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经验公式(希尔记法):
C21H21N3
化学文摘社编号:
分子量:
315.41
UNSPSC Code:
12161505
NACRES:
NA.32
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5107482
产品名称
二氢乙锭, BioReagent, suitable for fluorescence, ≥95% (HPCE)
InChI
1S/C21H21N3/c1-2-24-20-13-16(23)9-11-18(20)17-10-8-15(22)12-19(17)21(24)14-6-4-3-5-7-14/h3-13,21H,2,22-23H2,1H3
SMILES string
CCN1C(c2ccccc2)c3cc(N)ccc3-c4ccc(N)cc14
InChI key
XYJODUBPWNZLML-UHFFFAOYSA-N
product line
BioReagent
assay
≥95% (HPCE)
form
solid
Quality Level
mol wt
315.41 g/mol
solubility
acetonitrile: soluble
methanol: soluble
fluorescence
λex 358 nm; λem 461 nm
λex 392 nm; λem 410 nm in methanol
suitability
suitable for fluorescence
storage temp.
−20°C
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Application
二氢乙锭 (dHEt) 是一种荧光探针,用于检测活性氧自由基 (ROS) 的存在。
氧化还原指示剂。氧化为乙锭之前为蓝色荧光。
Other Notes
乙锭的B环还原型类似物
Packaging
无底玻璃瓶。内含物在插入的融合锥体内。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Journal of endodontics, 38(9), 1253-1256 (2012-08-16)
Root canal fillings are intended to prevent microbial proliferation over time in the canal after treatment. The objective of this study was to assess biofilm proliferation within the sealer-dentin interfaces of 2 methacrylate resin-based systems, self-etch (SE) and total-etch (TE)
Anna Rita Fetoni et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 33(9), 4011-4023 (2013-03-01)
This study addresses the relationship between cochlear oxidative damage and auditory cortical injury in a rat model of repeated noise exposure. To test the effect of increased antioxidant defenses, a water-soluble coenzyme Q10 analog (Qter) was used. We analyzed auditory
Francisco R M Laurindo et al.
Methods in enzymology, 441, 237-260 (2008-06-17)
Assessment of low-level superoxide in nonphagocytic cells is crucial for assessing redox-dependent signaling pathways and the role of enzymes such as the NADPH oxidase complex. However, most superoxide probes present inherent limitations. Particularly, assessment of dihydroethidium (DHE) fluorescence is limited
Laura Iarriccio et al.
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Dyskeratosis congenita is an inherited disease caused by mutations in genes coding for telomeric components. It was previously reported that expression of a dyskerin-derived peptide, GSE24.2, increases telomerase activity, regulates gene expression and decreases DNA damage and oxidative stress in
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