A4876
N-Acetyl-DL-proline
Sigma Grade
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About This Item
Empirical Formula (Hill Notation):
C7H11NO3
CAS Number:
Molecular Weight:
157.17
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
Product Name
N-Acetyl-DL-proline, Sigma Grade
SMILES string
CC(=O)N1CCCC1C(O)=O
grade
Sigma Grade
storage temp.
2-8°C
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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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
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
W L Mock et al.
The Journal of biological chemistry, 265(32), 19606-19610 (1990-11-15)
The pH dependence of Ki for inhibition of prolidase by acetylproline, proline, and trans-1,2-cyclopentanedicarboxylate follows a different pattern in each case, although deprotonation of an enzymic functional group with a pKa value of 6.6 perturbs ligand binding in every instance.
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
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