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Merck
CN

V2125

Val-Val

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经验公式(希尔记法):
C10H20N2O3
化学文摘社编号:
分子量:
216.28
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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SMILES string

CC(C)C(N)C(=O)NC(C(C)C)C(O)=O

storage temp.

−20°C

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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)

法规信息

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分析证书(COA)

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Joze Grdadolnik et al.
The journal of physical chemistry. B, 112(9), 2712-2718 (2008-02-12)
The NMR coupling constants ((3)J(H(N), H(alpha))) of dipeptides indicate that the backbone conformational preferences vary strikingly among dipeptides. These preferences are similar to those of residues in small peptides, denatured proteins, and the coil regions of native proteins. Detailed characterization
Alfredo E Cárdenas et al.
Biophysical journal, 85(5), 2919-2939 (2003-10-29)
An algorithm is described to compute approximate classical trajectories as a boundary value problem with an integration step in the arc length. High-frequency motions are filtered out when a large integration step is used, maintaining the stability of the algorithm.
R H Yun et al.
Protein engineering, 4(7), 761-766 (1991-10-01)
The conformational probability distribution of a valine residue in the valine dipeptide and of the valine side chain in an alpha-helix, as well as the change in helix stability for replacing alanine with valine, has been calculated by molecular dynamics
K Tamura et al.
Pharmaceutical research, 13(8), 1213-1218 (1996-08-01)
The purpose of this study was to determine whether the binding of the diastereomers of Val-Val to the apical oligopeptide transporter(s) could be correlated with their cellular uptake and transepithelial transport. The Caco-2 cell culture system was used for all
J Li et al.
Journal of drug targeting, 5(5), 317-327 (1998-10-15)
The objective of this study was to elucidate the structural features of the stereoisomers of Val-Val and Val-Val-Val that afford optimal binding affinity for the apical oligopeptide transporter in human intestinal Caco-2 cells. Three-dimensional conformations of cephalexin and Val stereoisomers

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