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S1650

Sigma-Aldrich

Seleno-DL-cystine

>98% (TLC), suitable for HPLC

Synonym(s):

3,3′-diselenobis- alanine,

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About This Item

Empirical Formula (Hill Notation):
C6H12N2O4Se2
CAS Number:
2897-21-4
Molecular Weight:
334.09
MDL number:
MFCD00055925
UNSPSC Code:
12352209
PubChem Substance ID:
24899489
NACRES:
NA.26

product name

Seleno-DL-cystine, powder

Assay

>98% (TLC)

Quality Level

200

form

powder

technique(s)

HPLC: suitable

mp

222 °C

storage temp.

−20°C

SMILES string

NC(C[Se][Se]CC(N)C(O)=O)C(O)=O

InChI

1S/C6H12N2O4Se2/c7-3(5(9)10)1-13-14-2-4(8)6(11)12/h3-4H,1-2,7-8H2,(H,9,10)(H,11,12)

InChI key

JULROCUWKLNBSN-UHFFFAOYSA-N

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Related Categories

Signal Word

Danger

Hazard Statements

H301 + H331,H373,H410

Hazard Classifications

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Pierre Burguière et al.
Journal of bacteriology, 186(15), 4875-4884 (2004-07-21)
The symporter YhcL and two ATP binding cassette transporters, YtmJKLMN and YckKJI, were shown to mediate L-cystine uptake in Bacillus subtilis. A triple DeltayhcL DeltaytmJKLMN DeltayckK mutant was unable to grow in the presence of L-cystine and to take up
Thomas Hofer et al.
Biochemistry, 48(50), 12047-12057 (2009-11-10)
Antibody conjugates have broad utility in basic, preclinical, and clinical applications. Conventional antibody conjugation through the amine group of lysine or the thiol group of cysteine residues yields heterogeneous products of undefined stoichiometry and considerable batch-to-batch variability. To preserve the
Mamoru Haratake et al.
Bioconjugate chemistry, 19(9), 1831-1839 (2008-08-19)
We synthesized nanoparticulate glutathione peroxidase (GPx) mimics in which selenocystine (SeCyst) was conjugated to a hydrophilic linear polysaccharide, pullulan (Pul). The SeCyst ester-conjugated Pul derivatives (SeCyst-Pul) in phosphate buffer (pH 7) were treated with a sonicator to spontaneously form particulate
Tianfeng Chen et al.
Journal of agricultural and food chemistry, 56(22), 10574-10581 (2008-10-31)
Selenocystine (SeC) is a nutritionally available selenoamino acid with selective anticancer effects on a number of human cancer cell lines. The present study shows that SeC inhibited the proliferation of human breast adenocarcinoma MCF-7 cells in a time- and dose-dependent
B Santhosh Kumar et al.
Radiation and environmental biophysics, 48(4), 379-384 (2009-09-17)
Organoselenium compounds belonging to the class of monoselenides, such as selenomethionine (SeM) and methylselenocysteine (MSeCys) and diselenides including selenocystine (SeCys) and selenopropionic acid (SePA), were examined for their comparative radioprotective effects using in vitro models. Effects of these compounds on
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