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Merck
CN

M0814

R(−)-Me5 hydriodide

solid

Synonym(s):

1-(2,6-Dimethylphenoxy)-3-methyl-2-butanamine hydriodide

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About This Item

Empirical Formula (Hill Notation):
C13H21NO · HI
Molecular Weight:
335.22
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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InChI

1S/C13H21NO.HI/c1-9(2)12(14)8-15-13-10(3)6-5-7-11(13)4;/h5-7,9,12H,8,14H2,1-4H3;1H

SMILES string

I[H].CC(C)C(N)COc1c(C)cccc1C

InChI key

AQLAXCGHPBMFIJ-UHFFFAOYSA-N

form

solid

color

white

solubility

H2O: 22 mg/mL

Gene Information

human ... SCN2A(6326)

Application

May be used as a sodium channel blocker in sketetal muscle.

Biochem/physiol Actions

Potent sodium channel antagonist.

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Stephan Bramow et al.
Brain : a journal of neurology, 133(10), 2983-2998 (2010-09-22)
The causes of incomplete remyelination in progressive multiple sclerosis are unknown, as are the pathological correlates of the different clinical characteristics of patients with primary and secondary progressive disease. We analysed brains and spinal cords from 51 patients with progressive
A De Luca et al.
Molecular pharmacology, 57(2), 268-277 (2000-01-29)
On the basis of the information about drug receptor on voltage-gated sodium channels, mexiletine (Mex) analogs with substitutions at either the asymmetric carbon atom or the aromatic ring were synthesized as pure enantiomers. The compounds were tested in vitro for
M Takanashi et al.
Gene therapy, 16(8), 982-989 (2009-05-29)
Recent advances of biotechnology have laid the groundwork for potent and specific molecular-targeting therapies including RNA interference. The largest remaining hurdle for widespread use of this technology in skin is an effective delivery system. Here, we demonstrate an effective topical
Leyla Sati et al.
Histochemistry and cell biology, 133(1), 85-93 (2009-10-15)
Pulmonary surfactant is a complex mixture of phospholipids and four surfactant-associated proteins (SP-A, SP-B, SP-C and SP-D). The biological functions of SP-A and SP-D are primarily twofold, namely surfactant homeostasis and host defense. The hydrophobic surfactant proteins, SP-B and SP-C
Marta Mellai et al.
Cancer genomics & proteomics, 6(4), 219-227 (2009-08-07)
To evaluate MGMT promoter hypermethylation as prognostic factor in a retrospective study of 104 cases of glioblastoma multiforme (GBM). The O(6)-methylguanine-DNA methyltransferase (MGMT) status was evaluated by methylation-specific PCR (MSP), immunohistochemistry and Western blotting analysis in formalin-fixed paraffin-embedded surgical samples.

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