotion Hyperactivity in Zebrafish Triggered by Arecoline Might Be Associated with Multiple Muscarinic Acetylcholine Receptors Activation.  Toxins,  13  (4): (259).  [PMID:33916832] [10.3390/toxins13040259]
Solution Calculators
Reviews

Customer Reviews

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