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:
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).
signalword
Danger
hcodes
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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L Chen et al.
Free radical biology & medicine, 19(6), 713-724 (1995-12-01)
A selenium (Se)-containing immunoconjugate of a human anti-erythrocyte membrane antibody (Ab-Se) has been synthesized via oxidation of the carbohydrate moieties of the antibody and covalent coupling with selenocystamine. The isolated Ab-Se immunoconjugate is shown to be more hemolytic than is
Wansik Cha et al.
Biomaterials, 28(1), 19-27 (2006-09-09)
Novel nitric oxide (NO) generating polymeric materials possessing immobilized organoselenium species are described. These materials mimic the capability of small organoselenium molecules as well as a known selenium-containing enzyme, glutathione peroxidase (GPx), by catalytically decomposing S-nitrosothiols (RSNO) into NO and
T Tabatabaie et al.
Toxicology and applied pharmacology, 141(2), 389-393 (1996-12-01)
Chronic benzaldehyde exposure is known to cause central nervous system (CNS) disturbances. Previous studies have shown that benzaldehyde causes the formation of reactive oxygen species (ROS) in rat synaptosomal fractions. Benzaldehyde has also been implicated in ROS formation in the
Global Trade Item Number
| SKU | GTIN |
|---|---|
| S0520-25MG | 04061832424460 |
| S0520-100MG | 04061832424453 |
| S0520-1G | 04061835359141 |
| S0520-250MG | 04061835359158 |