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Merck
CN

A4876

N-Acetyl-DL-proline

Sigma Grade

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经验公式(希尔记法):
C7H11NO3
化学文摘社编号:
分子量:
157.17
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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产品名称

N-Acetyl-DL-proline, Sigma Grade

SMILES string

CC(=O)N1CCCC1C(O)=O

grade

Sigma Grade

storage temp.

2-8°C

存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

新产品
此项目有

历史批次信息供参考:

分析证书(COA)

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Kyung-Koo Lee et al.
The journal of physical chemistry. B, 110(38), 18834-18843 (2006-09-22)
A few experimental and theoretical studies on the molecular structure of N-acetylproline amide (AP) in D2O solution have been reported recently. However, there is no consensus of the precise structure of AP in D2O because spectroscopically determined structures and a
R A Pfuetzner et al.
The Journal of biological chemistry, 263(9), 4056-4058 (1988-03-25)
We have investigated the interaction of ligands in the active site of the angiotensin-converting enzyme from rabbit lung by monitoring the concurrent effects of two inhibitors on enzyme activity. A strong synergism is found in the binding of N-acetyl-L-proline (an
Jeanette F Kheir et al.
The journal of physical chemistry. B, 115(49), 14846-14851 (2011-11-03)
In this study, the reactions of electrons with N-acetylproline are investigated by electron spin resonance (ESR) spectroscopy and density functional theory. Electrons are produced by γ irradiation or by photoionization of K(4)Fe(CN)(6) in neutral 7.5 M LiCl-D(2)O aqueous glasses at
Jiyun Liu et al.
Journal of the American Chemical Society, 127(7), 2044-2045 (2005-02-17)
Structure-based design of a bifunctional ligand for two protein pentamers, cholera toxin B pentamer (CTB) and human serum amyloid P component (SAP), leads to multivalent dimerization of CTB and SAP in solution. This multivalent heterodimerization of proteins significantly enhances the
Chiara Cappelli et al.
The journal of physical chemistry. B, 112(11), 3441-3450 (2008-02-26)
The structure and properties of (s)-N-acetylproline amide (NAP) in aqueous solution are studied by exploiting a continuum solvation model. The conformational preference of NAP as a function of the environment is discussed as well as data for a number of

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