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Merck
CN

P7637

聚-L-精氨酸 硫酸盐

mol wt 15,000-50,000

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化学文摘社编号:
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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SMILES string

OS(O)(=O)=O.NC(CCCNC(N)=N)C(O)=O

mol wt

15,000-50,000

storage temp.

−20°C

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Analysis Note

Molecular weight based on viscosity. Also assayed by MALLS.

Other Notes

有关聚氨基酸的其他技术信息,请访问 聚氨基酸常见问题解答资源

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Pinaki R Desai et al.
Pharmaceutical research, 30(4), 1037-1049 (2012-11-29)
To investigate the percutaneous permeation pathways of cell penetrating peptide modified lipid nanoparticles and oleic acid modified polymeric nanoparticles. Confocal microscopy was performed on skin cultures (EpiDermFT™) for modified and un-modified nanoparticles. Differential stripping was performed following in vitro skin
Xiao-Li Liu et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 47(4), 512-516 (2012-07-17)
The purpose of this study is to investigate the feasibility of poly(arginine)8 (R8) modified poly(lactic-co-glycolic acid) (PLGA) nanoparticles as a carrier for the oral delivery of insulin. Insulin-loaded PLGA nanoparticle (INS-NP) was prepared by a double emulsion-solvent evaporation method, and
Peter D Ngo et al.
Pediatric research, 73(4 Pt 1), 414-419 (2012-12-28)
Eosinophils reside in normal gastrointestinal tracts and increase during disease states. Receptors for eosinophil-derived granule proteins (EDGPs) have not been identified, but highly cationic molecules, similar to eosinophil proteins, bind extracellular calcium-sensing receptors (CaSRs). We hypothesized that stimulation of CaSRs
Weina Ju et al.
Journal of neurochemistry, 124(6), 869-879 (2012-10-31)
The N-type voltage-gated calcium channel (CaV2.2) is a clinically endorsed target in chronic pain treatments. As directly targeting the channel can lead to multiple adverse side effects, targeting modulators of CaV2.2 may prove better. We previously identified ST1-104, a short
Tsutomu Yamaki et al.
Biological & pharmaceutical bulletin, 36(3), 496-500 (2012-12-22)
We have already reported that poly-L-arginine (PLA) remarkably enhanced the in vivo nasal absorption of hydrophilic macromolecules without producing any significant epithelial damage in rats. In the present study, we examined whether PLA could enhance the absorption of a model

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