G3882
Gly-Gly-Gly-Gly
≥98% (TLC)
别名:
Glycyl-glycyl-glycyl-glycine, Tetraglycine, Triglycyl-glycine
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关于此项目
线性分子式:
NH2CH2CO(NHCH2CO)3OH
化学文摘社编号:
分子量:
246.22
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
211-303-4
MDL number:
Beilstein/REAXYS Number:
1715387
产品名称
Gly-Gly-Gly-Gly,
assay
≥98% (TLC)
Quality Level
form
powder
color
white to off-white
mp
300 °C
application(s)
peptide synthesis
storage temp.
−20°C
SMILES string
NCC(=O)NCC(=O)NCC(=O)NCC(O)=O
InChI
1S/C8H14N4O5/c9-1-5(13)10-2-6(14)11-3-7(15)12-4-8(16)17/h1-4,9H2,(H,10,13)(H,11,14)(H,12,15)(H,16,17)
InChI key
QMOQBVOBWVNSNO-UHFFFAOYSA-N
Biochem/physiol Actions
Tetraglycine is used with copper (Cu-II) to study mechanisms of hydrogen peroxide/bicarbonate free radical production and effect in vitro.
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)
Fabian Barthels et al.
ChemMedChem, 15(10), 839-850 (2020-03-03)
Staphylococcus aureus is one of the most frequent causes of nosocomial and community-acquired infections, with drug-resistant strains being responsible for tens of thousands of deaths per year. S. aureus sortase A inhibitors are designed to interfere with virulence determinants. We
María V Alipázaga et al.
Dalton transactions (Cambridge, England : 2003), (13)(13), 2036-2040 (2004-07-15)
The synergistic effect of Ni(II) and Co(II) on the sulfite induced autoxidation of Cu(II)/tetraglycine was investigated spectrophotometrically at 25.0 degrees C, pH = 9.0, 1 x 10(-5) mol dm(-3) < or = [S(IV)] < or = 8 x 10(-5) mol
Yanfeng Yao et al.
Emerging microbes & infections, 8(1), 45-54 (2019-03-15)
Current influenza vaccines provide hemagglutinin strain-specific protection, but rarely provide cross-protection against divergent strains. It is, therefore, particularly important to develop a universal vaccine against conserved proteins or conserved regions of the virus. In this study, we used N-terminal extracellular
Udo H Verkerk et al.
The journal of physical chemistry. A, 115(24), 6683-6687 (2011-05-21)
Collision-induced dissociations of protonated (18)O-labeled tetraglycines labeled separately at either the first or the second amide bond established that water loss from the backbone occurs from the N-terminal residue. Density functional theory at B3LYP/6-311++G(d,p) predicted that the low-energy [G(4) +
Travis Cooper et al.
Journal of the American Society for Mass Spectrometry, 17(12), 1654-1664 (2006-08-29)
Extensive 13C, 15N, and 2H labeling of tetraglycine was used to investigate the b3+ --> a3* reaction during low-energy collision-induced dissociation (CID) in a quadrupole ion-trap mass spectrometer. The patterns observed with respect to the retention or elimination of the
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| G3882-500MG | 04061832820514 |
| G3882-1G | 04061826284803 |
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