A16300
N-乙酰甘氨酸
ReagentPlus®, 99%
别名:
乙酰氨基乙酸, 醋尿酸
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关于此项目
线性分子式:
CH3CONHCH2CO2H
化学文摘社编号:
分子量:
117.10
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
208-839-6
MDL number:
Beilstein/REAXYS Number:
774114
InChI key
OKJIRPAQVSHGFK-UHFFFAOYSA-N
InChI
1S/C4H7NO3/c1-3(6)5-2-4(7)8/h2H2,1H3,(H,5,6)(H,7,8)
SMILES string
CC(=O)NCC(O)=O
product line
ReagentPlus®
assay
99%
form
powder or crystals
reaction suitability
reaction type: C-H Activation, reaction type: solution phase peptide synthesis, reagent type: ligand
reaction type: Peptide Synthesis
color
white
Quality Level
mp
207-209 °C (lit.)
application(s)
detection
peptide synthesis
functional group
amine, carboxylic acid
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Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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)
Y Chen et al.
Biochemistry, 37(28), 9976-9982 (1998-07-17)
A general approach to dissecting the complex photophysics of tryptophan is presented and used to elucidate the effects of amino acid functional groups on tryptophan fluorescence. We have definitively identified the amino acid side chains that quench tryptophan fluorescence and
Z Gu et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 138(2), 193-198 (1999-05-26)
Triple-resonance experiments capable of correlating directly bonded and proximate carbon and nitrogen backbone sites of uniformly 13C- and 15N-labeled peptides in stationary oriented samples are described. The pulse sequences integrate cross-polarization from 1H to 13C and from 13C to 15N
Anatoliy Volkov et al.
Journal of computational chemistry, 25(7), 921-934 (2004-03-18)
Accurate and fast evaluation of electrostatic interactions in molecular systems is still one of the most challenging tasks in the rapidly advancing field of macromolecular chemistry, including molecular recognition, protein modeling and drug design. One of the most convenient and
H K Ogawa et al.
Journal of chromatography, 612(1), 145-149 (1993-01-29)
A simple and sensitive method for the determination of N-acetylneuraminic acid and N-glycolylneuraminic acid in glycoproteins by high-performance liquid chromatography has been investigated. The best condition to release sialic acid from glycoproteins involved incubation at 80 degrees C for 1
Liangxing Wu et al.
Journal of the American Chemical Society, 130(12), 4089-4096 (2008-03-07)
Eight B-containing compounds, i.e., 1a-h, were prepared as mimics of the green fluorescent protein (GFP) fluorophore. The underlying concept was that synthetic GFP chromophore analogues are not fluorescent primarily because of free rotation about an aryl-alkene bond (Figure 1b). This
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