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Merck
CN

V2125

Sigma-Aldrich

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
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
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储存温度

−20°C

SMILES字符串

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

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储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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W Bode et al.
European journal of biochemistry, 144(1), 185-190 (1984-10-01)
Large orthorhombic crystals of the complex formed by bovine trypsinogen and a semisynthetic homologous bovine pancreatic trypsin inhibitor with the reactive-site lysine residue replaced by an arginine residue [( Arg15]PTI) have been obtained which are isomorphous with the crystals of
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
Ripal Gaudana et al.
Journal of microencapsulation, 28(1), 10-20 (2010-10-14)
The objective of this study was to develop and characterize a nanoparticulate-based sustained release formulation of a water soluble dipeptide prodrug of dexamethasone, valine-valine-dexamethasone (VVD). Being hydrophilic in nature, it readily leaches out in the external aqueous medium and hence
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
D T Thwaites et al.
Biochemical and biophysical research communications, 194(1), 432-438 (1993-07-15)
Direct demonstration of intact peptide transport by the intestinal H+/dipeptide carrier is limited both by luminal/cytosolic hydrolysis and the availability of suitable radiolabelled substrates. Perfusion of Val-Val (20mM) at the apical surface of human intestinal epithelial (Caco-2) cell monolayers resulted

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