Fmoc-Lys(Fmoc)-OH

Name: Fmoc-Lys(Fmoc)-OH
Brand: ALDRICH
Price: 288 USD
Availability: InStock

≥98.0% (HPLC)

Synonym(s):

N_α,N_ε-di-Fmoc-L-lysine

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About This Item

Empirical Formula (Hill Notation):

C₃₆H₃₄N₂O₆

CAS Number:

78081-87-5

Molecular Weight:

590.66

Beilstein/REAXYS Number:

6034060

MDL number:

MFCD00080275

UNSPSC Code:

12352209

PubChem Substance ID:

57650922

NACRES:

NA.26

Key Documents

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Quality Level

100

assay

≥98.0% (HPLC)

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

OC(=O)[C@H](CCCCNC(=O)OCC1c2ccccc2-c3ccccc13)NC(=O)OCC4c5ccccc5-c6ccccc46

InChI

1S/C36H34N2O6/c39-34(40)33(38-36(42)44-22-32-29-17-7-3-13-25(29)26-14-4-8-18-30(26)32)19-9-10-20-37-35(41)43-21-31-27-15-5-1-11-23(27)24-12-2-6-16-28(24)31/h1-8,11-18,31-33H,9-10,19-22H2,(H,37,41)(H,38,42)(H,39,40)/t33-/m0/s1

InChI key

BMJRTKDVFXYEFS-XIFFEERXSA-N

Related Categories

Amino Acids, Resins & Reagents for Peptide Synthesis

Building Blocks, Resins, and Coupling Reagents for GLP-1 Synthesis

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1 of 4

This Item	47577	29207	47624
Sigma-Aldrich 47317 Fmoc-Lys(Fmoc)-OH	Sigma-Aldrich 47577 Fmoc-Lys(Z)-OH	Sigma-Aldrich 29207 Fmoc-Lys(Ddiv)-OH	Sigma-Aldrich 47624 Fmoc-Lys(Boc)-OH
functional group Fmoc	functional group Fmoc	functional group Fmoc	functional group Boc, Fmoc
assay ≥98.0% (HPLC)	assay ≥98.0% (HPLC)	assay ≥96.0% (HPLC)	assay ≥98.0% (HPLC)
storage temp. 2-8°C	storage temp. 2-8°C	storage temp. 2-8°C	storage temp. 2-8°C
Quality Level 100	Quality Level 100	Quality Level 100	Quality Level 100
reaction suitability reaction type: Fmoc solid-phase peptide synthesis	reaction suitability reaction type: Fmoc solid-phase peptide synthesis	reaction suitability reaction type: Fmoc solid-phase peptide synthesis	reaction suitability reaction type: Fmoc solid-phase peptide synthesis
application(s) peptide synthesis	application(s) peptide synthesis	application(s) peptide synthesis	application(s) peptide synthesis

Storage Class

11 - 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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Synthesis and comparative evaluation of novel (64)Cu-labeled high affinity cell-specific peptides for positron emission tomography imaging of tumor vasculature.

Joseph R Merrill et al.

Biomaterials, 84, 241-249 (2016-02-04)

Tumor angiogenesis, the formation of new tumor blood supply, has been recognized as a hallmark of cancer and represents an important target for clinical management of various angiogenesis-dependent solid tumors. Previously, by screening a bacteriophage peptide library we have discovered

Metal- and Oxidant-Free Photoinduced Aromatic Trifluoromethylation Performed in Aerated Gel Media: Determining the Effects on Yield and Selectivity.

Alex Abramov et al.

Molecules (Basel, Switzerland), 24(1) (2018-12-24)

In this work we have investigated the potential benefits of using supramolecular gel networks as reaction media to carry out air-sensitive metal-free light-induced trifluoromethylation of six-membered (hetero)arenes under aerobic conditions. This reaction was performed at room temperature (RT) using sodium

Dendrimeric Poly(Epsilon-Lysine) Delivery Systems for the Enhanced Permeability of Flurbiprofen across the Blood-Brain Barrier in Alzheimer's Disease.

Shafq Al-Azzawi et al.

International journal of molecular sciences, 19(10) (2018-10-21)

Alzheimer's disease (AD) is a progressive brain disorder and age-related disease characterised by abnormal accumulation of β-amyloid (Aβ). The development of drugs to combat AD is hampered by the lack of therapeutically-active molecules able to cross the blood-brain barrier (BBB).

Molecular design and synthesis of self-assembling camptothecin drug amphiphiles.

Andrew G Cheetham et al.

Acta pharmacologica Sinica, 38(6), 874-884 (2017-03-07)

The conjugation of small molecular hydrophobic anticancer drugs onto a short peptide with overall hydrophilicity to create self-assembling drug amphiphiles offers a new prodrug strategy, producing well-defined, discrete nanostructures with a high and quantitative drug loading. Here we show the

Peptide dendrimer-conjugates of ketoprofen: Synthesis and ex vivo and in vivo evaluations of passive diffusion, sonophoresis and iontophoresis for skin delivery.

Aswathi R Hegde et al.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 102, 237-249 (2017-03-13)

The aim of this study was to evaluate skin delivery of ketoprofen when covalently tethered to mildly cationic (2

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Fmoc-Lys(Fmoc)-OH