253375
3-马来酰亚胺基-2,2,5,5-四甲基吡咯烷
free radical
别名:
3-马来酰亚胺-2,2,5,5-四甲基吡咯烷-1-氧自由基
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关于此项目
经验公式（希尔记法）:
C12H17N2O3
化学文摘社编号:
分子量:
237.27
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
InChI
1S/C12H17N2O3/c1-11(2)7-8(12(3,4)14(11)17)13-9(15)5-6-10(13)16/h5-6,8H,7H2,1-4H3
SMILES string
CC1(C)CC(N2C(=O)C=CC2=O)C(C)(C)N1[O]
InChI key
HGNHBHXFYUYUIA-UHFFFAOYSA-N
mp
111-113 °C (lit.)
functional group
imide, maleimide
storage temp.
2-8°C
Quality Level
Application
用于研究局部蛋白质结构以及确定红细胞膜中分子变化的自旋标记物。
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
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Angela Tseng et al.
Journal of food science, 77(9), H192-H201 (2012-08-23)
The effects of different drying methods (40 °C conventional and vacuum oven, 25 °C ambient air and freeze dry) on the stability of two red wine grape (Pinot Noir, PN and Merlot, M) byproducts, pomace containing skins and seeds (P)
A Wróbel et al.
Biochemistry and molecular biology international, 41(2), 349-357 (1997-02-01)
The sulfhydryl group specific spin labels have been used to study the membrane proteins in the bovine and human erythrocyte membranes treated with ozone. The ratio hw/hs, determined from the respective peak amplitudes of the resulting EPR spectra of 3-maleimido-1-oxyl-2,2,5,5-tetramethylpyrrolidine
P D Morse
Biochimica et biophysica acta, 844(3), 337-345 (1985-03-21)
In a recent paper, Daveloose et al. (Daveloose, D., Fabre, G., Berleur, F., Testylier, G. and Letterrier, F. (1983) Biochim. Biophys. Acta 763, 41-49) described a technique to measure the internal microviscosity of erythrocytes using the spin label MAL-3 (2,2,5,5-tetramethyl-3-malimidopyrrolidinyl-N-oxyl)
L Zhao et al.
Biophysical journal, 69(3), 994-999 (1995-09-01)
Electron paramagnetic resonance spectroscopy of a spin probe attached to cys-707 on myosin cross-bridges was used to monitor the orientation of the myosin catalytic domain at the beginning and end of the working power stroke in active muscle. Elevated concentrations
Brett A Colson et al.
Proceedings of the National Academy of Sciences of the United States of America, 113(12), 3233-3238 (2016-02-26)
We have used the site-directed spectroscopies of time-resolved fluorescence resonance energy transfer (TR-FRET) and double electron-electron resonance (DEER), combined with complementary molecular dynamics (MD) simulations, to resolve the structure and dynamics of cardiac myosin-binding protein C (cMyBP-C), focusing on the
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