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55788

Sigma-Aldrich

Nα-Fmoc-Nε-Dabcyl-L-lysine

technical, ≥90% (HPLC)

Synonym(s):

Nε-4-[4-(Dimethylamino)phenylazo)benzoyl]-Nα-Fmoc-L-lysine, Fmoc-Lys(Dabcyl)-OH

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About This Item

Empirical Formula (Hill Notation):
C36H37N5O5
CAS Number:
Molecular Weight:
619.71
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

grade

technical

Assay

≥90% (HPLC)

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

CN(C)c1ccc(cc1)\N=N\c2ccc(cc2)C(=O)NCCCC[C@H](NC(=O)OCC3c4ccccc4-c5ccccc35)C(O)=O

InChI

1S/C36H37N5O5/c1-41(2)27-20-18-26(19-21-27)40-39-25-16-14-24(15-17-25)34(42)37-22-8-7-13-33(35(43)44)38-36(45)46-23-32-30-11-5-3-9-28(30)29-10-4-6-12-31(29)32/h3-6,9-12,14-21,32-33H,7-8,13,22-23H2,1-2H3,(H,37,42)(H,38,45)(H,43,44)/b40-39+/t33-/m0/s1

InChI key

FPOPWTDBGMLRNG-JEFPPREJSA-N

Other Notes

Building block for the synthesis of fluorogenic protease substrates

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Product No.
Description
Pricing

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Q.M. Wang et al.
Antiviral Chem. Chemother., 8, 303-303 (1997)
Automated Synthesis of Fluorogenic Protease Substrates: Design of Probes for Alzheimers Disease-Associated Proteases.
Wang, G.T., et al.
Bioorganic & Medicinal Chemistry Letters, 2, 1665-1665 (1992)

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