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S0520

Selenocystamine dihydrochloride

>98% (TLC), suitable for ligand binding assays

Synonym(s):

2,2′-diselenobis-Ethanamine hydrochloride (1:2)

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About This Item

Empirical Formula (Hill Notation):
C4H12N2Se2 · 2HCl
CAS Number:
Molecular Weight:
318.99
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.26
MDL number:
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Product Name

Selenocystamine dihydrochloride, powder

assay

>98% (TLC)

Quality Level

form

powder

technique(s)

ligand binding assay: suitable

color

yellow to orange

solubility

H2O: soluble, clear to slightly hazy

SMILES string

NCC[Se][Se]CCN.[H]Cl.[H]Cl

InChI

1S/C4H12N2Se2.ClH/c5-1-3-7-8-4-2-6;/h1-6H2;1H

InChI key

PKRYDZYGNSZBHO-UHFFFAOYSA-N

General description

Selenocystamine dihydrochloride has a potential to block the activity of influenza A and B virus associated RNA-dependent RNA polymerase enzyme.

Application

Selenocystamine dihydrochloride has been used to determine its effect on PP2A phosphatase activity in vitro. It has also been used as a catalyst for a disulfide-cleaving reagent, dithiothreitol (DTT).

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This Item
A6262C3647L5751
form

powder

form

powder

form

powder

form

powder

assay

>98% (TLC)

assay

≥98.0% (TLC)

assay

≥98% (TLC)

assay

≥98% (HPLC)

technique(s)

ligand binding assay: suitable

technique(s)

ligand binding assay: suitable

technique(s)

ligand binding assay: suitable

technique(s)

ligand binding assay: suitable

solubility

H2O: soluble, clear to slightly hazy

solubility

-

solubility

-

solubility

-

Quality Level

200

Quality Level

100

Quality Level

200

Quality Level

200

color

yellow to orange

color

white to off-white

color

white

color

white to faint yellow


signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges



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Transferrin serves as a mediator to deliver organometallic ruthenium (II) anticancer complexes into cells
Guo W, et al.
Inorganic Chemistry, 52(9), 5328-5338 (2013)
Y Hou et al.
Biochemical and biophysical research communications, 228(1), 88-93 (1996-11-01)
Seleno compounds such as selenocystamine and seleno-D, L-cystine were found to catalyze the decomposition of S-nitrosothiols (e.g. S-nitroso-glutathione and S-nitroso-N-acetyl-D, L-penicillamine) in the presence of different thiols (e.g. glutathione, N-acetyl-D-penicillamine and 2-mercaptoethanol), and liberate nitric oxide. It was also found
Sodium selenate specifically activates PP2A phosphatase, dephosphorylates tau and reverses memory deficits in an Alzheimer?s disease model
Corcoran NM, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia, 17(8), 1025-1033 (2010)



Global Trade Item Number

SKUGTIN
S0520-250MG04061835359158
S0520-100MG04061832424453
S0520-1G04061835359141
S0520-25MG04061832424460

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