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Sigma-Aldrich

Fmoc-Lys(ivDde)-Wang resin (100-200 mesh)

Novabiochem®

Sinónimos:

Fmoc-Protected Lysine Resin

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About This Item

UNSPSC Code:
12352209
NACRES:
NA.22

Quality Level

form

beads

manufacturer/tradename

Novabiochem®

functional group

Fmoc

storage temp.

2-8°C

General description

Useful tool for the synthesis of side-chain modified, cyclic and branched peptides by Fmoc SPPS. Following chain extension, the side-chain ivDde group is removed with 2% hydrazine in DMF, enabling selective modification of the ε-lysine amino group.

Associated Protocols and Technical Articles
Cleavage and Deprotection Protocols for Fmoc SPPS
SelectingOrthogonal Building Blocks

Literature references:
[1] R. Chhabra, et al. (1998) Tetrahedron Lett., 39, 1603.

Application

Fmoc-Lys(ivDde)-Wang resin (100-200 mesh) has been used as a solid support to prepare a peptide bearing a hexacarbonyldiiron cluster, neoglycopeptides and lipopeptides as putative antifungal and cancer vaccines, respectively.

Analysis Note

Color (visual): white to yellow to beige
Appearance of substance (visual): beads
Loading (Photometric determination of the Fmoc-chromophore liberated upon treatment with DBU/DMF): 0.40 - 1.00 mmol/g
Swelling Volume (in DMF): lot specific result
Identity (of the substitution): passes test
The polymer matrix is copoly (styrene -1 % DVB), 100- 200 mesh.

Legal Information

Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Towards a fully synthetic MUC1-based anticancer vaccine: Efficient conjugation of glycopeptides with mono-, di-, and tetravalent lipopeptides using click chemistry
Cai H, et al.
Chemistry?A European Journal , 17, 6396-6406 (2011)
An appraisal of new variants of Dde amine protecting group for solid phase peptide synthesis
R. Chhabra, et al.
Tetrahedron Letters, 39, 1603-1603 (1998)
Artificial [FeFe]-Hydrogenase: On Resin Modification of an Amino Acid to Anchor a Hexacarbonyldiiron Cluster in a Peptide Framework
Roy S, et al.
European Journal of Inorganic Chemistry, 1050-1055 (2011)
Jonathan Cartmell et al.
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Selective strategies for the construction of novel three component glycoconjugate vaccines presenting Candida albicans cell wall glycan (β-1,2 mannoside) and polypeptide fragments on a tetanus toxoid carrier are described. The first of two conjugation strategies employed peptides bearing an N-terminal

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