43791
2,2′-二硫二吡啶
≥99.0% (GC)
别名:
2,2′-二吡啶基二硫醚
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关于此项目
经验公式（希尔记法）:
C10H8N2S2
化学文摘社编号:
分子量:
220.31
UNSPSC Code:
12352112
NACRES:
NA.25
PubChem Substance ID:
EC Number:
218-343-1
Beilstein/REAXYS Number:
154629
MDL number:
Other Notes
For the determination of sulfhydryl groups in biological materials
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Determination of sulfhydryl groups with 2,2'- or 4,4'-dithiodipyridine.
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Archives of biochemistry and biophysics, 119(1), 41-49 (1967-03-01)
Rachel Lubong Sabado et al.
PloS one, 4(1), e4256-e4256 (2009-01-24)
The requirements for priming of HIV-specific T cell responses initially seen in infected individuals remain to be defined. Activation of T cell responses in lymph nodes requires cell-cell contact between T cells and DCs, which can give concurrent activation of
T L Dutka et al.
The Journal of physiology, 589(Pt 9), 2181-2196 (2010-12-01)
S-Nitrosoglutathione (GSNO) is generated in muscle and may S-glutathionylate and/or S-nitrosylate various proteins involved in excitation–contraction (EC) coupling, such as Na+-K+-ATPases, voltage-sensors (VSs) and Ca2+ release channels (ryanodine receptors,RyRs), possibly changing their properties. Using mechanically skinned fibres from rat extensor
Sanae Haga et al.
Antioxidants & redox signaling, 11(10), 2563-2572 (2009-06-06)
Noninvasive evaluation of organ redox states provides invaluable information in many clinical settings. We evaluated a newly developed reduction/oxidation-sensitive green fluorescent protein (roGFP) probe that reports cellular redox potentials and their dynamic changes in live cells. On hypoxia/reoxygenation (H/R) of
Panagiotis Vagenas et al.
Journal of acquired immune deficiency syndromes (1999), 52(4), 433-442 (2009-09-26)
Although mucosal responses are important for preventing infections with HIV, the optimal strategies for inducing them remain unclear. To evaluate vaccine strategies targeting the oral mucosal lymphoid tissue inductive sites as an approach to provide immunity at distal sites, we
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