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Merck

531359

Sigma-Aldrich

Fmoc-Glycine, polymer-bound on Wang resin

extent of labeling: 1.0 mmol/g loading, 1 % cross-linked

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About This Item

Fórmula empírica (notación de Hill):
C32H29NO5
Número de CAS:
Peso molecular:
507.58
UNSPSC Code:
12352200
PubChem Substance ID:

crosslinking

1 % cross-linked

extent of labeling

1.0 mmol/g loading

application(s)

peptide synthesis

functional group

Fmoc

SMILES string

P=S.Cc1ccc(COc2ccc(COC(=O)CNC(=O)OCC3c4ccccc4-c5ccccc35)cc2)cc1

InChI

1S/C17H15NO4/c19-16(20)9-18-17(21)22-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15H,9-10H2,(H,18,21)(H,19,20)

InChI key

NDKDFTQNXLHCGO-UHFFFAOYSA-N

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Mechanotransduction in the regulation of cellular responses has been previously studied using elastic hydrogels. Because cells interact only with the surface of biomaterials, we are focusing on the molecular mobility at the outermost surface of biomaterials. In this study, surfaces
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The objective of this work was to compare the efficacy of self-assembling cyclic and linear RGD peptide amphiphiles as carriers for delivering paclitaxel to αvβ3 integrin overexpressing tumors. Linear (C18-ADA5-RGD) and cyclic (C18-ADA5-cRGDfK) peptide amphiphiles were synthesized and characterized for
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To address the downside of conventional photo-patterning which can alter the chemical composition of protein scaffolds, we developed a non-covalent photo-patterning strategy for gelatin (denatured collagen) hydrogels that utilizes UV activated triple helical hybridization of caged collagen mimetic peptide (caged

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