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47583

Fmoc-Lys(Alloc)-OH

Name: Fmoc-Lys(Alloc)-OH
Brand: ALDRICH

≥95.0% (HPLC), for peptide synthesis

Synonym(s):

N_α-Fmoc-N_ε-Alloc-L-lysine

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About This Item

Empirical Formula (Hill Notation):

C₂₅H₂₈N₂O₆

CAS Number:

146982-27-6

Molecular Weight:

452.50

UNSPSC Code:

12352209

eCl@ss:

32160406

PubChem Substance ID:

57651022

NACRES:

NA.26

Beilstein/REAXYS Number:

5893081

MDL number:

MFCD00190872

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Properties

Product Name

Fmoc-Lys(Alloc)-OH, ≥95.0% (HPLC)

Quality Level

100

assay

≥95.0% (HPLC)

form

powder

optical activity

[α]20/D −12±1°, c = 1% in DMF

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

technique(s)

NMR: suitable

color

beige

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

OC(=O)[C@H](CCCCNC(=O)OCC=C)NC(=O)OCC1c2ccccc2-c3ccccc13

InChI

1S/C25H28N2O6/c1-2-15-32-24(30)26-14-8-7-13-22(23(28)29)27-25(31)33-16-21-19-11-5-3-9-17(19)18-10-4-6-12-20(18)21/h2-6,9-12,21-22H,1,7-8,13-16H2,(H,26,30)(H,27,31)(H,28,29)/t22-/m0/s1

InChI key

OJBNDXHENJDCBA-QFIPXVFZSA-N

Description

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Regenerating Bone via Multifunctional Coatings: The Blending of Cell Integration and Bacterial Inhibition Properties on the Surface of Biomaterials.

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Cationic block amphiphiles show anti-mitochondrial activity in multi-drug resistant breast cancer cells.

Petro P Czupiel et al.

Journal of controlled release : official journal of the Controlled Release Society, 305, 210-219 (2019-05-10)

Currently, there are limited treatment options for multi-drug resistant breast cancer. Lipid-modified cationic peptides have the potential to reach the mitochondria, which are attractive targets for the treatment of multi-drug resistant (MDR) breast cancer; yet, little is known about their

Global Trade Item Number

SKU	GTIN
47583-5G-F	04061832361925
47583-1G-F	04061826222621