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Merck
CN

M3184

MG 624

≥98%

Synonym(s):

N,N,N-Triethyl-2-(4-trans-stilbenoxy)ethylammonium iodide

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About This Item

Empirical Formula (Hill Notation):
C22H30INO
CAS Number:
Molecular Weight:
451.38
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Assay:
≥98%
Quality level:
Technical Service
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Product Name

MG 624, ≥98%

InChI

1S/C22H30NO.HI/c1-4-23(5-2,6-3)18-19-24-22-16-14-21(15-17-22)13-12-20-10-8-7-9-11-20;/h7-17H,4-6,18-19H2,1-3H3;1H/q+1;/p-1/b13-12+;

SMILES string

[I-].CC[N+](CC)(CC)CCOc1ccc(cc1)\C=C\c2ccccc2

InChI key

RDTKUZXIHMTSJO-UEIGIMKUSA-M

assay

≥98%

solubility

DMSO: ≤22 mg/mL
H2O: insoluble

storage temp.

2-8°C

Quality Level

Gene Information

human ... CHRNA7(1139)

Biochem/physiol Actions

Nicotinic acetylcholine receptor antagonist; selectively inhibits neuronal nicotinic α-bungarotoxin sensitive receptors that contain the α7 subunit.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Glenn W Vicary et al.
Respiratory research, 18(1), 115-115 (2017-06-04)
Tobacco-related chronic lung diseases are characterized by alterations in lung architecture leading to decreased lung function. Knowledge of the exact mechanisms involved in tobacco-induced tissue remodeling and inflammation remains incomplete. We hypothesize that nicotine stimulates the expression of extracellular matrix
C Gotti et al.
British journal of pharmacology, 124(6), 1197-1206 (1998-08-28)
1. Starting from the structure of an old 4-oxystilbene derivate with ganglioplegic activity (MG624), we synthesized two further derivates (F2 and F3) and two stereoisomers of F3 (F3A and F3B), and studied their selective effect on neuronal nicotinic acetylcholine receptor

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