产品名称
N-乙酰基-L-丙氨酸, ~99%
SMILES string
C[C@H](NC(C)=O)C(O)=O
InChI
1S/C5H9NO3/c1-3(5(8)9)6-4(2)7/h3H,1-2H3,(H,6,7)(H,8,9)/t3-/m0/s1
InChI key
KTHDTJVBEPMMGL-VKHMYHEASA-N
assay
~99%
form
powder
color
white to off-white
application(s)
cell analysis
storage temp.
2-8°C
Quality Level
Application
N-乙酰基-L-丙氨酸已被用于研究其对胞质和线粒体还原-氧化敏感性绿色荧光蛋白(roGFP)的作用。
Biochem/physiol Actions
N-乙酰基-L-丙氨酸可以与其他L-氨基酰化氨基酸一起用作底物,用于鉴定、区分和表征氨基酰基酶/酰胺水解酶。
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)
Improved sensitivity of HSQC spectra of exchanging protons at short interscan delays using a new fast HSQC (FHSQC) detection scheme that avoids water saturation.
S Mori et al.
Journal of magnetic resonance. Series B, 108(1), 94-98 (1995-07-01)
S Mori et al.
Journal of biomolecular NMR, 7(1), 77-82 (1996-01-01)
A technique for separating intramolecular NOE and solvent-proton exchange peaks in exchange spectroscopy is demonstrated. This method utilizes the large differences in relaxation and coupling properties of water and macromolecules to separate the two effects. The spin-echo filter consists of
C Bruyneel et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56(3), 591-602 (2000-05-04)
The energies, vibrational frequencies and IR intensities of cis- and trans-N-acetyl-L-alanine (NAAL) are computed using the density functional theory (B3LYP) combined with the 6-311G(d, p) basis set. The trans conformer is characterized by an intramolecular NH ... O hydrogen bond
Water exchange filter with improved sensitivity (WEX II) to study solvent-exchangeable protons. Application to the consensus zinc finger peptide CP-1.
S Mori et al.
Journal of magnetic resonance. Series B, 110(1), 96-101 (1996-01-01)
Shouguo Wu et al.
Biosensors & bioelectronics, 23(12), 1776-1780 (2008-04-05)
A beta-cyclodextrin (CD) modified copolymer membrane of sulfanilic acid (p-ASA) and N-acetylaniline (SPNAANI) on glassy carbon electrode (GCE) was prepared and used to determine uric acid (UA) in the presence of a large excess of ascorbic acid (AA) by differential
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